dc.contributor.author | Kumar, A. Sunil | |
dc.contributor.author | Kudva, Jyothi | |
dc.contributor.author | Lahtinen, Manu | |
dc.contributor.author | Peuronen, Anssi | |
dc.contributor.author | Sadashiva, Rajitha | |
dc.contributor.author | Naral, Damodara | |
dc.date.accessioned | 2019-04-25T06:31:29Z | |
dc.date.available | 2021-08-16T21:35:07Z | |
dc.date.issued | 2019 | |
dc.identifier.citation | Kumar, A. S., Kudva, J., Lahtinen, M., Peuronen, A., Sadashiva, R., & Naral, D. (2019). Synthesis, characterization, crystal structures and biological screening of 4-amino quinazoline sulfonamide derivatives. <i>Journal of Molecular Structure</i>, <i>1190</i>, 29-36. <a href="https://doi.org/10.1016/j.molstruc.2019.04.050" target="_blank">https://doi.org/10.1016/j.molstruc.2019.04.050</a> | |
dc.identifier.other | CONVID_30121675 | |
dc.identifier.other | TUTKAID_81228 | |
dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/63609 | |
dc.description.abstract | Three quinazolin-4-ylamino derivatives containing phenylbenzenesulfonamides (7a-7c) were
synthesized by reacting (E)-N'-(2-cyanophenyl)-N,N-dimethyl formamidine (6) with different 4-
amino-N-(phenyl)benzenesulfonamides (4a-4c) and characterized by different techniques such as
HRMS, IR, 1H NMR and 13C NMR spectroscopy. The structural properties were further
examined by single crystal X-ray diffraction method. The X-ray data shows that compounds 7a
and 7c contain two molecules and 7b contains one molecule in the asymmetric unit. Comparison
of conformation of two distinct molecules, “A” and “B”, in the asymmetric unit of 7a and 7c
were studied with the aid of reported literature. The in vitro antiproliferative activity of the
compounds was tested against two breast cancer cell lines (MDA-MB-231 and MCF7).
Compound 7b observed as a highest potent candidate against MDA-MB-231with IC50 of 5.44
µg/mL. Antimicrobial activity was also screened against bacterial and fungal strains. Compound
7a with chloro substitution was observed as the most potent candidate against the Gram-negative
bacterial strains, whereas the compounds showed no significant activity against the fungal strain. | fi |
dc.format.mimetype | application/pdf | |
dc.language.iso | eng | |
dc.publisher | Elsevier BV | |
dc.relation.ispartofseries | Journal of Molecular Structure | |
dc.rights | CC BY-NC-ND 4.0 | |
dc.subject.other | X-ray-diffraction | |
dc.subject.other | quinazoline-sulfonamide | |
dc.subject.other | crystal structure | |
dc.subject.other | antimicrobial | |
dc.subject.other | antiproliferative activity | |
dc.title | Synthesis, characterization, crystal structures and biological screening of 4-amino quinazoline sulfonamide derivatives | |
dc.type | article | |
dc.identifier.urn | URN:NBN:fi:jyu-201904232241 | |
dc.contributor.laitos | Kemian laitos | fi |
dc.contributor.laitos | Department of Chemistry | en |
dc.contributor.oppiaine | Epäorgaaninen ja analyyttinen kemia | fi |
dc.contributor.oppiaine | Inorganic and Analytical Chemistry | en |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
dc.date.updated | 2019-04-23T09:15:28Z | |
dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
dc.description.reviewstatus | peerReviewed | |
dc.format.pagerange | 29-36 | |
dc.relation.issn | 0022-2860 | |
dc.relation.numberinseries | 0 | |
dc.relation.volume | 1190 | |
dc.type.version | acceptedVersion | |
dc.rights.copyright | ©2019 Published by Elsevier B.V. | |
dc.rights.accesslevel | openAccess | fi |
dc.relation.grantnumber | 277250 | |
dc.subject.yso | aromaattiset yhdisteet | |
dc.subject.yso | antimikrobiset yhdisteet | |
dc.subject.yso | kemiallinen synteesi | |
dc.subject.yso | solunsalpaajat | |
dc.format.content | fulltext | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p23502 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p21949 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p8468 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p9995 | |
dc.rights.url | https://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.relation.doi | 10.1016/j.molstruc.2019.04.050 | |
dc.relation.funder | Suomen Akatemia | fi |
dc.relation.funder | Research Council of Finland | en |
jyx.fundingprogram | Akatemiahanke, SA | fi |
jyx.fundingprogram | Academy Project, AoF | en |
jyx.fundinginformation | The authors are gratefully acknowledge the financial support provided by VGST-K-FIST (L1)/2017, GRD No. 557 and the Academy of Finland (Project No. 277250 and 315911). | |
dc.type.okm | A1 | |