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Items: 12

1.

Synthesis, anti-leishmanial and molecular docking study of bis-indole derivatives.

Taha M, Uddin I, Gollapalli M, Almandil NB, Rahim F, Farooq RK, Nawaz M, Ibrahim M, Alqahtani MA, Bamarouf YA, Selvaraj M.

BMC Chem. 2019 Aug 6;13(1):102. doi: 10.1186/s13065-019-0617-4. eCollection 2019 Dec.

2.

Indole bearing thiadiazole analogs: synthesis, β-glucuronidase inhibition and molecular docking study.

Almandil NB, Taha M, Gollapalli M, Rahim F, Ibrahim M, Mosaddik A, Anouar EH.

BMC Chem. 2019 Feb 4;13(1):14. doi: 10.1186/s13065-019-0522-x. eCollection 2019 Dec.

3.

2,5-Disubstituted thiadiazoles as potent β-glucuronidase inhibitors; Synthesis, in vitro and in silico studies.

Taha M, Barak Almandil N, Rashid U, Ali M, Ibrahim M, Gollapalli M, Mosaddik A, Mohammed Khan K.

Bioorg Chem. 2019 Oct;91:103126. doi: 10.1016/j.bioorg.2019.103126. Epub 2019 Jul 12.

PMID:
31349116
4.

Synthesis of new arylhydrazide bearing Schiff bases/thiazolidinone: α-Amylase, urease activities and their molecular docking studies.

Rahim F, Taha M, Ullah H, Wadood A, Selvaraj M, Rab A, Sajid M, Shah SAA, Uddin N, Gollapalli M.

Bioorg Chem. 2019 Oct;91:103112. doi: 10.1016/j.bioorg.2019.103112. Epub 2019 Jul 9.

PMID:
31349115
5.

Synthesis of oxadiazole-coupled-thiadiazole derivatives as a potent β-glucuronidase inhibitors and their molecular docking study.

Taha M, Imran S, Alomari M, Rahim F, Wadood A, Mosaddik A, Uddin N, Gollapalli M, Alqahtani MA, Bamarouf YA.

Bioorg Med Chem. 2019 Jul 15;27(14):3145-3155. doi: 10.1016/j.bmc.2019.05.049. Epub 2019 Jun 4.

PMID:
31196753
6.

Synthesis, in vitro urease inhibitory potential and molecular docking study of Benzimidazole analogues.

Zaman K, Rahim F, Taha M, Ullah H, Wadood A, Nawaz M, Khan F, Wahab Z, Shah SAA, Rehman AU, Kawde AN, Gollapalli M.

Bioorg Chem. 2019 Aug;89:103024. doi: 10.1016/j.bioorg.2019.103024. Epub 2019 May 31.

PMID:
31176853
7.

Synthesis, thymidine phosphorylase, angiogenic inhibition and molecular docking study of isoquinoline derivatives.

Zaman K, Rahim F, Taha M, Wadood A, Adnan Ali Shah S, Gollapalli M, Ullah F, Ahmed A.

Bioorg Chem. 2019 Aug;89:102999. doi: 10.1016/j.bioorg.2019.102999. Epub 2019 May 21.

PMID:
31151055
8.

Synthesis of Chromen-4-One-Oxadiazole Substituted Analogs as Potent β-Glucuronidase Inhibitors.

Taha M, Rahim F, Ali M, Khan MN, Alqahtani MA, Bamarouf YA, Gollapalli M, Farooq RK, Shah SAA, Ahmed QU, Zakaria ZA.

Molecules. 2019 Apr 18;24(8). pii: E1528. doi: 10.3390/molecules24081528.

9.

Synthesis of Thymidine Phosphorylase Inhibitor Based on Quinoxaline Derivatives and Their Molecular Docking Study.

Almandil NB, Taha M, Farooq RK, Alhibshi A, Ibrahim M, Anouar EH, Gollapalli M, Rahim F, Nawaz M, Shah SAA, Ahmed QU, Zakaria ZA.

Molecules. 2019 Mar 13;24(6). pii: E1002. doi: 10.3390/molecules24061002.

10.

Synthesis of novel quinoline-based thiadiazole, evaluation of their antileishmanial potential and molecular docking studies.

Almandil NB, Taha M, Rahim F, Wadood A, Imran S, Alqahtani MA, Bamarouf YA, Ibrahim M, Mosaddik A, Gollapalli M.

Bioorg Chem. 2019 Apr;85:109-116. doi: 10.1016/j.bioorg.2018.12.025. Epub 2018 Dec 21.

PMID:
30605884
11.

Synthesis of benzothiazole derivatives as a potent α-glucosidase inhibitor.

Gollapalli M, Taha M, Javid MT, Almandil NB, Rahim F, Wadood A, Mosaddik A, Ibrahim M, Alqahtani MA, Bamarouf YA.

Bioorg Chem. 2019 Apr;85:33-48. doi: 10.1016/j.bioorg.2018.12.021. Epub 2018 Dec 15.

PMID:
30599411
12.

Synthesis of Bis-indolylmethane sulfonohydrazides derivatives as potent α-Glucosidase inhibitors.

Gollapalli M, Taha M, Ullah H, Nawaz M, AlMuqarrabun LMR, Rahim F, Qureshi F, Mosaddik A, Ahmat N, Khan KM.

Bioorg Chem. 2018 Oct;80:112-120. doi: 10.1016/j.bioorg.2018.06.001. Epub 2018 Jun 2.

PMID:
29894890

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