isoobtusilactone A
isooblusilactonc A
 
Notes:
None found
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CAS Number: 56522-16-8Picture of molecule3D/inchi
XlogP3-AA: 6.70 (est)
Molecular Weight: 308.46164000
Formula: C19 H32 O3
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Soluble in:
 water, 1.091 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: natural substances and extractives
Recommendation for isoobtusilactone A usage levels up to:
 not for fragrance use.
 
Recommendation for isoobtusilactone A flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 6442493
National Institute of Allergy and Infectious Diseases: Data
 (3E,4S)-4-hydroxy-5-methylidene-3-tetradecylideneoxolan-2-one
Chemidplus: 0056522168
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References:
 (3E,4S)-4-hydroxy-5-methylidene-3-tetradecylideneoxolan-2-one
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 6442493
Pubchem (cas): 56522-16-8
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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
CHEMBL: View
HMDB (The Human Metabolome Database): HMDB30960
FooDB: FDB017731
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
EFSA Update of results on the monitoring of furan levels in food: Read Report
EFSA Previous report: Results on the monitoring of furan levels in food: Read Report
EFSA Report of the CONTAM Panel on provisional findings on furan in food: Read Report
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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
 persea borbonia
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Synonyms:
2(3H)-furanone, dihydro-4-hydroxy-5-methylene-3-tetradecylidene-, (3E,4S)-
(3E,4S)-4-hydroxy-5-methylidene-3-tetradecylideneoxolan-2-one
isooblusilactonc A
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Articles:
PubMed: Evaluation of the genotoxic activity of ethanol extract and secondary metabolites isolated from Aiouea trinervis Meisn. (Lauraceae).
PubMed: Isoobtusilactone A sensitizes human hepatoma Hep G2 cells to TRAIL-induced apoptosis via ROS and CHOP-mediated up-regulation of DR5.
PubMed: Isolation of new esters from the stems of Cinnamomum reticulatum Hay.
PubMed: Anticancer activity of isoobtusilactone A from Cinnamomum kotoense: involvement of apoptosis, cell-cycle dysregulation, mitochondria regulation, and reactive oxygen species.
PubMed: Isoobtusilactone A induces both caspase-dependent and -independent apoptosis in Hep G2 cells.
PubMed: Isoobtusilactone A induces cell cycle arrest and apoptosis through reactive oxygen species/apoptosis signal-regulating kinase 1 signaling pathway in human breast cancer cells.
PubMed: Isoobtusilactone A-induced apoptosis in human hepatoma Hep G2 cells is mediated via increased NADPH oxidase-derived reactive oxygen species (ROS) production and the mitochondria-associated apoptotic mechanisms.
PubMed: Cytotoxic and genotoxic butanolides and lignans from Aiouea trinervis.
PubMed: Antitubercular constituents from the stem wood of Cinnamomum kotoense.
PubMed: Cytotoxic butanolides and secobutanolides from the stem wood of Formosan Lindera communis.
PubMed: Biologically active gamma-lactones and methylketoalkenes from Lindera benzoin.
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