CAS 120211-98-5
:(1beta,2alpha,3alpha,5xi,18alpha)-1,2,3,19-tetrahydroxyurs-12-en-28-oic acid
Description:
The chemical substance known as (1beta,2alpha,3alpha,5xi,18alpha)-1,2,3,19-tetrahydroxyurs-12-en-28-oic acid, with the CAS number 120211-98-5, is a triterpenoid compound derived from the ursane skeleton, which is characterized by a fused cyclopentane and cyclohexane ring structure. This compound features multiple hydroxyl (-OH) groups, which contribute to its hydrophilicity and potential biological activity. The presence of these hydroxyl groups can enhance solubility in polar solvents and may influence the compound's interaction with biological systems, including potential antioxidant and anti-inflammatory properties. The specific stereochemistry indicated by the nomenclature suggests a complex three-dimensional arrangement that may affect its pharmacological profile. Triterpenoids are often studied for their therapeutic potential, including anti-cancer, anti-diabetic, and hepatoprotective effects. However, detailed studies on the specific biological activities and mechanisms of action of this particular compound may still be limited, necessitating further research to fully elucidate its properties and potential applications in medicine or pharmacology.
Formula:C30H48O6
InChI:InChI=1/C30H48O6/c1-16-10-13-30(24(34)35)15-14-26(4)17(21(30)29(16,7)36)8-9-19-27(26,5)12-11-18-25(2,3)22(32)20(31)23(33)28(18,19)6/h8,16,18-23,31-33,36H,9-15H2,1-7H3,(H,34,35)/t16-,18?,19+,20+,21+,22-,23-,26-,27-,28+,29-,30+/m1/s1
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Found 4 products.
1β-Hydroxyeuscaphic acid
CAS:1beta-Hydroxyeuscaphic acid demonstrates notable hepatoprotective activity, effectively minimizing the leakage of intracellular enzymes, attenuating proteinFormula:C30H48O6Purity:98%Color and Shape:SolidMolecular weight:504.71β-Hydroxyeuscaphic acid
CAS:Formula:C30H48O6Purity:95%~99%Color and Shape:PowderMolecular weight:504.7081Beta-Hydroxyeuscaphic acid
CAS:Controlled Product<p>1Beta-Hydroxyeuscaphic acid is a pentacyclic triterpenoid, which is a secondary metabolite predominantly isolated from various medicinal plants, including species from the Rosaceae and related families. This compound is characterized by its intricate molecular structure, which contributes to its multifaceted biological activities.</p>Formula:C30H48O6Purity:Min. 95%Molecular weight:504.7 g/mol




