Carbamodithioic acid, N,N-bis(2-hydroxyethyl)-

Details

Stereochemistry	ACHIRAL
Molecular Formula	C5H11NO2S2
Molecular Weight	181.276
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of Carbamodithioic acid, N,N-bis(2-hydroxyethyl)-

Structure Search

SMILES

OCCN(CCO)C(S)=S

InChI

InChIKey=PCBLZWZCGNKODY-UHFFFAOYSA-N

InChI=1S/C5H11NO2S2/c7-3-1-6(2-4-8)5(9)10/h7-8H,1-4H2,(H,9,10)

HIDE SMILES / InChI

Molecular Formula	C5H11NO2S2
Molecular Weight	181.276
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Cytochrome P450 catalyzed oxidation of monochlorobenzene, 1,2- and 1,4-dichlorobenzene in rat, mouse, and human liver microsomes.	1998 Aug 14	9817075
Neural overexcitation and implication of NMDA and AMPA receptors in a mouse model of temporal lobe epilepsy implying zinc chelation.	2006 May	16686654
SLC30A3 responds to glucose- and zinc variations in beta-cells and is critical for insulin production and in vivo glucose-metabolism during beta-cell stress.	2009 May 25	19492079

Substance Class	Chemical Created by `admin` on `Fri Dec 15 19:40:13 GMT 2023` Edited by `admin` on `Fri Dec 15 19:40:13 GMT 2023`
Record UNII	IP73T3KT1R
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

Carbamodithioic acid, N,N-bis(2-hydroxyethyl)-

Systematic Name

English

Dihydroxyethyldithiocarbamate

Systematic Name

English

Code System Code Type Description

CAS

1528-72-9

Created by admin on Fri Dec 15 19:40:13 GMT 2023 , Edited by admin on Fri Dec 15 19:40:13 GMT 2023

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MESH

C039353

Created by admin on Fri Dec 15 19:40:13 GMT 2023 , Edited by admin on Fri Dec 15 19:40:13 GMT 2023

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FDA UNII

IP73T3KT1R

Created by admin on Fri Dec 15 19:40:13 GMT 2023 , Edited by admin on Fri Dec 15 19:40:13 GMT 2023

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PUBCHEM

32064

Created by admin on Fri Dec 15 19:40:13 GMT 2023 , Edited by admin on Fri Dec 15 19:40:13 GMT 2023

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