Synthesis and biological evaluation of (S)-4-aminoquinazoline alcohols
| dc.authorid | Karabuga, semistan/0000-0001-9753-206X | |
| dc.authorid | Gulluce, Medine/0000-0002-5957-8259 | |
| dc.authorid | Cakici, Murat/0000-0002-7020-0302; | |
| dc.contributor.author | Cakici, Murat | |
| dc.contributor.author | Catir, Mustafa | |
| dc.contributor.author | Karabuga, Semistan | |
| dc.contributor.author | Kilic, Hamdullah | |
| dc.contributor.author | Ulukanli, Sabri | |
| dc.contributor.author | Gulluce, Medine | |
| dc.contributor.author | Orhan, Furkan | |
| dc.date.accessioned | 2025-08-12T08:25:07Z | |
| dc.date.issued | 2010 | |
| dc.department | Osmaniye Korkut Ata Üniversitesi | |
| dc.description.abstract | A simple synthetic method for the preparation of enantiomerically pure (S)-4-aminoquinazoline alcohols from (S)-quinazolinone alcohols by key steps including chlorination, nucleophilic ipso substitution, and deacetylation is presented. Mutagenic and antimutagenic properties of the (S)-4-aminoquinazoline alcohols were investigated by using Salmonella typhimurium TA1535, and Escherichia colt WP2uvrA tester strains at 0.01, 0.1, and 1 mu g/plate concentrations. (S)-4-aminoquinazoline alcohols were found to be genotoxically safe at the tested concentrations. Among the tested (S)-4-aminoquinazoline alcohols, the best antimutagenic activity was obtained with a methyl derivative at 0.1 mu g/plate dose. (C) 2010 Elsevier Ltd. All rights reserved. | |
| dc.description.sponsorship | Scientific and Technological Research Council of Turkey (TUBITAK) [TBAG-108T116] | |
| dc.description.sponsorship | The financial support from the Scientific and Technological Research Council of Turkey (TUBITAK) (TBAG-108T116) is gratefully acknowledged. In addition, the authors would like to thank Dr. Graham Eaton from the Leicester University for the HRMS measurements. | |
| dc.identifier.doi | 10.1016/j.tetasy.2010.05.040 | |
| dc.identifier.endpage | 2031 | |
| dc.identifier.issn | 0957-4166 | |
| dc.identifier.issue | 16 | |
| dc.identifier.scopusquality | N/A | |
| dc.identifier.startpage | 2027 | |
| dc.identifier.uri | https://doi.org/10.1016/j.tetasy.2010.05.040 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12502/4743 | |
| dc.identifier.volume | 21 | |
| dc.identifier.wos | WOS:000281977500013 | |
| dc.identifier.wosquality | N/A | |
| dc.indekslendigikaynak | Web of Science | |
| dc.language.iso | en | |
| dc.publisher | Pergamon-Elsevier Science Ltd | |
| dc.relation.ispartof | Tetrahedron-Asymmetry | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.snmz | KA_WOS_20250812 | |
| dc.subject | Microwave-Assisted Synthesis | |
| dc.subject | Vitro Antitumor-Activity | |
| dc.subject | 4-Aminoquinazoline Derivatives | |
| dc.subject | Inhibitors | |
| dc.subject | Alkaloids | |
| dc.title | Synthesis and biological evaluation of (S)-4-aminoquinazoline alcohols | |
| dc.type | Article |











