Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sonia R. Miranda"'
Publikováno v:
Molecules, Vol 22, Iss 1, p 142 (2017)
Silymarin is the most commonly used herbal medicine by patients with chronic liver disease. Silymarin flavonolignans undergo rapid first-pass metabolism primarily by glucuronidation. The aims of this investigation were: (1) to determine the associati
Externí odkaz:
https://doaj.org/article/15b92a8626c3440e914d7a5e7d535b4e
Autor:
Jun Tang, Kevin W. Brown, Jerry Jeffrey, Charlene B. McDanal, Brian A. Johns, Sonia R. Miranda, Stacey A. Jones, David M. Irlbeck, Cristin M. Galardi
Publikováno v:
Bioorganicmedicinal chemistry letters. 27(12)
A new class of betulin-derived α-keto amides was identified as HIV-1 maturation inhibitors. Through lead optimization, GSK8999 was identified with IC50 values of 17 nM, 23 nM, 25 nM, and 8 nM for wild type, Q369H, V370A, and T371A respectively. When
Publikováno v:
Molecules, Vol 22, Iss 1, p 142 (2017)
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules; Volume 22; Issue 1; Pages: 142
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules; Volume 22; Issue 1; Pages: 142
Silymarin is the most commonly used herbal medicine by patients with chronic liver disease. Silymarin flavonolignans undergo rapid first-pass metabolism primarily by glucuronidation. The aims of this investigation were: (1) to determine the associati
Autor:
Jun Tang, Erjuan Wang, Zhimin Jin, Kevin W. Brown, David M. Irlbeck, Jerry L. Jeffery, Rui Li, Heping Yang, Cristin M. Galardi, Sonia R. Miranda, Bin Shen, Charlene B. McDanal, Yajun Yu, Daxin Gao, Brian A. Johns, Chunyu Liu, Yongyong Wu, Yufei Sun, Caiming Xi, Nianhe Han, Stacey A. Jones
Publikováno v:
The Open Medicinal Chemistry Journal
A macrocycle provides diverse functionality and stereochemical complexity in a conformationally preorganized ring structure, and it occupies a unique chemical space in drug discovery. However, the synthetic challenge to access this structural class i
Cytotoxicity of chloroacetanilide herbicide alachlor in HepG2 cells independent of CYP3A4 and CYP3A7
Autor:
Sonia R. Miranda, Sharon A. Meyer
Publikováno v:
Food and Chemical Toxicology. 45:871-877
Alachlor is cytotoxic to human hepatoblastoma HepG2s, a cell line that expresses constitutive CYP3A7 and dexamethasone (DEX)-inducible CYP3A4 and CYP3A7. CYP3A4 catalyzes alachlor N-dealkylation to 2-chloro-N-(2,6-diethylphenyl)acetamide (CDEPA), pre
Autor:
Brian A. Johns, Emile Johann Velthuisen, Kendra E. Hightower, John W. Seal, Peter Gerondelis, Kevin K. Brown, Ming Li, Lisa A. Leesnitzer, Wenwen Zhang, Yan Chen, Sonia R. Miranda, Ke Mou
Publikováno v:
European journal of medicinal chemistry. 83
Using a structure based pharmacophore design, a weak inhibitor of RNase H, identified from a small library of two metal binding HIV-1 integrase inhibitors, was optimized for potency and physicochemical properties. This manuscript describes the SAR an
Publikováno v:
Journal of biochemical and molecular toxicology. 22(1)
Noncancerous adverse effects observed at the lowest dose for chloroacetanilide herbicides alachlor [2-chloro-2',6'-diethyl-N-(methoxymethyl)-acetanilide] and acetochlor [2-chloro-2'-methyl-6'-ethyl-N-(ethoxymethyl)acetanilide], but not metolachlor [2