heteronemin

D-homoandrostano(17,17a-c)furan-5',12,16-triol, 5',17a-dihydro-4,4,8-trimethyl-, 5',16-diacetate, (5alpha,5'alpha,12beta,16beta,17aalpha)-

CAS: 62008-04-2 C29 H44 O6 MW: 488.66488000

Identification

Nameheteronemin
IUPAC[(1S,4S,5aS,5bR,7aS,11aS,11bR,13R,13aR)-1-acetyloxy-13-hydroxy-5a,5b,8,8,11a,13a-hexamethyl-4,5,6,7,7a,9,10,11,11b,12,13,13b-dodecahydro-1H-phenanthro[2,1-e][2]benzofuran-4-yl] acetate
CAS Number62008-04-2
FDA UNIISearch
Molecular FormulaC29 H44 O6
Molecular Weight488.66488000

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 559.68 °C. @ 760.00 mm Hg (est)
Flash Point 341.00 °F. TCC ( 171.50 °C. ) (est)
logP (o/w) 5.804 (est)
Soluble in water, 0.1159 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Preferred SDSView
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 heteronemin usage levels up tonot for fragrance use.
Recommendation for heteronemin flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

found in nature

Synonyms

[(1S,4S,5aS,5bR,7aS,11aS,11bR,13R,13aR)-1- acetyloxy-13-hydroxy-5a,5b,8,8,11a,13a-hexamethyl-4,5,6,7,7a,9,10,11,11b,12,13,13b-dodecahydro-1H-phenanthro[2,1-e][2]benzofuran-4-yl] acetate D-homo androstano(17,17a-c)furan-5',12,16-triol, 5',17a-dihydro-4,4,8-trimethyl-, 5',16-diacetate, (5alpha,5'alpha,12beta,16beta,17aalpha)- PubMed: Antiproliferative effects of 12-oxoheteronemin vs heteronemin. PubMed: Heteronemin, a marine sponge terpenoid, targets TDP-43, a key factor in several neurodegenerative disorders. PubMed: In vitro characterisation of the anti-intravasative properties of the marine product heteronemin. PubMed: Heteronemin, a spongean sesterterpene, inhibits TNF alpha-induced NF-kappa B activation through proteasome inhibition and induces apoptotic cell death. PubMed: Scalarane sesterterpenoids: semisynthesis and biological activity. PubMed: Antitubercular sesterterpenes from the Thai sponge Brachiaster sp. PubMed: Marine natural products. XXXII. Absolute configurations of C-4 of the manoalide family, biologically active sesterterpenes from the marine sponge Hyrtios erecta.