javanicin
1,4-naphthalenedione, 5,8-dihydroxy-6-methoxy-2-methyl-3-(2-oxopropyl)-
 
Notes:
None found
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      Product(s):
      476-45-9 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione
       
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CAS Number: 476-45-9Picture of molecule3D/inchi
FDA UNII: YNR51WFW2R
Nikkaji Web: J5.976E
Beilstein Number: 2296055
XlogP3-AA: 2.00 (est)
Molecular Weight: 290.27178000
Formula: C15 H14 O6
BioActivity Summary: listing
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
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Melting Point: 208.00 °C. @ 760.00 mm Hg
Boiling Point: 616.50 °C. @ 760.00 mm Hg (est)
Flash Point: 456.00 °F. TCC ( 235.70 °C. ) (est)
logP (o/w): 1.510 (est)
Soluble in:
 water, 222.2 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:
BOC Sciences
For experimental / research use only.
5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione
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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:
intraperitoneal-mouse LD50  500 mg/kg
"CRC Handbook of Antibiotic Compounds," Vols.1- , Berdy, J., Boca Raton, FL, CRC Press, 1980Vol. 3, Pg. 217, 1980.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: natural substances and extractives
Recommendation for javanicin usage levels up to:
 not for fragrance use.
 
Recommendation for javanicin 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 : 10149
National Institute of Allergy and Infectious Diseases: Data
 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione
Chemidplus: 0000476459
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References:
 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 10149
Pubchem (sid): 134973499
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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): Search
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
 found in nature
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Synonyms:
3-acetonyl-5,8-dihydroxy-6-methoxy-2-methyl-1,4-naphthoquinone
5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione
1,4-naphthalenedione, 5,8-dihydroxy-6-methoxy-2-methyl-3-(2-oxopropyl)-
1,4-naphthoquinone, 3-acetonyl-5,8-dihydroxy-6-methoxy-2-methyl-
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Articles:
PubMed: Bioactive dihydronaphthoquinone derivatives from Fusarium solani.
PubMed: Screening and evaluation of new inhibitors of hepatic glucose production.
PubMed: Javanicin, an antibacterial naphthaquinone from an endophytic fungus of neem, Chloridium sp.
PubMed: [Biosynthesis of naphthoquinone pigments by fungi of the genus Fusarium].
PubMed: Fungal quinone pigments as oxidizers and inhibitors of mitochondrial NADH:ubiquinone reductase.
PubMed: Studies on the constituents of Indonesian Picrasma javanica. III. Structures of new quassinoids, javanicins A, C and D.
PubMed: NAPHTHAQUINONE BIOSYNTHESIS IN MOULDS: THE MECHANISM FOR FORMATION OF JAVANICIN.
PubMed: Production of antibiotics by fungi; javanicin; an antibacterial pigment from Fusarium javanicum.
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