isofuranodiene, 57566-47-9

Supplier Sponsors

Best of Chemicals Supplier
Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
BOC Sciences provides a wide range of services to support the pharmaceutical industry through all stages of drug discovery including Custom Synthesis of those chemicals that are not in stock, Isotope Labeling Service, Chiral Synthesis and Resolution, Bioconjugation, PEGylation services, analytical services.
BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies.
Email:	Marketing
US Email:	Marketing
Email:	Sales
US Email:	Sales
Voice: 1-631-485-4226
Fax: 1-631-614-7828
US Voice: 1-631-485-4226
US Fax: 1-631-614-7828
Europe	44-203-286-1088
Facebook
Twitter
Linkedin
Blog
Get the App!
CODE159627 CODE159627
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

Name:	(5Z,9Z)-3,6,10-trimethyl-4,7,8,11-tetrahydrocyclodeca[b]furan
CAS Number:	57566-47-9	3D/inchi
FDA UNII:	Search
Nikkaji Web:	J19.859E
XlogP3-AA:	3.70 (est)
Molecular Weight:	216.32360000
Formula:	C15 H20 O
NMR Predictor:	Predict (works with chrome, Edge 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

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)

Organoleptic Properties:

Odor and/or flavor descriptions from others (if found).

Cosmetic Information:

None found

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%

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

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.

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

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

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

Potential Blenders and core components note

None Found

Potential Uses:

None Found

Occurrence (nature, food, other):note

found in nature

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

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)].

Notes:

None found