144 related articles for article (PubMed ID: 35257437)
1. Novel hybrid isoindole-1,3(2H)-dione compounds containing a 1H-tetrazole moiety: Synthesis, biological evaluation, and molecular docking studies.
Tan A; Kizilkaya S; Noma SAA; Ates B; Kara Y
J Biochem Mol Toxicol; 2022 May; 36(5):e23015. PubMed ID: 35257437
[TBL] [Abstract][Full Text] [Related]
2. Synthesis and Carbonic Anhydrase Inhibition of Novel 2-(4-(Aryl)thiazole-2-yl)-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione Derivatives.
Kocyigit UM; Aslan ON; Gulcin I; Temel Y; Ceylan M
Arch Pharm (Weinheim); 2016 Dec; 349(12):955-963. PubMed ID: 27859585
[TBL] [Abstract][Full Text] [Related]
3. Synthesis, characterization, anticancer, antimicrobial and carbonic anhydrase inhibition profiles of novel (3aR,4S,7R,7aS)-2-(4-((E)-3-(3-aryl)acryloyl) phenyl)-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione derivatives.
Kocyigit UM; Budak Y; Gürdere MB; Tekin Ş; Köprülü TK; Ertürk F; Özcan K; Gülçin İ; Ceylan M
Bioorg Chem; 2017 Feb; 70():118-125. PubMed ID: 28043719
[TBL] [Abstract][Full Text] [Related]
4. Synthesis and Molecular Docking of New N-Acyl Hydrazones- Benzimidazole as hCA I and II Inhibitors.
Küçükoğlu K; Çevik UA; Nadaroglu H; Celik I; Işık A; Bostancı HE; Özkay Y; Kaplancıklı ZA
Med Chem; 2023; 19(5):485-494. PubMed ID: 36567289
[TBL] [Abstract][Full Text] [Related]
5. Novel 2-(2-arylmethylthio-4-chloro-5-methylbenzenesulfonyl)-1-(1,3,5-triazin-2-ylamino)guanidine derivatives: Inhibition of human carbonic anhydrase cytosolic isozymes I and II and the transmembrane tumor-associated isozymes IX and XII, anticancer activity, and molecular modeling studies.
Żołnowska B; Sławiński J; Szafrański K; Angeli A; Supuran CT; Kawiak A; Wieczór M; Zielińska J; Bączek T; Bartoszewska S
Eur J Med Chem; 2018 Jan; 143():1931-1941. PubMed ID: 29146134
[TBL] [Abstract][Full Text] [Related]
6. Synthesis, biological activity and multiscale molecular modeling studies of bis-coumarins as selective carbonic anhydrase IX and XII inhibitors with effective cytotoxicity against hepatocellular carcinoma.
Kurt BZ; Dag A; Doğan B; Durdagi S; Angeli A; Nocentini A; Supuran CT; Sonmez F
Bioorg Chem; 2019 Jun; 87():838-850. PubMed ID: 31003041
[TBL] [Abstract][Full Text] [Related]
7. Evaluation of some thiophene-based sulfonamides as potent inhibitors of carbonic anhydrase I and II isoenzymes isolated from human erythrocytes by kinetic and molecular modelling studies.
Alım Z; Köksal Z; Karaman M
Pharmacol Rep; 2020 Dec; 72(6):1738-1748. PubMed ID: 32748253
[TBL] [Abstract][Full Text] [Related]
8. Enzyme Inhibition Properties and Molecular Docking Studies of 4-Sulfonate Containing Aryl α-Hydroxyphosphonates Based Hybrid Molecules.
Şahin İ; Bingöl Z; Onur S; Güngör SA; Köse M; Gülçin İ; Tümer F
Chem Biodivers; 2022 May; 19(5):e202100787. PubMed ID: 35315972
[TBL] [Abstract][Full Text] [Related]
9. Microwave assisted synthesis of novel tetrazole/sulfonamide derivatives based on octahydroacridine, xanthene and chromene skeletons as inhibitors of the carbonic anhydrases isoforms I, II, IV and VII.
Esirden İ; Tanç M; Supuran CT; Kaya M
Bioorg Med Chem Lett; 2017 Jan; 27(1):86-89. PubMed ID: 27876475
[TBL] [Abstract][Full Text] [Related]
10. Novel 1,3,5-Triazinyl Aminobenzenesulfonamides Incorporating Aminoalcohol, Aminochalcone and Aminostilbene Structural Motifs as Potent Anti-VRE Agents, and Carbonic Anhydrases I, II, VII, IX, and XII Inhibitors.
Havránková E; Garaj V; Mascaretti Š; Angeli A; Soldánová Z; Kemka M; Motyčka J; Brázdová M; Csöllei J; Jampílek J; Supuran CT
Int J Mol Sci; 2021 Dec; 23(1):. PubMed ID: 35008657
[TBL] [Abstract][Full Text] [Related]
11. Design, synthesis and biological evaluation of novel carbohydrate-based sulfonamide derivatives as antitumor agents.
Hao S; Cheng X; Wang X; An R; Xu H; Guo M; Li C; Wang Y; Hou Z; Guo C
Bioorg Chem; 2020 Nov; 104():104237. PubMed ID: 32911194
[TBL] [Abstract][Full Text] [Related]
12. Identification of Novel and Potent Indole-Based Benzenesulfonamides as Selective Human Carbonic Anhydrase II Inhibitors: Design, Synthesis, In Vitro, and In Silico Studies.
Elkamhawy A; Woo J; Nada H; Angeli A; Bedair TM; Supuran CT; Lee K
Int J Mol Sci; 2022 Feb; 23(5):. PubMed ID: 35269684
[TBL] [Abstract][Full Text] [Related]
13. Effects of dopaminergic compounds on carbonic anhydrase isozymes I, II, and VI.
Sentürk M; Ekinci D; Göksu S; Supuran CT
J Enzyme Inhib Med Chem; 2012 Jun; 27(3):365-9. PubMed ID: 21699374
[TBL] [Abstract][Full Text] [Related]
14. Three-component synthesis and carbonic anhydrase inhibitory properties of novel octahydroacridines incorporating sulfaguanidine scaffold.
Ulus R; Kaya M; Demir D; Tunca E; Bülbül M
J Enzyme Inhib Med Chem; 2016; 31(sup2):63-69. PubMed ID: 27237188
[TBL] [Abstract][Full Text] [Related]
15. Calcium channel blockers: molecular docking and inhibition studies on carbonic anhydrase I and II isoenzymes.
Türkeş C; Demir Y; Beydemir Ş
J Biomol Struct Dyn; 2021 Mar; 39(5):1672-1680. PubMed ID: 32107977
[TBL] [Abstract][Full Text] [Related]
16. Novel indolin-2-one-based sulfonamides as carbonic anhydrase inhibitors: Synthesis, in vitro biological evaluation against carbonic anhydrases isoforms I, II, IV and VII and molecular docking studies.
Eldehna WM; Al-Ansary GH; Bua S; Nocentini A; Gratteri P; Altoukhy A; Ghabbour H; Ahmed HY; Supuran CT
Eur J Med Chem; 2017 Feb; 127():521-530. PubMed ID: 28109946
[TBL] [Abstract][Full Text] [Related]
17. S-substituted 2-mercaptoquinazolin-4(3H)-one and 4-ethylbenzensulfonamides act as potent and selective human carbonic anhydrase IX and XII inhibitors.
El-Azab AS; Abdel-Aziz AA; Bua S; Nocentini A; AlSaif NA; Alanazi MM; El-Gendy MA; Ahmed HEA; Supuran CT
J Enzyme Inhib Med Chem; 2020 Dec; 35(1):733-743. PubMed ID: 32189526
[TBL] [Abstract][Full Text] [Related]
18. Design, synthesis, characterization, in vitro and in silico evaluation of novel imidazo[2,1-b][1,3,4]thiadiazoles as highly potent acetylcholinesterase and non-classical carbonic anhydrase inhibitors.
Askin S; Tahtaci H; Türkeş C; Demir Y; Ece A; Akalın Çiftçi G; Beydemir Ş
Bioorg Chem; 2021 Aug; 113():105009. PubMed ID: 34052739
[TBL] [Abstract][Full Text] [Related]
19. Synthesis and carbonic anhydrase inhibition studies of sulfonamide based indole-1,2,3-triazole chalcone hybrids.
Singh P; Swain B; Thacker PS; Sigalapalli DK; Purnachander Yadav P; Angeli A; Supuran CT; Arifuddin M
Bioorg Chem; 2020 Jun; 99():103839. PubMed ID: 32289586
[TBL] [Abstract][Full Text] [Related]
20. Synthesis and selective inhibitory effects of some 2-oxindole benzenesulfonamide conjugates on human carbonic anhydrase isoforms CA I, CA II, CA IX and CAXII.
George RF; Said MF; Bua S; Supuran CT
Bioorg Chem; 2020 Jan; 95():103514. PubMed ID: 31887473
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
