Fatima I - Search Results

1

Novel Tetrazoles against Acanthamoeba castellanii Belonging to the T4 Genotype.

Wehelie YI, Khan NA, Fatima I, Anwar A, Kanwal K, Khan KM, Siddiqui R, Tong YK, Anwar A. Wehelie YI, et al. Among authors: fatima i. Chemotherapy. 2022;67(3):183-192. doi: 10.1159/000520585. Epub 2021 Nov 1. Chemotherapy. 2022. PMID: 34724675

2

Antiamoebic activity of synthetic tetrazoles against Acanthamoeba castellanii belonging to T4 genotype and effects of conjugation with silver nanoparticles.

Anwar A, Yi YP, Fatima I, Khan KM, Siddiqui R, Khan NA, Anwar A. Anwar A, et al. Among authors: fatima i. Parasitol Res. 2020 Jun;119(6):1943-1954. doi: 10.1007/s00436-020-06694-4. Epub 2020 May 9. Parasitol Res. 2020. Retraction in: Parasitol Res. 2022 Mar;121(3):1073. doi: 10.1007/s00436-022-07440-8. PMID: 32385711 Retracted.

3

Novel Azoles as Antiparasitic Remedies against Brain-Eating Amoebae.

Anwar A, Mungroo MR, Khan S, Fatima I, Rafique R, Kanwal, Khan KM, Siddiqui R, Khan NA. Anwar A, et al. Among authors: fatima i. Antibiotics (Basel). 2020 Apr 17;9(4):188. doi: 10.3390/antibiotics9040188. Antibiotics (Basel). 2020. PMID: 32316387 Free PMC article.

4

Retraction Note to: Antiamoebic activity of synthetic tetrazoles against Acanthamoeba castellanii belonging to T4 genotype and effects of conjugation with silver nanoparticles.

Anwar A, Yi YP, Fatima I, Khan KM, Siddiqui R, Khan NA, Anwar A. Anwar A, et al. Among authors: fatima i. Parasitol Res. 2022 Mar;121(3):1073. doi: 10.1007/s00436-022-07440-8. Parasitol Res. 2022. PMID: 35072801 No abstract available.

5

Synthesis, molecular docking and xanthine oxidase inhibitory activity of 5-aryl-1H-tetrazoles.

Fatima I, Zafar H, Khan KM, Saad SM, Javaid S, Perveen S, Choudhary MI. Fatima I, et al. Bioorg Chem. 2018 Sep;79:201-211. doi: 10.1016/j.bioorg.2018.04.021. Epub 2018 May 1. Bioorg Chem. 2018. PMID: 29772470

6

N'-(3-Chloro-benzyl-idene)-4-hy-droxy-benzohydrazide.

Saad SM, Fatima I, Perveen S, Khan KM, Yousuf S. Saad SM, et al. Among authors: fatima i. Acta Crystallogr Sect E Struct Rep Online. 2012 Dec 1;68(Pt 12):o3499. doi: 10.1107/S1600536812048325. Epub 2012 Nov 30. Acta Crystallogr Sect E Struct Rep Online. 2012. PMID: 23476306 Free PMC article.

7

2-Arylquinazolin-4(3H)-ones: A new class of α-glucosidase inhibitors.

Javaid K, Saad SM, Rasheed S, Moin ST, Syed N, Fatima I, Salar U, Khan KM, Perveen S, Choudhary MI. Javaid K, et al. Among authors: fatima i. Bioorg Med Chem. 2015 Dec 1;23(23):7417-21. doi: 10.1016/j.bmc.2015.10.038. Epub 2015 Oct 29. Bioorg Med Chem. 2015. PMID: 26552899

8

2-Aryl benzimidazoles: Synthesis, In vitro α-amylase inhibitory activity, and molecular docking study.

Adegboye AA, Khan KM, Salar U, Aboaba SA, Kanwal, Chigurupati S, Fatima I, Taha M, Wadood A, Mohammad JI, Khan H, Perveen S. Adegboye AA, et al. Among authors: fatima i. Eur J Med Chem. 2018 Apr 25;150:248-260. doi: 10.1016/j.ejmech.2018.03.011. Epub 2018 Mar 6. Eur J Med Chem. 2018. PMID: 29533872

9

Isolation of onosmins A and B, lipoxygenase inhibitors from Onosma hispida.

Ahmad I, Nawaz SA, Afza N, Malik A, Fatima I, Khan SB, Ahmad M, Choudhary MI. Ahmad I, et al. Among authors: fatima i. Chem Pharm Bull (Tokyo). 2005 Aug;53(8):907-10. doi: 10.1248/cpb.53.907. Chem Pharm Bull (Tokyo). 2005. PMID: 16079517 Free article.

10

Two new protease-inhibiting glycosphingolipids from Buddleja crispa.

Ahmad I, Anis I, Fatima I, Malik A, Khan S, Afza N, Tareen RB, Lodhi MA, Choudhary MI. Ahmad I, et al. Among authors: fatima i. Chem Biodivers. 2007 May;4(5):917-24. doi: 10.1002/cbdv.200790080. Chem Biodivers. 2007. PMID: 17510987

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