epifriedelanol
(3S,4R,4aS,6aS,6bR,8aR,12aR,12bS,14aS,14bS)-4,4a,6b,8a,11,11,12b,14a-octamethyldocosahydro-3-picenol
Identification
| Name | epifriedelanol |
| IUPAC | (3S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-ol |
| CAS Number | 16844-71-6 |
| FDA UNII | Search |
| Molecular Formula | C30 H52 O |
| Molecular Weight | 428.74364000 |
| Nikkaji Number | J16.165I |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 478.30 °C. @ 760.00 mm Hg (est) |
| Flash Point | 391.00 °F. TCC ( 199.60 °C. ) (est) |
| logP (o/w) | 11.450 (est) |
| Soluble in | water, 7.845e-005 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 epifriedelanol usage levels up to | not for fragrance use. |
| Recommendation for epifriedelanol flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
epi-
friedelanol
epi
friedelinol
(3S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-
octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-ol
(3S,4R,4aS,6aS,6bR,8aR,12aR,12bS,14aS,14bS)-4,4a,6b,8a,11,11,12b,14a-
octamethyldocosahydro-3-picenol
(3S,4R,4aS,6aS,6bR,8aR,12aR,12bS,14aS,14bS)-4,4a,6b,8a,11,11,12b,14a-
octamethyldocosahydropicen-3-ol
3-
picenol, docosahydro-4,4a,6b,8a,11,11,12b,14a-octamethyl-, (3S,4R,4aS,6aS,6bR,8aR,12aR,12bS,14aS,14bS)-
(3beta,4beta,5beta,8alpha,9beta,10alpha,13alha,14beta)-5,9,13-
trimethyl-24,25,26-trinoroleanan-3-ol
PubMed:
A new cycloartane nortriterpenoid from stem and leaf of Quercus variabilis.
PubMed:
Antimicrobial activity and cytotoxicity of triterpenes isolated from leaves of Maytenus undata (Celastraceae).
PubMed:
Six new phenolic glycosides and a new ceramide from the flowers of Wedelia biflora and their cytotoxicity against some cancer cell lines.
PubMed:
Phenolic contents, antioxidant and cytotoxic activities of Elaeocarpus floribundus Blume.
PubMed:
[Study on chemical constituents from Anoectochilus chapaensis].
PubMed:
A review on chemical and biological properties of Cayratia trifolia Linn. (Vitaceae).
PubMed:
Antiproliferative constituents of the roots of Conyza canadensis.
PubMed:
Lignans and other constituents from the roots of the Vietnamese medicinal plant Pseuderanthemum palatiferum.
PubMed:
Regulation of human pregnane X receptor and its target gene cytochrome P450 3A4 by Chinese herbal compounds and a molecular docking study.
PubMed:
Epifriedelanol from the root bark of Ulmus davidiana inhibits cellular senescence in human primary cells.
PubMed:
[Chemical constituents of stem barks of Mucuna birdwoodiana].
PubMed:
[Study on the chemical constituents of Humulus scandens].
PubMed:
[Study on the chemical constituents of Dichrocephala integrifolia].
PubMed:
Triterpenoids from Calophyllum inophyllum and their growth inhibitory effects on human leukemia HL-60 cells.
PubMed:
[Studies on chemical constituents of leaves of Aquilaria sinensis].
PubMed:
Composition of the epicuticular and intracuticular wax layers on Kalanchoe daigremontiana (Hamet et Perr. de la Bathie) leaves.
PubMed:
[Studies on chemical constituents of aerial roots of Ficus microcarpa].
PubMed:
Development of the cuticular wax during growth of Kalanchoe daigremontiana (Hamet et Perr. de la Bathie) leaves.
PubMed:
New triterpenoids isolated from the root bark of Ulmus pumila L.
PubMed:
Antitumor and antiinflammatory constituents from Celtis sinensis.
PubMed:
Pentacyclic triterpenoids from Mallotus apelta.
PubMed:
[Studies on the constituents from the herb of Vernonia patula].
PubMed:
Antitumor activity of epifriedelanol from Vitis trifolia.
PubMed:
[Chemical constituents of Parthenocissus thomsonii (Laws.) Planch].
PubMed:
[Chemical constituents in the stem of Premna crassa Hand. -Mazz].
PubMed:
Antitumor agents XXXVIII: Isolation and structural elucidation of novel germacranolides and triterpenes from Elephantopus mollis.