lubimin
spiro(4.5)decane-6-carboxaldehyde, 8-hydroxy-10-methyl-2-(1-methylethenyl)-, (5S-(5alpha(S*),6beta,8beta,10beta))-
Identification
| Name | lubimin |
| IUPAC | (3R,6R,8S,10S)-8-hydroxy-6-methyl-3-prop-1-en-2-ylspiro[4.5]decane-10-carbaldehyde |
| CAS Number | 35951-50-9 |
| FDA UNII | SIC6883O43 |
| Molecular Formula | C15 H24 O2 |
| Molecular Weight | 236.35468000 |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 352.05 °C. @ 760.00 mm Hg (est) |
| Flash Point | 302.00 °F. TCC ( 150.00 °C. ) (est) |
| logP (o/w) | 3.224 (est) |
| Soluble in | water, 32.04 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 lubimin usage levels up to | not for fragrance use. |
| Recommendation for lubimin flavor usage levels up to | not for flavor use. |
No supplier data available
Potential Uses
Natural Occurrence
Synonyms
(5S-(5alpha(S*),6beta,8beta,10beta))-8-
hydroxy-10-methyl-2-(1-methyl ethenyl) spiro(4.5)decane-6-carboxaldehyde
(3R,6R,8S,10S)-8-
hydroxy-6-methyl-3-prop-1-en-2-ylspiro[4.5]decane-10-carbaldehyde
spiro(4.5)decane-6-carboxaldehyde, 8-hydroxy-10-methyl-2-(1-methylethenyl)-, (5S-(5alpha(S*),6beta,8beta,10beta))-
PubMed:
Multi-platform metabolomic analyses of ergosterol-induced dynamic changes in Nicotiana tabacum cells.
PubMed:
Ergosterol-induced sesquiterpenoid synthesis in tobacco cells.
PubMed:
Anti-fungal sesquiterpenoid from the root exudate of Solanum abutiloides.
PubMed:
Enhanced production of antimicrobial sesquiterpenes and lipoxygenase metabolites in elicitor-treated hairy root cultures of Solanum tuberosum.
PubMed:
Effect of elicitation on growth, respiration, and nutrient uptake of root and cell suspension cultures of Hyoscyamus muticus.
PubMed:
An ATP-binding cassette multidrug-resistance transporter is necessary for tolerance of Gibberella pulicaris to phytoalexins and virulence on potato tubers.
PubMed:
Sesquiterpenoids in root exudates of Solanum aethiopicum.
PubMed:
Structural confirmation of 15-norlubiminol and 15-norepilubiminol, isolated from Solanum aethiopicum, by chemical conversion from lubimin and epilubimin, and their antifungal activity.
PubMed:
Induction of plant gp91 phox homolog by fungal cell wall, arachidonic acid, and salicylic acid in potato.
PubMed:
Sesquiterpenoids from the roots of Solanum aethiopicum.
PubMed:
Induction of a polyubiquitin gene (ubi1) by potato phytoalexins and heat shock in Gibberella pulicaris.
PubMed:
Phytoalexins from hairy roots of Hyoscyamus albus treated with methyl jasmonate.
PubMed:
Novel study on the elicitation of hypersensitive response by polyunsaturated fatty acids in potato tuber.
PubMed:
Abiotic factors elicit sesquiterpenoid phytoalexin production but not alkaloid production in transformed root cultures of Datura stramonium.
PubMed:
Studies on the biosynthesis and metabolism of the phytoalexin lubimin and related compounds in Datura stramonium L.
PubMed:
A role for ca in the elicitation of rishitin and lubimin accumulation in potato tuber tissue.
PubMed:
Involvement of 3-hydroxy-3-methylglutaryl coenzyme a reductase in the regulation of sesquiterpenoid phytoalexin synthesis in potato.
PubMed:
The effect of the phytoalexins, lubimin, (-)-maackiain, pinosylvin, and the related compounds dehydroloroglossol and hordatine M on human lymphoblastoid cell lines.
PubMed:
Biotransformation of potato stress metabolites rishitin, lubimin, and 15-dihydro lubimin by potato and soybean cell cultures.
PubMed:
Arachidonic acid-related elicitors of the hypersensitive response in potato and enhancement of their activities by glucans from Phytophthora infestans (Mont.) deBary.
PubMed:
Effects of Controlled Atmospheres on Production of Sesquiterpenoid Stress Metabolites by White Potato Tuber: Possible Involvement of Cyanide-resistant Respiration.