Structure via PubChem · Public domain (PubChem)
گویترین
Sign in to saveAlso known as goitrin, 5-vinyl-1,3-oxazolidine-2-thione, 5-ethenyl-1,3-oxazolidine-2-thione
Goitrin is an organosulfur compound classified as a derivative of oxazolidine and as a cyclic thiocarbamate. It reduces the production of thyroid hormones such as thyroxine. It is found in cruciferous vegetables such as cabbage, brussels sprouts and rapeseed oil, and is formed by the hydrolysis of a glucosinolate: progoitrin or 2-hydroxy-3-butenyl glucosinolate. The unstable isothiocyanate (2-hydroxy-3-butenyl isothiocyanate) derived from the latter glucosinolate spontaneously cyclizes to goitrin, because the hydroxy group is situated in proximity to the isothiocyanate group (allowing a five-m
Chemical data
- Formula
- C5H7NOS
- Molecular weight
- 129.18 g/mol
- IUPAC name
- 5-ethenyl-1,3-oxazolidine-2-thione
- SMILES
- C=CC1CNC(=S)O1
- InChIKey
- UZQVYLOFLQICCT-UHFFFAOYSA-N
- XLogP
- 1
- Polar surface area
- 53.4 Ų
- H-bond donors
- 1
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Mass
- 129.025
Show 4 more facts
- chemical formula
- C₅H₇NOS
- canonical SMILES
- C=CC1CNC(=S)O1
- has characteristic
- bitterness
- found in taxon
- Isatis tinctoria
via Wikidata · CC0