erythrabyssin II
Identification
| Name | erythrabyssin II |
| CAS Number | 77263-06-0 |
| FDA UNII | Search |
| Molecular Formula | C25 H28 O4 |
| Molecular Weight | 392.49496000 |
| Nikkaji Number | J524.533H |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Soluble in | water, 0.005721 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| 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. |
BOC Sciences
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 Molecul...
Potential Uses
Natural Occurrence
Synonyms
(6aR,11aR)-2,10-bis(3-
methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol
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.