Compounds > porphobilinogen

porphobilinogen and boron

porphobilinogen has been researched along with boron in 69 studies

Research

Studies (69)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's10 (14.49)29.6817
2010's30 (43.48)24.3611
2020's29 (42.03)2.80

Authors

AuthorsStudies
Amat-Guerri, F; Bañuelos Prieto, J; Costela, A; García-Moreno, I; Gómez, C; Liras, M; López Arbeloa, F; López Arbeloa, I; Sastre, R1
Bonardi, L; Retailleau, P; Ulrich, G; Ziessel, R1
Bonardi, L; Ulrich, G; Ziessel, R1
Fukuzumi, S; Hattori, S; Lemmetyinen, H; Nagano, T; Ohkubo, K; Sunahara, H; Tkachenko, NV; Urano, Y; Wada, Y1
Qian, X; Xiao, Y; Zhang, X1
Hirose, K; Iino, M; Inoue, T; Kikuchi, K; Mizushima, A; Nagano, T; Sunahara, H; Urano, Y; Yogo, T1
Descalzo, AB; Hoffmann, K; Rurack, K; Shen, Z; Weller, MG; Xu, HJ; Xue, ZL; You, XZ1
Descalzo, AB; Rurack, K; Shen, Z; Xu, HJ1
Bandichhor, R; Burgess, K; Hall, MJ; Loudet, A; McDonnell, SO; O'Shea, DF; Palma, A1
Goeb, S; Harriman, A; Mallon, LJ; Ulrich, G; Ziessel, R1
Benniston, AC; Clegg, W; Copley, G; Harriman, A; Harrington, RW; Howgego, D1
Burgess, K; Han, J; Lee, HB; Lim, SH; Nowak-Sliwinska, P; Thivierge, C; van den Bergh, H; Wagnières, G1
Ando, Y; Citterio, D; Hiruta, Y; Suzuki, K1
Bae, SW; Hong, JI; Kim, H; Shin, IS1
Chung, PH; Kuimova, MK; Levitt, JA; Qu, J; Suhling, K; Wang, Y; Yahioglu, G1
Bian, Y; Chen, Y; Jiang, J; Wan, L; Wang, H1
Madhu, S; Rao, MR; Ravikanth, M; Shaikh, MS1
Lakshmi, V; Ravikanth, M1
Gu, X; Liu, C; Zhu, YC; Zhu, YZ1
Liu, Y; Wu, W; Yang, P; Yu, X; Zhao, J1
Ermilov, EA; Huang, Y; Liu, JY; Menting, R; Ng, DK; Röder, B1
Ermilov, EA; Huang, YS; Liu, JY; Menting, R; Ng, DK; Röder, B1
Cao, J; Chae, WS; He, Y; Jung, H; Kang, C; Kim, JS; Lee, JH; Park, N; Peng, X; Suh, M; Yang, Z1
El-Khouly, ME; Fukuzumi, S; Ng, DK; Ohkubo, K; Shi, WJ1
Chen, TL; Leblebici, SY; Ma, B; Olalde-Velasco, P; Yang, W1
Liu, SR; Vedamalai, M; Wu, SP1
D'Souza, F; El-Khouly, ME; Fukuzumi, S1
Madhu, S; Ravikanth, M1
Hanaoka, K; Kamiya, M; Komatsu, T; Nagano, T; Takahashi, H; Terai, T; Ueno, T; Umeda, N; Urano, Y1
Banfi, S; Barbieri, P; Caruso, E; Orlandi, VT; Rybtke, M; Tolker-Nielsen, T1
Han, Z; Wang, C; Xiao, Y; Zhang, X1
Alnoman, RB; Black, FA; Clegg, W; Costello, B; Hall, MJ; Herrebout, W; Knight, JG; O'Connor, DC; Peacock, RD; Rihn, S; Waddell, PG1
Choi, M; Churchill, DG; Jang, YJ; Jon, S; Kim, Y; Mulay, SV1
Bulut, I; Chávez, P; Fall, S; Hébraud, A; Heinrich, B; Heiser, T; Huaulmé, Q; Leclerc, N; Lévêque, P; Méry, S; Mirloup, A1
Anna, JM; Chenoweth, DM; Das, S; Lee, Y; Malamakal, RM; Meloni, S1
Cheung, YK; Fong, WP; Gao, D; Lo, PC; Ma, C; Ng, DKP; Wong, KS; Zhao, S; Zhou, Y1
Cao, JJ; Li, XQ; Liu, JY; Su, D; Wang, ZW; Yang, DC1
Du, J; Fan, J; Peng, X; Sun, W; Zhao, X1
Bui, HT; Cho, S; Choi, KH; Kim, B; Kim, HJ; Mai, DK; Park, BJ1
Lo, PC; Wang, Q; Wong, RCH; Yu, L1
Ahmed, HA; Alnoman, RB; Hagar, M; Knight, JG; Parveen, S1
Avellanal-Zaballa, E; Bañuelos, J; García-Moreno, I; Gómez, AM; Lopez, JC; Permingeat, C; Uriel, C; Ventura, J1
Arbeloa, T; Bañuelos, J; Bautista-Hernández, CI; Becerra-González, JG; Enríquez-Palacios, E; López-Arbeloa, I; Peña-Cabrera, E1
Colombani-Garay, D; Duan, C; Han, G; Huang, L; Lin, W1
Chen, JA; Fu, W; Gu, X; Guo, W; Hu, W; Ouyang, Z; Pan, H; Sun, N; Tan, J; Wang, Y; Wang, Z1
Antina, E; Berezin, M; Boichuk, S; Guseva, G; Islamov, D; Kayumov, A; Lisovskaya, S; Lodochnikova, O; Nikitina, L; Pavelyev, R; Usachev, K1
Chan, BC; Dharmaratne, P; Fung, KP; Ip, M; Lau, CBS; Lau, KM; Ng, DK; Wang, B; Wong, RC; Yu, L1
Jois, SD; Kaufman, NEM; Singh, SS; Vicente, MDGH; Williams, TM; Zhou, Z1
Bai, Q; Choi, CHJ; Choi, CKK; Dai, G; Ng, DKP; Xiao, Y; Yang, C; Zhou, Y1
Li, Z; Xia, J; Xie, Z; Zheng, M1
Kong, H; Kong, X; Liu, J; Zhang, K; Zhang, Q; Zhang, Y; Zhang, YN; Zhao, R; Zhao, Y1
Chen, Z; Liu, H; Liu, R; Su, H; Zhu, H; Zhu, S1
Cao, J; Chen, B; Kong, X; Lu, J; Zhang, K; Zhang, Q; Zhang, YN; Zubair Iqbal, M1
Feng, L; Huangfu, C; Li, C; Wang, F; Zhang, X; Zhu, M1
Bentley, JN; Caputo, CB; Crilley, LR; Nodeh-Farahani, D; VandenBoer, TC1
Cheng, Q; Dang, H; Teng, C; Tian, Y; Xie, K; Yan, L1
Algi, F; Degirmenci, A; Karaduman, T; Sonkaya, Ö; Soylukan, C1
Andraud, C; Berginc, G; Bondar, MV; Chang, HJ; David, S; Hagan, DJ; Jacquemin, D; Le Guennic, B; Maury, O; Munera, N; Van Stryland, EW1
Benniston, AC; Harriman, A; Karlsson, JKG; Waddell, PG; Waly, SM1
Liu, ZF; Niu, LY; Teng, KX; Wang, LY; Yang, QZ1
Mou, C; Shi, Q; Xie, Z; Zheng, M1
Han, Y; Jia, J; Li, Z; Song, G; Song, Y; Wang, Y; Zhang, X; Zhou, W1
Dündar, E; Işık, M; Şahin, E; Tanyeli, C1
Durandin, N; Efimov, A; Ilina, P; Kähärä, I; Laaksonen, T; Lisitsyna, E; Vuorimaa-Laukkanen, E1
Lan, M; Li, B; Li, X; Pang, E; Song, X; Tan, S; Wang, B; Xing, X; Yang, K; Yi, J1
Chen, H; Chen, Y; Li, X; Liang, L; Wang, D; Xiang, H; You, C; Zhao, Y1
Du, L; Lin, Z; Liu, JY; Lu, ZY; Luo, CM; Wen, LF; Yang, DC1
Chen, Z; Hu, P; Huang, M; Liu, JY; Weng, XL; Yang, DC; Zhu, CH1
Fu, H; Lei, J; Shen, Z; Wu, F; Xu, Z; Zhu, D1

Reviews

4 review(s) available for porphobilinogen and boron

ArticleYear
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

65 other study(ies) available for porphobilinogen and boron

ArticleYear
Photophysical and lasing properties of new analogs of the boron-dipyrromethene laser dye pyrromethene 567 incorporated into or covalently bounded to solid matrices of poly(methyl methacrylate).
    Photochemistry and photobiology, 2003, Volume: 78, Issue:1

    Topics: Boron; Chelating Agents; Fluorescent Dyes; Fluorometry; Lasers; Photosensitizing Agents; Polymethyl Methacrylate; Porphobilinogen

2003
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
    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
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
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
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
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
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
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
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