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Merck
CN

294357

Sigma-Aldrich

DL -异苯丙氨酸

98%

别名:

(±)-2-氨基-4-苯基丁酸

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关于此项目

线性分子式:
C6H5(CH2CH2)CH(NH2)CO2H
化学文摘社编号:
分子量:
179.22
MDL编号:
UNSPSC代码:
12352209
eCl@ss:
32160406
PubChem化学物质编号:
NACRES:
NA.22
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方案

98%

反应适用性

reaction type: solution phase peptide synthesis

mp

282 °C (dec.) (lit.)

应用

peptide synthesis

SMILES字符串

NC(CCc1ccccc1)C(O)=O

InChI

1S/C10H13NO2/c11-9(10(12)13)7-6-8-4-2-1-3-5-8/h1-5,9H,6-7,11H2,(H,12,13)

InChI key

JTTHKOPSMAVJFE-UHFFFAOYSA-N

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储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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分析证书(COA)

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Rafael Notario et al.
The journal of physical chemistry. B, 115(30), 9401-9409 (2011-06-18)
Calorimetric measurements are expected to provide useful data regarding the relative stability of α- versus β-amino acid isomers, which, in turn, may help us to understand why nature chose α- instead of β-amino acids for the formation of the biomolecules
Anne Stürzebecher et al.
ChemMedChem, 2(7), 1043-1053 (2007-06-02)
A series of highly potent substrate-analogue factor Xa inhibitors containing D-homophenylalanine analogues as the P3 residue has been identified by systematic optimization of a previously described inhibitor structure. An initial lead, benzylsulfonyl-D-hPhe-Gly-4-amidinobenzylamide (3), inhibits fXa with an inhibition constant of
Kento Koketsu et al.
Applied and environmental microbiology, 79(7), 2201-2208 (2013-01-29)
L-Homophenylalanine (L-Hph) is a useful chiral building block for synthesis of several drugs, including angiotensin-converting enzyme inhibitors and the novel proteasome inhibitor carfilzomib. While the chemoenzymatic route of synthesis is fully developed, we investigated microbial production of L-Hph to explore
Millán Cortizo et al.
Journal of plant physiology, 166(10), 1069-1076 (2009-02-17)
Germination negatively affects adventitious shoot formation induced by cytokinins in pine cotyledons. To investigate the causes of this decrease in the organogenic response, uptake and metabolism of benzyladenine (BA) were studied in stone pine cotyledons (Pinus pinea) isolated from in
D Sobolewski et al.
The journal of peptide research : official journal of the American Peptide Society, 65(4), 465-471 (2005-04-09)
In continuation of our efforts to elucidate the role of positions 2 and 3 in arginine vasopressin (AVP) and its analogues, we designed and synthesized peptides modified in these positions with l-beta-homophenylalanine (beta-Hph). Two of them had just this single

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