DTV

(2S,3S)-1,4-DIMERCAPTOBUTANE-2,3-DIOL

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is present as a standalone ligand in 25 entries

as a non-polymer is covalently linked to polymer or other heterogen groups 8 entries

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Chemical Component Summary
Name	(2S,3S)-1,4-DIMERCAPTOBUTANE-2,3-DIOL
Identifiers	(2S,3S)-1,4-bis-sulfanylbutane-2,3-diol
Formula	C₄ H₁₀ O₂ S₂
Molecular Weight	154.251
Type	NON-POLYMER
Isomeric SMILES	C([C@H]([C@@H](CS)O)O)S
InChI	InChI=1S/C4H10O2S2/c5-3(1-7)4(6)2-8/h3-8H,1-2H2/t3-,4-/m1/s1
InChIKey	VHJLVAABSRFDPM-QWWZWVQMSA-N

Chemical Details
Formal Charge	0
Atom Count	18
Chiral Atom Count	2
Bond Count	17
Aromatic Bond Count	0

Drug Info: DrugBank

DrugBank ID	DB02184 ?
Name	D-1,4-dithiothreitol
Groups	experimental
Description	A reagent commonly used in biochemical studies as a protective agent to prevent the oxidation of SH (thiol) groups and for reducing disulphides to dithiols. [PubChem]
Synonyms	D-threo-1,4-dimercapto-2,3-butanediol D-1,4-dithiothreitol (2S,3S)-1,4-dimercaptobutane-2,3-diol D-DTT

Drug Targets

Name	Target Sequence	Pharmacological Action	Actions
6,7-dimethyl-8-ribityllumazine synthase	MKGGAGVPDLPSLDASGVRLAIVASSWHGKICDALLDGARKVAAGCGLDD...	unknown

Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS. Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682