
CAS: 116499-73-1
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Found 4 products.
3H-3,10b-Ethanonaphtho[1,2-c]-1,2-dioxin-7-carboxylic acid, 5,6,6a,7,8,9,10,10a-octahydro-7,10a-dimethyl-3-(1-methylethyl)-, (3R,6aR,7R,10aS,10bR)-
CAS:Formula:C20H30O4Purity:97.0%Molecular weight:334.44989α,13α-Epidioxyabiet-8(14)-en-18-oic acid
CAS:9alpha,13alpha-Epidioxyabiet-8(14)-en-18-oic acid shows potent inhibitory effects on Epstein-Barr virus early antigen (EBV-EA) activation induced by the tumorFormula:C20H30O4Purity:98%Color and Shape:SolidMolecular weight:334.459α,13α-Epidioxyabiet-8(14)-en-18-oic acid
CAS:9α,13α-Epidioxyabiet-8(14)-en-18-oic acid is a naturally occurring diterpenoid compound, which is derived from various terrestrial plant species, particularly those belonging to the Pinaceae family. This compound is characterized by its unique epidioxy structure, implicating its potential function in oxidative stress responses within the plant. The mode of action of 9α,13α-Epidioxyabiet-8(14)-en-18-oic acid is primarily associated with its ability to induce cytotoxic effects. It acts by generating reactive oxygen species (ROS), leading to oxidative stress within cells, thereby causing apoptosis or programmed cell death. This mechanism is particularly valuable in the study of potential anticancer agents. In terms of applications, 9α,13α-Epidioxyabiet-8(14)-en-18-oic acid is utilized predominantly within the realm of biochemical and pharmacological research. It serves as a molecular probe for understanding the pathways and cellular mechanisms involving oxidative stress and apoptosis. Furthermore, due to its cytotoxic attributes, it is also explored in the development and testing of novel anticancer therapeutics. Its role in medicinal chemistry underscores the importance of naturally derived compounds in the advancement of cancer treatment strategies.Formula:C20H30O4Purity:Min. 95%Molecular weight:334.4 g/mol9α,13α-Epidioxyabiet-8(14)-en-18-oic acid
CAS:Formula:C20H30O4Purity:95%~99%Color and Shape:PowderMolecular weight:334.456