isofuranodiene
 
Notes:
None found
  • BOC Sciences
    • BOC Sciences
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      Product(s):
      57566-47-9 isofuranodiene >95%
      Isofuranodiene is a natural sesquiterpenoid found in the herbs of Chloranthus spicatus, it has the activity of anticancer. Isofuranodiene protects GalN/LPS-induced liver injury anti-cancer
       
       
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CAS Number: 57566-47-9Picture of molecule3D/inchi
Nikkaji Web: J19.859E
XlogP3-AA: 3.70 (est)
Molecular Weight: 216.32360000
Formula: C15 H20 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
Boiling Point: 309.65 °C. @ 760.00 mm Hg (est)
Vapor Pressure: 0.001000 mmHg @ 25.00 °C. (est)
Flash Point: 279.00 °F. TCC ( 137.10 °C. ) (est)
logP (o/w): 5.369 (est)
Soluble in:
 water, 0.1005 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.
isofuranodiene >95%
Odor: characteristic
Use: Isofuranodiene is a natural sesquiterpenoid found in the herbs of Chloranthus spicatus, it has the activity of anticancer. Isofuranodiene protects GalN/LPS-induced liver injury anti-cancer
Coompo
For experimental / research use only.
isoFuranodiene from Plants ≥96%
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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 isofuranodiene usage levels up to:
 not for fragrance use.
 
Recommendation for isofuranodiene 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 : 5317424
National Institute of Allergy and Infectious Diseases: Data
 (5Z,9Z)-3,6,10-trimethyl-4,7,8,11-tetrahydrocyclodeca[b]furan
Chemidplus: 0057566479
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References:
 (5Z,9Z)-3,6,10-trimethyl-4,7,8,11-tetrahydrocyclodeca[b]furan
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 5317424
Pubchem (sid): 135154531
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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
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
 found in nature
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Synonyms:
(E,E)-4,7,8,11-tetrahydro-3,6,10-trimethyl cyclodeca(b)furan
3,6,10-trimethyl-4,7,8,11-tetrahydro-cyclodeca[b]furan
(5Z,9Z)-3,6,10-trimethyl-4,7,8,11-tetrahydrocyclodeca[b]furan
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Articles:
PubMed: Antiproliferative evaluation of isofuranodiene on breast and prostate cancer cell lines.
PubMed: Wild celery (Smyrnium olusatrum L.) oil and isofuranodiene induce apoptosis in human colon carcinoma cells.
PubMed: In vitro biological activity of essential oils and isolated furanosesquiterpenes from the neglected vegetable Smyrnium olusatrum L. (Apiaceae).
PubMed: A forgotten vegetable (Smyrnium olusatrum L., Apiaceae) as a rich source of isofuranodiene.
PubMed: Sesquiterpenes from the rhizomes of Curcuma ochrorhiza.
PubMed: Sesquiterpene metabolites of the antarctic gorgonian Dasystenella acanthina.
PubMed: Sequestered chemistry of the Arminacean nudibranch Leminda millecra in Algoa Bay, South Africa.
PubMed: [Conversion of isofuranodiene to germacranolids (author's transl)].
PubMed: [Conformation of the furanogermacran derivative isofuranodiene (author's transl)].
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