erythrabyssin II, 77263-06-0

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CODE183974 CODE183974
Product(s):
77263-06-0 Erythrabyssin II >95%
Erythrabyssin II is a phenolic compound found in the herbs of Erythrina arborescens. Erythrabyssin II inhibits bacterial neuraminidase in a dose-dependent manner with significant inhibition.

CAS Number:	77263-06-0	3D/inchi
FDA UNII:	Search
Nikkaji Web:	J524.533H
XlogP3-AA:	6.10 (est)
Molecular Weight:	392.49496000
Formula:	C25 H28 O4
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
Soluble in:
	water, 0.005721 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.

Erythrabyssin II >95%

Odor: characteristic

Use: Erythrabyssin II is a phenolic compound found in the herbs of Erythrina arborescens. Erythrabyssin II inhibits bacterial neuraminidase in a dose-dependent manner with significant inhibition.

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 erythrabyssin II usage levels up to:
	not for fragrance use.

Recommendation for erythrabyssin II 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 :10408212

National Institute of Allergy and Infectious Diseases:Data

(6aR,11aR)-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol

References:

	(6aR,11aR)-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol
NIST Chemistry WebBook:	Search Inchi
Pubchem (cid):	10408212
Pubchem (cas):	77263-06-0

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):	HMDB34003
FooDB:	FDB012237
VCF-Online:	VCF Volatile Compounds in Food
ChemSpider:	View

Potential Blenders and core components note

None Found

Potential Uses:

None Found

Occurrence (nature, food, other):note

phaseolus lunatus
Search Trop Picture

Synonyms:

(6aR,11aR)-2,10-bis(3-

methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol

Articles:

PubMed:Potent inhibition of bacterial neuraminidase activity by pterocarpans isolated from the roots of Lespedeza bicolor.

PubMed:Erythrina alkaloids and a pterocarpan from the bark of Erythrina subumbrans.

PubMed:Antibacterial pterocarpans from Erythrina subumbrans.

PubMed:Three isoflav-3-enes and a 2-arylbenzofuran from the root bark of Erythrina burttii.

PubMed:Phenolic constituents in Erythrina x bidwilli and their activity against oral microbial organisms.

Notes:

None found