longispinogenin
Identification
| Name | longispinogenin |
| CAS Number | 465-94-1 |
| FDA UNII | 71XG0082E9 |
| Molecular Formula | C30 H50 O3 |
| Molecular Weight | 458.72610000 |
| Nikkaji Number | J12.088J |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Soluble in | water, 0.003063 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 longispinogenin usage levels up to | not for fragrance use. |
| Recommendation for longispinogenin flavor usage levels up to | not for flavor use. |
No supplier data available
Potential Uses
Natural Occurrence
Synonyms
(3S,4aR,6aR,6bS,8S,8aS,12aS,14aR,14bR)-8a-(
hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,8-diol
(3S,4aR,5R,6aR,6bS,8S,8aR,12aS,14aR,14bR)-8,8a-bis-
hydroxymethyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-eicosahydro-picen-3-ol
olean-12-ene-3, 16 28-triol, (3beta,16beta)-
PubMed:
In vitro evaluation of potential bitterness-masking terpenoids from the Canada goldenrod (Solidago canadensis).
PubMed:
Chemical constituents from the stems of Gymnema sylvestre.
PubMed:
Two antiproliferative saponins of Tarenna grevei from the Madagascar dry forest [1].
PubMed:
Constituents of Compositae plants III. Anti-tumor promoting effects and cytotoxic activity against human cancer cell lines of triterpene diols and triols from edible chrysanthemum flowers.
PubMed:
Antisweet saponins from Gymnema sylvestre.
PubMed:
Oleanane saponins from Gymnema sylvestre.
PubMed:
Antisweet natural products. XII. Structures of sitakisosides XI-XX from Stephanotis lutchuensis Koidz. var. japonica.
PubMed:
Inhibitory effect of Di- and trihydroxy triterpenes from the flowers of compositae on 12-O-tetradecanoylphorbol-13-acetate-induced inflammation in mice.
PubMed:
Antisweet natural products. XI. Structures of sitakisosides VI-X from Stephanotis lutchuensis Koidz. var. japonica.
PubMed:
3 beta-O-palmityl longispinogenin from Trichocereus chilensis.