205 related articles for article (PubMed ID: 34255561)
1. Discovery of Natural Compounds as Potential Inhibitors of Human Carbonic Anhydrase II: An Integrated Virtual Screening, Docking, and Molecular Dynamics Simulation Study.
Anjum F; Ali F; Mohammad T; Shafie A; Akhtar O; Abdullaev B; Hassan I
OMICS; 2021 Aug; 25(8):513-524. PubMed ID: 34255561
[TBL] [Abstract][Full Text] [Related]
2. Implication of sulfonylurea derivatives as prospective inhibitors of human carbonic anhydrase II.
Idrees D; Hadianawala M; Mahapatra AD; Datta B; Roy S; Ahamad S; Khan P; Imtaiyaz Hassan M
Int J Biol Macromol; 2018 Aug; 115():961-969. PubMed ID: 29704602
[TBL] [Abstract][Full Text] [Related]
3. Virtual screening, molecular dynamics, and binding free energy calculations on human carbonic anhydrase IX catalytic domain for deciphering potential leads.
John A; Sivashanmugam M; Umashankar V; Natarajan SK
J Biomol Struct Dyn; 2017 Aug; 35(10):2155-2168. PubMed ID: 27373313
[TBL] [Abstract][Full Text] [Related]
4. Design, synthesis, in silico and biological evaluation of novel 2-(4-(4-substituted piperazin-1-yl)benzylidene)hydrazine carboxamides.
Kumari S; Mishra CB; Idrees D; Prakash A; Yadav R; Hassan MI; Tiwari M
Mol Divers; 2017 Feb; 21(1):163-174. PubMed ID: 28039637
[TBL] [Abstract][Full Text] [Related]
5. Development of a Fingerprint-Based Scoring Function for the Prediction of the Binding Mode of Carbonic Anhydrase II Inhibitors.
Poli G; Jha V; Martinelli A; Supuran CT; Tuccinardi T
Int J Mol Sci; 2018 Jun; 19(7):. PubMed ID: 29937490
[TBL] [Abstract][Full Text] [Related]
6. Searching for Novel Anaplastic Lymphoma Kinase Inhibitors: Structure-Guided Screening of Natural Compounds for a Tyrosine Kinase Therapeutic Target in Cancers.
Adnan M; Koli S; Mohammad T; Siddiqui AJ; Patel M; Alshammari N; Bardakci F; Elasbali AM; Hassan MI
OMICS; 2022 Aug; 26(8):461-470. PubMed ID: 35925819
[TBL] [Abstract][Full Text] [Related]
7. Identification of high-affinity inhibitors of pyruvate dehydrogenase kinase-3: towards therapeutic management of cancer.
Mohammad T; Arif K; Alajmi MF; Hussain A; Islam A; Rehman MT; Hassan I
J Biomol Struct Dyn; 2021 Feb; 39(2):586-594. PubMed ID: 31903847
[TBL] [Abstract][Full Text] [Related]
8. Identification of novel PI3Kδ inhibitors by docking, ADMET prediction and molecular dynamics simulations.
Liu YY; Feng XY; Jia WQ; Jing Z; Xu WR; Cheng XC
Comput Biol Chem; 2019 Feb; 78():190-204. PubMed ID: 30557817
[TBL] [Abstract][Full Text] [Related]
9. High-throughput virtual screening with e-pharmacophore and molecular simulations study in the designing of pancreatic lipase inhibitors.
Veeramachaneni GK; Raj KK; Chalasani LM; Bondili JS; Talluri VR
Drug Des Devel Ther; 2015; 9():4397-412. PubMed ID: 26273199
[TBL] [Abstract][Full Text] [Related]
10. Virtual Screening Approach to Identify High-Affinity Inhibitors of Serum and Glucocorticoid-Regulated Kinase 1 among Bioactive Natural Products: Combined Molecular Docking and Simulation Studies.
Mohammad T; Siddiqui S; Shamsi A; Alajmi MF; Hussain A; Islam A; Ahmad F; Hassan MI
Molecules; 2020 Feb; 25(4):. PubMed ID: 32070031
[TBL] [Abstract][Full Text] [Related]
11. Discovering novel carbonic anhydrase type IX (CA IX) inhibitors from seven million compounds using virtual screening and in vitro analysis.
Salmas RE; Senturk M; Yurtsever M; Durdagi S
J Enzyme Inhib Med Chem; 2016; 31(3):425-33. PubMed ID: 25950196
[TBL] [Abstract][Full Text] [Related]
12. Toward the Discovery of a Novel Class of Leads for High Altitude Disorders by Virtual Screening and Molecular Dynamics Approaches Targeting Carbonic Anhydrase.
Ali A; Ali A; Warsi MH; Rahman MA; Ahsan MJ; Azam F
Int J Mol Sci; 2022 May; 23(9):. PubMed ID: 35563445
[TBL] [Abstract][Full Text] [Related]
13. A selectivity study of benzenesulfonamide derivatives on human carbonic anhydrase II/IX by 3D-QSAR, Molecular Docking and Molecular Dynamics Simulation.
Wang Y; Guo H; Tang G; He Q; Zhang Y; Hu Y; Wang Y; Lin Z
Comput Biol Chem; 2019 Jun; 80():234-243. PubMed ID: 31009872
[TBL] [Abstract][Full Text] [Related]
14. Carbonic anhydrase II binds to and increases the activity of the epithelial sodium-proton exchanger, NHE3.
Krishnan D; Liu L; Wiebe SA; Casey JR; Cordat E; Alexander RT
Am J Physiol Renal Physiol; 2015 Aug; 309(4):F383-92. PubMed ID: 26041446
[TBL] [Abstract][Full Text] [Related]
15. Identification and evaluation of bioactive natural products as potential inhibitors of human microtubule affinity-regulating kinase 4 (MARK4).
Mohammad T; Khan FI; Lobb KA; Islam A; Ahmad F; Hassan MI
J Biomol Struct Dyn; 2019 Apr; 37(7):1813-1829. PubMed ID: 29683402
[TBL] [Abstract][Full Text] [Related]
16. Intramolecular proton shuttle supports not only catalytic but also noncatalytic function of carbonic anhydrase II.
Becker HM; Klier M; Schüler C; McKenna R; Deitmer JW
Proc Natl Acad Sci U S A; 2011 Feb; 108(7):3071-6. PubMed ID: 21282642
[TBL] [Abstract][Full Text] [Related]
17. Structure-Guided Approach to Discover Tuberosin as a Potent Activator of Pyruvate Kinase M2, Targeting Cancer Therapy.
Adnan M; Shamsi A; Elasbali AM; Siddiqui AJ; Patel M; Alshammari N; Alharethi SH; Alhassan HH; Bardakci F; Hassan MI
Int J Mol Sci; 2022 Oct; 23(21):. PubMed ID: 36361954
[TBL] [Abstract][Full Text] [Related]
18. Integrated virtual screening and MD simulation study to discover potential inhibitors of Lyn-kinase: targeting cancer therapy.
Hassan MI; Anjum D; Mohammad T; Alam M; Khan MS; Shahwan M; Shamsi A; Yadav DK
J Biomol Struct Dyn; 2023 Dec; 41(20):10558-10568. PubMed ID: 36495308
[TBL] [Abstract][Full Text] [Related]
19. Discovery of novel HDAC8 inhibitors from natural compounds by in silico high throughput screening.
Esther Rubavathy SM; Palanisamy K; Priyankha S; Thilagavathi R; Prakash M; Selvam C
J Biomol Struct Dyn; 2023 Nov; 41(19):9492-9502. PubMed ID: 36369945
[TBL] [Abstract][Full Text] [Related]
20. Structural aspects of isozyme selectivity in the binding of inhibitors to carbonic anhydrases II and IV.
Kim CY; Whittington DA; Chang JS; Liao J; May JA; Christianson DW
J Med Chem; 2002 Feb; 45(4):888-93. PubMed ID: 11831900
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
