139 related articles for article (PubMed ID: 32098709)
1. One-pot synthesis of thioxo-tetrahydropyrimidine derivatives as potent β-glucuronidase inhibitor, biological evaluation, molecular docking and molecular dynamics studies.
Iraji A; Nouri A; Edraki N; Pirhadi S; Khoshneviszadeh M; Khoshneviszadeh M
Bioorg Med Chem; 2020 Apr; 28(7):115359. PubMed ID: 32098709
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 2-Oxo-1,2,3,4-tetrahydropyrimidines Ethyl Esters as Potent β- Glucuronidase Inhibitors: One-pot Synthesis, In vitro and In silico Studies.
Iqbal S; Shaikh NN; Khan KM; Naz S; Ul-Haq Z; Perveen S; Choudhary MI
Med Chem; 2018; 14(8):818-830. PubMed ID: 29793412
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Evaluation of bisindole as potent β-glucuronidase inhibitors: synthesis and in silico based studies.
Khan KM; Rahim F; Wadood A; Taha M; Khan M; Naureen S; Ambreen N; Hussain S; Perveen S; Choudhary MI
Bioorg Med Chem Lett; 2014 Apr; 24(7):1825-9. PubMed ID: 24602903
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Thiazolidin-2-cyanamides derivatives as novel potent
Zhou TS; Wei B; He M; Li YS; Wang YK; Wang SJ; Chen JW; Zhang HW; Cui ZN; Wang H
J Enzyme Inhib Med Chem; 2020 Dec; 35(1):1736-1742. PubMed ID: 32928007
[TBL] [Abstract][Full Text] [Related]
10. Thiadiazole derivatives as New Class of β-glucuronidase inhibitors.
Salar U; Taha M; Ismail NH; Khan KM; Imran S; Perveen S; Wadood A; Riaz M
Bioorg Med Chem; 2016 Apr; 24(8):1909-18. PubMed ID: 26994638
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. 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]
15. Dihydropyrimidones: As novel class of β-glucuronidase inhibitors.
Ali F; Khan KM; Salar U; Iqbal S; Taha M; Ismail NH; Perveen S; Wadood A; Ghufran M; Ali B
Bioorg Med Chem; 2016 Aug; 24(16):3624-35. PubMed ID: 27325448
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Synthesis, in vitro β-glucuronidase inhibitory activity and in silico studies of novel (E)-4-Aryl-2-(2-(pyren-1-ylmethylene)hydrazinyl)thiazoles.
Salar U; Khan KM; Syed S; Taha M; Ali F; Ismail NH; Perveen S; Wadood A; Ghufran M
Bioorg Chem; 2017 Feb; 70():199-209. PubMed ID: 28069264
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Synthesis of pyrimidine-2,4,6-trione derivatives: Anti-oxidant, anti-cancer, α-glucosidase, β-glucuronidase inhibition and their molecular docking studies.
Barakat A; Islam MS; Al-Majid AM; Ghabbour HA; Yousuf S; Ashraf M; Shaikh NN; Iqbal Choudhary M; Khalil R; Ul-Haq Z
Bioorg Chem; 2016 Oct; 68():72-9. PubMed ID: 27454620
[TBL] [Abstract][Full Text] [Related]
20. Synthesis, in vitro β-glucuronidase inhibitory potential and molecular docking studies of quinolines.
Bano B; Arshia ; Khan KM; Kanwal ; Fatima B; Taha M; Ismail NH; Wadood A; Ghufran M; Perveen S
Eur J Med Chem; 2017 Oct; 139():849-864. PubMed ID: 28865280
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
