Improved pharmacophore description of P-glycoprotein modulators

被引:0
作者
Ferreira, R. J. [1 ]
dos Santos, D. J. [1 ]
Ferreira, M. U. [1 ]
Guedes, R. C. [1 ]
机构
[1] Univ Lisbon, Res Inst Med & Pharmaceut Sci iMed UL, Fac Farm, P-1600083 Lisbon, Portugal
关键词
P-glycoprotein; pharmacophore; modulators; lathyrane; macrocyclic diterpenes; MULTIDRUG-RESISTANCE;
D O I
暂无
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
引用
收藏
页码:1442 / 1443
页数:2
相关论文
共 4 条
[1]   New macrocyclic lathyrane diterpenes, from Euphorbia lagascae, as inhibitors of multidrug resistance of tumour cells [J].
Duarte, N ;
Gyémánt, N ;
Abreu, PM ;
Molnár, J ;
Ferreira, MJU .
PLANTA MEDICA, 2006, 72 (02) :162-168
[2]   Pharmacophore model of drugs involved in P-glycoprotein multidrug resistance: Explanation of structural variety (Hypothesis) [J].
Pajeva, IK ;
Wiese, M .
JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (26) :5671-5686
[3]   ESSENTIAL FEATURES OF THE P-GLYCOPROTEIN PHARMACOPHORE AS DEFINED BY A SERIES OF RESERPINE ANALOGS THAT MODULATE MULTIDRUG RESISTANCE [J].
PEARCE, HL ;
SAFA, AR ;
BACH, NJ ;
WINTER, MA ;
CIRTAIN, MC ;
BECK, WT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (13) :5128-5132
[4]  
TSURUO T, 1981, CANCER RES, V41, P1967