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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:
64090-98-8
Molecular Weight:
166.18
Beilstein:
4351583
MDL number:
MFCD00079676
UNSPSC Code:
12352200
PubChem Substance ID:
57653640
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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

94814-1G-F:
94814-VAR-F:
94814-BULK-F:

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Certificates of Analysis (COA)

Lot/Batch Number
BCBQ1408V
BCBK4686V
BCBH5671V
BCBD8295V
BCBC3871V

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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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