Tahtaci H - Search Results

1

Design, Synthesis, SAR and Molecular Modeling Studies of Novel Imidazo[2,1-b][1,3,4]Thiadiazole Derivatives as Highly Potent Antimicrobial Agents.

Tahtaci H, Karacık H, Ece A, Er M, Şeker MG. Tahtaci H, et al. Mol Inform. 2018 Mar;37(3). doi: 10.1002/minf.201700083. Epub 2017 Sep 6. Mol Inform. 2018. PMID: 28876536

2

Novel olefinic-centered macroacyclic compounds involving tetrasubstituted 4-hydroxybenzoic acid fragments: synthesis, structural characterization and comparison of experimental and computational results.

Er M, Değirmencioğlu İ, Tahtacı H. Er M, et al. Among authors: tahtaci h. Spectrochim Acta A Mol Biomol Spectrosc. 2015 Mar 15;139:68-74. doi: 10.1016/j.saa.2014.12.030. Epub 2014 Dec 18. Spectrochim Acta A Mol Biomol Spectrosc. 2015. PMID: 25554954

3

An integrated approach towards the development of novel antifungal agents containing thiadiazole: synthesis and a combined similarity search, homology modelling, molecular dynamics and molecular docking study.

Er M, Abounakhla AM, Tahtaci H, Bawah AH, Çınaroğlu SS, Onaran A, Ece A. Er M, et al. Among authors: tahtaci h. Chem Cent J. 2018 Nov 23;12(1):121. doi: 10.1186/s13065-018-0485-3. Chem Cent J. 2018. PMID: 30470928 Free PMC article.

4

Design, synthesis, characterization, in vitro and in silico evaluation of novel imidazo[2,1-b][1,3,4]thiadiazoles as highly potent acetylcholinesterase and non-classical carbonic anhydrase inhibitors.

Askin S, Tahtaci H, Türkeş C, Demir Y, Ece A, Akalın Çiftçi G, Beydemir Ş. Askin S, et al. Among authors: tahtaci h. Bioorg Chem. 2021 Aug;113:105009. doi: 10.1016/j.bioorg.2021.105009. Epub 2021 May 23. Bioorg Chem. 2021. PMID: 34052739

5

Synthesis, in vitro cytotoxicity, molecular docking and ADME study of some indolin-2-one linked 1,2,3-triazole derivatives.

Das A, Greco G, Kumar S, Catanzaro E, Morigi R, Locatelli A, Schols D, Alici H, Tahtaci H, Ravindran F, Fimognari C, Karki SS. Das A, et al. Among authors: tahtaci h. Comput Biol Chem. 2022 Apr;97:107641. doi: 10.1016/j.compbiolchem.2022.107641. Epub 2022 Feb 9. Comput Biol Chem. 2022. PMID: 35168158

6

Design and various in silico studies of the novel curcumin derivatives as potential candidates against COVID-19 -associated main enzymes.

Alici H, Tahtaci H, Demir K. Alici H, et al. Among authors: tahtaci h. Comput Biol Chem. 2022 Jun;98:107657. doi: 10.1016/j.compbiolchem.2022.107657. Epub 2022 Feb 26. Comput Biol Chem. 2022. PMID: 35259661 Free PMC article.

7

Novel Thioether-Bridged 2,6-Disubstituted and 2,5,6-Trisubstituted Imidazothiadiazole Analogues: Synthesis, Antiproliferative Activity, ADME, and Molecular Docking Studies.

Ozcan I, Akkoc S, Alici H, Capanlar S, Sahin O, Tahtaci H. Ozcan I, et al. Among authors: tahtaci h. Chem Biodivers. 2023 Jan;20(1):e202200884. doi: 10.1002/cbdv.202200884. Epub 2022 Dec 13. Chem Biodivers. 2023. PMID: 36445849

8

Synthesis, in silico ADME, molecular docking and in vitro cytotoxicity evaluation of stilbene linked 1,2,3-triazoles.

Das A, Kumar S, Persoons L, Daelemans D, Schols D, Alici H, Tahtaci H, Karki SS. Das A, et al. Among authors: tahtaci h. Heliyon. 2021 Jan 30;7(1):e05893. doi: 10.1016/j.heliyon.2020.e05893. eCollection 2021 Jan. Heliyon. 2021. PMID: 33553718 Free PMC article.

9

Imidazole-Derived Alkyl and Aryl Ethers: Synthesis, Characterization, In Vitro Anticancer and Antioxidant Activities, Carbonic Anhydrase I-II Inhibition Properties, and In Silico Studies.

Faris M, Bostancı HE, Özcan İ, Öztürk M, Koçyiğit ÜM, Erdoğan T, Tahtaci H. Faris M, et al. Among authors: tahtaci h. ACS Omega. 2024 May 3;9(19):20937-20956. doi: 10.1021/acsomega.4c00028. eCollection 2024 May 14. ACS Omega. 2024. PMID: 38764643 Free PMC article.

10

1-[2-(2,6-Dichloro-benz-yloxy)-2-(2-fur-yl)eth-yl]-1H-1,2,4-triazole.

Ozel Güven O, Tahtacı H, Coles SJ, Hökelek T. Ozel Güven O, et al. Among authors: tahtaci h. Acta Crystallogr Sect E Struct Rep Online. 2009 Dec 12;66(Pt 1):o107-8. doi: 10.1107/S1600536809052568. Acta Crystallogr Sect E Struct Rep Online. 2009. PMID: 21579997 Free PMC article.

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