Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Cheryl Wu"'
Publikováno v:
CPT: Pharmacometrics & Systems Pharmacology, Vol 10, Iss 8, Pp 953-961 (2021)
Abstract Although the use of excipients is widespread, a thorough understanding of the drug interaction potential of these compounds remains a frequent topic of current research. Not only can excipients alter the disposition of coformulated drugs, bu
Externí odkaz:
https://doaj.org/article/253be63d1edb4eceb745e2080720f664
Autor:
Fathi Sei Pahangai Akbar, Steven Yanuar Prasetyo Ginting, Giovanna Cheryl Wu, Said Achmad, Rhio Sutoyo
Publikováno v:
2022 4th International Conference on Cybernetics and Intelligent System (ICORIS).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37a1f7403a820f54975a48d03e8576f7
https://doi.org/10.1109/icoris56080.2022.10031554
https://doi.org/10.1109/icoris56080.2022.10031554
Publikováno v:
CPT: Pharmacometrics & Systems Pharmacology
CPT: Pharmacometrics & Systems Pharmacology, Vol 10, Iss 8, Pp 953-961 (2021)
CPT: Pharmacometrics & Systems Pharmacology, Vol 10, Iss 8, Pp 953-961 (2021)
While the use of excipients is widespread, a thorough understanding of the drug interaction potential of these compounds remains a frequent topic of current research. Not only can excipients alter the disposition of co-formulated drugs, but it is lik
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca34b1d55fd34526bf31a820fd057797
http://europepmc.org/articles/PMC8376134
http://europepmc.org/articles/PMC8376134
Autor:
Sandra Merrick, Frédérique Barbosa, Nicolas Froloff, Boryeu Mao, Wei Shi, Kelly Kamm, Cheryl Wu, Rafael Gozalbes, Eric Wong, Jacques Migeon, Chester Costales
Publikováno v:
Journal of Chemical Information and Modeling. 46:2125-2134
We report the QSAR modeling of cytochrome P450 3A4 (CYP3A4) enzyme inhibition using four large data sets of in vitro data. These data sets consist of marketed drugs and drug-like compounds all tested in four assays measuring the inhibition of the met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5e4c22145439ec52828e36a0cb57087
https://doi.org/10.1021/ci0600915
https://doi.org/10.1021/ci0600915
Autor:
Keiko Yonezawa, Tohru Sugimoto, Shigeru Furuta, Takeshi Omata, Tadashi Kurimoto, Yoshihiro Kawabata, Xiaochun Cheryl Wu, Emiko Kamada
Publikováno v:
European Journal of Pharmacology. 497:223-231
In the present study, the inhibitory properties of N-[2-(diisopropylamino)ethyl]-2-[(2-hydroxy-4,5-dimethoxybenzoyl)amino]-1,3-thiazole-4-carboxamide monohydrochloride trihydrate (Z-338), a novel gastroprokinetic agent, were investigated and compared
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74c15352b253c1c18ab4007adb4e47f3
https://doi.org/10.1016/j.ejphar.2004.06.040
https://doi.org/10.1016/j.ejphar.2004.06.040
Publikováno v:
The American journal of physiology. 277(4)
Although its primary function is monovalent anion exchange, the band 3 protein also cotransports divalent anions together with protons at low pH. The putative proton binding site, Glu-681 in human erythrocyte band 3, is conserved throughout the anion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::179268050687f16c8e643e398a945662
https://pubmed.ncbi.nlm.nih.gov/10516109
https://pubmed.ncbi.nlm.nih.gov/10516109