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Trametenolic acid

Names

[ CAS No. ]:
24160-36-9

[ Name ]:
Trametenolic acid

[Synonym ]:
Trametenolic acid
(+)-trametenolic acid B
Lanosta-8,24-dien-21-oic acid,3-hydroxy-,(3beta)
3beta-Hydroxylanosta-8,24-dien-21-oic acid

Biological Activity

[Description]:

Trametenolic acid is a lanostanol glycoside that isolated from the EtOH extract of the fruit bodies of Laetiporus versisporus[1].

[Related Catalog]:

Signaling Pathways >> Others >> Others
Research Areas >> Inflammation/Immunology

[Target]

ERK1

ERK2


[In Vitro]

Trametenolic acid (1 mg/mL; 15-30 mins) induces the upregulation of autophagy-related proteins (Beclin-1, Atg12, and LC3) in B16-F1 cells by activating the ERK1/2 signaling pathway[1]. Trametenolic acid (1 mg/mL; 24 hours; B16-F1 cells) has dual synergic mechanisms to exert an anti-melanogenetic effect[1]. Trametenolic acid (0.1-4 mg/mL; 52 hours; B16-F1 cells) increase melanin synthesis by approximately 20% and 40% in cells transfected with siRNAs against mTOR and Atg5, respectively[1]. Western Blot Analysis[1] Cell Line: B16-F1 cells Concentration: 1 mg/mL Incubation Time: 15 and 30 mins Result: Increased the expression levels of phospho-p38, phospho-ERK1/2, Beclin-1, Atg12 and LC3 by approximately 46%, 10%, 48%, 126% and 49%, respectively. Western Blot Analysis[1] Cell Line: B16-F1 cells Concentration: 1 mg/mL Incubation Time: 24 hours Result: Increased the expression of ERK1/2 and p-ERK1/2 and decreased MITF, tyrosinase, and TRP 1 levels.

[References]

[1]. K Yoshikawa, et al. New lanostanoid glycosides from the fruit body of laetiporus versisporus. J Nat Prod. 1999 Apr;62(4):543-5.

Chemical & Physical Properties

[ Density]:
1.07±0.1 g/cm3

[ Melting Point ]:
259-261 ºC

[ Molecular Formula ]:
C30H48O3

[ Molecular Weight ]:
456.70000

[ Exact Mass ]:
456.36000

[ PSA ]:
57.53000

[ LogP ]:
7.54380

[ Vapour Pressure ]:
3.26E-15mmHg at 25°C

[ Storage condition ]:
2-8℃

[ Water Solubility ]:
Insuluble (8.2E-6 g/L) (25 ºC)


Related Compounds