solavetivone
katahdinone
 
Notes:
None found
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CAS Number: 54878-25-0Picture of molecule3D/inchi
FDA UNII: HS8O8A7REZ
Nikkaji Web: J455.725E
XlogP3-AA: 4.00 (est)
Molecular Weight: 218.33954000
Formula: C15 H22 O
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Soluble in:
 water, 1.212 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 solavetivone usage levels up to:
 not for fragrance use.
 
Recommendation for solavetivone 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 : 442399
National Institute of Allergy and Infectious Diseases: Data
 (3R,5S,6R)-6,10-dimethyl-3-prop-1-en-2-ylspiro[4.5]dec-9-en-8-one
Chemidplus: 0054878250
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References:
 (3R,5S,6R)-6,10-dimethyl-3-prop-1-en-2-ylspiro[4.5]dec-9-en-8-one
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 442399
Pubchem (cas): 54878-25-0
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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
CHEBI: View
CHEMBL: View
KEGG (GenomeNet): C09737
HMDB (The Human Metabolome Database): HMDB35657
FooDB: FDB014372
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: 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
 solanum indicum
Search Trop  Picture
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Synonyms:
(3R,5S,6R)-6,10-dimethyl-3-prop-1-en-2-ylspiro[4.5]dec-9-en-8-one
 katahdinone
 spiro(4.5)dec-6-en-8-one, 6,10-dimethyl-2-(1-methylethenyl)-, (2R,5S,10R)-
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Articles:
PubMed: Volatile constituents from the leaves, fruits (berries), stems and roots of Solanum xanthocarpum from Nepal.
PubMed: Antibacterial activity of carob (Ceratonia siliqua L.) extracts against phytopathogenic bacteria Pectobacterium atrosepticum.
PubMed: Multi-platform metabolomic analyses of ergosterol-induced dynamic changes in Nicotiana tabacum cells.
PubMed: Anti-inflammatory components from the root of Solanum erianthum.
PubMed: FT-ICR/MS and GC-EI/MS metabolomics networking unravels global potato sprout's responses to Rhizoctonia solani infection.
PubMed: HPTLC and reverse phase HPLC methods for the simultaneous quantification and in vitro screening of antioxidant potential of isolated sesquiterpenoids from the rhizomes of Cyperus rotundus.
PubMed: Ergosterol-induced sesquiterpenoid synthesis in tobacco cells.
PubMed: Production of sesquiterpene-type phytoalexins by hairy roots of Hyoscyamus albus co-treated with cupper sulfate and methyl jasmonate.
PubMed: Induction of sesquiterpenes, phytoesterols and extracellular pathogenesis-related proteins in elicited cell cultures of Capsicum annuum.
PubMed: Functional characterization of premnaspirodiene oxygenase, a cytochrome P450 catalyzing regio- and stereo-specific hydroxylations of diverse sesquiterpene substrates.
PubMed: Anti-fungal sesquiterpenoid from the root exudate of Solanum abutiloides.
PubMed: Effect of mycorrhization on the accumulation of rishitin and solavetivone in potato plantlets challenged with Rhizoctonia solani.
PubMed: Effect of elicitation on growth, respiration, and nutrient uptake of root and cell suspension cultures of Hyoscyamus muticus.
PubMed: Sesquiterpenoids in root exudates of Solanum aethiopicum.
PubMed: Cytotoxic and novel compounds from Solanum indicum.
PubMed: Sesquiterpenoids from the roots of Solanum aethiopicum.
PubMed: Comparison of volatile compounds isolated from the skin and flesh of four potato cultivars after baking.
PubMed: Phytoalexins from hairy roots of Hyoscyamus albus treated with methyl jasmonate.
PubMed: Enhanced recovery of solavetivone from Agrobacterium transformed root cultures of Hyoscyamus muticus using integrated product extraction.
PubMed: Biotransformation of the potato stress metabolite, solavetivone, by cell suspension cultures of two solanaceous and three non-solanaceous species.
PubMed: Effects of Controlled Atmospheres on Production of Sesquiterpenoid Stress Metabolites by White Potato Tuber: Possible Involvement of Cyanide-resistant Respiration.
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