farnesiferol B

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CAS: 54990-68-0 C24 H30 O4 MW: 382.49990000
All Ingredients Aromatic Ingredients CAS Numbers Found in Nature

Identification

Namefarnesiferol B
CAS Number54990-68-0
FDA UNIIJJ74M033DI
Molecular FormulaC24 H30 O4
Molecular Weight382.49990000
Nikkaji NumberJ13.066D

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Soluble in water, 0.04394 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for farnesiferol B usage levels up tonot for fragrance use.
Recommendation for farnesiferol B flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

ferula assa-foetida

Synonyms

2H-1- benzopyran-2-one, 7-(((2E)-5-((1R,3S)-3-hydroxy-2,2-dimethyl-6-methylenecyclohexyl)-3-methyl-2-pentenyl)oxy)- 7-[(E)-5-[(1S,3R)-3- hydroxy-2,2-dimethyl-6-methylidenecyclohexyl]-3-methylpent-2-enoxy]chromen-2-one PubMed: Modulation of Multidrug Resistance Protein 2 Efflux in the Cisplatin Resistance Human Ovarian Carcinoma Cells A2780/RCIS by Sesquiterpene Coumarins. PubMed: Reversal of P-glycoprotein-mediated multidrug resistance in MCF-7/Adr cancer cells by sesquiterpene coumarins. PubMed: Disesquiterpene and sesquiterpene coumarins from Ferula pseudalliacea, and determination of their absolute configurations. PubMed: New sesquiterpene coumarins from the roots of Ferula flabelliloba. PubMed: Galbanic acid, a cytotoxic sesquiterpene from the gum resin of Ferula asafoetida, blocks protein farnesyltransferase. PubMed: Total synthesis of (+/-)-elegansidiol, (+/-)-farnesiferol B, and (+/-)-farnesiferol D. PubMed: First total synthesis of (-)-achilleol B: reassignment of its relative stereochemistry. PubMed: [Chemical constituents from roots of Ferula sinkiangensis]. PubMed: Structure-based virtual screening for the discovery of natural inhibitors for human rhinovirus coat protein. PubMed: Sesquiterpene coumarins from Ferula szowitsiana and in vitro antileishmanial activity of 7-prenyloxycoumarins against promastigotes.