Zobrazeno 1 - 10
of 13
pro vyhledávání: '"MARKO KALINIĆ"'
Publikováno v:
Journal of the Serbian Chemical Society, Vol 75, Iss 4, Pp 483-495 (2010)
Aqueous solubility is an important factor influencing several aspects of the pharmacokinetic profile of a drug. Numerous publications present different methodologies for the development of reliable computational models for the prediction of solubilit
Externí odkaz:
https://doaj.org/article/0522278569e74f988f14051add49c185
Deep learning has demonstrated significant potential in advancing state of the art in many problem domains, especially those benefiting from automated feature extraction. Yet the methodology has seen limited adoption in the field of ligand-based virt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89e332269173658706d300b679dfc935
https://doi.org/10.26434/chemrxiv.12412694.v1
https://doi.org/10.26434/chemrxiv.12412694.v1
Autor:
Marko Kalinić, Peter Komar
DNA-encoded libraries (DELs) are large, pooled collections of compounds in which every library member is attached to a stretch of DNA encoding its complete synthetic history. DEL-based hit discovery involves affinity selection of the library against
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::390badb33e44320ed9546384fded28bd
https://doi.org/10.26434/chemrxiv.11573427.v2
https://doi.org/10.26434/chemrxiv.11573427.v2
Autor:
Ana B. Damjanović, Slavica Erić, Jelena Antić-Stanković, Marko Kalinić, Vladimir Savic, Milena Simic, Gordana Tasic
Publikováno v:
Journal of the Serbian Chemical Society, Vol 81, Iss 2, Pp 103-123 (2016)
Journal of the Serbian Chemical Society
Journal of the Serbian Chemical Society
A novel and efficient synthetic route has been developed for the preparation of protoberberine derivatives. The methodology designed to control, primarily, substitution patterns on the terminal rings, was used to access a small array of these compoun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ed3179d87196b5088d863efa905e705
http://www.doiserbia.nb.rs/img/doi/0352-5139/2016/0352-51391500090S.pdf
http://www.doiserbia.nb.rs/img/doi/0352-5139/2016/0352-51391500090S.pdf
Publikováno v:
Journal of Chromatography A
The aim of this study was to examine the interaction of the chaotropic salts of different position in Hofmeister series (CF3COONa, NaClO4, NaPF6) added to the mobile phase with the stationary phases of different hydrophobicity (C8 and C18 XTerra (R)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b15b3ffbf9f7a89a1ce3d85b65b9e9f5
https://doi.org/10.1016/j.chroma.2015.01.078
https://doi.org/10.1016/j.chroma.2015.01.078
Publikováno v:
Advances in Chromatography
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cad868b02c493b0b1642af83063a8f26
https://doi.org/10.1201/9781315116372-1
https://doi.org/10.1201/9781315116372-1
Publikováno v:
Journal of Chromatography A
In this study, we present novel insights into the pH-dependent retention behavior of protonated basic solutes in chaotropic chromatography. To this end, two sets of experiments were performed to distinguish between mobile phase pH and ionic strength
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3eb9edad52f0d2ceaa7a84a39ace7a5a
https://pubmed.ncbi.nlm.nih.gov/28697932
https://pubmed.ncbi.nlm.nih.gov/28697932
Publikováno v:
Journal of Chromatography A
The aim of this study was to systematically investigate the phenomena affecting the retention behavior of structurally diverse basic drugs in ion-interaction chromatographic systems with chaotropic additives. To this end, the influence of three facto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e8f94cf5099d21b5c7cec170c5ab151
https://pubmed.ncbi.nlm.nih.gov/26610616
https://pubmed.ncbi.nlm.nih.gov/26610616
Autor:
Slavica Erić, Marko Kalinić
Publikováno v:
Arhiv za farmaciju (2015) 65(2):89-114
Arhiv za farmaciju
Arhiv za farmaciju, Vol 65, Iss 2, Pp 89-114 (2015)
Arhiv za farmaciju
Arhiv za farmaciju, Vol 65, Iss 2, Pp 89-114 (2015)
P-glycoprotein (Pgp) is a transmembrane transporter which can, by transporting structurally diverse compounds, influence the absorption, distribution and efficacy of a number of drugs. Pgp overexpression in cells is a major contributing factor to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84b04bb7e98e0ed066d00d89982c194c
http://scindeks.ceon.rs/article.aspx?artid=0004-19631502089E
http://scindeks.ceon.rs/article.aspx?artid=0004-19631502089E
Publikováno v:
Saudi Pharmaceutical Journal
P-glycoprotein (P-gp/ABCB1) and breast cancer resistance protein (BCRP/ABCG2) are two members of the adenosine triphosphate (ATP) binding cassette (ABC) family of transporters which function as membrane efflux transporters and display considerable su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab33e8733c77e6b76d76843bc20c5857
https://pubmed.ncbi.nlm.nih.gov/25435255
https://pubmed.ncbi.nlm.nih.gov/25435255