Tarikogullari AH - Search Results

1

Design, synthesis, and biological evaluation of some novel naphthoquinone-glycine/β-alanine anilide derivatives as noncovalent proteasome inhibitors.

Tatar I, Uysal S, Yilmaz S, Tarikogullari AH, Ballar Kirmizibayrak P, Soyer Z. Tatar I, et al. Among authors: tarikogullari ah. Chem Biol Drug Des. 2023 Jun;101(6):1283-1298. doi: 10.1111/cbdd.14212. Epub 2023 Feb 17. Chem Biol Drug Des. 2023. PMID: 36762979

2

Design, synthesis and biological evaluation of novel naphthoquinone-4-aminobenzensulfonamide/carboxamide derivatives as proteasome inhibitors.

Uysal S, Soyer Z, Saylam M, Tarikogullari AH, Yilmaz S, Kirmizibayrak PB. Uysal S, et al. Among authors: tarikogullari ah. Eur J Med Chem. 2021 Jan 1;209:112890. doi: 10.1016/j.ejmech.2020.112890. Epub 2020 Oct 3. Eur J Med Chem. 2021. PMID: 33039723

3

Synthesis, biological evaluation, and docking studies of some 5-chloro-2(3H)-benzoxazolone Mannich bases derivatives as cholinesterase inhibitors.

Uysal S, Parlar S, Tarikogullari AH, Aydin Kose F, Alptuzun V, Soyer Z. Uysal S, et al. Among authors: tarikogullari ah. Arch Pharm (Weinheim). 2018 Apr;351(3-4):e1700273. doi: 10.1002/ardp.201700273. Epub 2018 Mar 12. Arch Pharm (Weinheim). 2018. PMID: 29527733

4

Synthesis, Biological Evaluation and Molecular Docking Study of Hydrazone-Containing Pyridinium Salts as Cholinesterase Inhibitors.

Parlar S, Bayraktar G, Tarikogullari AH, Alptüzün V, Erciyas E. Parlar S, et al. Among authors: tarikogullari ah. Chem Pharm Bull (Tokyo). 2016;64(9):1281-7. doi: 10.1248/cpb.c16-00221. Chem Pharm Bull (Tokyo). 2016. PMID: 27581632 Free article.

5

Synthesis, biological activity and molecular modeling studies on 1H-benzimidazole derivatives as acetylcholinesterase inhibitors.

Alpan AS, Parlar S, Carlino L, Tarikogullari AH, Alptüzün V, Güneş HS. Alpan AS, et al. Among authors: tarikogullari ah. Bioorg Med Chem. 2013 Sep 1;21(17):4928-37. doi: 10.1016/j.bmc.2013.06.065. Epub 2013 Jul 10. Bioorg Med Chem. 2013. PMID: 23891231

6

Multifunctional cholinesterase inhibitors for Alzheimer's disease: Synthesis, biological evaluations, and docking studies of o/p-propoxyphenylsubstituted-1H-benzimidazole derivatives.

Sarıkaya G, Çoban G, Parlar S, Tarikogullari AH, Armagan G, Erdoğan MA, Alptüzün V, Alpan AS. Sarıkaya G, et al. Among authors: tarikogullari ah. Arch Pharm (Weinheim). 2018 Jul 8. doi: 10.1002/ardp.201800076. Online ahead of print. Arch Pharm (Weinheim). 2018. PMID: 29984517

7

Design, synthesis, acetylcholinesterase, butyrylcholinesterase, and amyloid-β aggregation inhibition studies of substituted 4,4'-diimine/4,4'-diazobiphenyl derivatives.

Fidan GS, Parlar S, Tarikogullari AH, Alptuzun V, Alpan AS. Fidan GS, et al. Among authors: tarikogullari ah. Arch Pharm (Weinheim). 2022 Dec;355(12):e2200152. doi: 10.1002/ardp.202200152. Epub 2022 Aug 17. Arch Pharm (Weinheim). 2022. PMID: 35976708

8

Synthesis and anticonvulsant activity of some alkanamide derivatives.

Tarikogullari AH, Kilic FS, Erol K, Pabuccuoglu V. Tarikogullari AH, et al. Arzneimittelforschung. 2010;60(10):593-8. doi: 10.1055/s-0031-1296331. Arzneimittelforschung. 2010. PMID: 21125808

9

N-Substituted piperidine-3-carbohydrazide-hydrazones against Alzheimer's disease: Synthesis and evaluation of cholinesterase, beta-amyloid inhibitory activity, and antioxidant capacity.

Parlar S, Sayar G, Tarikogullari AH, Karadagli SS, Alan E, Sevin G, Erciyas E, Holzgrabe U, Alptuzun V. Parlar S, et al. Among authors: tarikogullari ah. Arch Pharm (Weinheim). 2023 Mar;356(3):e2200519. doi: 10.1002/ardp.202200519. Epub 2022 Dec 3. Arch Pharm (Weinheim). 2023. PMID: 36461719

10

Exploring enzyme inhibition profiles of novel halogenated chalcone derivatives on some metabolic enzymes: Synthesis, characterization and molecular modeling studies.

Anil DA, Polat MF, Saglamtas R, Tarikogullari AH, Alagoz MA, Gulcin I, Algul O, Burmaoglu S. Anil DA, et al. Among authors: tarikogullari ah. Comput Biol Chem. 2022 Oct;100:107748. doi: 10.1016/j.compbiolchem.2022.107748. Epub 2022 Jul 28. Comput Biol Chem. 2022. PMID: 35917597

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