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94814

Sigma-Aldrich

3-(3-Pyridyl)-L-alanine

≥98.0% (HPLC)

Synonym(s):

(S)-2-Amino-3-(3-pyridyl)propionic acid, 3′-Aza-L-phenylalanine

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About This Item

Empirical Formula (Hill Notation):
C8H10N2O2
CAS Number:
Molecular Weight:
166.18
Beilstein/REAXYS Number:
4351583
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22

assay

≥98.0% (HPLC)

form

powder

reaction suitability

reaction type: solution phase peptide synthesis

application(s)

peptide synthesis

SMILES string

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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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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