kuwanon J
 
Notes:
None found
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CAS Number: 83709-26-6Picture of molecule3D/inchi
Nikkaji Web: J696.393E
XlogP3-AA: 7.80 (est)
Molecular Weight: 678.73486000
Formula: C40 H38 O10
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Soluble in:
 water, 2.221e-006 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 kuwanon J usage levels up to:
 not for fragrance use.
 
Recommendation for kuwanon J 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 : 13194889
National Institute of Allergy and Infectious Diseases: Data
 (E)-1-[3-[(1R,5R,6S)-6-[2,4-dihydroxy-3-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one
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References:
 (E)-1-[3-[(1R,5R,6S)-6-[2,4-dihydroxy-3-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 13194889
Pubchem (cas): 83709-26-6
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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): Search
FooDB: FDB001913
VCF-Online: VCF Volatile Compounds in Food
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
 morus alba
Search Trop  Picture
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Synonyms:
(E)-1-[3-[(1R,5R,6S)-6-[2,4-dihydroxy-3-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one
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Articles:
PubMed: Isoprenylated phenolic compounds with tyrosinase inhibition from Morus nigra.
PubMed: Chiral Boron Complex-Promoted Asymmetric Diels-Alder Cycloaddition and Its Application in Natural Product Synthesis.
PubMed: Enantioselective biomimetic total syntheses of kuwanons I and J and brosimones A and B.
PubMed: [Chemical constituents from cell cultures of Morus alba].
PubMed: Chalcone-derived Diels-Alder adducts as NF-κB inhibitors from Morus alba.
PubMed: Synthetic studies towards the mulberry Diels-Alder adducts: H-bond accelerated cycloadditions of chalcones.
PubMed: [Flavonoids from the leaves of Morus alba L].
PubMed: Chemistry and biosynthesis of isoprenylated flavonoids from Japanese mulberry tree.
PubMed: Protein tyrosine phosphatase 1B inhibitors isolated from Morus bombycis.
PubMed: Guangsangons F-J, anti-oxidant and anti-inflammatory Diels-Alder type adducts, from Morus macroura Miq.
PubMed: A new phenolic glycoside from Sorocea ilicifolia stem bark.
PubMed: Sorocein L and sorocein M: two Diels-Alder type adducts from Sorocea ilicifolia.
PubMed: [Chemistry and biosynthesis of prenylflavonoids].
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