obtusilactone A

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CAS: 56522-15-7 C19 H32 O3 MW: 308.46164000
All Ingredients Aromatic Ingredients CAS Numbers Found in Nature

Identification

Nameobtusilactone A
CAS Number56522-15-7
FDA UNIISearch
Molecular FormulaC19 H32 O3
Molecular Weight308.46164000
Nikkaji NumberJ12.712D

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Soluble in water, 1.091 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for obtusilactone A usage levels up tonot for fragrance use.
Recommendation for obtusilactone A flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

persea borbonia

Synonyms

(S)-4,5- dihydro-4-hydroxy-5-methylene-3-((Z)-tetradecan-1-ylidene)furan-2(3H)-one 2(3H)- furanone, dihydro-4-hydroxy-5-methylene-3-tetradecylidene-, (3Z,4S)- (3Z,4S)-4- hydroxy-5-methylidene-3-tetradecylideneoxolan-2-one PubMed: Enhancement of Bone Marrow-Derived Mesenchymal Stem Cell Osteogenesis and New Bone Formation in Rats by Obtusilactone A. PubMed: Evaluation of the genotoxic activity of ethanol extract and secondary metabolites isolated from Aiouea trinervis Meisn. (Lauraceae). PubMed: Obtusilactone A and (-)-sesamin induce apoptosis in human lung cancer cells by inhibiting mitochondrial Lon protease and activating DNA damage checkpoints. PubMed: Antioxidants from the leaves of Cinnamomum kotoense. PubMed: Isolation of new esters from the stems of Cinnamomum reticulatum Hay. PubMed: Cytotoxic and genotoxic butanolides and lignans from Aiouea trinervis. PubMed: Biologically active gamma-lactones and methylketoalkenes from Lindera benzoin.