首页> 外国专利> IRREVERSIBLE INHIBITOR OF SARCOPLASMIC RETICULUM Ca2+-ADENOSINE TRIPHOSPHATASE

IRREVERSIBLE INHIBITOR OF SARCOPLASMIC RETICULUM Ca2+-ADENOSINE TRIPHOSPHATASE

机译:钙质网Ca 2 + -腺苷三磷酸酶的不可逆抑制剂

摘要

FIELD: biochemistry, organic chemistry. SUBSTANCE: invention relates to the use of derivatives of 1,2-benzisothiazole-3-one of the general formula given in the invention where R1 means lower alkyl or phenyl and R2 is H or NO2 which are used as irreversible inhibitor of Ca2+-adenosine triphosphatase of sarcoplasmic reticulum (SERCA). Derivatives of 1,2-benzisothiaxole- -3-one of the general formula given in the invention exhibit the more expressed irreversible effect on SERCA as compared with its analog, i. e. 7-chloro-4-nitrobenz-2,1,3- oxadiazole (NBD-Cl). NBD-Cl under close conditions inhibits enzyme irreversibly also but its effect eliciting in concentration 0.75 mM is compared with effect of 6-nitro-2-phenyl-1,2- -benzisothiazole-3-one in concentration 0.15 mM. EFFECT: valuable biochemical properties of inhibitor. 1 tbl, 1 dwg
机译:领域:生物化学,有机化学。物质:本发明涉及在本发明中给出的通式1,2-苯并噻唑-3-的衍生物的用途,其中R 1 表示低级烷基或苯基,R 2 是H或NO 2 ,用作肌浆网(SERCA)的Ca 2 + -腺苷三磷酸酶的不可逆抑制剂。与本发明的类似物相比,本发明给出的通式的1,2-苯并噻唑-3-的衍生物对SERCA表现出更明显的不可逆作用。 e。 7-氯-4-硝基苯-2,1,3-恶二唑(NBD-Cl)。 NBD-Cl在接近条件下也不可逆地抑制酶,但是将其在浓度为0.75 mM时引起的作用与浓度为0.15 mM的6-硝基-2-苯基-1,2--苯并噻唑-3-酮的作用进行了比较。效果:抑制剂的重要生化特性。 1桶,1桶

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