Isolation and characterization of larvicidal principle of garlicProtective effect of diallyl trisulfide on liver in rats with sepsis and the mechanismAntioxidant effects of diallyl trisulfide on high glucose-induced apoptosis are mediated by the PI3K/Akt-dependent activation of Nrf2 in cardiomyocytesEffect of diallyl trisulfide derivatives on the induction of apoptosis in human prostate cancer PC-3 cells.Reversion of P-glycoprotein-mediated multidrug resistance by diallyl trisulfide in a human osteosarcoma cell line.Reversion of p-glycoprotein-mediated multidrug resistance in human leukemic cell line by diallyl trisulfideDiallyl trisulfide-induced prostate cancer cell death is associated with Akt/PKB dephosphorylation mediated by P-p66shc.Critical role for reactive oxygen species in apoptosis induction and cell migration inhibition by diallyl trisulfide, a cancer chemopreventive component of garlicInhibiting invasion into human bladder carcinoma 5637 cells with diallyl trisulfide by inhibiting matrix metalloproteinase activities and tightening tight junctions.Keap1 cysteine 288 as a potential target for diallyl trisulfide-induced Nrf2 activation.Diallyl trisulfide inhibits estrogen receptor-α activity in human breast cancer cells.Diallyl trisulfide suppresses the adipogenesis of 3T3-L1 preadipocytes through ERK activation.Apoptotic pathway induced by diallyl trisulfide in pancreatic cancer cellsDiallyl trisulfide-induced apoptosis of bladder cancer cells is caspase-dependent and regulated by PI3K/Akt and JNK pathways.Diallyl trisulfide is more cytotoxic to prostate cancer cells PC-3 than to noncancerous epithelial cell line PNT1A: a possible role of p66Shc signaling axis.Antiparasitic activity of diallyl trisulfide (Dasuansu) on human and animal pathogenic protozoa (Trypanosoma sp., Entamoeba histolytica and Giardia lamblia) in vitro.Diallyl trisulfide induces apoptosis and inhibits proliferation of A549 cells in vitro and in vivo.Diallyl trisulfide as an inhibitor of benzo(a)pyrene-induced precancerous carcinogenesis in MCF-10A cells.Apoptosis induction of U937 human leukemia cells by diallyl trisulfide induces through generation of reactive oxygen species.Effect of diallyl trisulfide on human ovarian cancer SKOV- 3/DDP cell apoptosis.Arsenic-induced hepatic mitochondrial toxicity in rats and its amelioration by diallyl trisulfide.Diallyl trisulfide inhibits proliferation, invasion and angiogenesis of osteosarcoma cells by switching on suppressor microRNAs and inactivating of Notch-1 signaling.Spermicidal effect in vitro by the active principle of garlic.Diallyl trisulfide attenuates carbon tetrachloride-caused liver injury and fibrogenesis and reduces hepatic oxidative stress in rats.Diallyl trisulfide suppresses dextran sodium sulfate-induced mouse colitis: NF-κB and STAT3 as potential targets.A role for diallyl trisulfide in mitochondrial antioxidative stress contributes to its protective effects against vascular endothelial impairment.Effect of garlic (Allium sativum) on blood lipids, blood sugar, fibrinogen and fibrinolytic activity in patients with coronary artery disease.Inhibition by diallyl trisulfide, a garlic component, of intracellular Ca(2+) mobilization without affecting inositol-1,4, 5-trisphosphate (IP(3)) formation in activated platelets.Diallyl trisulfide induces apoptosis in human primary colorectal cancer cells.Diallyl trisulfide and diallyl disulfide ameliorate cardiac dysfunction by suppressing apoptotic and enhancing survival pathways in experimental diabetic rats.Inhibition of cholesterol biosynthesis by organosulfur compounds derived from garlic
P921
Q28250625-72D949C3-D726-4597-8685-033BF5B3C339Q28568647-30BF1799-018B-40C7-8EC2-108C7AB2827BQ28575791-93B8860E-5CED-47FF-A65A-D727A8C17FEFQ34092131-B9D66416-2AB5-4D11-8391-F8A598BC636AQ35161807-FE84C1C3-A75C-4AE5-958E-0EEE90798269Q36163183-30536189-399D-410D-AE16-E3BA13ED1A42Q36275402-8696856E-9F72-4F3D-9680-22C4A562D79BQ36674992-0895FB89-1ED4-4071-8F68-ED5DE8D9EB0FQ37291210-0A2ADADD-E1AE-4BC3-8F6C-D26DF231D458Q37525077-59C85359-0978-419C-B3BE-B14E770EF33CQ37615049-5C41FC69-AF43-454D-AC8A-E7FFADCCD702Q38329805-953AA7F2-E49F-43E9-8C9B-C8AA1BCB779FQ39035155-D98C31DD-E383-4721-8978-BD58688FF20EQ39048147-0648B3BA-2F81-412B-A76C-E3874A1BB992Q39125250-1F5AEAF7-DAF9-4842-BE55-A8277003FD0AQ39193980-EE633B04-7FE3-4E58-862B-B655F761B710Q39346612-6EB24993-8DD8-44EA-B00A-6DBE17F72C19Q39360493-747384E5-6414-4A11-81D2-3420FEDF2760Q42249675-A9DA5536-D058-4106-967D-2F2F87D41A7AQ42707200-00984A37-FE68-4DEA-B9B7-4C900625D78FQ42708106-177877E6-122E-4C83-BB14-989360ECA7CDQ42712813-8085E125-27CB-434F-98E9-B908377D38D4Q43772842-35A3E926-4DD1-41EE-B15C-9FCCA795ED0BQ44703471-816B9488-F0C4-4FD1-89C3-D04F87593BD8Q44801292-569D7784-C926-4DCC-86AB-882ED9296AE4Q46944621-89E77587-EF5F-411F-9704-D7D11B0361C1Q47880029-C004C2B6-7C12-4405-987D-116041769B1AQ52583141-7501FE36-CF1C-402F-8E87-37301DAD8A88Q52739762-DA0BEF51-66A6-4855-B98D-2D60AADA6929Q52745734-25748415-9F4E-4ABE-9759-6E0A428A896AQ73658458-A0A84036-7B8E-4659-BA87-DEF33DE403A5
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
allyl trisulfide
@en
type
label
allyl trisulfide
@en
altLabel
(CH2=CHCH2S)2S
@en
DATS
@en
di-2-propenyl trisulfide
@en
prefLabel
allyl trisulfide
@en
P2868
P486
P592
P6366
P661
P662
P683
P1579
P2057
HMDB0031154
P2067
P231
P232
P233
C=CCSSSCC=C
P234
1S/C6H10S3/c1-3-5-7-9-8-6-4-2/h3-4H,1-2,5-6H2
P235
UBAXRAHSPKWNCX-UHFFFAOYSA-N
P2566
100.016.462
P274
P279
P2868
P3117
DTXSID9045972
P486
P592
CHEMBL123040
P6366
2781220098
2910094252