18296-44-1
18296-44-1
Chemical Structure
Valepotriate
Synonym(s): Valtrate
- CAS No.: 18296-44-1
- Formula:C22H30O8
- Molecular Weight:422.47
IUPAC Name: (1S,6S,7R,7aS)-4-(acetoxymethyl)-6,7a-dihydro-1H-spiro[cyclopenta[c]pyran-7,2'-oxirane]-1,6-diyl bis(3-methylbutanoate)
InChIKey: BDIAUFOIMFAIPU-KVJIRVJXSA-N
SMILES: O=C(CC(C)C)O[C@@H]1[C@]2(CO2)[C@]([C@@H]3OC(CC(C)C)=O)([H])C(C(COC(C)=O)=CO3)=C1
Biological Activity: Valepotriate can be isolated from Valeriana jatamansi Jones, has anti-epileptic and anti-cancer activities[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Valepotriate | 99.40% | Valepotriate can be isolated from Valeriana jatamansi Jones, has anti-epileptic and anti-cancer activities. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Valepotriate (Standard) | ≥98% | Valepotriate (Standard) is the analytical standard of Valepotriate. This product is intended for research and analytical applications. Valepotriate can be isolated from Valeriana jatamansi Jones, has anti-epileptic and anti-cancer activities. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Yan YY, et al. A novel derivative of valepotriate inhibits the PI3K/AKT pathway and causes Noxa-dependent apoptosis in human pancreatic cancer cells. Acta Pharmacol Sin. 2020 Feb 11. [Content Brief]
- [2]. Wu A, et al. Anti-epileptic Effects of Valepotriate Isolated from Valeriana jatamansi Jones and Its Possible Mechanisms. Pharmacogn Mag. 2017 Jul-Sep;13(51):512-516. [Content Brief]
Keywords
