568-76-3 Usage
Description
Gamma-hydroxyphenylbutazone, also known as γ-Hydroxy Phenylbutazone, is a metabolite of the antirheumatic drug Kebuzone. It is characterized by its chemical structure and pharmacological properties, which contribute to its potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
Gamma-hydroxyphenylbutazone is used as an active metabolite for its anti-inflammatory and analgesic properties. It is particularly effective in the treatment of rheumatic conditions, where it helps to alleviate pain and reduce inflammation.
Used in Research and Development:
In the field of pharmaceutical research and development, gamma-hydroxyphenylbutazone serves as a valuable compound for studying the mechanisms of action and potential therapeutic applications of related drugs. Its metabolite status allows researchers to investigate the pharmacokinetics, pharmacodynamics, and safety profiles of its parent drug, Kebuzone, and other similar compounds.
Used in Drug Metabolism Studies:
Gamma-hydroxyphenylbutazone is utilized as a model compound in drug metabolism studies, providing insights into the metabolic pathways and enzyme interactions involved in the conversion of prodrugs to their active metabolites. This information is crucial for the design and optimization of new drugs with improved efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 568-76-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,6 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 568-76:
(5*5)+(4*6)+(3*8)+(2*7)+(1*6)=93
93 % 10 = 3
So 568-76-3 is a valid CAS Registry Number.
InChI:InChI=1/C19H20N2O3/c1-14(22)12-13-17-18(23)20(15-8-4-2-5-9-15)21(19(17)24)16-10-6-3-7-11-16/h2-11,14,17,22H,12-13H2,1H3
568-76-3Relevant articles and documents
Contraceptive method
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, (2008/06/13)
Contraceptive method comprises maintaining in the genital tract of a female mammal a pyrazolone derivative in a concentration effective to inhibit the fertilization of ova. In addition to effectively inhibiting the enzymes or other sperm components necessary for conception, the compounds used in the method of the invention are advantageous in having low toxic, caustic or irritating properties, so that the contraceptive compositions are suitable for long-term use without adverse side-effects.