Design, Synthesis, and Biological Evaluation of Novel Nonsteroidal Farnesoid X Receptor (FXR) Antagonists: Molecular Basis of FXR Antagonism.
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Novel chemoenzymatic oxidation of amines into oximes based on hydrolase-catalysed peracid formation.Synthesis and Molecular Modeling Studies of N'-Hydroxyindazolecarboximidamides as Novel Indoleamine 2,3-Dioxygenase 1 (IDO1) Inhibitors.Reagent-controlled regiodivergent intermolecular cyclization of 2-aminobenzothiazoles with β-ketoesters and β-ketoamides.
P2860
Design, Synthesis, and Biological Evaluation of Novel Nonsteroidal Farnesoid X Receptor (FXR) Antagonists: Molecular Basis of FXR Antagonism.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Design, Synthesis, and Biologi ...... cular Basis of FXR Antagonism.
@en
Design, Synthesis, and Biologi ...... cular Basis of FXR Antagonism.
@nl
type
label
Design, Synthesis, and Biologi ...... cular Basis of FXR Antagonism.
@en
Design, Synthesis, and Biologi ...... cular Basis of FXR Antagonism.
@nl
prefLabel
Design, Synthesis, and Biologi ...... cular Basis of FXR Antagonism.
@en
Design, Synthesis, and Biologi ...... cular Basis of FXR Antagonism.
@nl
P2093
P2860
P356
P1433
P1476
Design, Synthesis, and Biologi ...... ecular Basis of FXR Antagonism
@en
P2093
Hualiang Jiang
P2860
P304
P356
10.1002/CMDC.201500136
P50
P577
2015-05-15T00:00:00Z