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(24R)-20,24-Epoxy-5α-dammarane-3α,25-diol is a naturally occurring triterpenoid compound belonging to the dammarane family. It is distinguished by its unique chemical structure, featuring a 20,24-epoxy group and a 3α,25-diol group. (24R)-20,24-Epoxy-5α-dammarane-3α,25-diol has been isolated from various plant sources and is known for its diverse biological activities, such as anti-inflammatory, anti-cancer, and anti-diabetic properties. Ongoing research suggests its potential as a therapeutic agent for treating a range of diseases and conditions.

35761-53-6

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35761-53-6 Usage

Uses

Used in Pharmaceutical Industry:
(24R)-20,24-Epoxy-5α-dammarane-3α,25-diol is used as a potential therapeutic agent for its anti-inflammatory, anti-cancer, and anti-diabetic properties. Its diverse biological activities make it a candidate for the development of treatments for various diseases and conditions.
Used in Cancer Research:
In cancer research, (24R)-20,24-Epoxy-5α-dammarane-3α,25-diol is utilized as a compound with anti-cancer properties. It may be studied for its potential to inhibit tumor growth and progression, as well as its possible synergistic effects when combined with conventional chemotherapeutic drugs, thereby enhancing chemo-sensitivity and efficacy in resistant cases.
Used in Diabetes Research:
(24R)-20,24-Epoxy-5α-dammarane-3α,25-diol is used in diabetes research for its anti-diabetic properties. It may be investigated for its potential to regulate blood sugar levels and improve insulin sensitivity, contributing to the development of treatments for diabetes and related metabolic disorders.
Used in Inflammation Research:
In the field of inflammation research, (24R)-20,24-Epoxy-5α-dammarane-3α,25-diol is employed for its anti-inflammatory properties. It may be explored for its capacity to reduce inflammation and alleviate symptoms associated with inflammatory conditions, offering a potential avenue for the development of new anti-inflammatory therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 35761-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,7,6 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35761-53:
(7*3)+(6*5)+(5*7)+(4*6)+(3*1)+(2*5)+(1*3)=126
126 % 10 = 6
So 35761-53-6 is a valid CAS Registry Number.

35761-53-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name epiocotillol

1.2 Other means of identification

Product number -
Other names (24R)-20,24-epoxydammarane-3α,25-diol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:35761-53-6 SDS

35761-53-6Relevant academic research and scientific papers

TRITERPENOIDS FROM THE LEAVES OF Betula lanata

Pokhilo, N. D.,Malinovskaya, G. V.,Makhan'kov, V. V.,Anufriev, V. F.,Uvarova, N. I.

, p. 368 - 372 (2007/10/02)

From the unsaponifiable fraction of an ethereal extract of the leaves of Betula lanata, in addition to 3-epiocotillol (I) we have isolated a new triterpene, 20(S),24(R)-epoxydammarane-3α,11α,25-triol (V) and also derivatives of it - the monoacetates at C-3 (II) and C-11 (III), and the monoketone at C-3 (IV).The structures of compounds (I-V) have been established on the basis of the results of physicochemical investigations.

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