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Details

Stereochemistry ABSOLUTE
Molecular Formula C3H8N2O
Molecular Weight 88.1084
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ALANINAMIDE, L-

SMILES

C[C@H](N)C(N)=O

InChI

InChIKey=HQMLIDZJXVVKCW-REOHCLBHSA-N
InChI=1S/C3H8N2O/c1-2(4)3(5)6/h2H,4H2,1H3,(H2,5,6)/t2-/m0/s1

HIDE SMILES / InChI

Molecular Formula C3H8N2O
Molecular Weight 88.1084
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Chemically modified chiral monolithic silica column prepared by a sol-gel process for enantiomeric separation by micro high-performance liquid chromatography.
2002 Jan 4
Chemically modified "polar patch" mutants of subtilisin in peptide synthesis with remarkably broad substrate acceptance: designing combinatorial biocatalysts.
2002 Sep 16
Design of chiral monochloro-s-triazine reagents for the liquid chromatographic separation of amino acid enantiomers.
2003 May 23
Single peptide bonds exhibit poly(pro)II ("random coil") circular dichroism spectra.
2005 Jul 13
Visual enantiomeric recognition of amino acid derivatives in protic solvents.
2005 Jun 10
Application of Fourier transform infrared spectroscopy for monitoring hydrolysis and synthesis reactions catalyzed by a recombinant amidase.
2005 Nov 1
Effect of betulonic acid and its derivative [3-oxo-20(29)-lupene-28-oyl]-3-aminopropionic acid on liver structure in mice with RLS lymphoma.
2005 Sep
Pharmacological and molecular characterization of the mechanisms involved in prostaglandin E2-induced mouse paw edema.
2006 Aug
Complexes of Cu(II) ions and noncovalent interactions in systems with L-aspartic acid and cytidine-5'-monophosphate.
2008
Complete genome sequence of Gordonia bronchialis type strain (3410).
2010 Jan 28
Efficient synthesis of a small molecule, nonpeptide inhibitor of LFA-1.
2010 Oct 1
Complete genome sequence of Marinobacter adhaerens type strain (HP15), a diatom-interacting marine microorganism.
2010 Sep 28
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:48:56 GMT 2023
Edited
by admin
on Fri Dec 15 19:48:56 GMT 2023
Record UNII
GOD06L4T27
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ALANINAMIDE, L-
Systematic Name English
(S)-(+)-2-AMINOPROPANAMIDE
Systematic Name English
ALANINE AMIDE
Common Name English
L-ALANINAMIDE
Systematic Name English
PROPANAMIDE, 2-AMINO-, (S)-
Systematic Name English
Code System Code Type Description
PUBCHEM
444939
Created by admin on Fri Dec 15 19:48:56 GMT 2023 , Edited by admin on Fri Dec 15 19:48:56 GMT 2023
PRIMARY
CAS
7324-05-2
Created by admin on Fri Dec 15 19:48:56 GMT 2023 , Edited by admin on Fri Dec 15 19:48:56 GMT 2023
PRIMARY
CHEBI
21217
Created by admin on Fri Dec 15 19:48:56 GMT 2023 , Edited by admin on Fri Dec 15 19:48:56 GMT 2023
PRIMARY
EPA CompTox
DTXSID60223470
Created by admin on Fri Dec 15 19:48:56 GMT 2023 , Edited by admin on Fri Dec 15 19:48:56 GMT 2023
PRIMARY
CHEBI
74169
Created by admin on Fri Dec 15 19:48:56 GMT 2023 , Edited by admin on Fri Dec 15 19:48:56 GMT 2023
PRIMARY
FDA UNII
GOD06L4T27
Created by admin on Fri Dec 15 19:48:56 GMT 2023 , Edited by admin on Fri Dec 15 19:48:56 GMT 2023
PRIMARY