L-1,4-dithiothreitol (CHEBI:42106)

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ChEBI Name	L-1,4-dithiothreitol

ChEBI ID	CHEBI:42106

ChEBI ASCII Name	L-1,4-dithiothreitol

Stars	This entity has been manually annotated by the ChEBI Team.

Secondary ChEBI IDs	CHEBI:42102, CHEBI:32885

Supplier Information	ChemicalBook:CB5481183, eMolecules:537809, ZINC000000895149

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Formula

C4H10O2S2

Net Charge

Average Mass

154.25300

Monoisotopic Mass

154.01222

InChI

InChI=1S/C4H10O2S2/c5-3(1-7)4(6)2-8/h3-8H,1-2H2/t3-,4-/m0/s1

InChIKey

VHJLVAABSRFDPM-IMJSIDKUSA-N

SMILES

O[C@@H](CS)[C@@H](O)CS

Roles Classification
Chemical Role(s):	reducing agent The element or compound in a reduction-oxidation (redox) reaction that donates an electron to another species. (via 1,4-dithiothreitol ) chelator A ligand with two or more separate binding sites that can bind to a single metallic central atom, forming a chelate. (via 1,4-dithiothreitol )

Biological Role(s):	human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). (via 1,4-dithiothreitol )

ChEBI Ontology
Outgoing	L-1,4-dithiothreitol (CHEBI:42106) is a 1,4-dithiothreitol (CHEBI:18320) L-1,4-dithiothreitol (CHEBI:42106) is enantiomer of D-1,4-dithiothreitol (CHEBI:42170)

Incoming	D-1,4-dithiothreitol (CHEBI:42170) is enantiomer of L-1,4-dithiothreitol (CHEBI:42106)

IUPAC Name

(2R,3R)-1,4-disulfanylbutane-2,3-diol

Synonyms	Sources
(2R,3R)-1,4-dimercaptobutane-2,3-diol	PDBeChem
1,4-Dithiothreitol	KEGG COMPOUND
2,3-DIHYDROXY-1,4-DITHIOBUTANE	PDBeChem
DL-threo-1,4-Dimercapto-2,3-butanediol	KEGG COMPOUND
L-1,4-dithiothreitol	ChemIDplus
L-dithiothreitol	ChemIDplus
L-DTT	ChemIDplus
L-threo-1,4-dimercapto-2,3-butanediol	ChemIDplus
threo-1,4-Dimercapto-2,3-butanediol	KEGG COMPOUND

Last Modified

28 July 2014