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Details

Stereochemistry ABSOLUTE
Molecular Formula C4H7NO2
Molecular Weight 101.1039
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-AZETIDINECARBOXYLIC ACID, (S)-

SMILES

OC(=O)[C@@H]1CCN1

InChI

InChIKey=IADUEWIQBXOCDZ-VKHMYHEASA-N
InChI=1S/C4H7NO2/c6-4(7)3-1-2-5-3/h3,5H,1-2H2,(H,6,7)/t3-/m0/s1

HIDE SMILES / InChI

Molecular Formula C4H7NO2
Molecular Weight 101.1039
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Substrate specificity and functional characterisation of the H+/amino acid transporter rat PAT2 (Slc36a2).
2005 Jan
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 08:50:25 GMT 2023
Edited
by admin
on Sat Dec 16 08:50:25 GMT 2023
Record UNII
5GZ3E0L9ZU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-AZETIDINECARBOXYLIC ACID, (S)-
Common Name English
L-2-AZETIDINECARBOXYLIC ACID
Common Name English
(S)-2-AZETIDINECARBOXYLIC ACID
Systematic Name English
2-AZETIDINECARBOXYLIC ACID, (2S)-
Systematic Name English
L-AZETIDINE-2-CARBOXYLIC ACID
Common Name English
AZETIDINE-2-CARBOXYLIC ACID, L-
Systematic Name English
AZETIDINECARBOXYLIC ACID
Systematic Name English
(-)-AZETIDINECARBOXYLIC ACID
Systematic Name English
(2S)-AZETIDINE-2-CARBOXYLIC ACID
Systematic Name English
AZETIDYL-2-CARBOXYLIC ACID [HSDB]
Common Name English
(L)-AZETIDINE-2-CARBOXYLIC ACID
Common Name English
(S)-(-)-2-AZETIDINE CARBOXYLIC ACID
Systematic Name English
(S)-AZETIDINE-2-CARBOXYLIC ACID
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID0044020
Created by admin on Sat Dec 16 08:50:26 GMT 2023 , Edited by admin on Sat Dec 16 08:50:26 GMT 2023
PRIMARY
ECHA (EC/EINECS)
218-362-5
Created by admin on Sat Dec 16 08:50:26 GMT 2023 , Edited by admin on Sat Dec 16 08:50:26 GMT 2023
PRIMARY
WIKIPEDIA
Azetidine-2-carboxylic acid
Created by admin on Sat Dec 16 08:50:26 GMT 2023 , Edited by admin on Sat Dec 16 08:50:26 GMT 2023
PRIMARY
PUBCHEM
16486
Created by admin on Sat Dec 16 08:50:26 GMT 2023 , Edited by admin on Sat Dec 16 08:50:26 GMT 2023
PRIMARY
FDA UNII
5GZ3E0L9ZU
Created by admin on Sat Dec 16 08:50:26 GMT 2023 , Edited by admin on Sat Dec 16 08:50:26 GMT 2023
PRIMARY
CAS
2133-34-8
Created by admin on Sat Dec 16 08:50:26 GMT 2023 , Edited by admin on Sat Dec 16 08:50:26 GMT 2023
PRIMARY
HSDB
3465
Created by admin on Sat Dec 16 08:50:26 GMT 2023 , Edited by admin on Sat Dec 16 08:50:26 GMT 2023
PRIMARY
CHEBI
6198
Created by admin on Sat Dec 16 08:50:26 GMT 2023 , Edited by admin on Sat Dec 16 08:50:26 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
n many species, including man,L-Aze is mis-incorporated into protein in place of proline, altering collagen, keratin, hemoglobin, and protein folding. L-Aze was found to be present in the root of garden beets. the plant part ordinarily consumed by humans.The ratio of the free amino acidsL-Aze2toL-proline was determined to be from 5% to 20%, the result depending on the amino acid extraction method.