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Agathic acid dimethyl ester, also known as methyl agathate, is a naturally occurring organic compound derived from the Agathosma genus of plants, particularly in the South African plant Agathosma betulina, commonly known as buchu. Agathicaciddimethylester is a monoterpene ester with the chemical formula C12H20O2, featuring a methyl ester group attached to a cyclohexane ring. It is known for its aromatic properties and is used in the fragrance industry for its pleasant scent. Additionally, agathic acid dimethyl ester has been studied for its potential anti-inflammatory and antimicrobial properties, although further research is needed to fully understand its therapeutic applications.

1757-85-3

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1757-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1757-85-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,5 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1757-85:
(6*1)+(5*7)+(4*5)+(3*7)+(2*8)+(1*5)=103
103 % 10 = 3
So 1757-85-3 is a valid CAS Registry Number.

1757-85-3Relevant academic research and scientific papers

Antimicrobial activity of terpenoids from Copaifera langsdorffii Desf. against cariogenic bacteria

Souza, Ariana B.,Martins, Carlos H. G.,Souza, Maria G. M.,Furtado, Niege A. J. C.,Heleno, Vladimir C. G.,De Sousa, Joao P. B.,Rocha, Erilda M. P.,Bastos, Jairo K.,Cunha, Wilson R.,Veneziani, Rodrigo C. S.,Ambrosio, Sergio R.

experimental part, p. 215 - 220 (2012/01/12)

In the present work, the anticariogenic activities of nine labdane type-diterpenes and four sesquiterpenes were investigated. Among these metabolites, (-)-copalic acid (CA) was the most active compound displaying MIC values very promising (ranging from 2.0 to 6.0 μg/mL) against the main microorganisms responsible for dental caries: Streptococcus salivarius, S. sobrinus, S. mutans, S. mitis, S. sanguinis and Lactobacillus casei. Time kill assays performed with CA against the primary causative agent (S. mutans) revealed that, in the first 12 h, this compound only inhibits the growth of the inoculum (bacteriostatic effect). However, its bactericidal effect is clearly noted thereafter (between 12 and 24 h). Also, CA did not show a synergistic effect when combined with the anticariogenic gold standard (chlorhexidine, CHD) in the checkerboard assays against S. mutans. In conclusion, the results points out CA as an important metabolite in the search for new effective anticariogenic agents.

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