AFFINITY-CHROMATOGRAPHY OF SOLUBILIZED OPIOID BINDING-SITES USING CH-SEPHAROSE MODIFIED WITH A NEW NALTREXONE DERIVATIVE

被引：18

作者：

GIOANNINI, TL ^{[1
]}

HOWARD, A ^{[1
]}

HILLER, JM ^{[1
]}

SIMON, EJ ^{[1
]}

机构：

[1] NYU MED CTR,DEPT PHARMACOL,NEW YORK,NY 10016

来源：

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | 1984年 / 119卷 / 02期

关键词：

D O I：

10.1016/S0006-291X(84)80295-8

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：624 / 629

页数：6

共 11 条

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[2] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3] ISOLATION OF OPIATE BINDING-COMPONENTS BY AFFINITY-CHROMATOGRAPHY AND RECONSTITUTION OF BINDING ACTIVITIES
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[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (17): : 5176 - 5180
[4] ISOLATION OF INSULIN RECEPTOR OF LIVER AND FAT-CELL MEMBRANES
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[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1972, 69 (02) : 318 - +
[5] LECTIN BINDING OF SOLUBILIZED OPIATE RECEPTORS - EVIDENCE FOR THEIR GLYCOPROTEIN NATURE
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HATTEN, ME
SIMON, EJ
[J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1982, 105 (03) : 1128 - 1134
[6] HOWELLS RD, 1982, J PHARMACOL EXP THER, V222, P629
[7] STEREOCHEMICAL STUDIES ON MEDICINAL AGENTS .23. SYNTHESIS AND BIOLOGICAL EVALUATION OF 6-AMINO DERIVATIVES OF NALOXONE AND NALTREXONE
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TAKEMORI, AE
[J]. JOURNAL OF MEDICINAL CHEMISTRY, 1977, 20 (08) : 1100 - 1102
[8] PHOSPHOLIPASE-A INHIBITION OF OPIATE RECEPTOR-BINDING CAN BE REVERSED BY ALBUMIN
LIN, HK
SIMON, EJ
[J]. NATURE, 1978, 271 (5643) : 383 - 384
[9] MANECKJEE R, 1983, JUL INT NARC RES C
[10] SYNTHESIS AND PHARMACOLOGIC CHARACTERIZATION OF AN ALKYLATING ANALOG (CHLORNALTREXAMINE) OF NALTREXONE WITH ULTRA-LONG-LASTING NARCOTIC-ANTAGONIST PROPERTIES
PORTOGHESE, PS
LARSON, DL
JIANG, JB
CARUSO, TP
TAKEMORI, AE
[J]. JOURNAL OF MEDICINAL CHEMISTRY, 1979, 22 (02) : 168 - 173

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