136 related articles for article (PubMed ID: 26526743)
1. Synthesis of novel benzohydrazone-oxadiazole hybrids as β-glucuronidase inhibitors and molecular modeling studies.
Taha M; Ismail NH; Imran S; Selvaraj M; Rahim A; Ali M; Siddiqui S; Rahim F; Khan KM
Bioorg Med Chem; 2015 Dec; 23(23):7394-404. PubMed ID: 26526743
[TBL] [Abstract][Full Text] [Related]
2. Novel 2,5-disubtituted-1,3,4-oxadiazoles with benzimidazole backbone: a new class of β-glucuronidase inhibitors and in silico studies.
Zawawi NK; Taha M; Ahmat N; Wadood A; Ismail NH; Rahim F; Ali M; Abdullah N; Khan KM
Bioorg Med Chem; 2015 Jul; 23(13):3119-25. PubMed ID: 26001340
[TBL] [Abstract][Full Text] [Related]
3. Synthesis and in silico studies of novel sulfonamides having oxadiazole ring: As β-glucuronidase inhibitors.
Taha M; Baharudin MS; Ismail NH; Selvaraj M; Salar U; Alkadi KA; Khan KM
Bioorg Chem; 2017 Apr; 71():86-96. PubMed ID: 28160943
[TBL] [Abstract][Full Text] [Related]
4. Synthesis of Chromen-4-One-Oxadiazole Substituted Analogs as Potent
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; 24(8):. PubMed ID: 31003424
[TBL] [Abstract][Full Text] [Related]
5. Synthesis and molecular modelling studies of phenyl linked oxadiazole-phenylhydrazone hybrids as potent antileishmanial agents.
Taha M; Ismail NH; Imran S; Anouar EH; Selvaraj M; Jamil W; Ali M; Kashif SM; Rahim F; Khan KM; Adenan MI
Eur J Med Chem; 2017 Jan; 126():1021-1033. PubMed ID: 28012342
[TBL] [Abstract][Full Text] [Related]
6. 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; 27(14):3145-3155. PubMed ID: 31196753
[TBL] [Abstract][Full Text] [Related]
7. Synthesis, β-glucuronidase inhibition and molecular docking studies of cyano-substituted bisindole hydrazone hybrids.
Abid O; Imran S; Taha M; Ismail NH; Jamil W; Kashif SM; Khan KM; Yusoff J
Mol Divers; 2021 May; 25(2):995-1009. PubMed ID: 32301032
[TBL] [Abstract][Full Text] [Related]
8. Synthesis, Molecular Docking and β-Glucuronidase Inhibitory Potential of Indole Base Oxadiazole Derivatives.
Anouar EH; Moustapha ME; Taha M; Geesi MH; Farag ZR; Rahim F; Almandil NB; Farooq RK; Nawaz M; Mosaddik A
Molecules; 2019 Mar; 24(5):. PubMed ID: 30857263
[TBL] [Abstract][Full Text] [Related]
9. Synthesis of indole analogs as potent β-glucuronidase inhibitors.
Baharudin MS; Taha M; Imran S; Ismail NH; Rahim F; Javid MT; Khan KM; Ali M
Bioorg Chem; 2017 Jun; 72():323-332. PubMed ID: 28505547
[TBL] [Abstract][Full Text] [Related]
10. Synthesis: Small library of hybrid scaffolds of benzothiazole having hydrazone and evaluation of their β-glucuronidase activity.
Taha M; Arbin M; Ahmat N; Imran S; Rahim F
Bioorg Chem; 2018 Apr; 77():47-55. PubMed ID: 29331764
[TBL] [Abstract][Full Text] [Related]
11. Synthesis, β-glucuronidase inhibition and molecular docking studies of hybrid bisindole-thiosemicarbazides analogs.
Taha M; Ismail NH; Imran S; Rahim F; Wadood A; Khan H; Ullah H; Salar U; Khan KM
Bioorg Chem; 2016 Oct; 68():56-63. PubMed ID: 27454618
[TBL] [Abstract][Full Text] [Related]
12. Synthesis of bis-indolylmethanes as new potential inhibitors of β-glucuronidase and their molecular docking studies.
Taha M; Ullah H; Al Muqarrabun LMR; Khan MN; Rahim F; Ahmat N; Ali M; Perveen S
Eur J Med Chem; 2018 Jan; 143():1757-1767. PubMed ID: 29133042
[TBL] [Abstract][Full Text] [Related]
13. Synthesis of benzimidazole derivatives as potent β-glucuronidase inhibitors.
Taha M; Ismail NH; Imran S; Selvaraj M; Rashwan H; Farhanah FU; Rahim F; Kesavanarayanan KS; Ali M
Bioorg Chem; 2015 Aug; 61():36-44. PubMed ID: 26073618
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 31349116
[TBL] [Abstract][Full Text] [Related]
15. Synthesis and biological evaluation of novel N-arylidenequinoline-3-carbohydrazides as potent β-glucuronidase inhibitors.
Taha M; Sultan S; Nuzar HA; Rahim F; Imran S; Ismail NH; Naz H; Ullah H
Bioorg Med Chem; 2016 Aug; 24(16):3696-704. PubMed ID: 27312423
[TBL] [Abstract][Full Text] [Related]
16. Synthesis, thymidine phosphorylase inhibition and molecular modeling studies of 1,3,4-oxadiazole-2-thione derivatives.
Shahzad SA; Yar M; Bajda M; Shahzadi L; Khan ZA; Naqvi SA; Mutahir S; Mahmood N; Khan KM
Bioorg Chem; 2015 Jun; 60():37-41. PubMed ID: 25920005
[TBL] [Abstract][Full Text] [Related]
17. Synthesis of novel disulfide and sulfone hybrid scaffolds as potent β-glucuronidase inhibitor.
Taha M; Ismail NH; Imran S; Wadood A; Rahim F; Al Muqarrabin LM; Zaki HM; Ahmat N; Nasir A; Khan F
Bioorg Chem; 2016 Oct; 68():15-22. PubMed ID: 27414468
[TBL] [Abstract][Full Text] [Related]
18. Synthesis, thymidine phosphorylase inhibitory and computational study of novel 1,3,4-oxadiazole-2-thione derivatives as potential anticancer agents.
Bajaj S; Roy PP; Singh J
Comput Biol Chem; 2018 Oct; 76():151-160. PubMed ID: 30015176
[TBL] [Abstract][Full Text] [Related]
19. Synthesis of 6-chloro-2-Aryl-1H-imidazo[4,5-b]pyridine derivatives: Antidiabetic, antioxidant, β-glucuronidase inhibiton and their molecular docking studies.
Taha M; Ismail NH; Imran S; Rashwan H; Jamil W; Ali S; Kashif SM; Rahim F; Salar U; Khan KM
Bioorg Chem; 2016 Apr; 65():48-56. PubMed ID: 26855413
[TBL] [Abstract][Full Text] [Related]
20. Synthesis and biological evaluation of novel oxadiazole derivatives: a new class of thymidine phosphorylase inhibitors as potential anti-tumor agents.
Shahzad SA; Yar M; Bajda M; Jadoon B; Khan ZA; Naqvi SA; Shaikh AJ; Hayat K; Mahmmod A; Mahmood N; Filipek S
Bioorg Med Chem; 2014 Feb; 22(3):1008-15. PubMed ID: 24411198
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
