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Details

Stereochemistry ACHIRAL
Molecular Formula C6H10S3
Molecular Weight 178.339
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ALLYL TRISULFIDE

SMILES

C=CCSSSCC=C

InChI

InChIKey=UBAXRAHSPKWNCX-UHFFFAOYSA-N
InChI=1S/C6H10S3/c1-3-5-7-9-8-6-4-2/h3-4H,1-2,5-6H2

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
In vitro efficacy of a compound derived from garlic against Pneumocystis carinii.
1996 Nov
Protective effect of three diallyl sulphides against glucose-induced erythrocyte and platelet oxidation, and ADP-induced platelet aggregation.
2002 Dec 15
Diallyl trisulfide inhibits tumor necrosis factor-alpha expression in inflammed mucosa of ulcerative colitis.
2005 Aug
Microarray analysis of altered gene expression in diallyl trisulfide-treated HepG2 cells.
2005 Nov-Dec
Effects of allitridi on cell cycle arrest of human gastric cancer cells.
2005 Sep 21
A proteomic investigation into a human gastric cancer cell line BGC823 treated with diallyl trisulfide.
2006 Jun
[Effect of diallyl trisulfide on tumor necrosis factor-alpha expression and nuclear factor-KappaB activity in mice with acute lung injury induced by lipopolysaccharide].
2007 Apr
Mitochondria-mediated apoptosis by diallyl trisulfide in human prostate cancer cells is associated with generation of reactive oxygen species and regulated by Bax/Bak.
2007 May
Allium compounds, dipropyl and dimethyl thiosulfinates as antiproliferative and differentiating agents of human acute myeloid leukemia cell lines.
2008 Dec
In vitro anti-Helicobacter pylori activity of diallyl sulphides and protocatechuic acid.
2008 Jan
Transcriptional repression and inhibition of nuclear translocation of androgen receptor by diallyl trisulfide in human prostate cancer cells.
2009 Aug 1
Neuroprotective potential of phase II enzyme inducer diallyl trisulfide.
2009 Feb
Diallylpolysulfides induce growth arrest and apoptosis.
2010 Mar
Diallyl trisulfide suppresses the adipogenesis of 3T3-L1 preadipocytes through ERK activation.
2012 Mar
Diallyl sulfide, diallyl disulfide and diallyl trisulfide affect drug resistant gene expression in colo 205 human colon cancer cells in vitro and in vivo.
2012 May 15
Effect of diallyl trisulfide on human ovarian cancer SKOV- 3/DDP cell apoptosis.
2013
Diallyl trisulfide inhibits proliferation, invasion and angiogenesis of osteosarcoma cells by switching on suppressor microRNAs and inactivating of Notch-1 signaling.
2013 Jul
Diallyl sulfide, diallyl disulfide, and diallyl trisulfide inhibit migration and invasion in human colon cancer colo 205 cells through the inhibition of matrix metalloproteinase-2, -7, and -9 expressions.
2013 Sep
Antioxidant effects of diallyl trisulfide on high glucose-induced apoptosis are mediated by the PI3K/Akt-dependent activation of Nrf2 in cardiomyocytes.
2013 Sep 30
Allitridin reduces I Kr current by disrupting the trafficking of human ether-à-go-go-related gene channels.
2014
Keap1 cysteine 288 as a potential target for diallyl trisulfide-induced Nrf2 activation.
2014
Name Type Language
ALLYL TRISULFIDE
Systematic Name English
ALLITRIDE
Common Name English
Diallyl trisulfide [WHO-DD]
Common Name English
DIALLYL TRISULPHIDE
Systematic Name English
ALLITRIDUM
Common Name English
DIALLYL TRISULFIDE [MI]
Common Name English
DIALLYL TRISULFIDE
FHFI   MI  
Systematic Name English
DIALLYL TRISULFIDE [FHFI]
Common Name English
FEMA NO. 3265
Code English
DI-2-PROPENYL TRISULFIDE
Systematic Name English
NSC-651936
Code English
TRISULFIDE, DI-2-PROPENYL
Systematic Name English
ALLITRIDIN
Common Name English
Classification Tree Code System Code
JECFA EVALUATION DIALLYL TRISULFIDE
Created by admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
NCI_THESAURUS C68520
Created by admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
Code System Code Type Description
CHEBI
78492
Created by admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
PRIMARY
PUBCHEM
16315
Created by admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
PRIMARY
MERCK INDEX
m4246
Created by admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C68525
Created by admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
PRIMARY
CAS
2050-87-5
Created by admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
PRIMARY
MESH
C042577
Created by admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
PRIMARY
FDA UNII
0ZO1U5A3XX
Created by admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
PRIMARY
EPA CompTox
DTXSID9045972
Created by admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
PRIMARY
JECFA MONOGRAPH
153
Created by admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
PRIMARY
ECHA (EC/EINECS)
218-107-8
Created by admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
PRIMARY
NSC
651936
Created by admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
PRIMARY
WIKIPEDIA
Diallyl trisulfide
Created by admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
PRIMARY