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3β,22α-Dihydroxyolean-12-en-29-oic acid is a triterpenoid compound belonging to the oleanolic acids class. It features an oleanane skeleton with a dammarane-type structure and is known for its diverse biological activities. This naturally occurring chemical is derived from oleanane triterpenoids and is prevalent in numerous plant species. It has garnered interest in pharmacological research, particularly for its potential therapeutic applications in anti-inflammatory and antitumor activities.

84108-17-8

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84108-17-8 Usage

Uses

Used in Pharmaceutical Research:
3β,22α-Dihydroxyolean-12-en-29-oic acid is utilized as a research compound for exploring its potential in pharmaceutical applications, specifically due to its anti-inflammatory and antitumor properties. Its presence in various plants makes it a valuable candidate for the development of novel therapeutic agents.
Used in Anti-inflammatory Applications:
In the field of medicine, 3β,22α-Dihydroxyolean-12-en-29-oic acid is employed as an anti-inflammatory agent, leveraging its natural biological activities to mitigate inflammation and related conditions. Its effectiveness in this area is currently under investigation, with the aim of harnessing its properties for the treatment of various inflammatory diseases.
Used in Antitumor Applications:
3β,22α-Dihydroxyolean-12-en-29-oic acid is also used as an antitumor agent, with research focusing on its ability to inhibit tumor growth and progression. Its potential role in cancer therapy is being explored, with the goal of integrating 3β,22α-Dihydroxyolean-12-en-29-oic acid into future cancer treatment strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 84108-17-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,1,0 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84108-17:
(7*8)+(6*4)+(5*1)+(4*0)+(3*8)+(2*1)+(1*7)=118
118 % 10 = 8
So 84108-17-8 is a valid CAS Registry Number.
InChI:InChI=1/C30H48O4/c1-25(2)20-10-13-30(7)21(28(20,5)12-11-22(25)31)9-8-18-19-16-26(3,24(33)34)17-23(32)27(19,4)14-15-29(18,30)6/h8,19-23,31-32H,9-17H2,1-7H3,(H,33,34)/t19-,20-,21+,22-,23-,26?,27+,28-,29+,30+/m0/s1

84108-17-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3β,22α)-3,22-Dihydroxyolean-12-en-29-oic acid

1.2 Other means of identification

Product number -
Other names maytenfolic acid

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:84108-17-8 SDS

84108-17-8Upstream product

84108-17-8Relevant academic research and scientific papers

Isolation and Structure Elucidation of Abruslactone A: a New Oleanene-type Triterpene from the Roots and Vines of Abrus precatorius L.

Chang, Hson-Mou,Chiang, Teh-Chang,Mak, Thomas C. W.

, p. 1197 - 1198 (2007/10/02)

Abruslactone A, a new triterpenoid sapogenin isolated from the roots and vines of Abrus precatorius L., has been characterized by spectral and X-ray analysis as the γ-lactone of 3β,22α-dihydroxy-olean-12-en-29α-oic acid, with ring E in an unusual boat conformation.

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