INCREASED POTENCY OF ANTAGONISTS OF THE LUTEINIZING-HORMONE-RELEASING HORMONE WHICH HAVE D-3-PAL IN POSITION-6

被引：18

作者：

FOLKERS, K ^{[1
]}

BOWERS, C ^{[1
]}

XIAO, SB ^{[1
]}

TANG, PFL ^{[1
]}

KUBOTA, M ^{[1
]}

机构：

[1] TULANE UNIV,SCH MED,ENDOCRINE UNIT,NEW ORLEANS,LA 70112

来源：

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | 1986年 / 137卷 / 02期

关键词：

D O I：

10.1016/0006-291X(86)91136-8

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：709 / 715

页数：7

共 11 条

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[2]

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[3]

HO TL, 1984, INT J PEPT PROT RES, V24, P79

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[5]

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[6]

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[8]

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[9] LUTEINIZING-HORMONE-RELEASING HORMONE ANTAGONISTS CONTAINING VERY HYDROPHOBIC AMINO-ACIDS [J].

NESTOR, JJ ;

TAHILRAMANI, R ;

HO, TL ;

MCRAE, GI ;

VICKERY, BH .

JOURNAL OF MEDICINAL CHEMISTRY, 1984, 27 (09) :1170-1174

[10] SYNTHESIS OF A NOVEL CLASS OF HETEROAROMATIC AMINO-ACIDS AND THEIR USE IN THE PREPARATION OF ANALOGS OF LUTEINIZING-HORMONE-RELEASING HORMONE [J].

NESTOR, JJ ;

HORNER, BL ;

HO, TL ;

JONES, GH ;

MCRAE, GI ;

VICKERY, BH .

JOURNAL OF MEDICINAL CHEMISTRY, 1984, 27 (03) :320-325

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