M. Balbaa, G. Yacout, Taysseer Ghonaim, Doaa Othman
{"title":"苯巴比妥衍生物对天冬氨酸转氨基甲酰基酶的抑制作用","authors":"M. Balbaa, G. Yacout, Taysseer Ghonaim, Doaa Othman","doi":"10.1080/14756360109162374","DOIUrl":null,"url":null,"abstract":"Mammalian and hepatic aspartate transcarbamylase is inhibited by phenobarbital p-nitrophenylhydra-zone in a reversible and non-competitive type with Ki values 8.45 × 10−5 and 9.64×10−5 M in the reactions toward carbamyl phosphate and aspartate, respectively. In vivo inhibition occurred in a dose-dependent manner in which less than 50% of the activity was retained. These observations suggest that this inhibitor may interfere with the in vivo regulation of this enzyme and lead to an additional biological effect of phenobarbitals.","PeriodicalId":15776,"journal":{"name":"Journal of enzyme inhibition","volume":"16 1","pages":"259 - 267"},"PeriodicalIF":0.0000,"publicationDate":"2001-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Inhibition of Aspartate Transcarbamylase by a Phenobarbital Derivative\",\"authors\":\"M. Balbaa, G. Yacout, Taysseer Ghonaim, Doaa Othman\",\"doi\":\"10.1080/14756360109162374\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Mammalian and hepatic aspartate transcarbamylase is inhibited by phenobarbital p-nitrophenylhydra-zone in a reversible and non-competitive type with Ki values 8.45 × 10−5 and 9.64×10−5 M in the reactions toward carbamyl phosphate and aspartate, respectively. In vivo inhibition occurred in a dose-dependent manner in which less than 50% of the activity was retained. These observations suggest that this inhibitor may interfere with the in vivo regulation of this enzyme and lead to an additional biological effect of phenobarbitals.\",\"PeriodicalId\":15776,\"journal\":{\"name\":\"Journal of enzyme inhibition\",\"volume\":\"16 1\",\"pages\":\"259 - 267\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2001-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of enzyme inhibition\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/14756360109162374\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of enzyme inhibition","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/14756360109162374","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Inhibition of Aspartate Transcarbamylase by a Phenobarbital Derivative
Mammalian and hepatic aspartate transcarbamylase is inhibited by phenobarbital p-nitrophenylhydra-zone in a reversible and non-competitive type with Ki values 8.45 × 10−5 and 9.64×10−5 M in the reactions toward carbamyl phosphate and aspartate, respectively. In vivo inhibition occurred in a dose-dependent manner in which less than 50% of the activity was retained. These observations suggest that this inhibitor may interfere with the in vivo regulation of this enzyme and lead to an additional biological effect of phenobarbitals.