Cycloastragenol

Modify Date: 2025-08-23 08:58:44

Cycloastragenol Structure
Cycloastragenol structure
Common Name Cycloastragenol
CAS Number 84605-18-5 Molecular Weight 490.715
Density 1.2±0.1 g/cm3 Boiling Point 617.2±55.0 °C at 760 mmHg
Molecular Formula C30H50O5 Melting Point N/A
MSDS USA Flash Point 327.1±31.5 °C

 Use of Cycloastragenol


Cycloastragenol, a natural tetracyclic triterpenoid, was first identified when screening Astragalus membranaceus extracts for active ingredients with antiaging properties. IC50 value:Target:In vitro: In the study of Cycloastragenolon the treatment of degenerative diseases, the result showed that first-pass intestinal metabolism of cycloastragenol might occur upon passage through the intestinal epithelium. Cycloastragenol underwent extensive metabolism in rat and human liver microsomes with only 17.4% and 8.2%, respectively, of the starting amount of Cycloastragenol remaining after 30 min of incubation [1]. The present study demonstrates that cycloastragenol stimulates telomerase activity and cell proliferation in human neonatal keratinocytes. In particular, cycloastragenol promotes scratch wound closure of human neonatal keratinocyte monolayers in vitro [3]. In vivo: Rats were treated with Cycloastragenol (40 mg·kg- 1·d- 1) for 7 days to induce hepatic microsomal enzyme. The result showed that compared with the control, cycloastragenol obviously activated CYP2E1, and remarkably inhibited CYP3A4 [2].

 Names

Name cycloastragenol
Synonym More Synonyms

 Cycloastragenol Biological Activity

Description Cycloastragenol, a natural tetracyclic triterpenoid, was first identified when screening Astragalus membranaceus extracts for active ingredients with antiaging properties. IC50 value:Target:In vitro: In the study of Cycloastragenolon the treatment of degenerative diseases, the result showed that first-pass intestinal metabolism of cycloastragenol might occur upon passage through the intestinal epithelium. Cycloastragenol underwent extensive metabolism in rat and human liver microsomes with only 17.4% and 8.2%, respectively, of the starting amount of Cycloastragenol remaining after 30 min of incubation [1]. The present study demonstrates that cycloastragenol stimulates telomerase activity and cell proliferation in human neonatal keratinocytes. In particular, cycloastragenol promotes scratch wound closure of human neonatal keratinocyte monolayers in vitro [3]. In vivo: Rats were treated with Cycloastragenol (40 mg·kg- 1·d- 1) for 7 days to induce hepatic microsomal enzyme. The result showed that compared with the control, cycloastragenol obviously activated CYP2E1, and remarkably inhibited CYP3A4 [2].
Related Catalog
References

[1]. Jing Zhu, et al. In vitro Intestinal Absorption and First-pass Intestinal and Hepatic Metabolism of Cycloastragenol, a Potent Small Molecule Telomerase Activator. Drug Metabolism and Pharmacokinetics Volume 25, Issue 5, 2010, Pages 477-486

[2]. WEI Bao-hong, et al. Effect of continuous oral cycloastragenol on the activity of cytochrome P450 enzymes in rats. Chinese New Drugs Journal, 2014 -04

[3]. Ip FC, et al. Cycloastragenol is a potent telomerase activator in neuronal cells: implications for depression management. Neurosignals. 2014;22(1):52-63.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 617.2±55.0 °C at 760 mmHg
Molecular Formula C30H50O5
Molecular Weight 490.715
Flash Point 327.1±31.5 °C
Exact Mass 490.365814
PSA 90.15000
LogP 3.82
Vapour Pressure 0.0±4.0 mmHg at 25°C
Index of Refraction 1.582
Storage condition -20°C

 Safety Information

HS Code 2942000000

 Synthetic Route

 Customs

HS Code 2942000000

 Synonyms

9,19-Cyclolanostane-3,6,16,25-tetrol, 20,24-epoxy-, (3β,6α,9β,16β,20R,24S)-
Astramembrangenin
Cycloastragenol
(3β,6α,9β,16β,20R,24S)-20,24-Epoxy-9,19-cyclolanostane-3,6,16,25-tetrol
Cyclogalegigenin
cycloartenol trans-ferulate
Cycloartenol ferulic acid ester
CYCLOGALEGENIN
Oryzanol A
3-O-ferulylcycloartenol
cycloartenyl ferulate
Ring astragalus alcohol
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