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Cerberinic acid methyl, also known as 3β,23-dihydroxylanost-8,24-dien-21-oic acid methyl ester, is a natural triterpenoid compound derived from various medicinal plants. It is a methyl ester derivative of cerberinic acid, characterized by its anti-inflammatory, antioxidant, and anti-tumor properties. Cerberinic acid methyl's pharmacological effects are attributed to its ability to modulate inflammatory pathways and oxidative stress, positioning it as a promising candidate for the development of therapeutic agents.

65597-42-4

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65597-42-4 Usage

Uses

Used in Pharmaceutical Industry:
Cerberinic acid methyl is used as a therapeutic agent for its anti-inflammatory, antioxidant, and anti-tumor effects. It modulates inflammatory pathways and oxidative stress, making it a potential treatment for various diseases.
Used in Anti-inflammatory Applications:
Cerberinic acid methyl is used as an anti-inflammatory agent, targeting the modulation of inflammatory pathways. Its ability to reduce inflammation makes it a candidate for treating conditions associated with excessive inflammation.
Used in Antioxidant Applications:
Cerberinic acid methyl is used as an antioxidant, protecting cells from oxidative stress and damage. Its antioxidant properties contribute to its potential use in preventing and treating diseases related to oxidative stress.
Used in Antitumor Applications:
Cerberinic acid methyl is used as an anti-tumor agent, exhibiting potential in the treatment of various types of cancer. Its anti-tumor effects are attributed to its ability to modulate pathways involved in tumor growth and progression.
Used in Drug Development:
Cerberinic acid methyl is used in the development of new therapeutic agents, given its promising potential in preclinical studies. Further research and development are necessary to explore its full potential in treating various diseases and improving patient outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 65597-42-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,9 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 65597-42:
(7*6)+(6*5)+(5*5)+(4*9)+(3*7)+(2*4)+(1*2)=164
164 % 10 = 4
So 65597-42-4 is a valid CAS Registry Number.

65597-42-4SDS

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 Cerbinal

1.2 Other means of identification

Product number -
Other names -

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:65597-42-4 SDS

65597-42-4Downstream Products

65597-42-4Relevant academic research and scientific papers

An Efficient Synthesis of Cerbinal, a 10 ? Aromatic Iridoid

Ge, Yuting,Isoe, Sachihiko

, p. 139 - 140 (1992)

Cerbinal, an unusual iridoid with 10 ?-system, was synthesized from (+)-genipin in 6 steps via dehydration of the hemiacetal and subsequent dehydrogenation with DDQ.

Method for fully synthesizing natural product cerbinal and application ofcerbinal

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Paragraph 0019-0021; 0024-0032; 0033; 0036, (2019/11/13)

The invention relates to a method for fully synthesizing natural product cerbinal and application in plant protection, and belongs to the technical field of pesticides. The method comprise the steps that genipin is used as a raw material; the first step, the raw material genipin is oxidized by IBX to obtain a compound 1; and the second step, DDQ and acid are added, and the compound 1 is oxidized and dehydrated to obtain the cerbinal. The method does not adopt a protecting group strategy, first, IBX only oxidizes a primary hydroxyl group and does not react with an acetal hydroxyl group to obtain an intermediate 1; and then, oxidative dehydrogenation and elimination of dehydration are completed simultaneously, the natural product cerbinal is synthesized only in two steps, a synthetic route is significantly shortened, and the application prospects are good. It is found the first time that the natural product cerbinal has anti-plant virus, insecticidal and bactericidal activity by the method, and the cerbinal can be developed as a novel plant-derived pesticide or as a lead compound.

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