IRREVERSIBLE OPIATE AGONISTS AND ANTAGONISTS .5. HYDRAZONE AND ACYLHYDRAZONE DERIVATIVES OF NALTREXONE

被引：48

作者：

LUKE, MC

HAHN, EF

PRICE, M

PASTERNAK, GW

机构：

[1] CORNELL UNIV,MED CTR,COLL MED,DEPT NEUROL,NEW YORK,NY 10021

[2] CORNELL UNIV,MED CTR,COLL MED,DEPT PHARMACOL,NEW YORK,NY 10021

[3] ROCKEFELLER UNIV,BIOCHEM ENDOCRINOL LAB,NEW YORK,NY 10021

来源：

关键词：

D O I：

10.1016/0024-3205(88)90215-9

中图分类号：

R-3 [医学研究方法]; R3 [基础医学];

学科分类号：

1001 ;

摘要：

引用

页码：1249 / 1256

页数：8

共 9 条

[1] CLARK JA, IN PRESS MOL PHARM
[2] HAHN EF, 1985, J PHARMACOL EXP THER, V235, P846
[3] NALOXONAZINE, A POTENT, LONG-LASTING INHIBITOR OF OPIATE BINDING-SITES
HAHN, EF
PASTERNAK, GW
[J]. LIFE SCIENCES, 1982, 31 (12-1) : 1385 - 1388
[4] HAHN EF, 1982, J NEUROSCI, V2, P572
[5] HAHN EF, 1985, J PHARMACOL EXP THER, V235, P839
[6] NALOXONAZINE ACTIONS INVIVO
LING, GSF
SIMANTOV, R
CLARK, JA
PASTERNAK, GW
[J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1986, 129 (1-2) : 33 - 38
[7] MINIREVIEW - MULTIPLE MU OPIATE RECEPTORS
PASTERNAK, GW
WOOD, PJ
[J]. LIFE SCIENCES, 1986, 38 (21) : 1889 - 1898
[8] PASTERNAK GW, 1980, J MED CHEM, V23, P674, DOI 10.1021/jm00180a019
[9] PRICE M, IN PRESS MOL PHARM