D-1,4-dithiothreitol (CHEBI:42170)

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ChEBI Name	D-1,4-dithiothreitol

ChEBI ID	CHEBI:42170

ChEBI ASCII Name	D-1,4-dithiothreitol

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

Secondary ChEBI IDs	CHEBI:42166, CHEBI:32886

Supplier Information

Download	Molfile XML SDF

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-/m1/s1

InChIKey

VHJLVAABSRFDPM-QWWZWVQMSA-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	D-1,4-dithiothreitol (CHEBI:42170) is a 1,4-dithiothreitol (CHEBI:18320) D-1,4-dithiothreitol (CHEBI:42170) is enantiomer of L-1,4-dithiothreitol (CHEBI:42106)

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

IUPAC Name

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

Synonyms	Sources
(2S,3S)-1,4-dimercaptobutane-2,3-diol	PDBeChem
D-DTT	ChEBI
D-threo-1,4-dimercapto-2,3-butanediol	ChEBI

Registry Number	Type	Source
1847519	Beilstein Registry Number	Beilstein

Last Modified

13 September 2007