porphobilinogen and dipyrromethene

porphobilinogen has been researched along with dipyrromethene in 138 studies

Research

Studies (138)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	23 (16.67)	29.6817
2010's	72 (52.17)	24.3611
2020's	43 (31.16)	2.80

Authors

Authors	Studies
Daub, J; Röhr, H; Rurack, K; Trieflinger, C	2
Chen, X; Dalgleish, ND; Okamoto, Y; Power, ED; Ross, AC; Thompson, A; Wood, TE	1
Bonardi, L; Retailleau, P; Ulrich, G; Ziessel, R	1
Bittman, R; Liu, Y	1
Bonardi, L; Ulrich, G; Ziessel, R	2
Fukuzumi, S; Hattori, S; Lemmetyinen, H; Nagano, T; Ohkubo, K; Sunahara, H; Tkachenko, NV; Urano, Y; Wada, Y	1
Goze, C; Ulrich, G; Ziessel, R	1
Hashimoto, T; Maeda, H	1
Daub, J; Koval'chuck, A; Rurack, K; Trieflinger, C	1
Bittman, R; Li, Z	1
Qian, X; Xiao, Y; Zhang, X	1
Hirose, K; Iino, M; Inoue, T; Kikuchi, K; Mizushima, A; Nagano, T; Sunahara, H; Urano, Y; Yogo, T	1
Descalzo, AB; Hoffmann, K; Rurack, K; Shen, Z; Weller, MG; Xu, HJ; Xue, ZL; You, XZ	1
Prasad, PN; Xu, G; Zheng, Q	1
Descalzo, AB; Rurack, K; Shen, Z; Xu, HJ	1
Campagna, S; Diring, S; Nastasi, F; Puntoriero, F; Ziessel, R	1
Dehaen, W; Janssen, D; Orlewska, C; Radecka, H; Rohand, T; Stobiecka, M; Szymańska, I	1
Bandichhor, R; Burgess, K; Hall, MJ; Loudet, A; McDonnell, SO; O'Shea, DF; Palma, A	1
Goeb, S; Harriman, A; Mallon, LJ; Ulrich, G; Ziessel, R	1
Garg, V; Gust, D; Kodis, G; Liddell, PA; Moore, AL; Moore, TA; Terazono, Y	1
Esswein, AJ; Gray, TG; Teets, TS; Updegraff, JB	1
Gouloumis, A; Guldi, DM; Rio, Y; Seitz, W; Sessler, JL; Torres, T; Vázquez, P	1
Benniston, AC; Clegg, W; Copley, G; Harriman, A; Harrington, RW; Howgego, D	1
Burgess, K; Han, J; Lee, HB; Lim, SH; Nowak-Sliwinska, P; Thivierge, C; van den Bergh, H; Wagnières, G	1
Ando, Y; Citterio, D; Hiruta, Y; Suzuki, K	1
O'Shea, DF; Tasior, M	1
Elliott, K; Harriman, A; Mula, S; Ziessel, R	1
Bae, SW; Hong, JI; Kim, H; Shin, IS	1
Bane, SL; Dilek, O	1
Andraud, C; Aronica, C; Bellier, Q; Le Guennic, B; Maury, O; Pégaz, S	1
Cao, J; Feng, P; Lin, Q; Zhang, Y; Zhao, C; Zhou, Y; Zhu, L	1
Chung, PH; Kuimova, MK; Levitt, JA; Qu, J; Suhling, K; Wang, Y; Yahioglu, G	1
Bian, Y; Chen, Y; Jiang, J; Wan, L; Zhang, D	1
Fong, WP; He, H; Lo, PC; Ng, DK; Yeung, SL	1
Bian, Y; Chen, Y; Jiang, J; Wan, L; Wang, H	1
Madhu, S; Rao, MR; Ravikanth, M; Shaikh, MS	1
Lakshmi, V; Ravikanth, M	1
Gu, X; Liu, C; Zhu, YC; Zhu, YZ	1
Borisov, SM; Jokic, T; Klimant, I; Kühl, M; Nielsen, DA; Saf, R	1
Liu, Y; Wu, W; Yang, P; Yu, X; Zhao, J	1
Deligonul, N; Gao, L; Gray, TG	1
Hanaoka, K; Komatsu, T; Myochin, T; Nagano, T; Terai, T	1
Grossi, M; Hall, MJ; McDonnell, SO; Muldoon, J; O'Shea, DF; Palma, A; Rai, DK	1
Chen, J; Pan, T; Qin, Y; Xie, Y; Xu, Y; Zhai, J; Zhu, J	1
Mukherjee, S; Swamy, CA; Thilagar, P	1
Ermilov, EA; Huang, Y; Liu, JY; Menting, R; Ng, DK; Röder, B	1
Ermilov, EA; Huang, YS; Liu, JY; Menting, R; Ng, DK; Röder, B	1
Chujo, Y; Tanaka, K; Yamane, H; Yoshii, R	1
Cao, J; Chae, WS; He, Y; Jung, H; Kang, C; Kim, JS; Lee, JH; Park, N; Peng, X; Suh, M; Yang, Z	1
El-Khouly, ME; Fukuzumi, S; Ng, DK; Ohkubo, K; Shi, WJ	1
Cauët, E; De Winter, J; Dehaen, W; Gerbaux, P; Kirsch-De Mesmaeker, A; Lambermont, J; Moucheron, C; Ovaere, M; Servaty, K; Thomas, F; Vaeck, N; Van Meervelt, L; Volker, L	1
Aksenova, YV; Berezin, MB; Cherepanov, VN; Kuznetsova, RT; Semeikin, AS; Sinelnikov, AN; Valiev, RR	1
Chen, TL; Leblebici, SY; Ma, B; Olalde-Velasco, P; Yang, W	1
Fong, WP; Ke, MR; Lo, PC; Ng, DK; Yeung, SL	1
Liu, SR; Vedamalai, M; Wu, SP	1
D'Souza, F; El-Khouly, ME; Fukuzumi, S	1
Ding, Y; Hao, E; Jiao, L; Mu, X; Wang, S; Wei, Y; Wu, Y; Yu, C; Zhang, P	1
Madhu, S; Ravikanth, M	1
Chen, X; Hou, J; Li, F; Liu, W; Wu, YW; Yi, L	1
Akhtar, M; Azim, N; Coker, A; Cooper, JB; Deery, E; Erskine, P; Warren, MJ; Wolfenden, BA; Wood, SP	1
Callan, JF; Cusido, J; Fowley, C; McCaughan, B; Raymo, FM; Swaminathan, S	1
Hanaoka, K; Kamiya, M; Komatsu, T; Nagano, T; Takahashi, H; Terai, T; Ueno, T; Umeda, N; Urano, Y	1
Banfi, S; Barbieri, P; Caruso, E; Orlandi, VT; Rybtke, M; Tolker-Nielsen, T	1
Han, Z; Wang, C; Xiao, Y; Zhang, X	1
Guan, J; Jiang, XD; Li, S; Sun, CL; Xi, D; Xiao, LJ; Yu, H; Zhao, J	1
Jia, H; Lv, J; Pang, S; Shang, J; Zha, X; Zhang, Y	1
Cui, Z; Fan, C; Fei, Q; Huang, Q; Luo, S; Pan, D; Pan, L; Tian, H; Wang, F; Wang, R; Zhao, C; Zhou, L; Zhu, Y	1
Dehaen, W; Góra-Sochacka, A; Jarocka, U; Porębska, A; Radecka, H; Radecki, J; Sączyńska, V; Sawicka, R; Sirko, A; Stachyra, A; Zagórski-Ostoja, W	1
Dehaen, W; Kurzątkowska, K; Radecka, H; Radecki, J; Sirko, A; Zagórski-Ostoja, W	1
Barbon, SM; Gilroy, JB; Groom, H; Luyt, LG; Maar, RR; Sharma, N	1
Chen, ZL; Cheung, S; Devocelle, M; O'Shea, DF; Wu, D; Zhang, LJ	1
Alnoman, RB; Black, FA; Clegg, W; Costello, B; Hall, MJ; Herrebout, W; Knight, JG; O'Connor, DC; Peacock, RD; Rihn, S; Waddell, PG	1
Dehaen, W; Grabowska, I; Radecka, H; Radecki, J	1
Esmaeili Mohsen Abadi, S; Imani-Nejad, M; Johns, M; Kwon, G; Lee, J; Malik, N; McPherson, T; Neumann, WL; Rausaria, S; Schober, J	1
Liu, Y; Miao, JY; Zhao, BX; Zhao, ZM	1
Choi, M; Churchill, DG; Jang, YJ; Jon, S; Kim, Y; Mulay, SV	1
Alberto Juárez, L; Costero, AM; Gaviña, P; Gil, S; Martínez-Máñez, R; Parra, M; Sancenón, F	1
Bulut, I; Chávez, P; Fall, S; Hébraud, A; Heinrich, B; Heiser, T; Huaulmé, Q; Leclerc, N; Lévêque, P; Méry, S; Mirloup, A	1
Bon, C; Cahill, RA; Daly, HC; Ismail, G; O'Shea, DF; Sampedro, G; Wu, D	1
Chen, H; He, X; Li, C; Su, M; Zhai, W; Zhang, H	1
Anna, JM; Chenoweth, DM; Das, S; Lee, Y; Malamakal, RM; Meloni, S	1
Burgess, K; Chung, LY; Kamkaew, A; Kiew, LV; Kue, CS; Lee, HB; Misran, M; Tiew, SX; Voon, SH	1
Cheung, YK; Fong, WP; Gao, D; Lo, PC; Ma, C; Ng, DKP; Wong, KS; Zhao, S; Zhou, Y	1
Bergese, P; Cheung, S; Ducoli, S; Ffrench, B; Monopoli, MP; Nolan, J; O'Shea, DF; Piskareva, O; Sampedro, G; Stalings, RL; Wu, D; Zendrini, A	1
Cahill, RA; Conroy, E; Daly, HC; Gallagher, WM; Li, B; O'Shea, DF; Wu, D	1
Cao, JJ; Li, XQ; Liu, JY; Su, D; Wang, ZW; Yang, DC	1
Du, J; Fan, J; Peng, X; Sun, W; Zhao, X	1
Miao, F; Phan, H; Wu, J	1
Bui, HT; Cho, S; Choi, KH; Kim, B; Kim, HJ; Mai, DK; Park, BJ	1
Lo, PC; Wang, Q; Wong, RCH; Yu, L	1
Aikman, B; Casini, A; Döllerer, D; Jones, AT; Kühn, FE; Sayers, EJ; Wenzel, MN; Woods, B	1
Bartelmess, J; Bell, J; Chauhan, VP; Rurack, K; Tillo, A	1
Guo, X; Lo, PC; Ng, DKP; Wong, RCH; Zhou, Y	1
Ahmed, HA; Alnoman, RB; Hagar, M; Knight, JG; Parveen, S	1
Avellanal-Zaballa, E; Bañuelos, J; García-Moreno, I; Gómez, AM; Lopez, JC; Permingeat, C; Uriel, C; Ventura, J	1
Arbeloa, T; Bañuelos, J; Bautista-Hernández, CI; Becerra-González, JG; Enríquez-Palacios, E; López-Arbeloa, I; Peña-Cabrera, E	1
Colombani-Garay, D; Duan, C; Han, G; Huang, L; Lin, W	1
Cao, JJ; Li, XQ; Liu, JY; Xu, G; Yang, DC; Zhang, MS	1
Amaral, C; Argerich, J; Ciruela, F; Fernández-Dueñas, V; Qian, M; Risseeuw, MDP; Van Calenbergh, S	1
Biazzotto, JC; Castro, KADF; Costa, LD; da Neves, MGPMS; da Silva, RS; Faustino, MAF; Guieu, S; Tomé, AC	1
Chen, JA; Fu, W; Gu, X; Guo, W; Hu, W; Ouyang, Z; Pan, H; Sun, N; Tan, J; Wang, Y; Wang, Z	1
Guo, W; Liu, J; Liu, M; Sun, YQ; Zhang, H	1
Antina, E; Berezin, M; Boichuk, S; Guseva, G; Islamov, D; Kayumov, A; Lisovskaya, S; Lodochnikova, O; Nikitina, L; Pavelyev, R; Usachev, K	1
Andrioletti, B; Guérin, C; Jean-Gérard, L; Michel, C; Steinmann, S; Zhang, Z	1
Chen, XF; Ma, Q; Ma, Y; Song, Y; Wang, Z; Xie, Z; Yang, Z; Zhao, X	1
Chan, BC; Dharmaratne, P; Fung, KP; Ip, M; Lau, CBS; Lau, KM; Ng, DK; Wang, B; Wong, RC; Yu, L	1
Feng, T; Feng, W; Li, F; Li, M; Liu, S; Xu, Y; Zhao, M; Zhao, Q	1
Jois, SD; Kaufman, NEM; Singh, SS; Vicente, MDGH; Williams, TM; Zhou, Z	1
Al-Taher, M; Aonghusa, PM; Barberio, M; Cahill, R; Curtin, N; Diana, M; Marescaux, J; O'Shea, DF; Sarkar, A; Wu, D; Zhuk, S	1
Bai, Q; Choi, CHJ; Choi, CKK; Dai, G; Ng, DKP; Xiao, Y; Yang, C; Zhou, Y	1
Li, Z; Xia, J; Xie, Z; Zheng, M	1
Kong, H; Kong, X; Liu, J; Zhang, K; Zhang, Q; Zhang, Y; Zhang, YN; Zhao, R; Zhao, Y	1
Chen, Z; Liu, H; Liu, R; Su, H; Zhu, H; Zhu, S	1
Cao, J; Chen, B; Kong, X; Lu, J; Zhang, K; Zhang, Q; Zhang, YN; Zubair Iqbal, M	1
Feng, L; Huangfu, C; Li, C; Wang, F; Zhang, X; Zhu, M	1
Bentley, JN; Caputo, CB; Crilley, LR; Nodeh-Farahani, D; VandenBoer, TC	1
Cheng, Q; Dang, H; Teng, C; Tian, Y; Xie, K; Yan, L	1
Algi, F; Degirmenci, A; Karaduman, T; Sonkaya, Ö; Soylukan, C	1
Mizukami, K; Muraoka, T; Shiozaki, S; Tobita, S; Yoshihara, T	1
Andraud, C; Berginc, G; Bondar, MV; Chang, HJ; David, S; Hagan, DJ; Jacquemin, D; Le Guennic, B; Maury, O; Munera, N; Van Stryland, EW	1
Benniston, AC; Harriman, A; Karlsson, JKG; Waddell, PG; Waly, SM	1
Liu, ZF; Niu, LY; Teng, KX; Wang, LY; Yang, QZ	1
He, LN; Li, XY; Qiu, LQ; Yang, ZW; Yao, X	1
Mou, C; Shi, Q; Xie, Z; Zheng, M	1
Han, Y; Jia, J; Li, Z; Song, G; Song, Y; Wang, Y; Zhang, X; Zhou, W	1
Dündar, E; Işık, M; Şahin, E; Tanyeli, C	1
Durandin, N; Efimov, A; Ilina, P; Kähärä, I; Laaksonen, T; Lisitsyna, E; Vuorimaa-Laukkanen, E	1
Chen, F; Li, Y; Lin, X; Qiu, H; Stang, PJ; Wang, H; Yin, S; Yu, X	1
Lan, M; Li, B; Li, X; Pang, E; Song, X; Tan, S; Wang, B; Xing, X; Yang, K; Yi, J	1
Chen, H; Chen, Y; Li, X; Liang, L; Wang, D; Xiang, H; You, C; Zhao, Y	1
Du, L; Lin, Z; Liu, JY; Lu, ZY; Luo, CM; Wen, LF; Yang, DC	1
Chen, Z; Hu, P; Huang, M; Liu, JY; Weng, XL; Yang, DC; Zhu, CH	1
Fu, H; Lei, J; Shen, Z; Wu, F; Xu, Z; Zhu, D	1
Aksenova, I; Pomogaev, V	1
Firmansyah, D; Juliawaty, LD; Qolby, DS; Yuliarto, B	1
Cheung, PCK; Lo, PC; Ng, DKP; Tam, LKB	1

Reviews

4 review(s) available for porphobilinogen and dipyrromethene

Article	Year
Red/near-infrared boron-dipyrromethene dyes as strongly emitting fluorophores. Annals of the New York Academy of Sciences, 2008, Volume: 1130 Topics: Boron; Boron Compounds; Fluorescent Dyes; Hydrogen-Ion Concentration; Ions; Metals; Models, Chemical; Molecular Structure; Phenanthrenes; Porphobilinogen; Solvents; Spectrophotometry; Spectroscopy, Near-Infrared; Temperature	2008
Photosynthetic antenna-reaction center mimicry by using boron dipyrromethene sensitizers. Chemphyschem : a European journal of chemical physics and physical chemistry, 2014, Jan-13, Volume: 15, Issue:1 Topics: Biomimetic Materials; Biomimetics; Boron; Electrons; Energy Transfer; Photochemical Processes; Photosynthesis; Porphobilinogen; Solar Energy	2014
Boron Dipyrromethene Nano-Photosensitizers for Anticancer Phototherapies. Small (Weinheim an der Bergstrasse, Germany), 2019, Volume: 15, Issue:32 Topics: Animals; Antineoplastic Agents; Boron; Humans; Neoplasms; Photosensitizing Agents; Phototherapy; Porphobilinogen	2019
Tailoring nanoparticles based on boron dipyrromethene for cancer imaging and therapy. Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology, 2020, Volume: 12, Issue:4 Topics: Animals; Boron; Diagnostic Imaging; Drug Compounding; Humans; Nanoparticles; Neoplasms; Porphobilinogen	2020

Other Studies

134 other study(ies) available for porphobilinogen and dipyrromethene

Article	Year
Multiple switching and photogated electrochemiluminescence expressed by a dihydroazulene/boron dipyrromethene dyad. Angewandte Chemie (International ed. in English), 2005, Oct-28, Volume: 44, Issue:42 Topics: Azulenes; Boron Compounds; Electrochemistry; Fluorescent Dyes; Luminescence; Luminescent Measurements; Molecular Structure; Photochemistry; Porphobilinogen; Ultraviolet Rays	2005
Proton- and redox-controlled switching of photo- and electrochemiluminescence in thiophenyl-substituted boron-dipyrromethene dyes. Chemistry (Weinheim an der Bergstrasse, Germany), 2006, Jan-11, Volume: 12, Issue:3 Topics: Boron Compounds; Electrochemistry; Fluorescent Dyes; Heterocyclic Compounds, 2-Ring; Luminescent Measurements; Phenols; Porphobilinogen; Sulfhydryl Compounds	2006
Dinuclear zinc(II) double-helicates of homochirally substituted bis(dipyrromethene)s. The Journal of organic chemistry, 2005, Nov-25, Volume: 70, Issue:24 Topics: Molecular Structure; Organometallic Compounds; Porphobilinogen; Stereoisomerism; Zinc	2005
Isocyanate-, isothiocyanate-, urea-, and thiourea-substituted boron dipyrromethene dyes as fluorescent probes. The Journal of organic chemistry, 2006, Apr-14, Volume: 71, Issue:8 Topics: Boron; Crystallography, X-Ray; Electrochemistry; Fluorescent Dyes; Isocyanates; Models, Molecular; Molecular Structure; Porphobilinogen; Solutions; Sulfhydryl Compounds; Temperature; Urea	2006
Synthesis of fluorescent lactosylceramide stereoisomers. Chemistry and physics of lipids, 2006, Volume: 142, Issue:1-2 Topics: Animals; Antigens, CD; Boron Compounds; Caveolae; Cell Membrane; Endocytosis; Fluorescent Dyes; Glycosphingolipids; Lactosylceramides; Microscopy, Fluorescence; Models, Chemical; Porphobilinogen; Stereoisomerism	2006
Boron dipyrromethene dyes: a rational avenue for sensing and light emitting devices. Dalton transactions (Cambridge, England : 2003), 2006, Jun-21, Issue:23 Topics: Boron; Boron Compounds; Chemistry; Electrons; Fluorescence; Fluorescent Dyes; Light; Models, Chemical; Molecular Structure; Nitrobenzenes; Photochemistry; Porphobilinogen; X-Rays	2006
Charge separation in a nonfluorescent donor-acceptor dyad derived from boron dipyrromethene dye, leading to photocurrent generation. The journal of physical chemistry. B, 2005, Aug-18, Volume: 109, Issue:32 Topics: Boron; Coloring Agents; Electrochemistry; Electrons; Ions; Molecular Structure; Oxidation-Reduction; Photochemistry; Porphobilinogen; Spectrophotometry	2005
Unusual fluorescent monomeric and dimeric dialkynyl dipyrromethene-borane complexes. Organic letters, 2006, Sep-28, Volume: 8, Issue:20 Topics: Boranes; Dimerization; Fluorescent Dyes; Models, Molecular; Porphobilinogen; Spectrum Analysis	2006
Nanoscale metal coordination macrocycles fabricated by using "dimeric" dipyrrins. Chemistry (Weinheim an der Bergstrasse, Germany), 2007, Volume: 13, Issue:28 Topics: Dimerization; Ligands; Metal Nanoparticles; Porphobilinogen; Stereoisomerism; Zinc	2007
An ionically driven molecular IMPLICATION gate operating in fluorescence mode. Chemistry (Weinheim an der Bergstrasse, Germany), 2007, Volume: 13, Issue:32 Topics: Boron Compounds; Fluorescence; Fluorescent Dyes; Ions; Molecular Structure; Porphobilinogen; Quantum Theory	2007
Synthesis and spectral properties of cholesterol- and FTY720-containing boron dipyrromethene dyes. The Journal of organic chemistry, 2007, Oct-26, Volume: 72, Issue:22 Topics: Boron Compounds; Cholesterol; Fingolimod Hydrochloride; Fluorescent Dyes; Molecular Structure; Porphobilinogen; Propylene Glycols; Spectrophotometry, Ultraviolet; Sphingosine; Stereoisomerism	2007
Highly efficient energy transfer in the light harvesting system composed of three kinds of boron-dipyrromethene derivatives. Organic letters, 2008, Jan-03, Volume: 10, Issue:1 Topics: Absorption; Boron; Energy Transfer; Light; Models, Molecular; Molecular Structure; Porphobilinogen; Solar Energy	2008
Selective photoinactivation of protein function through environment-sensitive switching of singlet oxygen generation by photosensitizer. Proceedings of the National Academy of Sciences of the United States of America, 2008, Jan-08, Volume: 105, Issue:1 Topics: Animals; Boron; Boron Compounds; Cell Line; Chickens; Cytosol; Fluorescent Dyes; Inositol 1,4,5-Trisphosphate Receptors; Light; Models, Biological; Oxygen; Photochemistry; Photosensitizing Agents; Porphobilinogen; Protein Binding; Singlet Oxygen	2008
Phenanthrene-fused boron-dipyrromethenes as bright long-wavelength fluorophores. Organic letters, 2008, Apr-17, Volume: 10, Issue:8 Topics: Boron; Fluorescence Resonance Energy Transfer; Fluorescent Dyes; Magnetic Resonance Spectroscopy; Microscopy, Confocal; Models, Molecular; Phenanthrenes; Porphobilinogen	2008
Tailoring the properties of boron-dipyrromethene dyes with acetylenic functions at the 2,6,8 and 4-B substitution positions. Organic letters, 2008, Jun-05, Volume: 10, Issue:11 Topics: Acetylene; Boron Compounds; Fluorescent Dyes; Porphobilinogen	2008
Conformationally restricted dipyrromethene boron difluoride (BODIPY) dyes: highly fluorescent, multicolored probes for cellular imaging. Chemistry (Weinheim an der Bergstrasse, Germany), 2008, Volume: 14, Issue:19 Topics: Boron Compounds; Cells; Crystallography, X-Ray; Fluorescent Dyes; Image Interpretation, Computer-Assisted; Molecular Conformation; Porphobilinogen; Spectrometry, Fluorescence	2008
Photoinduced intercomponent processes in multichromophoric species made of Pt(II)-terpyridine-acetylide and dipyrromethene-BF2 subunits. Physical chemistry chemical physics : PCCP, 2008, Jul-21, Volume: 10, Issue:27 Topics: Energy Transfer; Fluorescent Dyes; Luminescence; Molecular Structure; Organoplatinum Compounds; Oxidation-Reduction; Photochemistry; Porphobilinogen; Pyridinium Compounds; Ruthenium; Ultraviolet Rays	2008
Electroactive dipyrromethene-Cu(II) self-assembled monolayers: complexation reaction on the surface of gold electrodes. Langmuir : the ACS journal of surfaces and colloids, 2008, Oct-07, Volume: 24, Issue:19 Topics: Copper; Electrochemistry; Electrodes; Electrons; Gold; Microscopy, Atomic Force; Molecular Structure; Porphobilinogen; Surface Properties	2008
B,O-chelated azadipyrromethenes as near-IR probes. Organic letters, 2008, Nov-06, Volume: 10, Issue:21 Topics: Aza Compounds; Boron; Chelating Agents; Crystallography, X-Ray; Models, Molecular; Molecular Probes; Molecular Structure; Oxygen; Photochemistry; Porphobilinogen; Solvents; Spectrometry, Fluorescence; Spectroscopy, Near-Infrared	2008
Electronic energy transfer to the S2 level of the acceptor in functionalised boron dipyrromethene dyes. Chemistry (Weinheim an der Bergstrasse, Germany), 2009, Volume: 15, Issue:18 Topics: Boron; Electrons; Energy Transfer; Fluorescent Dyes; Hydrocarbons, Fluorinated; Perylene; Porphobilinogen; Spectrometry, Fluorescence	2009
Multiantenna artificial photosynthetic reaction center complex. The journal of physical chemistry. B, 2009, May-21, Volume: 113, Issue:20 Topics: Absorption; Anthracenes; Benzene; Biomimetics; Electrons; Energy Transfer; Fullerenes; Furans; Light; Metalloporphyrins; Models, Molecular; Molecular Conformation; Photosynthetic Reaction Center Complex Proteins; Porphobilinogen; Spectrum Analysis; Time Factors	2009
Three-coordinate, phosphine-ligated azadipyrromethene complexes of univalent group 11 metals. Inorganic chemistry, 2009, Sep-07, Volume: 48, Issue:17 Topics: Aza Compounds; Computer Simulation; Crystallography, X-Ray; Ligands; Models, Chemical; Models, Molecular; Molecular Structure; Organometallic Compounds; Phosphines; Porphobilinogen; Stereoisomerism; Transition Elements	2009
A panchromatic supramolecular fullerene-based donor-acceptor assembly derived from a peripherally substituted bodipy-zinc phthalocyanine dyad. Chemistry (Weinheim an der Bergstrasse, Germany), 2010, Feb-08, Volume: 16, Issue:6 Topics: Boron Compounds; Dimerization; Electrochemistry; Fluorescence; Fullerenes; Indoles; Isoindoles; Models, Chemical; Organometallic Compounds; Photochemistry; Porphobilinogen; Spectrometry, Fluorescence; Spectrophotometry, Ultraviolet; Zinc Compounds	2010
Cofacial boron dipyrromethene (Bodipy) dimers: synthesis, charge delocalization, and exciton coupling. The Journal of organic chemistry, 2010, Mar-19, Volume: 75, Issue:6 Topics: Boron; Crystallography, X-Ray; Dimerization; Fluorescent Dyes; Magnetic Resonance Spectroscopy; Molecular Structure; Porphobilinogen	2010
In vitro and in vivo photocytotoxicity of boron dipyrromethene derivatives for photodynamic therapy. Journal of medicinal chemistry, 2010, Apr-08, Volume: 53, Issue:7 Topics: Animals; Apoptosis; Biological Transport; Blood Vessels; Boron; Boron Compounds; Cell Cycle; Cell Line, Tumor; Chickens; Chorioallantoic Membrane; Humans; Intracellular Space; Photochemotherapy; Photosensitizing Agents; Porphobilinogen; Singlet Oxygen; Structure-Activity Relationship	2010
A fast-response pH optode based on a fluoroionophore immobilized to a mesoporous silica thin film. Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 2010, Volume: 26, Issue:3 Topics: Boron; Fluorescent Dyes; Hydrogen-Ion Concentration; Membranes, Artificial; Porosity; Porphobilinogen; Silicon Dioxide; Surface Properties	2010
BF2-chelated tetraarylazadipyrromethenes as NIR fluorochromes. Bioconjugate chemistry, 2010, Jul-21, Volume: 21, Issue:7 Topics: Aza Compounds; Boron Compounds; Chelating Agents; Fluorescent Dyes; Lysine; Molecular Structure; Muramidase; Porphobilinogen; Spectroscopy, Near-Infrared; Stereoisomerism; Trypsin	2010
Energy transfer by way of an exciplex intermediate in flexible boron dipyrromethene-based allosteric architectures. The journal of physical chemistry. A, 2010, Oct-07, Volume: 114, Issue:39 Topics: Boron Compounds; Electrochemistry; Energy Transfer; Fluorescent Dyes; Molecular Structure; Porphobilinogen; Stereoisomerism	2010
Electrogenerated chemiluminescent anion sensing: selective recognition and sensing of pyrophosphate. Analytical chemistry, 2010, Oct-01, Volume: 82, Issue:19 Topics: Amines; Anions; Boron; Coordination Complexes; Diphosphates; Electrochemical Techniques; Luminescent Measurements; Picolinic Acids; Porphobilinogen; Thermodynamics; Zinc	2010
Synthesis and spectroscopic characterization of fluorescent boron dipyrromethene-derived hydrazones. Journal of fluorescence, 2011, Volume: 21, Issue:1 Topics: Boron Compounds; Electrophoresis, Polyacrylamide Gel; Hydrazones; Kinetics; Magnetic Resonance Spectroscopy; Porphobilinogen	2011
Near-infrared nitrofluorene substitued aza-Boron-dipyrromethenes dyes. Organic letters, 2011, Jan-07, Volume: 13, Issue:1 Topics: Aza Compounds; Boron Compounds; Fluorenes; Models, Molecular; Molecular Structure; Porphobilinogen; Spectroscopy, Near-Infrared	2011
Development of an indole-based boron-dipyrromethene fluorescent probe for benzenethiols. The journal of physical chemistry. B, 2011, Feb-03, Volume: 115, Issue:4 Topics: Boron Compounds; Buffers; Fluorescent Dyes; Hydrogen-Ion Concentration; Indoles; Molecular Structure; Phenols; Porphobilinogen; Spectrometry, Fluorescence; Sulfhydryl Compounds	2011
Fluorescence anisotropy of molecular rotors. Chemphyschem : a European journal of chemical physics and physical chemistry, 2011, Feb-25, Volume: 12, Issue:3 Topics: Boron; Fluorescence Polarization; Fluorescent Dyes; Models, Theoretical; Nitriles; Porphobilinogen; Quantum Theory; Quinolizines; Solvents; Spectrometry, Fluorescence; Viscosity	2011
Modulation of the spectroscopic property of Bodipy derivates through tuning the molecular configuration. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2011, Volume: 10, Issue:6 Topics: Boron Compounds; Crystallography, X-Ray; Electrochemical Techniques; Fluorescent Dyes; Molecular Conformation; Oxidation-Reduction; Porphobilinogen; Quantum Theory; Spectrometry, Fluorescence	2011
Synthesis and in vitro photodynamic activities of pegylated distyryl boron dipyrromethene derivatives. Journal of medicinal chemistry, 2011, Apr-28, Volume: 54, Issue:8 Topics: Humans; Photochemotherapy; Polyethylene Glycols; Porphobilinogen	2011
8-Hydroxyquinoline-substituted boron-dipyrromethene compounds: synthesis, structure, and OFF-ON-OFF type of pH-sensing properties. The Journal of organic chemistry, 2011, May-20, Volume: 76, Issue:10 Topics: Boron; Crystallography, X-Ray; Drug Design; Electron Transport; Fluorescent Dyes; Hydrogen-Ion Concentration; Models, Molecular; Molecular Conformation; Oxyquinoline; Photochemical Processes; Porphobilinogen	2011
3,5-Diformylboron dipyrromethenes as fluorescent pH sensors. Inorganic chemistry, 2011, May-16, Volume: 50, Issue:10 Topics: Benzoquinones; Biosensing Techniques; Boron; Boron Compounds; Crystallography, X-Ray; Dimethylformamide; Fluorescence; Fluorescent Dyes; Formamides; Hydrogen Bonding; Hydrogen-Ion Concentration; Magnetic Resonance Spectroscopy; Molecular Structure; Porphobilinogen; Pyrroles; Spectrometry, Fluorescence; Thermodynamics	2011
Synthesis of sterically crowded polyarylated boron-dipyrromethenes. The Journal of organic chemistry, 2011, Oct-21, Volume: 76, Issue:20 Topics: Boron; Boron Compounds; Crystallography, X-Ray; Fluorescence; Fluorescent Dyes; Magnetic Resonance Spectroscopy; Molecular Conformation; Molecular Imaging; Molecular Probes; Oxidation-Reduction; Porphobilinogen; Spectrometry, Fluorescence	2011
A boron-dipyrromethene-based fluorescent probe for colorimetric and ratiometric detection of sulfite. Journal of agricultural and food chemistry, 2011, Nov-23, Volume: 59, Issue:22 Topics: Boron; Boron Compounds; Colorimetry; Fluorescent Dyes; Porphobilinogen; Spectrometry, Fluorescence; Sulfites	2011
Highly photostable near-infrared fluorescent pH indicators and sensors based on BF2-chelated tetraarylazadipyrromethene dyes. Analytical chemistry, 2012, Aug-07, Volume: 84, Issue:15 Topics: Chelating Agents; Dental Cements; Electron Transport; Fluorescent Dyes; Fluorides, Topical; Hydrogen-Ion Concentration; Indicators and Reagents; Kinetics; Porphobilinogen; Spectrometry, Fluorescence	2012
Accessing the long-lived triplet excited states in bodipy-conjugated 2-(2-hydroxyphenyl) benzothiazole/benzoxazoles and applications as organic triplet photosensitizers for photooxidations. The Journal of organic chemistry, 2012, Jul-20, Volume: 77, Issue:14 Topics: Benzothiazoles; Benzoxazoles; Boron; Molecular Structure; Oxidation-Reduction; Phenols; Photochemical Processes; Photosensitizing Agents; Porphobilinogen; Quantum Theory	2012
Gold(I) complexes of brominated azadipyrromethene ligands. Inorganic chemistry, 2012, Jul-16, Volume: 51, Issue:14 Topics: Aza Compounds; Crystallography, X-Ray; Ligands; Models, Molecular; Molecular Structure; Organogold Compounds; Porphobilinogen; Quantum Theory	2012
Design strategy for a near-infrared fluorescence probe for matrix metalloproteinase utilizing highly cell permeable boron dipyrromethene. Journal of the American Chemical Society, 2012, Aug-22, Volume: 134, Issue:33 Topics: Animals; Boron Compounds; Cell Line, Tumor; Cell Membrane Permeability; Cell Survival; Fluorescence; Fluorescence Resonance Energy Transfer; Fluorescent Dyes; Humans; Matrix Metalloproteinases; Mice; Microscopy, Fluorescence; Neoplasms; Porphobilinogen; Whole Body Imaging	2012
Mechanistic insight into the formation of tetraarylazadipyrromethenes. The Journal of organic chemistry, 2012, Oct-19, Volume: 77, Issue:20 Topics: Molecular Structure; Porphobilinogen; Stereoisomerism	2012
Boronic acid functionalized boron dipyrromethene fluorescent probes: preparation, characterization, and saccharides sensing applications. Analytical chemistry, 2012, Dec-04, Volume: 84, Issue:23 Topics: Biosensing Techniques; Boron Compounds; Boronic Acids; Fluorescence; Fluorescent Dyes; Glycogen; Monosaccharides; Porphobilinogen	2012
Dual emissive borane-BODIPY dyads: molecular conformation control over electronic properties and fluorescence response towards fluoride ions. Chemical communications (Cambridge, England), 2013, Feb-01, Volume: 49, Issue:10 Topics: Boranes; Electrons; Fluorescence; Fluorides; Ions; Molecular Conformation; Molecular Structure; Porphobilinogen; Quantum Theory	2013
A boron dipyrromethene-phthalocyanine pentad as an artificial photosynthetic model. Chemical communications (Cambridge, England), 2013, Apr-14, Volume: 49, Issue:29 Topics: Biomimetic Materials; Boron; Energy Transfer; Indoles; Organosilicon Compounds; Photosynthetic Reaction Center Complex Proteins; Porphobilinogen; Spectrophotometry	2013
Photoinduced energy and charge transfer in a p-phenylene-linked dyad of boron dipyrromethene and monostyryl boron dipyrromethene. Physical chemistry chemical physics : PCCP, 2013, May-14, Volume: 15, Issue:18 Topics: Boron; Porphobilinogen; Solvents; Spectrophotometry, Ultraviolet; Thermodynamics	2013
Efficient light absorbers based on thiophene-fused boron dipyrromethene (BODIPY) dyes. Bioorganic & medicinal chemistry, 2013, May-15, Volume: 21, Issue:10 Topics: Boron Compounds; Fluorescent Dyes; Molecular Structure; Porphobilinogen; Spectrometry, Fluorescence	2013
A self-calibrating bipartite viscosity sensor for mitochondria. Journal of the American Chemical Society, 2013, Jun-19, Volume: 135, Issue:24 Topics: Biosensing Techniques; Boron; Coumarins; Fluorescent Dyes; HeLa Cells; Humans; Mitochondria; Porphobilinogen; Spectrometry, Fluorescence; Viscosity	2013
Photosynthetic antenna-reaction center mimicry with a covalently linked monostyryl boron-dipyrromethene-aza-boron-dipyrromethene-C60 triad. Chemistry (Weinheim an der Bergstrasse, Germany), 2013, Aug-19, Volume: 19, Issue:34 Topics: Aza Compounds; Biocompatible Materials; Boron; Electron Transport; Electrons; Energy Transfer; Fullerenes; Photosynthetic Reaction Center Complex Proteins; Porphobilinogen; Quantum Theory	2013
Peculiar properties of homoleptic Cu complexes with dipyrromethene derivatives. Dalton transactions (Cambridge, England : 2003), 2013, Oct-21, Volume: 42, Issue:39 Topics: Coordination Complexes; Copper; Crystallography, X-Ray; Molecular Conformation; Oxidation-Reduction; Porphobilinogen	2013
The computational and experimental investigations of photophysical and spectroscopic properties of BF2 dipyrromethene complexes. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 2014, Jan-03, Volume: 117 Topics: Computer Simulation; Electrons; Light; Models, Molecular; Molecular Structure; Photochemistry; Porphobilinogen; Quantum Theory; Spectrometry, Fluorescence	2014
Reducing exciton binding energy by increasing thin film permittivity: an effective approach to enhance exciton separation efficiency in organic solar cells. ACS applied materials & interfaces, 2013, Oct-23, Volume: 5, Issue:20 Topics: Boron; Fullerenes; Oxygen; Porphobilinogen; Quantum Theory; Solar Energy	2013
Preparation and in vitro photodynamic activities of folate-conjugated distyryl boron dipyrromethene based photosensitizers. Journal of medicinal chemistry, 2013, Nov-14, Volume: 56, Issue:21 Topics: Boron Compounds; Cell Survival; Dose-Response Relationship, Drug; Folic Acid; Humans; KB Cells; MCF-7 Cells; Models, Biological; Molecular Structure; Photosensitizing Agents; Porphobilinogen; Structure-Activity Relationship	2013
Hypochlorous acid turn-on boron dipyrromethene probe based on oxidation of methyl phenyl sulfide. Analytica chimica acta, 2013, Oct-24, Volume: 800 Topics: Animals; Boron; Cell Line; Electron Transport; Fluorescent Dyes; Hypochlorous Acid; Mice; Microscopy, Confocal; Oxidation-Reduction; Porphobilinogen; Quantum Theory; Reactive Nitrogen Species; Reactive Oxygen Species; Sulfides	2013
Conformationally restricted aza-dipyrromethene boron difluorides (aza-BODIPYs) with high fluorescent quantum yields. Chemistry, an Asian journal, 2014, Volume: 9, Issue:3 Topics: Aza Compounds; Boron Compounds; Fluorescence; Fluorescent Dyes; Fluorides; Molecular Conformation; Molecular Structure; Porphobilinogen; Quantum Theory; Solvents	2014
Boron-dipyrromethene based reversible and reusable selective chemosensor for fluoride detection. Inorganic chemistry, 2014, Feb-03, Volume: 53, Issue:3 Topics: Benzimidazoles; Boron; Boron Compounds; Crystallography, X-Ray; Fluorescent Dyes; Fluorides; Models, Molecular; Phenylenediamines; Porphobilinogen; Spectrometry, Fluorescence	2014
A rapid and fluorogenic TMP-AcBOPDIPY probe for covalent labeling of proteins in live cells. Journal of the American Chemical Society, 2014, Mar-26, Volume: 136, Issue:12 Topics: Cell Survival; Escherichia coli; Fluorescent Dyes; HeLa Cells; Heterocyclic Compounds, 3-Ring; Humans; Porphobilinogen; Staining and Labeling; Tetrahydrofolate Dehydrogenase; Time Factors; Trimethoprim	2014
Structural evidence for the partially oxidized dipyrromethene and dipyrromethanone forms of the cofactor of porphobilinogen deaminase: structures of the Bacillus megaterium enzyme at near-atomic resolution. Acta crystallographica. Section D, Biological crystallography, 2014, Volume: 70, Issue:Pt 3 Topics: Amino Acid Sequence; Bacillus megaterium; Crystallization; Crystallography, X-Ray; Hydroxymethylbilane Synthase; Molecular Sequence Data; Oxidation-Reduction; Porphobilinogen	2014
Intracellular guest exchange between dynamic supramolecular hosts. Journal of the American Chemical Society, 2014, Jun-04, Volume: 136, Issue:22 Topics: Anthracenes; Cell Membrane; Energy Transfer; HeLa Cells; Humans; Nanoparticles; Polyethylene Glycols; Polymethacrylic Acids; Porphobilinogen	2014
Boron dipyrromethene as a fluorescent caging group for single-photon uncaging with long-wavelength visible light. ACS chemical biology, 2014, Oct-17, Volume: 9, Issue:10 Topics: Boron; Boron Compounds; Fluorescent Dyes; HeLa Cells; Humans; Light; Molecular Structure; Photons; Porphobilinogen	2014
Antimicrobial and anti-biofilm effect of a novel BODIPY photosensitizer against Pseudomonas aeruginosa PAO1. Biofouling, 2014, Volume: 30, Issue:8 Topics: Anti-Bacterial Agents; Biofilms; Boron; Microscopy, Confocal; Photosensitizing Agents; Porphobilinogen; Pseudomonas aeruginosa	2014
A photostable near-infrared fluorescent tracker with pH-independent specificity to lysosomes for long time and multicolor imaging. ACS applied materials & interfaces, 2014, Dec-10, Volume: 6, Issue:23 Topics: Boron; Cell Tracking; Diagnostic Imaging; Fluorescent Dyes; Humans; Lysosomes; Porphobilinogen; Spectroscopy, Near-Infrared	2014
A new water-soluble phosphorus-dipyrromethene and phosphorus-azadipyrromethene dye: PODIPY/aza-PODIPY. Chemistry (Weinheim an der Bergstrasse, Germany), 2015, Apr-13, Volume: 21, Issue:16 Topics: Aza Compounds; Fluorescent Dyes; Hep G2 Cells; Humans; Models, Molecular; Optical Imaging; Organophosphorus Compounds; Porphobilinogen; Solubility; Water	2015
Synthesis and melanogenesis evaluation of 3',4',7-trihydroxyflavanone derivatives and characterization of flavanone-BODIPY. Bioorganic & medicinal chemistry letters, 2015, Apr-01, Volume: 25, Issue:7 Topics: Animals; Boron Compounds; Cell Line, Tumor; Endoplasmic Reticulum; Flavanones; Fluorescent Dyes; Melanoma; Mice; Mice, Inbred C57BL; Porphobilinogen	2015
Fluorescent In Situ Targeting Probes for Rapid Imaging of Ovarian-Cancer-Specific γ-Glutamyltranspeptidase. Angewandte Chemie (International ed. in English), 2015, Jun-15, Volume: 54, Issue:25 Topics: Boron Compounds; Cell Line, Tumor; Enzyme Assays; Female; Fluorescent Dyes; gamma-Glutamyltransferase; Human Umbilical Vein Endothelial Cells; Humans; Microscopy, Confocal; Optical Imaging; Ovarian Neoplasms; Ovary; Porphobilinogen	2015
A biosensor based on electroactive dipyrromethene-Cu(II) layer deposited onto gold electrodes for the detection of antibodies against avian influenza virus type H5N1 in hen sera. Analytical and bioanalytical chemistry, 2015, Volume: 407, Issue:25 Topics: Animals; Antibodies, Viral; Biosensing Techniques; Chickens; Copper; Electrochemical Techniques; Electrodes; Female; Gold; Hemagglutinin Glycoproteins, Influenza Virus; Immunoassay; Influenza A Virus, H5N1 Subtype; Influenza in Birds; Limit of Detection; Porphobilinogen	2015
Electrochemical label-free and reagentless genosensor based on an ion barrier switch-off system for DNA sequence-specific detection of the avian influenza virus. Analytical chemistry, 2015, Oct-06, Volume: 87, Issue:19 Topics: Animals; Biosensing Techniques; Birds; Cobalt; Coordination Complexes; Copper; DNA, Single-Stranded; Electrochemical Techniques; Electrodes; Gold; Influenza A Virus, H5N1 Subtype; Influenza in Birds; Limit of Detection; Nucleic Acid Hybridization; Porphobilinogen	2015
Evaluation of Anisole-Substituted Boron Difluoride Formazanate Complexes for Fluorescence Cell Imaging. Chemistry (Weinheim an der Bergstrasse, Germany), 2015, Oct-26, Volume: 21, Issue:44 Topics: Anisoles; Boron Compounds; Crystallography, X-Ray; Diagnostic Imaging; Diamines; Fibroblasts; Fluorescence; Indoles; Models, Molecular; Molecular Structure; Porphobilinogen	2015
Synthesis and assessment of a maleimide functionalized BF2 azadipyrromethene near-infrared fluorochrome. Chemical communications (Cambridge, England), 2015, Dec-04, Volume: 51, Issue:93 Topics: Animals; Aza Compounds; Fluorescence; Fluorescent Dyes; Glutathione; HeLa Cells; Humans; Infrared Rays; Maleimides; Mice; Molecular Structure; Neoplasms, Experimental; Peptides, Cyclic; Porphobilinogen; Sulfhydryl Compounds	2015
Circularly Polarized Luminescence from Helically Chiral N,N,O,O-Boron-Chelated Dipyrromethenes. Chemistry (Weinheim an der Bergstrasse, Germany), 2016, Jan-04, Volume: 22, Issue:1 Topics: Boron; Chelating Agents; Circular Dichroism; Fluorescent Dyes; Luminescence; Luminescent Measurements; Molecular Structure; Porphobilinogen; Solutions; Stereoisomerism	2016
Exploring of protein - protein interactions at the solid - aqueous interface by means of contact angle measurements. Colloids and surfaces. B, Biointerfaces, 2016, May-01, Volume: 141 Topics: Algorithms; Copper; Histidine; Models, Chemical; Models, Molecular; Nickel; Porphobilinogen; Protein Binding; Protein Domains; Protein Interaction Mapping; Receptor for Advanced Glycation End Products; S100 Calcium Binding Protein beta Subunit; Surface Properties; Water	2016
Oral administration of SR-110, a peroxynitrite decomposing catalyst, enhances glucose homeostasis, insulin signaling, and islet architecture in B6D2F1 mice fed a high fat diet. Archives of biochemistry and biophysics, 2016, 04-15, Volume: 596 Topics: Administration, Oral; Animals; Blood Glucose; Dietary Fats; Homeostasis; Insulin; Insulin-Secreting Cells; Mice; Peroxynitrous Acid; Porphobilinogen; Rats; Rats, Sprague-Dawley; Signal Transduction	2016
A ratiometric fluorescent probe based on boron dipyrromethene and rhodamine Förster resonance energy transfer platform for hypochlorous acid and its application in living cells. Analytica chimica acta, 2016, 05-19, Volume: 921 Topics: Animals; Boron Compounds; Fluorescence Resonance Energy Transfer; Fluorescent Dyes; Hypochlorous Acid; Limit of Detection; Mice; Optical Imaging; Porphobilinogen; RAW 264.7 Cells; Rhodamines; Spectrometry, Fluorescence	2016
Enhanced Fluorescence Turn-on Imaging of Hypochlorous Acid in Living Immune and Cancer Cells. Chemistry (Weinheim an der Bergstrasse, Germany), 2016, Jul-04, Volume: 22, Issue:28 Topics: Boron; Cell Line; Fluorescence; Fluorescent Dyes; Humans; Hypochlorous Acid; Limit of Detection; MCF-7 Cells; Microscopy, Confocal; Oxidation-Reduction; Porphobilinogen; Selenium	2016
NO Chemical communications (Cambridge, England), 2017, 01-03, Volume: 53, Issue:3 Topics: Molecular Structure; Nanoparticles; Nitrogen Dioxide; Oxidation-Reduction; Particle Size; Porosity; Porphobilinogen; Rhodamines; Silicon Dioxide; Surface Properties	2017
Rational Engineering of BODIPY-Bridged Trisindole Derivatives for Solar Cell Applications. ChemSusChem, 2017, 05-09, Volume: 10, Issue:9 Topics: Boron; Chemical Engineering; Electric Power Supplies; Fluorescent Dyes; Fullerenes; Indoles; Molecular Conformation; Porphobilinogen; Solar Energy	2017
BF European journal of medicinal chemistry, 2017, Jul-28, Volume: 135 Topics: Aza Compounds; Boron Compounds; Colon; Dose-Response Relationship, Drug; Fluorescent Dyes; Humans; Molecular Structure; Porphobilinogen; Spectroscopy, Near-Infrared; Structure-Activity Relationship	2017
A General Strategy Toward Highly Fluorogenic Bioprobes Emitting across the Visible Spectrum. Journal of the American Chemical Society, 2017, 07-26, Volume: 139, Issue:29 Topics: Biosensing Techniques; Boron Compounds; Cell Survival; Electrons; Fluorescent Dyes; HeLa Cells; Humans; Hydrogen Peroxide; Mitochondria; Molecular Structure; Optical Imaging; Peptide Hydrolases; Porphobilinogen; Spectrometry, Fluorescence; Spectrophotometry, Ultraviolet	2017
Ultrafast Solvation Dynamics and Vibrational Coherences of Halogenated Boron-Dipyrromethene Derivatives Revealed through Two-Dimensional Electronic Spectroscopy. Journal of the American Chemical Society, 2017, 10-18, Volume: 139, Issue:41 Topics: Boron; Boron Compounds; Electrons; Porphobilinogen; Quantum Theory; Solubility; Solvents; Spectrum Analysis; Vibration	2017
Chitosan-Coated Poly(lactic-co-glycolic acid)-Diiodinated boron-Dipyrromethene Nanoparticles Improve Tumor Selectivity and Stealth Properties in Photodynamic Cancer Therapy. Journal of biomedical nanotechnology, 2016, Volume: 12, Issue:7 Topics: Animals; Antineoplastic Agents; Boron Compounds; Cell Line, Tumor; Cell Survival; Chitosan; Drug Carriers; Female; Humans; Iodine; Lactic Acid; Mice; Mice, Inbred BALB C; Nanoparticles; Photochemotherapy; Polyglycolic Acid; Polylactic Acid-Polyglycolic Acid Copolymer; Porphobilinogen; Tissue Distribution	2016
Endoplasmic Reticulum-Localized Two-Photon-Absorbing Boron Dipyrromethenes as Advanced Photosensitizers for Photodynamic Therapy. Journal of medicinal chemistry, 2018, 05-10, Volume: 61, Issue:9 Topics: Absorption, Radiation; Boron; Endoplasmic Reticulum; HeLa Cells; Hep G2 Cells; Humans; Photochemotherapy; Photons; Photosensitizing Agents; Porphobilinogen; Reactive Oxygen Species; Singlet Oxygen; Structure-Activity Relationship	2018
Endogenous exosome labelling with an amphiphilic NIR-fluorescent probe. Chemical communications (Cambridge, England), 2018, Jun-26, Volume: 54, Issue:52 Topics: Aza Compounds; Boron Compounds; Cell Line, Tumor; Exosomes; Fluorescent Dyes; Humans; Infrared Rays; Optical Imaging; Porphobilinogen; Surface-Active Agents	2018
PEGylated BF European journal of medicinal chemistry, 2019, Jan-01, Volume: 161 Topics: Animals; Aza Compounds; Boron Compounds; Breast Neoplasms; Cell Line, Tumor; Dose-Response Relationship, Drug; Female; Fluorescent Dyes; Humans; Mammary Neoplasms, Experimental; Mice; Mice, Inbred BALB C; Molecular Structure; Optical Imaging; Polyethylene Glycols; Porphobilinogen; Renal Elimination; Spectrometry, Fluorescence; Structure-Activity Relationship	2019
A H₂O₂-Responsive Boron Dipyrromethene-Based Photosensitizer for Imaging-Guided Photodynamic Therapy. Molecules (Basel, Switzerland), 2018, Dec-21, Volume: 24, Issue:1 Topics: Biological Transport; Boron; Cell Line; Humans; Hydrogen Peroxide; Molecular Structure; Photochemistry; Photochemotherapy; Photosensitizing Agents; Porphobilinogen; Reactive Oxygen Species; Spectrometry, Fluorescence	2018
A BODIPY-Bridged Bisphenoxyl Diradicaloid: Solvent-Dependent Diradical Character and Physical Properties. Molecules (Basel, Switzerland), 2019, Apr-12, Volume: 24, Issue:8 Topics: Boron Compounds; Crystallography, X-Ray; Models, Molecular; Molecular Structure; Porphobilinogen	2019
Effect of Substituents on the Photophysical Properties and Bioimaging Application of BODIPY Derivatives with Triphenylamine Substituents. The journal of physical chemistry. B, 2019, 07-05, Volume: 123, Issue:26 Topics: Animals; Boron; Cells, Cultured; Density Functional Theory; Mice; Molecular Structure; Photochemical Processes; Porphobilinogen; Spectrophotometry, Ultraviolet	2019
Construction of cathepsin B-responsive fluorescent probe and photosensitizer using a ferrocenyl boron dipyrromethene dark quencher. European journal of medicinal chemistry, 2019, Oct-01, Volume: 179 Topics: Animals; Boron; Cathepsin B; Cell Survival; Dose-Response Relationship, Drug; Female; Ferrous Compounds; Fluorescent Dyes; Hep G2 Cells; HT29 Cells; Humans; Mice; Mice, Inbred BALB C; Mice, Nude; Molecular Structure; Optical Imaging; Photosensitizing Agents; Porphobilinogen; Structure-Activity Relationship; Tumor Cells, Cultured	2019
Highly luminescent metallacages featuring bispyridyl ligands functionalised with BODIPY for imaging in cancer cells. Journal of inorganic biochemistry, 2019, Volume: 199 Topics: Antineoplastic Agents; Boron Compounds; Cell Line, Tumor; Cell Proliferation; Cell Survival; Cisplatin; Coordination Complexes; Glutathione; Humans; Magnetic Resonance Spectroscopy; Microscopy, Confocal; Microscopy, Fluorescence; Palladium; Porphobilinogen	2019
Microfluidic Device for the Determination of Water Chlorination Levels Combining a Fluorescent Analytical chemistry, 2019, 10-15, Volume: 91, Issue:20 Topics: Boron Compounds; Charcoal; Chlorides; Drinking Water; Fluorescence; Fluorescent Dyes; Halogenation; Humans; Microfluidic Analytical Techniques; Porphobilinogen; Spectrometry, Fluorescence	2019
A novel distyryl boron dipyrromethene with two functional tags for site-specific bioorthogonal photosensitisation towards targeted photodynamic therapy. Chemical communications (Cambridge, England), 2019, Nov-07, Volume: 55, Issue:90 Topics: Animals; Antineoplastic Agents; Boron Compounds; Cell Line, Tumor; Cell Proliferation; Cell Survival; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Humans; Mice; Mice, Nude; Molecular Structure; Neoplasms, Experimental; Optical Imaging; Photochemotherapy; Photosensitizing Agents; Porphobilinogen; Reactive Oxygen Species; Structure-Activity Relationship	2019
A new chiral boron-dipyrromethene (BODIPY)-based fluorescent probe: molecular docking, DFT, antibacterial and antioxidant approaches. Journal of biomolecular structure & dynamics, 2020, Volume: 38, Issue:18 Topics: Anti-Bacterial Agents; Anti-Infective Agents; Antioxidants; Boron; Fluorescent Dyes; Molecular Docking Simulation; Porphobilinogen	2020
BODIPYs as Chemically Stable Fluorescent Tags for Synthetic Glycosylation Strategies towards Fluorescently Labeled Saccharides. Chemistry (Weinheim an der Bergstrasse, Germany), 2020, Apr-24, Volume: 26, Issue:24 Topics: Boron; Boron Compounds; Fluorescence; Fluorescent Dyes; Glycosylation; Light; Porphobilinogen	2020
Ready Access to Molecular Rotors Based on Boron Dipyrromethene Dyes-Coumarin Dyads Featuring Broadband Absorption. Molecules (Basel, Switzerland), 2020, Feb-12, Volume: 25, Issue:4 Topics: Boron; Coumarins; Fluorescence; Fluorescent Dyes; Molecular Conformation; Porphobilinogen; Spectrometry, Fluorescence	2020
A glutathione-responsive photosensitizer with fluorescence resonance energy transfer characteristics for imaging-guided targeting photodynamic therapy. European journal of medicinal chemistry, 2020, May-01, Volume: 193 Topics: Animals; Antineoplastic Agents; Boron Compounds; Cell Line, Tumor; Cell Proliferation; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Female; Fluorescence Resonance Energy Transfer; Glutathione; Humans; Mice; Mice, Inbred Strains; Molecular Structure; Neoplasms, Experimental; Optical Imaging; Photochemotherapy; Photosensitizing Agents; Porphobilinogen; Structure-Activity Relationship	2020
Design, Synthesis and Characterization of a New Series of Fluorescent Metabotropic Glutamate Receptor Type 5 Negative Allosteric Modulators. Molecules (Basel, Switzerland), 2020, Mar-27, Volume: 25, Issue:7 Topics: Allosteric Regulation; Allosteric Site; Binding Sites; Bioluminescence Resonance Energy Transfer Techniques; Boron Compounds; Calcium; Drug Discovery; Fluorescent Dyes; HEK293 Cells; Humans; Ligands; Porphobilinogen; Protein Binding; Receptor, Metabotropic Glutamate 5	2020
Photodynamic treatment of melanoma cells using aza-dipyrromethenes as photosensitizers. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2020, Jul-01, Volume: 19, Issue:7 Topics: Animals; Antineoplastic Agents; Aza Compounds; Cell Proliferation; Cell Survival; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Melanoma; Mice; Molecular Structure; Photochemotherapy; Photosensitizing Agents; Porphobilinogen; Structure-Activity Relationship; Tumor Cells, Cultured	2020
Analytical chemistry, 2020, 09-15, Volume: 92, Issue:18 Topics: Animals; Atherosclerosis; beta-Galactosidase; Boron; Cellular Senescence; Fluorescent Dyes; Male; Mice; Mice, Inbred C57BL; Molecular Structure; Nanoparticles; Porphobilinogen; Rats; Rats, Sprague-Dawley	2020
Carbon-Dipyrromethenes: Bright Cationic Fluorescent Dyes and Potential Application in Revealing Cellular Trafficking of Mitochondrial Glutathione Conjugates. Journal of the American Chemical Society, 2020, 10-07, Volume: 142, Issue:40 Topics: A549 Cells; Boron Compounds; Carbon; Cations; Cell Membrane; Cell Movement; Electrochemical Techniques; Fluorescent Dyes; Glutathione; Glutathione Transferase; Humans; Mitochondria; Molecular Structure; Optical Imaging; Photochemical Processes; Porphobilinogen; Solubility; Solvents; Spectrometry, Fluorescence	2020
Spectroscopic and In Vitro Investigations of Boron(III) Complex with Molecules (Basel, Switzerland), 2020, Oct-03, Volume: 25, Issue:19 Topics: Boron; Boron Compounds; Candida albicans; Cell Line, Tumor; Crystallography, X-Ray; Diagnostic Imaging; Doxorubicin; Electrons; Fusarium; Humans; Porphobilinogen; Solvents; Spectrometry, Fluorescence; Subcellular Fractions; Ultraviolet Rays	2020
Strong Affinity of Triazolium-Appended Dipyrromethenes (TADs) for BF Molecules (Basel, Switzerland), 2020, Oct-05, Volume: 25, Issue:19 Topics: Boron Compounds; Fluorides; Porphobilinogen; Triazoles	2020
A Boron Dipyrromethene-Based Fluorescence 'OFF-ON' Probe for Sensitive and Selective Detection of Palladium(II) Ions and Its Application in Live Cell Imaging. Chemistry, an Asian journal, 2020, Dec-01, Volume: 15, Issue:23 Topics: A549 Cells; Boron Compounds; Fluorescent Dyes; Humans; Palladium; Porphobilinogen; Sensitivity and Specificity; Single-Cell Analysis	2020
A Novel Dicationic Boron Dipyrromethene-based Photosensitizer for Antimicrobial Photodynamic Therapy against Methicillin-Resistant Staphylococcus aureus. Current medicinal chemistry, 2021, Volume: 28, Issue:21 Topics: Animals; Anti-Bacterial Agents; Anti-Infective Agents; Boron; Humans; Methicillin-Resistant Staphylococcus aureus; Mice; Microbial Sensitivity Tests; Photochemotherapy; Photosensitizing Agents; Porphobilinogen	2021
Rational Design of Near-Infrared-Absorbing Pt(II)-Chelated Azadipyrromethene Dyes as a New Generation of Photosensitizers for Synergistic Phototherapy. Inorganic chemistry, 2020, Dec-21, Volume: 59, Issue:24 Topics: Furans; HeLa Cells; Humans; Infrared Rays; Molecular Structure; Photosensitizing Agents; Phototherapy; Platinum Compounds; Porphobilinogen; Spectrophotometry, Infrared	2020
Click Conjugation of Boron Dipyrromethene (BODIPY) Fluorophores to EGFR-Targeting Linear and Cyclic Peptides. Molecules (Basel, Switzerland), 2021, Jan-23, Volume: 26, Issue:3 Topics: Boron; Boron Compounds; Cell Line, Tumor; ErbB Receptors; Fluorescent Dyes; Humans; Ligands; Peptides, Cyclic; Porphobilinogen; Protein Binding; Surface Plasmon Resonance	2021
Dual Color Imaging from a Single BF International journal of medical sciences, 2021, Volume: 18, Issue:7 Topics: Animals; Endoscopy; Female; Fluorescent Dyes; HeLa Cells; Humans; Intraoperative Care; Intravital Microscopy; Lymph Nodes; Lymphatic Metastasis; Male; Models, Animal; Neoplasms; Optical Imaging; Porphobilinogen; Rats; Spectrophotometry, Infrared; Sus scrofa; Toxicity Tests, Subacute	2021
Immobilising hairpin DNA-conjugated distyryl boron dipyrromethene on gold@polydopamine core-shell nanorods for microRNA detection and microRNA-mediated photodynamic therapy. Nanoscale, 2021, Apr-07, Volume: 13, Issue:13 Topics: Animals; Boron; DNA; Gold; HEK293 Cells; Humans; Indoles; Mice; Mice, Nude; MicroRNAs; Nanotubes; Photochemotherapy; Polymers; Porphobilinogen	2021
Near-Infrared absorbing J-Aggregates of boron dipyrromethene for high efficient photothermal therapy. Journal of colloid and interface science, 2021, Volume: 599 Topics: Boron; Nanoparticles; Phototherapy; Photothermal Therapy; Polymers; Porphobilinogen	2021
Hierarchical nano-to-molecular disassembly of boron dipyrromethene nanoparticles for enhanced tumor penetration and activatable photodynamic therapy. Biomaterials, 2021, Volume: 275 Topics: Boron; Cell Line, Tumor; Nanoparticles; Photochemotherapy; Photosensitizing Agents; Porphobilinogen	2021
Meso-substituted boron-dipyrromethene compounds: synthesis, tunable solid-state emission, and application in blue-driven LEDs. Luminescence : the journal of biological and chemical luminescence, 2021, Volume: 36, Issue:7 Topics: Boron; Boron Compounds; Luminescence; Porphobilinogen	2021
Synergistic photodynamic and photothermal therapy of BODIPY-conjugated hyaluronic acid nanoparticles. Journal of biomaterials science. Polymer edition, 2021, Volume: 32, Issue:15 Topics: Boron; Cell Line, Tumor; Hyaluronic Acid; Nanoparticles; Photochemotherapy; Photothermal Therapy; Porphobilinogen	2021
The BODIPY-based chemosensor for the fluorometric determination of organochlorine pesticide dicofol. Food chemistry, 2022, Feb-15, Volume: 370 Topics: Boron; Dicofol; Humans; Pesticides; Porphobilinogen	2022
A boron dipyrromethene (BODIPY) based probe for selective passive sampling of atmospheric nitrous acid (HONO) indoors. The Analyst, 2021, Sep-13, Volume: 146, Issue:18 Topics: Air Pollution, Indoor; Boron; Humans; Nitrites; Nitrous Acid; Porphobilinogen	2021
Galactose conjugated boron dipyrromethene and hydrogen bonding promoted J-aggregates for efficiently targeted NIR-II fluorescence assistant photothermal therapy. Journal of colloid and interface science, 2022, Apr-15, Volume: 612 Topics: Boron; Cell Line, Tumor; Fluorescence; Galactose; Hydrogen Bonding; Nanoparticles; Phototherapy; Photothermal Therapy; Porphobilinogen	2022
BODIPY and 2,3-Dihydrophthalazine-1,4-Dione Conjugates As Heavy Atom-Free Chemiluminogenic Photosensitizers. ACS applied bio materials, 2021, 06-21, Volume: 4, Issue:6 Topics: Boron; Boron Compounds; Luminol; Photochemotherapy; Photosensitizing Agents; Porphobilinogen; Singlet Oxygen	2021
Near-Infrared Emitting Ir(III) Complexes Bearing a Dipyrromethene Ligand for Oxygen Imaging of Deeper Tissues Analytical chemistry, 2022, 02-15, Volume: 94, Issue:6 Topics: Iridium; Ligands; Oxygen; Porphobilinogen	2022
Femtosecond Spectroscopy and Nonlinear Optical Properties of aza-BODIPY Derivatives in Solution. Chemistry (Weinheim an der Bergstrasse, Germany), 2022, Mar-22, Volume: 28, Issue:17 Topics: Boron; Boron Compounds; Fluorescent Dyes; Porphobilinogen; Spectrum Analysis	2022
Light-Harvesting Crystals Formed from BODIPY-Proline Biohybrid Conjugates: Antenna Effects and Excitonic Coupling. The journal of physical chemistry. A, 2022, Mar-10, Volume: 126, Issue:9 Topics: Boron; Boron Compounds; Porphobilinogen; Proline	2022
Circularly polarized luminescence from helical N,O-boron-chelated dipyrromethene (BODIPY) derivatives. Chemical communications (Cambridge, England), 2022, Mar-18, Volume: 58, Issue:23 Topics: Boron; Boron Compounds; Luminescence; Porphobilinogen	2022
Highly Robust Rhenium(I) Bipyridyl Complexes Containing Dipyrromethene-BF ChemSusChem, 2022, Jul-21, Volume: 15, Issue:14 Topics: 2,2'-Dipyridyl; Carbon Dioxide; Light; Oxidation-Reduction; Porphobilinogen; Rhenium	2022
Exploring BODIPY derivatives as photosensitizers for antibacterial photodynamic therapy. Photodiagnosis and photodynamic therapy, 2022, Volume: 39 Topics: Animals; Anti-Bacterial Agents; Anti-Infective Agents; Bacteria; Boron; Boron Compounds; Mice; Photochemotherapy; Photosensitizing Agents; Porphobilinogen; Reactive Oxygen Species; Staphylococcus aureus	2022
Enhancement of Two-Photon Absorption in Boron-Dipyrromethene (BODIPY) Derivatives. Molecules (Basel, Switzerland), 2022, Apr-29, Volume: 27, Issue:9 Topics: Boron; Boron Compounds; Fluorescent Dyes; Porphobilinogen	2022
A boron dipyrromethene chiral at boron and carbon with a bent geometry: synthesis, resolution and chiroptical properties. Chemical communications (Cambridge, England), 2022, Jun-23, Volume: 58, Issue:51 Topics: Boron; Carbon; Circular Dichroism; Porphobilinogen	2022
Phototoxicity of BODIPY in long-term imaging can be reduced by intramolecular motion. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2022, Volume: 21, Issue:9 Topics: Boron; Boron Compounds; Molecular Probes; Oxygen; Porphobilinogen	2022
Phenylthiol-BODIPY-based supramolecular metallacycles for synergistic tumor chemo-photodynamic therapy. Proceedings of the National Academy of Sciences of the United States of America, 2022, 07-19, Volume: 119, Issue:29 Topics: Boron Compounds; Cell Line, Tumor; Coordination Complexes; Drug Synergism; Humans; Neoplasms; Photochemotherapy; Platinum; Porphobilinogen	2022
Boron Dipyrromethene-Based Phototheranostics for Near Infrared Fluorescent and Photoacoustic Imaging-Guided Synchronous Photodynamic and Photothermal Therapy of Cancer. The journal of physical chemistry letters, 2022, Sep-01, Volume: 13, Issue:34 Topics: Boron; Boron Compounds; HeLa Cells; Humans; Nanoparticles; Neoplasms; Photoacoustic Techniques; Photothermal Therapy; Porphobilinogen	2022
Self-Assembled Aza-Boron-Dipyrromethene for Ferroptosis-Boosted Sonodynamic Therapy. Angewandte Chemie (International ed. in English), 2022, 10-10, Volume: 61, Issue:41 Topics: Boron; Cell Line, Tumor; Cysteine; Ferroptosis; Humans; Nanoparticles; Neoplasms; Porphobilinogen; Reactive Oxygen Species; Singlet Oxygen	2022
A Hypoxia-Activated Prodrug Conjugated with a BODIPY-Based Photothermal Agent for Imaging-Guided Chemo-Photothermal Combination Therapy. ACS applied materials & interfaces, 2022, Sep-14, Volume: 14, Issue:36 Topics: Azo Compounds; Boron; Boron Compounds; Camptothecin; Cell Line, Tumor; Humans; Hyperthermia, Induced; Hypoxia; Nanoparticles; Neoplasms; Phototherapy; Photothermal Therapy; Porphobilinogen; Prodrugs	2022
Mitochondria-Targeting Boron Dipyrromethene Based Photosensitizers for Enhanced Photodynamic Therapy: Synthesis, Optical Properties, and in vitro Biological Activity. ChemPlusChem, 2022, Volume: 87, Issue:9 Topics: Boron; Coloring Agents; Mitochondria; Photochemotherapy; Photosensitizing Agents; Porphobilinogen; Singlet Oxygen	2022
BODIPY-based metal-organic frameworks as efficient electrochemiluminescence emitters for telomerase detection. Chemical communications (Cambridge, England), 2022, Oct-13, Volume: 58, Issue:82 Topics: Biosensing Techniques; Boron; Boron Compounds; Electrochemical Techniques; Limit of Detection; Luminescent Measurements; Metal-Organic Frameworks; Porphobilinogen; Telomerase	2022
Stability of Dibromo-Dipyrromethene Complexes Coordinated with B, Zn, and Cd in Solutions of Various Acidities. Molecules (Basel, Switzerland), 2022, Dec-12, Volume: 27, Issue:24 Topics: Cadmium; Ethanol; Porphobilinogen; Solvents; Zinc	2022
Cinnamoyl Dipyrromethenes as Fluorescence Zinc(II) Ion Sensor. Chemistry, an Asian journal, 2023, Jun-15, Volume: 18, Issue:12 Topics: Chelating Agents; Fluorescence; Fluorescent Dyes; Ions; Porphobilinogen; Spectrometry, Fluorescence; Zinc	2023
A Tetrazine-Caged Carbon-Dipyrromethene as a Bioorthogonally Activatable Fluorescent Probe. Chemistry, an Asian journal, 2023, Sep-01, Volume: 18, Issue:17 Topics: Cycloaddition Reaction; Fluorescent Dyes; Heterocyclic Compounds; Humans; Porphobilinogen	2023