echinocystic acid-3-O-glucoside
eclalbasaponin II
Identification
| Name | echinocystic acid-3-O-glucoside |
| CAS Number | 78285-90-2 |
| EINECS | 278-887-0 |
| FDA UNII | Search |
| Molecular Formula | C36 H58 O9 |
| Molecular Weight | 634.85106000 |
| MDL Number | MFCD00017386 |
| Nikkaji Number | J319.751D |
| Beilstein | 1613820 |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 752.60 °C. @ 760.00 mm Hg (est) |
| Flash Point | 443.00 °F. TCC ( 228.60 °C. ) (est) |
| logP (o/w) | 5.610 (est) |
| Soluble in | water, 0.03096 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 | information only not used for fragrances or flavors |
| Recommendation for echinocystic acid-3-O-glucoside usage levels up to | not for fragrance use. |
| Recommendation for echinocystic acid-3-O-glucoside flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
eclalbasaponin II
(3beta,16alpha)-3-(beta-D-
glucopyranosyloxy)-16-hydroxyolean-12-en-28-oic acid
PubMed:
Eclalbasaponin II induces autophagic and apoptotic cell death in human ovarian cancer cells.
PubMed:
Echinocystic acid isolated from Eclipta prostrata suppresses lipopolysaccharide-induced iNOS, TNF-α, and IL-6 expressions via NF-κB inactivation in RAW 264.7 macrophages.
PubMed:
Antiproliferative activity of triterpenoids from Eclipta prostrata on hepatic stellate cells.