matricin
proazulene
 
Notes:
None found
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CAS Number: 29041-35-8Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 249-384-3
FDA UNII: O034C3549S
Nikkaji Web: J286.506H
MDL: MFCD08460273
XlogP3-AA: 1.00 (est)
Molecular Weight: 306.35834000
Formula: C17 H22 O5
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, 3994 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:
Sigma-Aldrich
For experimental / research use only.
Matricin analytical standard
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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 matricin usage levels up to:
 not for fragrance use.
 
Recommendation for matricin flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 92265
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 [(3S,3aR,4S,9R,9aS,9bS)-9-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl] acetate
Chemidplus: 0029041358
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References:
 [(3S,3aR,4S,9R,9aS,9bS)-9-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl] acetate
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 92265
Pubchem (cas): 29041-35-8
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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
CHEBI: View
CHEMBL: View
KEGG (GenomeNet): C09499
HMDB (The Human Metabolome Database): HMDB36643
FooDB: FDB015565
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: 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
 matricaria chamomilla
Search Trop  Picture
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Synonyms:
(3S-(3alpha,3aalpha,4alpha,9alpha,9aalpha,9bbeta))-3a,4,5,9,9a,9b-hexahydro-9-hydroxy-3,6,9-trimethyl-2-oxoazuleno(4,5-b)-3H-furan-4-yl acetate
[(3S,3aR,4S,9R,9aS,9bS)-9-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl] acetate
 proazulene
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Articles:
PubMed: Amaranthus leucocarpus lectin recognizes a moesin-like O-glycoprotein and costimulates murine CD3-activated CD4(+) T cells.
PubMed: Revisited anti-inflammatory activity of matricine in vitro: Comparison with chamazulene.
PubMed: Anglo-Saxon pharmacopoeia revisited: a potential treasure in drug discovery.
PubMed: Chamazulene carboxylic acid and matricin: a natural profen and its natural prodrug, identified through similarity to synthetic drug substances.
PubMed: Supercritical carbon dioxide extraction of chamomile flowers: extraction efficiency, stability, and in-line inclusion of chamomile-carbon dioxide extract in beta-cyclodextrin.
PubMed: Absolute stereochemistry of guaianolides, of matricin and its epimers, of yarrow proazulenes, and of chamazulene carboxylic acid.
PubMed: On the absolute configuration of matricin.
PubMed: Chamazulene: an antioxidant-type inhibitor of leukotriene B4 formation.
PubMed: [Sesquiterpenelactones of Achillea setacea with antiphlogistic activity].
PubMed: Alkylating agent interactions with the nuclear matrix.
PubMed: [Pharmacologic studies on chamomile compounds. VI. Studies on the antiphlogistic effect of chamazulene and matricine].
PubMed: Comparative studies of rat liver and sea urchin embryo nuclear matrices: partial fractionation and protein kinase activity distribution.
PubMed: Fractionation of the nuclear matrix. I. Partial separation into matrix protein fibrils and a residual ribonucleoprotein fraction.
PubMed: Matricin fibrils: isolation of the primary nuclear matrix polypeptides.
PubMed: Isolation of matricin from Artemisia caruthii.
PubMed: [Pharmacodynamic effects of artabasine & matricine].
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