Dammar-20(21)-ene-3beta,24,25-triol

Dammar-20(21)-ene-3beta,24,25-triol - Names and Identifiers

Name	Dammar-20(21)-ene-3β,24,25-triol
Synonyms	Dammar-20(21)-en-3,24,25-triol DaMMar-20(21)-ene-3β,24,25-triol Dammar-20(21)-ene-3β,24,25-triol (24R)-Dammar-20-ene-3β,24,25-triol Dammar-20(21)-ene-3beta,24,25-triol (24R)-5α-Dammara-20-ene-3β,24,25-triol Dammar-20-ene-3,24,25-triol, (3β,24R)-
CAS	55050-69-6

Dammar-20(21)-ene-3beta,24,25-triol - Physico-chemical Properties

Molecular Formula	C30H52O3
Molar Mass	460.73
Melting Point	165-167℃
Storage Condition	2-8℃

Dammar-20(21)-ene-3beta,24,25-triol - Introduction

Dammar-20(21)-ene-3β,24,25-triol (also known as Dammar-20(21)-ene-3β,24,25-triol) is a natural triterpenoid. Its structure contains four rings, one of which is a five-membered ring and the other three rings are six-membered rings. This compound has a plurality of hydroxyl substitution sites at carbon number 3, carbon number 24 and carbon number 25.

Dammar-20(21)-ene-3β,24,25-triol is present in some plants, such as the resin tree brain (dammar resin) and some pine resin plants. It has a variety of biological activities, including antibacterial, anti-inflammatory, antioxidant and so on. Therefore, it has certain application value in traditional Chinese medicine, drug research and development and natural pharmaceutical chemistry.

The method for preparing Dammar-20(21)-ene-3β,24,25-triol is usually extracted from natural plants or synthesized. The extraction methods mainly include solvent extraction, methanol extraction and so on. The synthesis method can be through organic synthesis reaction, such as oxidation, ketone reduction, etc.

Last Update：2024-04-09 02:00:52