69926-31-4

Basic information

• Product Name: 20(S),24(R)-Ocotillol
• Synonyms: 20(S),24(R)-Ocotillol;(3beta,6alpha,12beta,24R)-20,24-Epoxydammarane-3,6,12,25-tetrol
• CAS NO: 69926-31-4
• Molecular Formula: C30H52O5
• Molecular Weight: 492.73
• EINECS: 2017-001-1
• Mol File: 69926-31-4.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 594.5±50.0 °C(Predicted)
• Appearance: /
• Density: 1.126±0.06 g/cm3(Predicted)
• PKA: 14.57±0.29(Predicted)
• CAS DataBase Reference: 20(S),24(R)-Ocotillol(CAS DataBase Reference)
• NIST Chemistry Reference: 20(S),24(R)-Ocotillol(69926-31-4)
• EPA Substance Registry System: 20(S),24(R)-Ocotillol(69926-31-4)

Safety Data

• Hazardous Substances Data: 69926-31-4(Hazardous Substances Data)

Usage

Description

20(S),24(R)-Ocotillol is a tetracyclic triterpenoid, a type of chemical compound typically derived from plants. It is known for its diverse biological activities, including anti-inflammatory, antiviral, and anticancer properties. 20(S),24(R)-Ocotillol has been specifically isolated from the root of the plant Panax japonicus, and research indicates its potential to combat various diseases. However, further comprehensive studies are needed to fully comprehend its impact and benefits on human health.

Uses

Used in Pharmaceutical Industry:
20(S),24(R)-Ocotillol is used as a potential therapeutic agent for its anti-inflammatory properties, which can help in reducing inflammation and associated symptoms in various conditions.
Used in Antiviral Applications:
20(S),24(R)-Ocotillol is used as an antiviral agent, leveraging its ability to inhibit viral replication and activity, potentially offering a treatment option for viral infections.
Used in Anticancer Research:
20(S),24(R)-Ocotillol is used as a subject of anticancer research, with studies exploring its potential to target and inhibit cancer cell growth, offering a new avenue for cancer treatment strategies.
Used in Nutraceutical Industry:
20(S),24(R)-Ocotillol is used as a nutraceutical ingredient, benefiting from its health-promoting properties, which may include immune support and overall wellness enhancement.

Upstream product

• 1453-93-6 20S-protopanaxatriol 

Relevant articles and documents

With antibacterial activity (20 S, 24 R) - ocotillol-type Ginseng saponin derivatives, their preparation and use

The invention relates to the fields of organic synthesis and pharmaceutical chemistry, in particular to a (20S, 24R)-ocotillol type ginsenoside derivative having represented in a structural formula (I). The invention further discloses a reparation method of the (20S, 24R)-ocotillol type ginsenoside derivative, pharmaceutical compositions containing the derivative and anti-bacterial and anti-infection application.

Biotransformation of 20(S)-protopanaxatriol by Aspergillus niger and the cytotoxicity of the resulting metabolites

The microbial transformation of 20(S)-protopanaxatriol by cell suspension cultures of Aspergillus niger AS 3.1858 yielded metabolites 1-13. The chemical structures of these transformed products were elucidated based on various spectroscopic analyses, incl

Synthesis, structural determination of a new ocotillol derivative and its epimer

Epimeric 20S, 24-epoxy-dammarane-3β, 6α, 12β, 25-tetraol acetic ester was synthesized from 20(S)-protopanaxatriol in the presence of acetic anhydride and the product oxidated by m-CPBA. 20S, 24R-epoxy dammarane-3β, 6α, 12β, 25-tetraol (ocotillol derivative) and its epimer were synthesized by saponification in the presence of sodium hydroxide in 1:1 molar ratio. The structures of the two compounds were characterized by X-ray diffraction method. The results showed the configuration of C-24 of two epimers as S-form (4, ocotillol derivative) and R-form (3, epimer), respectively.