Rational design and synthesis of 2,2-bisheterocycle tandem derivatives as non-nucleoside hepatitis B virus inhibitors.
about
Potent and orally efficacious bisthiazole-based histone deacetylase inhibitorsEmergence of Chinese drug discovery research: impact of hit and lead identification.Isothiafludine, a novel non-nucleoside compound, inhibits hepatitis B virus replication through blocking pregenomic RNA encapsidation.Synthesis and anti-hepatitis B virus activity of a novel class of thiazolylbenzimidazole derivatives.Antimicrobial activity of thiophene derivatives derived from ethyl (E)-5-(3-(dimethylamino)acryloyl)-4-methyl-2-(phenylamino)thiophene-3-carboxylate
P2860
Rational design and synthesis of 2,2-bisheterocycle tandem derivatives as non-nucleoside hepatitis B virus inhibitors.
description
2008 nî lūn-bûn
@nan
2008 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Rational design and synthesis ...... hepatitis B virus inhibitors.
@ast
Rational design and synthesis ...... hepatitis B virus inhibitors.
@en
type
label
Rational design and synthesis ...... hepatitis B virus inhibitors.
@ast
Rational design and synthesis ...... hepatitis B virus inhibitors.
@en
prefLabel
Rational design and synthesis ...... hepatitis B virus inhibitors.
@ast
Rational design and synthesis ...... hepatitis B virus inhibitors.
@en
P2093
P356
P1433
P1476
Rational design and synthesis ...... hepatitis B virus inhibitors.
@en
P2093
Fa-Jun Nan
Feng-Hua Zhu
Gui-Feng Wang
Hai-Jun Chen
Jian-Ping Zuo
Li-Fei Hou
Li-Ping Shi
Pei-Lan He
P2860
P304
P356
10.1002/CMDC.200800136
P577
2008-09-01T00:00:00Z