Nonsymmetric P2/P2' cyclic urea HIV protease inhibitors. Structure-activity relationship, bioavailability, and resistance profile of monoindazole-substituted P2 analogues.
about
Identification of novel HIV 1--protease inhibitors: application of ligand and structure based pharmacophore mapping and virtual screening4,6-Bis(4-fluoro-phen-yl)-2-phenyl-1H-indazol-3(2H)-one.Propan-2-yl r-4-(4-fluoro-phen-yl)-3-hy-droxy-c-6-methyl-2-phenyl-4,5-dihydro-2H-indazole-t-5-carboxyl-ate.Claisen-Schmidt condensation: Synthesis of (1S,6R)/(1R,6S)-2-oxo-N,4,6-triarylcyclohex-3-enecarboxamide derivatives with different substituents in H2 O/EtOH.
P2860
Nonsymmetric P2/P2' cyclic urea HIV protease inhibitors. Structure-activity relationship, bioavailability, and resistance profile of monoindazole-substituted P2 analogues.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Nonsymmetric P2/P2' cyclic ure ...... zole-substituted P2 analogues.
@en
type
label
Nonsymmetric P2/P2' cyclic ure ...... zole-substituted P2 analogues.
@en
prefLabel
Nonsymmetric P2/P2' cyclic ure ...... zole-substituted P2 analogues.
@en
P2093
P356
P1476
Nonsymmetric P2/P2' cyclic ure ...... zole-substituted P2 analogues.
@en
P2093
Bacheler LT
De Lucca GV
Erickson-Viitanen S
P304
P356
10.1021/JM980103G
P407
P577
1998-06-01T00:00:00Z