thiacremonone
 
Notes:
None found
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CAS Number: 96504-28-8Picture of molecule3D/inchi
Nikkaji Web: J2.366.398H
XlogP3-AA: 0.50 (est)
Molecular Weight: 160.19236000
Formula: C6 H8 O3 S
NMR Predictor: Predict (works with chrome or firefox)
Category: information only not used for fragrances or flavors
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
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Google Scholar: with word "odor"Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Soluble in:
 water, 1786 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
 None found
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Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: information only not used for fragrances or flavors
Recommendation for thiacremonone usage levels up to:
 not for fragrance use.
 
Recommendation for thiacremonone flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 539170
National Institute of Allergy and Infectious Diseases: Data
 2,4-dihydroxy-2,5-dimethylthiophen-3-one
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References:
 2,4-dihydroxy-2,5-dimethylthiophen-3-one
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 539170
Pubchem (cas): 96504-28-8
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
HMDB (The Human Metabolome Database): HMDB35901
FooDB: FDB014686
ChemSpider: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
2,4-dihydroxy-2,5-dimethylthiophen-3-one
2,5-dimethyl-2,4-dihydroxy-3(2H)-thiophenone
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Articles:
PubMed: Inhibitory effect of thiacremonone on MPTP-induced dopaminergic neurodegeneration through inhibition of p38 activation.
PubMed: Physiological Activities of Thiacremonone Produced in High Temperature and High Pressure Treated Garlic.
PubMed: Thiacremonone Potentiates Anti-Oxidant Effects to Improve Memory Dysfunction in an APP/PS1 Transgenic Mice Model.
PubMed: Enhanced cell growth inhibition by thiacremonone in paclitaxel-treated lung cancer cells.
PubMed: Anti-cancer effect of thiacremonone through down regulation of peroxiredoxin 6.
PubMed: Curative Effects of Thiacremonone against Acetaminophen-Induced Acute Hepatic Failure via Inhibition of Proinflammatory Cytokines Production and Infiltration of Cytotoxic Immune Cells and Kupffer Cells.
PubMed: Thiacremonone, a sulfur compound isolated from garlic, attenuates lipid accumulation partially mediated via AMPK activation in 3T3-L1 adipocytes.
PubMed: Anti-amyloidogenic effect of thiacremonone through anti-inflamation in vitro and in vivo models.
PubMed: Antiobesity effects of a sulfur compound thiacremonone mediated via down-regulation of serum triglyceride and glucose levels and lipid accumulation in the liver of db/db mice.
PubMed: Anti-inflammatory and arthritic effects of thiacremonone, a novel sulfur compound isolated from garlic via inhibition of NF-kappaB.
PubMed: Thiacremonone augments chemotherapeutic agent-induced growth inhibition in human colon cancer cells through inactivation of nuclear factor-{kappa}B.
PubMed: Inhibition of cell growth and induction of apoptosis via inactivation of NF-kappaB by a sulfurcompound isolated from garlic in human colon cancer cells.
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