Structure via PubChem · Public domain (PubChem)
timonacic
Sign in to saveAlso known as Thiazolidinecarboxylic acid, DL-Thiaproline, DL-Thiazolidinecarboxylic acid, 4-Thiazolidinecarboxylic acid, Thiazolidine-4-carboxylic acid, Thiaproline, 4-Carboxythiazolidine
Thioproline is a nonproteinogenic amino acid with the formula , although it crystallizes as the zwitterion . It consists of a 1,3-thiazolidine ring ( ) substituted with a carboxylic acid. It is synthesized by reaction of formaldehyde and cysteine. It occurs in nature, but rarely. It forms a coordination complex with cobalt.
Chemical data
- Formula
- C4H7NO2S
- Molecular weight
- 133.17 g/mol
- IUPAC name
- 1,3-thiazolidine-4-carboxylic acid
- SMILES
- C1C(NCS1)C(=O)O
- InChIKey
- DZLNHFMRPBPULJ-UHFFFAOYSA-N
- XLogP
- -2.3
- Polar surface area
- 74.6 Ų
- H-bond donors
- 2
- H-bond acceptors
- 4
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Mass
- 133.02
Show 7 more facts
- found in taxon
- Lentinula edodes
- subject has role
- antioxidant
- canonical SMILES
- C1C(NCS1)C(=O)O
- chemical formula
- C₄H₇NO₂S
- pKa
- 1.51
- World Health Organisation international non-proprietary name
- timonacic
- Commons category
- 1,3-Thiazolidine-4-carboxylic acid
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
Thioproline is a nonproteinogenic amino acid with the formula , although it crystallizes as the zwitterion . It consists of a 1,3-thiazolidine ring ( ) substituted with a carboxylic acid. It is synthesized by reaction of formaldehyde and cysteine. It occurs in nature, but rarely. It forms a coordination complex with cobalt.
== References ==
Excerpted from Wikipedia’s “timonacic” article, available under the CC BY-SA 4.0 licence.