Page last updated: 2024-08-18

pyrroles and pyrroloquinoline

pyrroles has been researched along with pyrroloquinoline in 62 studies

Research

Studies (62)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	17 (27.42)	29.6817
2010's	36 (58.06)	24.3611
2020's	9 (14.52)	2.80

Authors

Authors	Studies
Ennis, MD; Nieman, JA	1
Alcaraz, MJ; Gonzalez-Tejero, A; Molina, P; Rioja, I; Tárraga, A; Terencio, MC; Ubeda, A	1
Cheng, M; Hua, H; Li, X; Pei, Y	1
Katz, E; Willner, I	1
Kubota, LT; Pessôa, CA; Yamashita, M	1
Adachi, O; Matsushita, K; Tanasupawat, S; Toyama, H; Yoshihara, N	1
Dalla Via, L; Ferlin, MG; Gia, OM	1
Dixit, A; Gaur, S; Kashaw, SK; Saxena, AK	1
Chilin, A; Dalla Via, L; Ferlin, MG; Guiotto, A; Marzano, C; Moro, S; Zagotto, G	1
Delfourne, E; Legentil, L; Lesur, B	1
Benel, L; Bertrand, V; Delfourne, E; Legentil, L; Lesur, B	1
Abdullah, WN; Al-Said, NH; Shawakfeh, KQ	1
Deng, C; Dong, L; Gu, J; Liu, T; Shen, X; Wang, J; Wu, H; Xue, R; Zhang, S	1
Kyrychenko, A; Waluk, J	1
Ariga, H; Iguchi-Ariga, S; Miyazaki, S; Nakano, M; Nunome, K	1
Chiarelotto, G; Dalla Via, L; Ferlin, MG; Gia, O	1
Chen, X; Jabri, S; Jin, H; Kim, CU; Lansdown, R; Metobo, S; Mish, M; Tsiang, M; Wright, M	1
Chen, K; Heasley, SE; Hopkins, TA; Knechtel, ML; Nair, SK; Nieman, JA; Nugent, RA; Oien, NL; Schultz, BL; Stephanski, KJ; Wathen, MW; Wieber, JL; Zerth, HM	1
Barraja, P; Brun, P; Caracausi, L; Carbone, A; Castagliuolo, I; Cirrincione, G; Dall'acqua, F; Diana, P; Montalbano, A; Palù, G; Salvador, A; Vedaldi, D	1
Basso, G; Bortolozzi, R; Brun, P; Castagliuolo, I; Ferlin, MG; Hamel, E; Viola, G	1
Chu, YH; Chu, YW; Hwang, J; Lin, CM; Tsai, HP; Tseng, MC	1
He, B; Li, HH; Liu, SQ	1
Gerth, K; Jansen, R; Mohr, KI; Müller, R; Okanya, PW	1
Barraja, P; Brun, P; Caracausi, L; Carbone, A; Castagliuolo, I; Cirrincione, G; Dall'Acqua, F; Diana, P; Montalbano, A; Salvador, A; Tisi, S; Vedaldi, D	1
Barbieri, L; Carter, GT; Eustáquio, AS; Feng, X; Fielding, EN; He, M; Janso, JE; Jensen, PR; Koehn, FE; Leighton, M; Liu, H; McDonald, L; Miyanaga, A; Moore, BS	1
Dagousset, G; Masson, G; Retailleau, P; Zhu, J	1
Liu, J; Wu, J; Ye, S	1
Jiang, B; Li, G; Li, TJ; Tu, SJ; Wang, XS; Yao, CS; Yin, HM	1
Kong, L; Smith, W; Yang, C; Yu, L; Zhu, J; Zhu, Q; Zhu, S	1
Cao, Z; Ding, F; Ding, M; Ke, K; Zhang, J; Zhang, Q	1
Nagasawa, K; Takayama, Y; Tatekabe, S; Yamada, T	1
Chen, K; Li, JR; Li, X; Zhu, HL	1
Aisa, HA; Chen, QB; Lee, SS; Xin, XL; Yang, Y	1
He, B; Li, H; Liu, S; Tao, H; Wei, A	1
Fang, Q; Fei, G; Gong, N; Jin, L; Liu, M; Pan, X; Sang, S; Sun, X; Xu, T; Yu, Z; Zhao, L; Zhao, N; Zhong, C	1
Chen, GQ; Liu, CJ; Wang, Z; Yu, GP	1
Appun, J; Boomhoff, M; Schneider, C; Yadav, AK	1
Jeganmohan, M; Manoharan, R	1
Balasso, A; Caliceti, P; Carta, D; Ferlin, MG	1
Chen, F; Chen, T; Chen, W; Shao, Y; Wang, B	1
Chen, X; He, Z; Tang, T; Yang, C	1
Kogler, H; Pulte, A; Spiteller, P; Wagner, S	1
He, J; Ma, C; Ran, T; Wang, W; Wei, Q; Xu, D	1
Agrawal, A; Bajpai, P; Darra, A	1
Abdel-Mogib, M; Al-Mourabit, A; Atanasov, AG; Bishayee, A; El-Demerdash, A; Hooper, JNA	1
Bansal, A; Bhardwaj, V; Chattopadhyay, P; Nehra, S; Saraswat, D	1
Lohmann, JS; Pulte, A; Spiteller, P; Steglich, W; von Nussbaum, M; Wagner, S	1
Chao, B; Chen, J; David, LL; Li, BX; Xiao, X	1
Bojarski, AJ; Dubiel, K; Grychowska, K; Kurczab, R; Matłoka, M; Moszczyński-Pętkowski, R; Pieczykolan, J; Satała, G; Śliwa, P; Zajdel, P	1
Sugimoto, K	1
Almansour, AI; Arumugam, N; Mahalingam, SM; Maruoka, K; Suresh Kumar, R; Thangamani, S; Villa, P	1
Chi, Y; Han, N; Li, Y; Wang, B; Wang, Z; Zhao, K	1
Funk, MA; Gonen, T; Halaby, SL; Ting, CP; van der Donk, WA; Zhang, Z	1
Backenköhler, J; Himstedt, R; Jaeger, RJR; Lieunang Watat, ML; Rupcic, Z; Spiteller, P; Stadler, M; Wagner, S	1
Bobers, J; Brunschweiger, A; Dinter, R; Gramse, C; Kockmann, N; Neukirch, L; Sakthithasan, P; Škopić, MK; Weberskirch, R	1
Gantseva, A; Gantseva, E; Ilin, I; Krysin, M; Kutov, D; Ledenyova, I; Novichikhina, N; Podoplelova, N; Shikhaliev, K; Sulimov, A; Sulimov, V; Tashchilova, A	1
Annadurai, B; Geetha Thanuja, K; Thankappan, S; Uthandi, S	1
Delfourne, E; Levy, T; Marchand, L; Pilotte, L; Rodriguez, F; Stroobant, V; Van den Eynde, B	1
Adhikari, A; Dong, LB; Luo, J; Rader, C; Shen, B; Yan, X; Yang, D; Ye, F	1
Chen, L; Dai, X; Miao, D; Tao, J; Wang, Y; Wu, J; Xia, W; Yi, X	1
Gu, XF; Shi, YJ; Wang, F; Xu, YX; Yang, B; Zhou, J	1
Dong, R; Li, W; Liu, JY; Shi, L; Sun, LP; Wang, C; Wang, CM; Wang, M; Wang, YW; Xu, Y; Zhang, C; Zhang, HE; Zhang, Y	1

Reviews

4 review(s) available for pyrroles and pyrroloquinoline

Article	Year
A functional scaffold in marine alkaloid: an anticancer moiety for human. Current medicinal chemistry, 2013, Volume: 20, Issue:31 Topics: Alkaloids; Animals; Antineoplastic Agents; Humans; Indoles; Neoplasms; Oxazoles; Pyridines; Pyrroles; Quinolines	2013
Microbe-mitochondrion crosstalk and health: An emerging paradigm. Mitochondrion, 2018, Volume: 39 Topics: Fatty Acids, Volatile; Fermentation; Health; Humans; Metabolism; Microbiota; Mitochondria; Pyrroles; Quinolines	2018
Batzella, Crambe and Monanchora: Highly Prolific Marine Sponge Genera Yielding Compounds with Potential Applications for Cancer and Other Therapeutic Areas. Nutrients, 2018, Jan-02, Volume: 10, Issue:1 Topics: Alkaloids; Animals; Antineoplastic Agents; Crambe Sponge; Guanidines; Humans; Molecular Mimicry; Molecular Structure; Neoplasms; Porifera; Pyrroles; Quinolines; Structure-Activity Relationship	2018
[Development of Novel Preparations for Nitrogen Heterocycles Based on Cascade Reactions]. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 2018, Volume: 138, Issue:9 Topics: Azo Compounds; Catalysis; Cyclization; Gold; Heterocyclic Compounds; Nitrogen Compounds; Organic Chemistry Phenomena; Pyrroles; Pyrrolizidine Alkaloids; Quinolines; Thiosemicarbazones	2018

Other Studies

58 other study(ies) available for pyrroles and pyrroloquinoline

Article	Year
Enantioselective synthesis of the pyrroloquinoline core of the martinellines. Organic letters, 2000, May-18, Volume: 2, Issue:10 Topics: Crystallography, X-Ray; Indicators and Reagents; Models, Molecular; Molecular Structure; Plants, Medicinal; Pyrroles; Quinolines; Stereoisomerism	2000
A pyrroloquinazoline derivative with anti-inflammatory and analgesic activity by dual inhibition of cyclo-oxygenase-2 and 5-lipoxygenase. European journal of pharmacology, 2002, Jan-11, Volume: 434, Issue:3 Topics: Analgesics; Animals; Anti-Inflammatory Agents, Non-Steroidal; Arachidonate 5-Lipoxygenase; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Cyclooxygenase Inhibitors; Dose-Response Relationship, Drug; Edema; Enzyme Inhibitors; Female; Humans; Isoenzymes; Lipoxygenase Inhibitors; Membrane Proteins; Mice; Monocytes; Pain Measurement; Prostaglandin-Endoperoxide Synthases; Pyrroles; Quinazolines; Quinolines; Sheep	2002
A new pyrroloquinazoline alkaloid from Linaria vulgaris. Chemical & pharmaceutical bulletin, 2002, Volume: 50, Issue:10 Topics: Alkaloids; Drugs, Chinese Herbal; Linaria; Plant Components, Aerial; Pyrroles; Quinolines	2002
A biofuel cell with electrochemically switchable and tunable power output. Journal of the American Chemical Society, 2003, Jun-04, Volume: 125, Issue:22 Topics: Bioelectric Energy Sources; Copper; Cytochrome c Group; Electrochemistry; Electrodes; Flavin-Adenine Dinucleotide; Glucose; Glucose Oxidase; Oxidation-Reduction; PQQ Cofactor; Pyrroles; Quinolines; Quinolones; Quinones	2003
Electrochemical behavior of pyrroloquinoline quinone immobilized on silica gel modified with zirconium oxide. Journal of colloid and interface science, 2003, Jul-01, Volume: 263, Issue:1 Topics: Benzoquinones; Calcium; Carbon; Electrochemistry; Hydrogen-Ion Concentration; Ions; Models, Chemical; NAD; Pyrroles; Quinolines; Silicon Dioxide; Spectrophotometry; Ultraviolet Rays; Zirconium	2003
Purification and characterization of membrane-bound quinoprotein quinate dehydrogenase. Bioscience, biotechnology, and biochemistry, 2003, Volume: 67, Issue:10 Topics: Acinetobacter; Alcohol Oxidoreductases; Bacteria, Aerobic; Bacterial Proteins; Gluconobacter; Membrane Proteins; Methods; Pyrroles; Quinolines	2003
Synthesis and antiproliferative activity of some new DNA-targeted alkylating pyrroloquinolines. Bioorganic & medicinal chemistry, 2004, Feb-15, Volume: 12, Issue:4 Topics: Alkylating Agents; Alkylation; Animals; Cell Division; Cell Line; Circular Dichroism; DNA; Humans; Inhibitory Concentration 50; Molecular Structure; Pyrroles; Quinolines; Salmon; Substrate Specificity	2004
Development of CoMFA, advance CoMFA and CoMSIA models in pyrroloquinazolines as thrombin receptor antagonist. Bioorganic & medicinal chemistry, 2004, Jul-01, Volume: 12, Issue:13 Topics: Catalysis; Hydrogen Bonding; Hydrophobic and Hydrophilic Interactions; Models, Chemical; Models, Molecular; Molecular Structure; Pyrroles; Quantitative Structure-Activity Relationship; Quinolines; Receptors, Thrombin	2004
New water soluble pyrroloquinoline derivatives as new potential anticancer agents. Bioorganic & medicinal chemistry, 2005, Aug-01, Volume: 13, Issue:15 Topics: Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Humans; Hydrogen-Ion Concentration; Magnetic Resonance Spectroscopy; Molecular Structure; Pyrroles; Quinolines; Solubility; Water	2005
Aza-analogues of the marine pyrroloquinoline alkaloids wakayin and tsitsikammamines: synthesis and topoisomerase inhibition. Bioorganic & medicinal chemistry letters, 2006, Jan-15, Volume: 16, Issue:2 Topics: Animals; Aza Compounds; Cyclization; Humans; Indole Alkaloids; Molecular Structure; Pyrroles; Quinolines; Structure-Activity Relationship; Topoisomerase I Inhibitors	2006
Synthesis and antitumor characterization of pyrazolic analogues of the marine pyrroloquinoline alkaloids: wakayin and tsitsikammamines. Journal of medicinal chemistry, 2006, May-18, Volume: 49, Issue:10 Topics: Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Drug Screening Assays, Antitumor; Humans; Indole Alkaloids; Pyrazoles; Pyrroles; Quinolines; Structure-Activity Relationship; Topoisomerase I Inhibitors; Topoisomerase II Inhibitors	2006
Cyclization of free radicals at the C-7 position of ethyl indole-2-carboxylate derivatives: an entry to a new class of Duocarmycin Analogues. Molecules (Basel, Switzerland), 2005, Dec-31, Volume: 10, Issue:12 Topics: Alkylating Agents; Cyclization; Duocarmycins; Free Radicals; Indoles; Molecular Structure; Pyrroles; Quinolines	2005
Simultaneous determination of blood glucose and isoleucine levels in rats after chronic alcohol exposure by microwave-assisted derivatization and isotope dilution gas chromatography/mass spectrometry. Rapid communications in mass spectrometry : RCM, 2008, Volume: 22, Issue:2 Topics: Administration, Oral; Alcoholism; Animals; Biomarkers; Blood Glucose; Disease Models, Animal; Drug Therapy, Combination; Ethanol; Gas Chromatography-Mass Spectrometry; Isoleucine; Isotope Labeling; Male; Microwaves; Pyrroles; Quinolines; Rats; Rats, Sprague-Dawley	2008
Distribution and favorable binding sites of pyrroloquinoline and its analogues in a lipid bilayer studied by molecular dynamics simulations. Biophysical chemistry, 2008, Volume: 136, Issue:2-3 Topics: Binding Sites; Computer Simulation; Hydrogen Bonding; Lipid Bilayers; Molecular Structure; Protons; Pyrroles; Quinolines; Solvents; Water	2008
Pyrroloquinoline quinone prevents oxidative stress-induced neuronal death probably through changes in oxidative status of DJ-1. Biological & pharmaceutical bulletin, 2008, Volume: 31, Issue:7 Topics: Animals; Antioxidants; Ascorbic Acid; Blotting, Western; Cell Death; Cell Survival; Dose-Response Relationship, Drug; Female; Hydrogen Peroxide; Microtubule-Associated Proteins; Neurons; Oxidants; Oxidation-Reduction; Oxidative Stress; Oxidopamine; Pregnancy; Protein Binding; Protein Deglycase DJ-1; Pyrroles; Quinolines; Rats; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Tetrazolium Salts; Thiazoles; Tumor Cells, Cultured; Vitamin E	2008
DNA-targeting pyrroloquinoline-linked butenone and chalcones: synthesis and biological evaluation. European journal of medicinal chemistry, 2009, Volume: 44, Issue:7 Topics: Antineoplastic Agents; Butanones; Cell Line, Tumor; Cell Proliferation; Chalcones; DNA; Humans; Pyrroles; Quinolines; Topoisomerase II Inhibitors	2009
Tricyclic HIV integrase inhibitors: VI. SAR studies of 'benzyl flipped' C3-substituted pyrroloquinolines. Bioorganic & medicinal chemistry letters, 2009, Feb-15, Volume: 19, Issue:4 Topics: Administration, Oral; Animals; Anti-HIV Agents; Dogs; Drug Design; HIV Integrase Inhibitors; Humans; Molecular Structure; Pyrroles; Quinolines; Rats; Structure-Activity Relationship	2009
Modifications of C-2 on the pyrroloquinoline template aimed at the development of potent herpesvirus antivirals with improved aqueous solubility. Bioorganic & medicinal chemistry letters, 2010, May-15, Volume: 20, Issue:10 Topics: Antiviral Agents; Cytomegalovirus; DNA-Directed DNA Polymerase; Herpesviridae; Herpesvirus 1, Human; Herpesvirus 3, Human; Humans; Nucleic Acid Synthesis Inhibitors; Pyrroles; Quinolines; Solubility; Structure-Activity Relationship	2010
Synthesis of pyrrolo[3,2-h]quinolinones with good photochemotherapeutic activity and no DNA damage. Bioorganic & medicinal chemistry, 2010, Jul-01, Volume: 18, Issue:13 Topics: Cell Line, Tumor; DNA Damage; Furocoumarins; Humans; Membrane Potential, Mitochondrial; Phosphatidylserines; Photosensitizing Agents; Pyrroles; Quinolines; Reactive Oxygen Species	2010
Synthesis and in vitro evaluation of 3h-pyrrolo[3,2-f]-quinolin-9-one derivatives that show potent and selective anti-leukemic activity. ChemMedChem, 2010, Aug-02, Volume: 5, Issue:8 Topics: Antineoplastic Agents; Apoptosis; Cell Division; Cell Line, Tumor; Drug Screening Assays, Antitumor; G2 Phase; Humans; Leukemia; Pyrroles; Quinolines; Reactive Oxygen Species; Structure-Activity Relationship; Tubulin; Tubulin Modulators	2010
One-pot synthesis of luotonin A and its analogues. Organic letters, 2011, Mar-04, Volume: 13, Issue:5 Topics: DNA Topoisomerases, Type I; Humans; Molecular Structure; Peganum; Pyrroles; Quinazolines; Quinolines; Quinones; Topoisomerase I Inhibitors	2011
[The extracellular signal-regulated kinase was promoted by pyrroloquinoline quinine in cultured Schwann cells]. Zhonghua zheng xing wai ke za zhi = Zhonghua zhengxing waike zazhi = Chinese journal of plastic surgery, 2010, Volume: 26, Issue:6 Topics: Animals; Cell Proliferation; Cells, Cultured; Extracellular Signal-Regulated MAP Kinases; Mitogen-Activated Protein Kinases; Pyrroles; Quinolines; Rats; Rats, Sprague-Dawley; Schwann Cells; Signal Transduction	2010
Marinoquinolines A-F, pyrroloquinolines from Ohtaekwangia kribbensis (Bacteroidetes). Journal of natural products, 2011, Apr-25, Volume: 74, Issue:4 Topics: Anti-Bacterial Agents; Antifungal Agents; Antimalarials; Antineoplastic Agents; Bacteroidetes; Drug Screening Assays, Antitumor; Female; Humans; India; Inhibitory Concentration 50; Microbial Sensitivity Tests; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Plasmodium falciparum; Pyrroles; Quinolines	2011
Pyrrolo[3,2-h]quinazolines as photochemotherapeutic agents. ChemMedChem, 2011, Jul-04, Volume: 6, Issue:7 Topics: Apoptosis; Cell Line, Tumor; Drug Screening Assays, Antitumor; Furocoumarins; Humans; Photosensitizing Agents; Pyrroles; Quinolines; Reactive Oxygen Species; Structure-Activity Relationship; Ultraviolet Rays	2011
Discovery and assembly-line biosynthesis of the lymphostin pyrroloquinoline alkaloid family of mTOR inhibitors in Salinispora bacteria. Journal of the American Chemical Society, 2011, Aug-31, Volume: 133, Issue:34 Topics: Actinomycetales; Alkaloids; Enzyme Inhibitors; Pyrroles; Quinolines; TOR Serine-Threonine Kinases	2011
Chiral phosphoric acid-catalyzed enantioselective three-component Povarov reaction using cyclic enethioureas as dienophiles: stereocontrolled access to enantioenriched hexahydropyrroloquinolines. Chemistry (Weinheim an der Bergstrasse, Germany), 2012, May-07, Volume: 18, Issue:19 Topics: Aldehydes; Aniline Compounds; Bignoniaceae; Catalysis; Combinatorial Chemistry Techniques; Molecular Structure; Phosphoric Acids; Pyrroles; Quinolines; RNA, Plant; Stereoisomerism; Thiourea	2012
Generation of 4-polyfluoroaryl pyrrolo[1,2-a]quinolines via C-H bond activation. Chemical communications (Cambridge, England), 2012, May-21, Volume: 48, Issue:41 Topics: Catalysis; Halogenation; Palladium; Pyrroles; Quinolines	2012
A one-pot multicomponent strategy for stereospecific construction of tricyclic pyrrolo[1,2-a]quinolines. Chemical communications (Cambridge, England), 2012, Dec-21, Volume: 48, Issue:98 Topics: Models, Molecular; Molecular Structure; Pyrroles; Quinolines; Stereoisomerism	2012
Pyrroloquinoline quinine inhibits RANKL-mediated expression of NFATc1 in part via suppression of c-Fos in mouse bone marrow cells and inhibits wear particle-induced osteolysis in mice. PloS one, 2013, Volume: 8, Issue:4 Topics: Acid Phosphatase; Animals; Bone Marrow Cells; Cell Death; Cell Differentiation; Gene Expression Regulation; Isoenzymes; Mice; Mice, Inbred C57BL; NFATC Transcription Factors; Osteoclasts; Osteogenesis; Osteolysis; Polyethylenes; Proto-Oncogene Proteins c-fos; Pyrroles; Quinine; Quinolines; RANK Ligand; RNA, Messenger; Skull; Tartrate-Resistant Acid Phosphatase; X-Ray Microtomography	2013
Pyrroloquinoline quinine protects rat brain cortex against acute glutamate-induced neurotoxicity. Neurochemical research, 2013, Volume: 38, Issue:8 Topics: Animals; Apoptosis; Base Sequence; Cerebral Cortex; DNA Primers; Glutamic Acid; Glutathione; In Situ Nick-End Labeling; Male; Malondialdehyde; Nerve Tissue Proteins; Neuroprotective Agents; Phosphorylation; Pyrroles; Quinolines; Rats; Rats, Sprague-Dawley; Reactive Oxygen Species; Real-Time Polymerase Chain Reaction; RNA, Messenger; Superoxide Dismutase	2013
A tandem Friedel-Crafts based method for the construction of a tricyclic pyrroloquinoline skeleton and its application in the synthesis of ammosamide B. Chemical communications (Cambridge, England), 2013, Jul-25, Volume: 49, Issue:58 Topics: Amides; Heterocyclic Compounds, 3-Ring; Molecular Structure; Pyrroles; Quinolines	2013
Highly conjugated norditerpenoid and pyrroloquinoline alkaloids with potent PTP1B inhibitory activity from Nigella glandulifera. Journal of natural products, 2014, Apr-25, Volume: 77, Issue:4 Topics: Alkaloids; Circular Dichroism; Diterpenes; Drug Screening Assays, Antitumor; Molecular Structure; Nigella; Protein Tyrosine Phosphatase, Non-Receptor Type 1; Pyrroles; Quinolines	2014
[Effects of pyrroloquinoline quinine on oxidative stress-induced apoptosis of Schwann cells and its mechanism]. Zhonghua zheng xing wai ke za zhi = Zhonghua zhengxing waike zazhi = Chinese journal of plastic surgery, 2014, Volume: 30, Issue:2 Topics: Apoptosis; Benzimidazoles; Cell Nucleus; DNA Fragmentation; Fluorescent Dyes; Humans; Hydrogen Peroxide; Malondialdehyde; Oxidants; Oxidative Stress; Pyrroles; Quinine; Quinolines; Schwann Cells; Superoxide Dismutase	2014
Beneficial synergistic effects of microdose lithium with pyrroloquinoline quinone in an Alzheimer's disease mouse model. Neurobiology of aging, 2014, Volume: 35, Issue:12 Topics: Alzheimer Disease; Amyloid beta-Peptides; Animals; Antidepressive Agents; Antioxidants; Disease Models, Animal; Dose-Response Relationship, Drug; Drug Synergism; Drug Therapy, Combination; Glycogen Synthase Kinase 3; Learning; Lithium Compounds; Long-Term Potentiation; Memory; Mice, Transgenic; Pyrroles; Quinolines; tau Proteins	2014
Pyrroloquinoline quinone protects mouse brain endothelial cells from high glucose-induced damage in vitro. Acta pharmacologica Sinica, 2014, Volume: 35, Issue:11 Topics: Animals; Antioxidants; Apoptosis; Brain; Cell Line; Cell Survival; Cytoprotection; Dose-Response Relationship, Drug; Endothelial Cells; Glucose; Hypoxia-Inducible Factor 1, alpha Subunit; JNK Mitogen-Activated Protein Kinases; Mice; Microvessels; Mitochondria; Oxidative Stress; Phosphorylation; Protein Kinase Inhibitors; Pyrroles; Quinolines; Reactive Oxygen Species; Signal Transduction	2014
Modular, flexible, and stereoselective synthesis of pyrroloquinolines: rapid assembly of complex heterocyclic scaffolds. Organic letters, 2014, Dec-05, Volume: 16, Issue:23 Topics: Catalysis; Imines; Molecular Structure; Pyrroles; Quinolines; Stereoisomerism	2014
Ruthenium-catalyzed cyclization of N-carbamoyl indolines with alkynes: an efficient route to pyrroloquinolinones. Organic & biomolecular chemistry, 2015, Sep-21, Volume: 13, Issue:35 Topics: Alkynes; Benzoquinones; Catalysis; Cyclization; Indoles; Models, Molecular; Molecular Conformation; Pyrroles; Quinolines; Ruthenium	2015
Design, Synthesis, and Photophysical Properties of Pyrroloquinoline-Based Compounds Showing Strong Blue Fluorescence as Potential Dyes for Biomedical Applications. ChemMedChem, 2015, Volume: 10, Issue:11 Topics: Cell Survival; Cell Tracking; Dose-Response Relationship, Drug; Drug Design; Fluorescence; Fluorescent Dyes; Humans; MCF-7 Cells; Molecular Structure; Photochemical Processes; Pyrroles; Quinolines; Structure-Activity Relationship	2015
Global insights into acetic acid resistance mechanisms and genetic stability of Acetobacter pasteurianus strains by comparative genomics. Scientific reports, 2015, Dec-22, Volume: 5 Topics: Acetic Acid; Acetobacter; Adaptation, Physiological; Alcohol Dehydrogenase; Amino Acids; Chromosomes, Bacterial; Fermentation; Genes, Bacterial; Genes, Essential; Genomics; Metabolic Networks and Pathways; Plasmids; Pyrroles; Quinolines; Sequence Homology, Nucleic Acid	2015
Annulation Reaction of 3-Acylmethylidene Oxindoles with Huisgen Zwitterions and Its Applications in the Syntheses of Pyrrolo[4,3,2-de]quinolinones and Marine Alkaloids Ammosamides. Organic letters, 2016, Mar-18, Volume: 18, Issue:6 Topics: Alkaloids; Amides; Biological Products; Heterocyclic Compounds, 3-Ring; Indoles; Marine Biology; Molecular Structure; Oxindoles; Pyrroles; Quinolines; Quinolones; Structure-Activity Relationship	2016
Pelianthinarubins A and B, Red Pyrroloquinoline Alkaloids from the Fruiting Bodies of the Mushroom Mycena pelianthina. Journal of natural products, 2016, Apr-22, Volume: 79, Issue:4 Topics: Agaricales; Alkaloids; Betaine; Fruiting Bodies, Fungal; Germany; Histidine; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Pyrroles; Quinolines	2016
Crystal Structure and Function of PqqF Protein in the Pyrroloquinoline Quinone Biosynthetic Pathway. The Journal of biological chemistry, 2016, 07-22, Volume: 291, Issue:30 Topics: Bacterial Proteins; Crystallography, X-Ray; Protein Domains; Pyrroles; Quinolines; Serratia	2016
Nanocurcumin-pyrroloquinoline formulation prevents hypertrophy-induced pathological damage by relieving mitochondrial stress in cardiomyocytes under hypoxic conditions. Experimental & molecular medicine, 2017, 12-01, Volume: 49, Issue:12 Topics: Animals; Cell Survival; Cells, Cultured; Curcumin; Hypertrophy; Hypertrophy, Right Ventricular; Hypoxia; Male; Mitochondria; Myocytes, Cardiac; Pyrroles; Quinolines; Rats; Rats, Sprague-Dawley	2017
Mycenaflavin A, B, C, and D: Pyrroloquinoline Alkaloids from the Fruiting Bodies of the Mushroom Mycena haematopus. Chemistry (Weinheim an der Bergstrasse, Germany), 2018, Jun-18, Volume: 24, Issue:34 Topics: Agaricales; Alkaloids; Anti-Bacterial Agents; Azoarcus; Dinitrocresols; Fruiting Bodies, Fungal; Molecular Structure; Pyrroles; Quinolines; Structure-Activity Relationship	2018
Anticancer Pyrroloquinazoline LBL1 Targets Nuclear Lamins. ACS chemical biology, 2018, 05-18, Volume: 13, Issue:5 Topics: Actins; Antineoplastic Agents; Cell Nucleus; HEK293 Cells; Humans; Intermediate Filament Proteins; Lamins; Pyrroles; Quinolines	2018
Pyrroloquinoline scaffold-based 5-HT Bioorganic & medicinal chemistry, 2018, 07-23, Volume: 26, Issue:12 Topics: Binding Sites; HEK293 Cells; Humans; Hydrogen Bonding; Ligands; Molecular Dynamics Simulation; Nitrogen; Protein Structure, Tertiary; Pyrroles; Quantum Theory; Quinolines; Receptors, Serotonin; Structure-Activity Relationship	2018
Benzimidazole tethered pyrrolo[3,4-b]quinoline with broad-spectrum activity against fungal pathogens. Bioorganic & medicinal chemistry letters, 2019, 03-01, Volume: 29, Issue:5 Topics: Antifungal Agents; Benzimidazoles; Biofilms; Candida albicans; Cryptococcus; Microbial Sensitivity Tests; Pyrroles; Quinolines	2019
Protective effects of pyrroloquinoline quinine against oxidative stress-induced cellular senescence and inflammation in human renal tubular epithelial cells via Keap1/Nrf2 signaling pathway. International immunopharmacology, 2019, Volume: 72 Topics: Anti-Inflammatory Agents; Antioxidants; Cell Line; Cellular Senescence; Epithelial Cells; Humans; Kelch-Like ECH-Associated Protein 1; Kidney; NF-E2-Related Factor 2; Oxidative Stress; Pyrroles; Quinolines; Signal Transduction	2019
Use of a scaffold peptide in the biosynthesis of amino acid-derived natural products. Science (New York, N.Y.), 2019, 07-19, Volume: 365, Issue:6450 Topics: Amino Acids; Biological Products; Escherichia coli; Multigene Family; Peptide Biosynthesis; Peptides; Pseudomonas syringae; Pyrroles; Quinolines	2019
Formaldehyde as a Chemical Defence Agent of Fruiting Bodies of Mycena rosea and its Role in the Generation of the Alkaloid Mycenarubin C. Chembiochem : a European journal of chemical biology, 2020, 06-02, Volume: 21, Issue:11 Topics: Agaricales; Alkaloids; Amino Acids; Antibiosis; Formaldehyde; Fruiting Bodies, Fungal; Gallic Acid; Inactivation, Metabolic; Magnetic Resonance Spectroscopy; Molecular Structure; Mucorales; Pyrroles; Quinolines	2020
Design of an Automated Reagent-Dispensing System for Reaction Screening and Validation with DNA-Tagged Substrates. ACS combinatorial science, 2020, 03-09, Volume: 22, Issue:3 Topics: Amides; Amines; Automation; Carboxylic Acids; Combinatorial Chemistry Techniques; DNA; Drug Design; Drug Evaluation, Preclinical; Molecular Structure; Pyrroles; Quinolines	2020
Synthesis, Docking, and In Vitro Anticoagulant Activity Assay of Hybrid Derivatives of Pyrrolo[3,2,1- Molecules (Basel, Switzerland), 2020, Apr-19, Volume: 25, Issue:8 Topics: Anticoagulants; Drug Design; Factor Xa; Factor Xa Inhibitors; Factor XIa; Hydrogen Bonding; Inhibitory Concentration 50; Molecular Docking Simulation; Pyrroles; Quinolines; Structure-Activity Relationship	2020
Non-rhizobial endophytic (NRE) yeasts assist nodulation of Rhizobium in root nodules of blackgram (Vigna mungo L.). Archives of microbiology, 2020, Volume: 202, Issue:10 Topics: Candida glabrata; Candida tropicalis; Carbon-Carbon Lyases; Endophytes; Microbial Interactions; Nitrogen Fixation; Phylogeny; Plant Development; Plant Root Nodulation; Pyrroles; Quinolines; Rhizobium; Root Nodules, Plant; Symbiosis; Vigna; Volatile Organic Compounds	2020
IDO1 and TDO inhibitory evaluation of analogues of the marine pyrroloiminoquinone alkaloids: Wakayin and Tsitsikammamines. Bioorganic & medicinal chemistry letters, 2021, 05-15, Volume: 40 Topics: Alkaloids; Aquatic Organisms; Enzyme Inhibitors; HEK293 Cells; Humans; Indole Alkaloids; Indoleamine-Pyrrole 2,3,-Dioxygenase; Molecular Docking Simulation; Protein Binding; Protein Conformation; Pyrroles; Pyrroloiminoquinones; Quinolines; Small Molecule Libraries; Structure-Activity Relationship; Tryptophan Oxygenase	2021
Discovery of ammosesters by mining the Streptomyces uncialis DCA2648 genome revealing new insight into ammosamide biosynthesis. Journal of industrial microbiology & biotechnology, 2021, Jun-04, Volume: 48, Issue:3-4 Topics: Amides; Biological Products; Genome, Bacterial; Humans; Multigene Family; Pyrroles; Quinolines; Streptomyces	2021
PQQ Dietary Supplementation Prevents Alkylating Agent-Induced Ovarian Dysfunction in Mice. Frontiers in endocrinology, 2022, Volume: 13 Topics: Alkylating Agents; Animals; Dietary Supplements; Female; Male; Mice; Ovarian Follicle; Pregnancy; Pyrroles; Quinine; Quinolines	2022
Selective detection of HSO Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 2022, Volume: 38, Issue:8 Topics: Fluorescent Dyes; HeLa Cells; Humans; Pyrroles; Quinolines; Sulfites	2022
Design, synthesis, and anticancer evaluation of ammosamide B with pyrroloquinoline derivatives as novel BRD4 inhibitors. Bioorganic chemistry, 2022, Volume: 127 Topics: Amides; Epigenesis, Genetic; Heterocyclic Compounds, 3-Ring; Nuclear Proteins; Pyrroles; Quinolines; Structure-Activity Relationship	2022