所有图片(1)
别名:
(S)-2-氨基-3-(3-吡啶基)丙酸, 3′-氮杂-L-苯丙氨酸
经验公式（希尔记法）:
C8H10N2O2
CAS号:
分子量:
166.18
Beilstein:
4351583
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.22
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检测方案
≥98.0% (HPLC)
形式
powder
反应适用性
reaction type: solution phase peptide synthesis
应用
peptide synthesis
SMILES字符串
N[C@@H](Cc1cccnc1)C(O)=O
InChI
1S/C8H10N2O2/c9-7(8(11)12)4-6-2-1-3-10-5-6/h1-3,5,7H,4,9H2,(H,11,12)/t7-/m0/s1
InChI key
DFZVZEMNPGABKO-ZETCQYMHSA-N
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
P N Rao et al.
International journal of peptide and protein research, 29(1), 118-125 (1987-01-01)
The DL-arylamino acid ethyl ester derivatives of beta-(3-pyridyl)-DL-alanine, and beta-(3-benzo[b]thienyl)-DL-alanine were synthesized by diethyl acetamidomalonate condensation with the respective arylmethyl halides followed by partial hydrolysis to the monoethyl ester and decarboxylation. Each derivative was enzymatically resolved to a separable mixture
H Shimeno et al.
Journal of enzyme inhibition, 2(1), 57-66 (1987-01-01)
Single doses of DL-alpha-amino-beta-(2-pyridine)propanoic acid (2-PA, 100 mg/kg) significantly decreased the holoenzyme and apoenzyme activities of rat liver tryptophan pyrrolase (TP) and increased brain tryptophan, serotonin (5-HT) and 5-hydroxyindole-3-ylacetic acid concentrations. 2-PA had no inhibitory effect on either of the
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