SYNTHESIS OF SUBSTITUTED 2-METHYL-3-(3,4-DIMETHOXY-DIHYDROXYPHENYLETHYL)-4-QUINAZOLONES AS POSSIBLE ANTI-PARKINSON DRUGS

被引:23
作者
PARMAR, SS
SINGH, SP
机构
[1] Department of Physiology, University of North Dakota, Grand Forks, North Dakota
关键词
D O I
10.1002/jhet.5570160307
中图分类号
O62 [有机化学];
学科分类号
070303 [有机化学]; 081704 [应用化学];
摘要
Several substituted 2‐methyl‐3‐(3,4‐dimethoxy/dihydroxyphenylethyl)‐4‐quinazolones were synthesized as possible antiparkinsonism agents. The structure of these compounds were confirmed by their elemental and spectral analysis. Copyright © 1979 Journal of Heterocyclic Chemistry
引用
收藏
页码:449 / 452
页数:4
相关论文
共 7 条
[1]
MEYERS FH, 1976, REV MEDICAL PHARMACO, P311
[2]
SYNTHESIS OF SUBSTITUTED QUINAZOLONE ALLYL ETHERS AND ALLYL PHENOLS AND THEIR EFFECT ON OXIDATION OF PYRUVIC ACID BY RAT BRAIN HOMOGENATE [J].
PARMAR, SS ;
RASTOGI, VK ;
ARORA, RC .
JOURNAL FUR PRAKTISCHE CHEMIE, 1970, 312 (05) :958-&
[3]
INTERRELATIONSHIP OF CHEMICAL STRUCTURE AND ANTIACETYLCHOLINESTERASE ACTIVITY OF DISUBSTITUTED QUINAZOLONES [J].
PARMAR, SS ;
JOSHI, LD ;
KISHOR, K ;
KUMAR, R .
BIOCHEMICAL PHARMACOLOGY, 1966, 15 (06) :723-&
[4]
SOME 2,3,6,8- TETRASUBSTITUTED QUINAZOLONE HYDRAZIDES AS MONOAMINE OXIDASE INHIBITORS [J].
PARMAR, SS ;
ARORA, RC .
JOURNAL OF MEDICINAL CHEMISTRY, 1967, 10 (06) :1182-&
[5]
PARMAR SS, 1968, CAN J CHEMISTRY, V46, P2519
[6]
PINDER RN, 1976, DRUGS, V11
[7]
INTERRELATIONSHIP BETWEEN MONOAMINE OXIDASE INHIBITION AND CENTRAL NERVOUS SYSTEM DEPRESSANT ACTIVITY OF SUBSTITUTED QUINAZOLONE HYDRAZIDES [J].
RASTOGI, VK ;
ARORA, RC ;
SINHA, JN ;
PARMAR, SS .
JOURNAL FUR PRAKTISCHE CHEMIE, 1970, 312 (05) :744-&