Found: 24
Select item for more details and to access through your institution.
Development of quinoline‐based hybrid as inhibitor of methionine aminopeptidase 1 from Leishmania donovani.
- Published in:
- Chemical Biology & Drug Design, 2021, v. 97, n. 2, p. 315, doi. 10.1111/cbdd.13783
- By:
- Publication type:
- Article
An efficient and facile green synthesis of bisindole methanes as potential Mtb FtsZ inhibitors.
- Published in:
- Chemical Biology & Drug Design, 2018, v. 92, n. 6, p. 1933, doi. 10.1111/cbdd.13363
- By:
- Publication type:
- Article
Design, Synthesis and Biological Assessment of Rhodanine-Linked Benzenesulfonamide Derivatives as Selective and Potent Human Carbonic Anhydrase Inhibitors.
- Published in:
- Molecules, 2022, v. 27, n. 22, p. 8028, doi. 10.3390/molecules27228028
- By:
- Publication type:
- Article
Werner transition‐metal complex (WTMC)‐mediated mild and efficient chemo‐selective acylation of phenols and anilines under solvent‐free condition.
- Published in:
- Journal of the Chinese Chemical Society, 2018, v. 65, n. 9, p. 1104, doi. 10.1002/jccs.201800013
- By:
- Publication type:
- Article
Ureidosulfocoumarin Derivatives As Selective and Potent Carbonic Anhydrase IX and XII Inhibitors.
- Published in:
- ChemMedChem, 2022, v. 17, n. 5, p. 1, doi. 10.1002/cmdc.202100725
- By:
- Publication type:
- Article
Coumarin‐Thiourea Hybrids Show Potent Carbonic Anhydrase IX and XIII Inhibitory Action.
- Published in:
- ChemMedChem, 2021, v. 16, n. 8, p. 1252, doi. 10.1002/cmdc.202000915
- By:
- Publication type:
- Article
Synthesis and Biological Evaluation of 4‐Sulfamoylphenyl/Sulfocoumarin Carboxamides as Selective Inhibitors of Carbonic Anhydrase Isoforms hCA II, IX, and XII.
- Published in:
- ChemMedChem, 2018, v. 13, n. 12, p. 1165, doi. 10.1002/cmdc.201800180
- By:
- Publication type:
- Article
Design, synthesis, and biological evaluation of 3‐benzenesulfonamide‐linked 3‐hydrazinoisatin derivatives as carbonic anhydrase inhibitors.
- Published in:
- Archiv der Pharmazie, 2024, v. 357, n. 6, p. 1, doi. 10.1002/ardp.202300718
- By:
- Publication type:
- Article
Exploration of 3‐aryl pyrazole‐tethered sulfamoyl carboxamides as carbonic anhydrase inhibitors.
- Published in:
- Archiv der Pharmazie, 2023, v. 356, n. 11, p. 1, doi. 10.1002/ardp.202300309
- By:
- Publication type:
- Article
6‐Aminocoumarin oxime‐ether/sulfonamides as selective hCA IX and XII inhibitors: Synthesis, evaluation, and molecular dynamics studies.
- Published in:
- Archiv der Pharmazie, 2023, v. 356, n. 10, p. 1, doi. 10.1002/ardp.202300316
- By:
- Publication type:
- Article
Design, synthesis, and structure–activity studies of new rhodanine derivatives as carbonic anhydrase II, IX inhibitors.
- Published in:
- Archiv der Pharmazie, 2023, v. 356, n. 9, p. 1, doi. 10.1002/ardp.202300205
- By:
- Publication type:
- Article
Synthesis and biological evaluation of coumarin‐thiazole hybrids as selective carbonic anhydrase IX and XII inhibitors.
- Published in:
- Archiv der Pharmazie, 2022, v. 355, n. 12, p. 1, doi. 10.1002/ardp.202200232
- By:
- Publication type:
- Article
Design, synthesis, SAR, and biological evaluation of saccharin‐based hybrids as carbonic anhydrase inhibitors.
- Published in:
- Archiv der Pharmazie, 2022, v. 355, n. 8, p. 1, doi. 10.1002/ardp.202200019
- By:
- Publication type:
- Article
Design and development of novel series of indole‐3‐sulfonamide ureido derivatives as selective carbonic anhydrase II inhibitors.
- Published in:
- Archiv der Pharmazie, 2022, v. 355, n. 1, p. 1, doi. 10.1002/ardp.202100333
- By:
- Publication type:
- Article
Design and synthesis of benzenesulfonamide‐linked imidazo[2,1‐b][1,3,4]thiadiazole derivatives as carbonic anhydrase I and II inhibitors.
- Published in:
- Archiv der Pharmazie, 2021, v. 354, n. 7, p. 1, doi. 10.1002/ardp.202100028
- By:
- Publication type:
- Article
Sulfocoumarin-, Coumarin-, 4-Sulfamoylphenyl-Bearing Indazole-3-carboxamide Hybrids: Synthesis and Selective Inhibition of Tumor-Associated Carbonic Anhydrase Isozymes IX and XII.
- Published in:
- ChemMedChem, 2017, v. 12, n. 19, p. 1578, doi. 10.1002/cmdc.201700446
- By:
- Publication type:
- Article
A COMPREHENSIVE ANALYSIS OF CLINICAL CHARACTERISTICS, MICROBIAL PROFILE, PROGNOSTIC INDICATORS, AND TREATMENT IN PATIENTS WITH TYPE 2 DIABETES MELLITUS AND ACUTE PYELONEPHRITIS.
- Published in:
- Journal of Cardiovascular Disease Research (Journal of Cardiovascular Disease Research), 2024, v. 15, n. 1, p. 496
- By:
- Publication type:
- Article
EFFECTS OF TUBERCULOSIS ON GENITOURINARY SYSTEM.
- Published in:
- Journal of Cardiovascular Disease Research (Journal of Cardiovascular Disease Research), 2023, v. 14, n. 12, p. 2291
- By:
- Publication type:
- Article
Microwave‐Assisted Copper‐Catalyzed One‐Pot Synthesis of 2‐Aryl/Heteroaryl‐4‐Quinolones via Sequential Intramolecular Aza‐Michael Addition and Oxidation.
- Published in:
- Asian Journal of Organic Chemistry, 2022, v. 11, n. 7, p. 1, doi. 10.1002/ajoc.202200181
- By:
- Publication type:
- Article
Metal-Free C−C Bond Cleavage: One-Pot Access to 1,4-Benzoquinone-linked N-Formyl Amides/Sulfonamides/Carbamates using Oxone.
- Published in:
- Asian Journal of Organic Chemistry, 2017, v. 6, n. 8, p. 1008, doi. 10.1002/ajoc.201700266
- By:
- Publication type:
- Article
Synthesis and Biological Evaluation of Coumarin-Linked 4-Anilinomethyl-1,2,3-Triazoles as Potent Inhibitors of Carbonic Anhydrases IX and XIII Involved in Tumorigenesis.
- Published in:
- Metabolites (2218-1989), 2021, v. 11, n. 4, p. 225, doi. 10.3390/metabo11040225
- By:
- Publication type:
- Article
Design, Synthesis, and Biological Evaluation of 1,2,3-Triazole-linked triazino[5,6-b]indole-benzene sulfonamide Conjugates as Potent Carbonic Anhydrase I, II, IX, and XIII Inhibitors.
- Published in:
- Metabolites (2218-1989), 2020, v. 10, n. 5, p. 200, doi. 10.3390/metabo10050200
- By:
- Publication type:
- Article
Synthesis and Biological Evaluation of Imidazo[2,1-b]Thiazole based Sulfonyl Piperazines as Novel Carbonic Anhydrase II Inhibitors.
- Published in:
- Metabolites (2218-1989), 2020, v. 10, n. 4, p. 136, doi. 10.3390/metabo10040136
- By:
- Publication type:
- Article
DABCO mediated one pot synthesis of 2‐(3‐benzyl‐2, 6‐dioxo‐3, 6‐dihydropyrimidin‐1[2H]‐yl)‐N‐(4‐(1, 3‐dioxo‐1H‐benzo [de]isoquinolin‐2[3H]‐yl) aryl) acetamides as antimicrobial agents
- Published in:
- Journal of Heterocyclic Chemistry, 2020, v. 57, n. 9, p. 3375, doi. 10.1002/jhet.4055
- By:
- Publication type:
- Article