N-BENZYLOXYCARBONYL-L-AMINOSUCCINYL-L-PHENYLALANINAMIDE (Z-L-ASU-L-PHE-NH2)

被引：11

作者：

MAZZARELLA, L ^{[1
]}

SCHON, I ^{[1
]}

SICA, F ^{[1
]}

ZAGARI, A ^{[1
]}

机构：

[1] CHEM WORKS GEDEON RICHTER,H-1475 BUDAPEST 10,HUNGARY

来源：

关键词：

D O I：

10.1107/S0108270187011831

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：880 / 882

页数：3

共 16 条

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[3] CAPASSO S, 1984, INT J PEPT PROT RES, V23, P248
[4] CAPASSO S, 1984, INT J PEPT PROT RES, V24, P588
[5] TERT-BUTYLOXYCARBONYL-L-AMINOSUCCINYL-GLYCYL-L-ALANINE METHYL-ESTER (BOC-L-ASU-GLY-L-ALA-OME)
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[J]. ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS, 1987, 43 : 1607 - 1610
[6] CAPASSO S, 1984, INT J PEPT PROT RES, V24, P85
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[J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1985, 54 : 479 - 506
[8] CREMER D, 1975, J AM CHEM SOC, V97, P1345
[9] ENZYMATIC PROTEIN CARBOXYL METHYLATION AT PHYSIOLOGICAL PH - CYCLIC IMIDE FORMATION EXPLAINS RAPID METHYL TURNOVER
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ASWAD, DW
[J]. BIOCHEMISTRY, 1985, 24 (10) : 2581 - 2586
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