Jan MS - Search Results

1

2-Hydroxybenzohydrazide as a novel potential candidate against nociception, inflammation, and pyrexia: in vitro, in vivo, and computational approaches.

Ali G, Islam NU, Qaim M, Ullah R, Jan MS, Shabbiri K, Shafique M, Ayaz M. Ali G, et al. Among authors: jan ms. Inflammopharmacology. 2024 Feb;32(1):643-656. doi: 10.1007/s10787-023-01356-0. Epub 2023 Oct 21. Inflammopharmacology. 2024. PMID: 37864684

2

Synthesis, anticholinesterase and antioxidant potentials of ketoesters derivatives of succinimides: a possible role in the management of Alzheimer's.

Sadiq A, Mahmood F, Ullah F, Ayaz M, Ahmad S, Haq FU, Khan G, Jan MS. Sadiq A, et al. Among authors: jan ms. Chem Cent J. 2015 May 26;9:31. doi: 10.1186/s13065-015-0107-2. eCollection 2015. Chem Cent J. 2015. PMID: 26064188 Free PMC article.

3

Anticholinesterase and antioxidant potentials of Nonea micrantha Bioss. & Reut along with GC-MS analysis.

Imran M, Ullah F, Ayaz M, Sadiq A, Shah MR, Jan MS, Ullah F. Imran M, et al. Among authors: jan ms. BMC Complement Altern Med. 2017 Nov 23;17(1):499. doi: 10.1186/s12906-017-2004-9. BMC Complement Altern Med. 2017. PMID: 29169349 Free PMC article.

4

HPLC-DAD finger printing, antioxidant, cholinesterase, and α-glucosidase inhibitory potentials of a novel plant Olax nana.

Ovais M, Ayaz M, Khalil AT, Shah SA, Jan MS, Raza A, Shahid M, Shinwari ZK. Ovais M, et al. Among authors: jan ms. BMC Complement Altern Med. 2018 Jan 3;18(1):1. doi: 10.1186/s12906-017-2057-9. BMC Complement Altern Med. 2018. PMID: 29295712 Free PMC article.

5

Ethyl 3-oxo-2-(2,5-dioxopyrrolidin-3-yl)butanoate Derivatives: Anthelmintic and Cytotoxic Potentials, Antimicrobial, and Docking Studies.

Mahmood F, Jan MS, Ahmad S, Rashid U, Ayaz M, Ullah F, Hussain F, Ahmad A, Khan AU, Aasim M, Sadiq A. Mahmood F, et al. Among authors: jan ms. Front Chem. 2017 Dec 12;5:119. doi: 10.3389/fchem.2017.00119. eCollection 2017. Front Chem. 2017. PMID: 29312926 Free PMC article.

6

Synthesis, in-vitro α-glucosidase inhibition, antioxidant, in-vivo antidiabetic and molecular docking studies of pyrrolidine-2,5-dione and thiazolidine-2,4-dione derivatives.

Hussain F, Khan Z, Jan MS, Ahmad S, Ahmad A, Rashid U, Ullah F, Ayaz M, Sadiq A. Hussain F, et al. Among authors: jan ms. Bioorg Chem. 2019 Oct;91:103128. doi: 10.1016/j.bioorg.2019.103128. Epub 2019 Jul 18. Bioorg Chem. 2019. PMID: 31369977

7

Design, synthesis, in-vitro, in-vivo and in-silico studies of pyrrolidine-2,5-dione derivatives as multitarget anti-inflammatory agents.

Jan MS, Ahmad S, Hussain F, Ahmad A, Mahmood F, Rashid U, Abid OU, Ullah F, Ayaz M, Sadiq A. Jan MS, et al. Eur J Med Chem. 2020 Jan 15;186:111863. doi: 10.1016/j.ejmech.2019.111863. Epub 2019 Nov 10. Eur J Med Chem. 2020. PMID: 31740050

8

Pharmacological Evaluation of Aldehydic-Pyrrolidinedione Against HCT-116, MDA-MB231, NIH/3T3, MCF-7 Cancer Cell Lines, Antioxidant and Enzyme Inhibition Studies.

Ahmad A, Ullah F, Sadiq A, Ayaz M, Rahim H, Rashid U, Ahmad S, Jan MS, Ullah R, Shahat AA, Mahmood HM. Ahmad A, et al. Among authors: jan ms. Drug Des Devel Ther. 2019 Dec 10;13:4185-4194. doi: 10.2147/DDDT.S226080. eCollection 2019. Drug Des Devel Ther. 2019. PMID: 31849450 Free PMC article.

9

Mechanistic evaluation of a novel cyclohexenone derivative's functionality against nociception and inflammation: An in-vitro, in-vivo and in-silico approach.

Khan J, Ali G, Rashid U, Khan R, Jan MS, Ullah R, Ahmad S, Abbasi SW, Khan Khalil AA, Sewell RE. Khan J, et al. Among authors: jan ms. Eur J Pharmacol. 2021 Jul 5;902:174091. doi: 10.1016/j.ejphar.2021.174091. Epub 2021 Apr 16. Eur J Pharmacol. 2021. PMID: 33865830

10

Neuroprotective potentials of selected natural edible oils using enzyme inhibitory, kinetic and simulation approaches.

Mahnashi MH, Alyami BA, Alqahtani YS, Alqarni AO, Jan MS, Ayaz M, Ullah F, Shahid M, Rashid U, Sadiq A. Mahnashi MH, et al. Among authors: jan ms. BMC Complement Med Ther. 2021 Oct 2;21(1):248. doi: 10.1186/s12906-021-03420-0. BMC Complement Med Ther. 2021. PMID: 34600509 Free PMC article.

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