References of 2-[2-[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]acetyl]oxyacetic
acid
Title: Acemetacin
CAS Registry Number: 53164-05-9
CAS Name: 1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1
H-indole-3-acetic acid carboxymethyl ester
Synonyms: [[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]acetoxy]acetic acid
Manufacturers' Codes: TV-1322
Trademarks: Acemix (Bioprogress); Emflex (Merck KGaA); Rantudil (Bayer); Solart (Bioindustria)
Molecular Formula: C21H18ClNO6
Molecular Weight: 415.82
Percent Composition: C 60.66%, H 4.36%, Cl 8.53%, N 3.37%, O 23.09%
Literature References: Deriv of indomethacin,
q.v. Prepn: K. H. Boltze
et al., DE 2234651;
eidem, US 3910952 (1972, 1975 both to Troponwerke). Series of articles on chemistry, analysis, pharmacodynamics, toxicology and clinical trials:
Arzneim.-Forsch. 30, 1313-1468 (1980). Toxicity data: H. Jacobi, H.-D. Dell,
ibid. 1398.
Properties: Very fine pale yellow crystals from petr ether, mp 150-153°. LD50 in male, female mice, male, female rats (mg/kg): 55.5, 18.42, 24.2, 30.1 orally; 34.1, 51.1, 38.1, 28.3 i.v. (Jacobi, Dell).
Melting point: mp 150-153°
Toxicity data: LD50 in male, female mice, male, female rats (mg/kg): 55.5, 18.42, 24.2, 30.1 orally; 34.1, 51.1, 38.1, 28.3 i.v. (Jacobi, Dell)
Therap-Cat: Anti-inflammatory.
Keywords: Anti-inflammatory (Nonsteroidal); Arylacetic Acid Derivatives.