Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Christopher T. Meta"'
Autor:
Chen Christine Hiu-Tung, Remiszewski Stacy W, Jianmei Fan, Alex Fekete, Brant Firestone, Joseph D. Growney, Christopher T. Meta, Joe Eckman, Dyuti Majumdar, Ping Wang, Peter Atadja, Vinita Uttamsingh, Liping Zhou, Laszlo Urban, Qiang Lu, Meier Hsu, Suzanne Skolnik, Lei Jiang, Tim Ramsey, Martin Traebert, Yan Yan-Neale, Minying Pu, Julie Flynn, Lawrence Blas Perez, Yung-Mae Yao, Xueying Cao, Franco Lombardo, Steven Whitebread, Mats Holmqvist, Lewis Whitehead, Young Shin Cho, Paul Kwon, N Davis, Jack Green, Daniel Jansson, Michael Shultz, Gang Liu
Publikováno v:
Journal of Medicinal Chemistry. 54:4752-4772
Histone deacetylase (HDAC) inhibitors have shown promise in treating various forms of cancer. However, many HDAC inhibitors from diverse structural classes have been associated with QT prolongation in humans. Inhibition of the human ether a-go-go rel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c444090ceb6d32a590072a95df83c006
https://doi.org/10.1021/jm200388e
https://doi.org/10.1021/jm200388e
Autor:
Kazunori Koide, Christopher T. Meta
Publikováno v:
ChemInform. 35
γ-Hydroxy-α,β-acetylenic esters are used as precursors to prepare γ-hydroxy-α,β-alkenoic esters by means of trans-selective additions of two hydrogen atoms or one hydrogen atom and one iodine atom across the triple bonds. These methods allow fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::690b838ee59d89bc3c05c304fdb6ef64
https://doi.org/10.1002/chin.200441074
https://doi.org/10.1002/chin.200441074
Autor:
Christopher T, Meta, Kazunori, Koide
Publikováno v:
Organic letters. 6(11)
Gamma-hydroxy-alpha,beta-acetylenic esters are used as precursors to prepare gamma-hydroxy-alpha,beta-alkenoic esters by means of trans-selective additions of two hydrogen atoms or one hydrogen atom and one iodine atom across the triple bonds. These
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5b1e5b068d735f81056dae58b322fe1f
https://pubmed.ncbi.nlm.nih.gov/15151414
https://pubmed.ncbi.nlm.nih.gov/15151414
Autor:
Robert M. Cicchillo, Peter Norris, Matthew D. Bernardina, Jason L. Mccartney, Timothy R. Wagner, Christopher T. Meta
Publikováno v:
The Journal of organic chemistry. 68(26)
Addition of PhLi and lithiated dithianes to 2,3-O-isopropylidene-d-erythronolactone affords lactols, which are reduced with Et3SiH to the corresponding C-glycosides, the structures of two of which have been solved by X-ray diffraction. The use of a d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af9eb20549c40e4204fa9d5f5d388ff5
https://pubmed.ncbi.nlm.nih.gov/14682713
https://pubmed.ncbi.nlm.nih.gov/14682713