khusinol

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isolongifolan-7-alpha-ol

CAS: 24268-34-6 C15 H24 O MW: 220.35548000
All Ingredients Aromatic Ingredients CAS Numbers Found in Nature

Identification

Namekhusinol
CAS Number24268-34-6
FDA UNIISearch
Molecular FormulaC15 H24 O
Molecular Weight220.35548000
Nikkaji NumberJ16.396A

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No

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 khusinol usage levels up tonot for fragrance use.
Recommendation for khusinol flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

cirsium japonicum rhizomes

Synonyms

iso longifolan-7-alpha-ol iso longifolol PubMed: Chemical composition, antinociceptive and anti-inflammatory properties of essential oil from the roots of Illicium lanceolatum. PubMed: Essential oil from aerial parts of of Betonica grandiflora Willd. from Iran. PubMed: Microbial transformation of (-)-isolongifolol by plant pathogenic fungus Glomerella cingulata. PubMed: Terpene conjugates of diaminedichloridoplatinum(II) complexes: antiproliferative effects in HL-60 leukemia, 518A2 melanoma, and HT-29 colon cancer cells. PubMed: Stereochemical and steric control of the UDP-glucuronosyltransferase-catalyzed conjugation reaction: a rational approach for the design of inhibitors for the human UGT2B7. PubMed: Eudismic analysis of tricyclic sesquiterpenoid alcohols: lead structures for the design of potent inhibitors of the human UDP-glucuronosyltransferase 2B7. PubMed: Biotransformation of (+)-cycloisolongifolol by plant pathogenic fungus Glomerella cingulata. PubMed: Isoform-selective inhibition of the human UDP-glucuronosyltransferase 2B7 by isolongifolol derivatives. PubMed: Microbial transformation of (-)-isolongifolol and butyrylcholinesterase inhibitory activity of transformed products.