BARBITURIC ACID DERIVATIVE AND PREVENTIVE AND THERAPEUTIC AGENT OF BONE AND CARTILAGE

PROBLEM TO BE SOLVED: To provide the subject novel compound that is useful as an active ingredient for pharmaceutical composition that is useful for prevention and treatment of diseases of bone and cartilage. SOLUTION: This novel compound is represented by formula I [R and R are each H, a 1-15C (sub...

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Hauptverfasser: SAKAI KUNIKAZU, SATO SUKENORI
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creator SAKAI KUNIKAZU
SATO SUKENORI
description PROBLEM TO BE SOLVED: To provide the subject novel compound that is useful as an active ingredient for pharmaceutical composition that is useful for prevention and treatment of diseases of bone and cartilage. SOLUTION: This novel compound is represented by formula I [R and R are each H, a 1-15C (substituted) alkyl or alkenyl; a (substituted) arylmethyl or a (substituted) arly; R is a 1-15C (substituted) alkyl or alkenyl; a (substituted) arylmethyl or a (substituted) aryl], typically 1,3-dibenzyl-5-(3-methyl-1-oxobutyl) barbituric acid. The compound of formula I is prepared, for example, by condensation reaction of a barbituric acid derivative of formula II with an acylating agent of formula III. The daily dose of the compound of formula I is 0.01-2 g (about 0.15-30 mg/kg/day).
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SOLUTION: This novel compound is represented by formula I [R and R are each H, a 1-15C (substituted) alkyl or alkenyl; a (substituted) arylmethyl or a (substituted) arly; R is a 1-15C (substituted) alkyl or alkenyl; a (substituted) arylmethyl or a (substituted) aryl], typically 1,3-dibenzyl-5-(3-methyl-1-oxobutyl) barbituric acid. The compound of formula I is prepared, for example, by condensation reaction of a barbituric acid derivative of formula II with an acylating agent of formula III. 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SOLUTION: This novel compound is represented by formula I [R and R are each H, a 1-15C (substituted) alkyl or alkenyl; a (substituted) arylmethyl or a (substituted) arly; R is a 1-15C (substituted) alkyl or alkenyl; a (substituted) arylmethyl or a (substituted) aryl], typically 1,3-dibenzyl-5-(3-methyl-1-oxobutyl) barbituric acid. The compound of formula I is prepared, for example, by condensation reaction of a barbituric acid derivative of formula II with an acylating agent of formula III. 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SOLUTION: This novel compound is represented by formula I [R and R are each H, a 1-15C (substituted) alkyl or alkenyl; a (substituted) arylmethyl or a (substituted) arly; R is a 1-15C (substituted) alkyl or alkenyl; a (substituted) arylmethyl or a (substituted) aryl], typically 1,3-dibenzyl-5-(3-methyl-1-oxobutyl) barbituric acid. The compound of formula I is prepared, for example, by condensation reaction of a barbituric acid derivative of formula II with an acylating agent of formula III. The daily dose of the compound of formula I is 0.01-2 g (about 0.15-30 mg/kg/day).</abstract><edition>6</edition><oa>free_for_read</oa></addata></record>
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subjects CHEMISTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
title BARBITURIC ACID DERIVATIVE AND PREVENTIVE AND THERAPEUTIC AGENT OF BONE AND CARTILAGE
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