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875585-30-1

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875585-30-1 Usage

Description

Ent-14,15-Dir-13-oxolabda-8(17),11-dien-18-oic acid is a diterpenoid compound belonging to the labdane family. It is a carboxylic acid with a complex molecular structure, featuring a 13-oxolabda-8(17),11-dien-18-oic acid backbone. This chemical compound has been identified to possess a range of biological activities, such as anti-inflammatory, antiviral, and anticancer properties. Additionally, it has potential therapeutic applications in the treatment of inflammatory and autoimmune diseases. The unique chemical structure and potential medicinal properties of ent-14,15-Dir-13-oxolabda-8(17),11-dien-18-oic acid make it a promising candidate for further research and development in drug discovery and pharmaceuticals.

Uses

Used in Pharmaceutical Industry:
Ent-14,15-Dir-13-oxolabda-8(17),11-dien-18-oic acid is used as a pharmaceutical agent for its anti-inflammatory properties, making it a potential treatment for inflammatory diseases. Its antiviral and anticancer properties also contribute to its potential use in developing medications for viral infections and cancer treatment, respectively.
Used in Drug Discovery:
Ent-14,15-Dir-13-oxolabda-8(17),11-dien-18-oic acid serves as a target for drug discovery due to its diverse biological activities. Researchers are interested in exploring its potential as a lead compound for the development of new drugs that can address various health conditions, including inflammation, viral infections, and cancer.
Used in Autoimmune Disease Treatment:
Ent-14,15-Dir-13-oxolabda-8(17),11-dien-18-oic acid is used as a therapeutic agent for the treatment of autoimmune diseases. Its anti-inflammatory properties make it a candidate for managing conditions where the immune system mistakenly attacks the body's own tissues, potentially leading to the development of novel treatments for such diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 875585-30-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,5,5,8 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 875585-30:
(8*8)+(7*7)+(6*5)+(5*5)+(4*8)+(3*5)+(2*3)+(1*0)=221
221 % 10 = 1
So 875585-30-1 is a valid CAS Registry Number.

875585-30-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,4aR,5R,8aS)-1,4a-Dimethyl-6-methylene-5-[(1E)-3-oxo-1-buten-1 -yl]decahydro-1-naphthalenecarboxylic acid

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:875585-30-1 SDS

875585-30-1Downstream Products

875585-30-1Relevant articles and documents

Asymmetric synthesis of methyl (-)-13-oxo-15,16-dinorlabda-8(17),11E-dien- 19-oate, methyl ester of a potent suppressor toward carcinogenic promotor

Katoh, Takahiro,Mizumoto, Shinsuke,Fudesaka, Masato,Kajimoto, Tetsuya,Node, Manabu

, p. 1333 - 1337 (2006)

Asymmetric synthesis of methyl ester (4) of (-)-13-oxo-15,16-dinorlabda- 8(17),11E-dien-19-oic acid (1), which exhibited the most potent activity for the prevention of incipient carcinogenesis among the isolated diterpenes from Thuja standishii and its related plants, was achieved by using methyl (-)-1,4a-dimethyl-5-oxodecahydronaphthalene-1-carboxylate (5) as a strating material, which was easily prepared on gram scale by baker's yeast-catalyzed asymmetric reduction.

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