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咪瑞司他

更新时间:2025-08-25 16:03:00

咪瑞司他结构式
咪瑞司他结构式
品牌特惠专场
常用名 咪瑞司他 英文名 IMIRESTAT
CAS号 89391-50-4 分子量 286.23300
密度 1.58g/cm3 沸点 N/A
分子式 C15H8F2N2O2 熔点 N/A
MSDS N/A 闪点 N/A

 咪瑞司他用途


IMIRESTAT 是一种 aldose reductase 抑制剂,可用于治疗糖尿病。

 咪瑞司他名称

中文名 咪瑞司他
英文名 2,7-difluorospiro[fluorene-9,5'-imidazolidine]-2',4'-dione
英文别名 更多

 咪瑞司他生物活性

描述 Imirestat (AL 1576) 是一种 aldose reductase 抑制剂,可用于治疗糖尿病。
相关类别
体内研究 Imirestat(1 mg/kg)可改善神经传导速度,但不会影响对缺氧传导阻滞的抵抗或胰岛素刺激的对人体敏感的ATP酶活性的缺陷[1]。
参考文献

[1]. Carrington AL, et al. Aldose reductase inhibition with imirestat-effects on impulse conduction and insulin-stimulation of Na+/K(+)-adenosine triphosphatase activity in sciatic nerves of streptozotocin-diabetic rats. Diabetologia. 1991 Jun;34(6):397-401.

 咪瑞司他物理化学性质

密度 1.58g/cm3
分子式 C15H8F2N2O2
分子量 286.23300
精确质量 286.05500
PSA 58.20000
LogP 2.68580
InChIKey QCCHBHSAIQIQGO-UHFFFAOYSA-N
SMILES O=C1NC(=O)C2(N1)c1cc(F)ccc1-c1ccc(F)cc12
折射率 1.692
储存条件 2-8℃

 咪瑞司他毒性和生态

 咪瑞司他合成线路

~%

咪瑞司他结构式

咪瑞司他

89391-50-4

文献:Alcon Laboratories, Inc. Patent: US4436745 A1, 1984 ; Title/Abstract Full Text Show Details Alcon Laboratories, Inc. Patent: US4540700 A1, 1985 ;

 咪瑞司他上下游产品

咪瑞司他上游产品  1

咪瑞司他下游产品  0

 咪瑞司他靶点实验

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实验名称:In vivo inhibition of SCoR2 in ischemia/reperfusion induced acute kidney injury mouse...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL5340500
实验名称:Protection against ischemia/reperfusion induced acute kidney injury in mouse assessed...
来源:ChEMBL
靶标:Mus musculus
External Id:CHEMBL5340501
实验名称:Protection against ischemia/reperfusion induced acute kidney injury in mouse assessed...
来源:ChEMBL
靶标:Mus musculus
External Id:CHEMBL5340498
实验名称:Protection against ischemia/reperfusion induced acute kidney injury in mouse assessed...
来源:ChEMBL
靶标:Mus musculus
External Id:CHEMBL5340499
实验名称:Selectivity as ratio of IC50 for rat lens and kidney aldose reductase
来源:ChEMBL
靶标:Aldo-keto reductase family 1 member B1
External Id:CHEMBL851664
实验名称:In vivo inhibition of SCoR2 in mouse assessed as reduction in SNO-CoA metabolic activ...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL5340496
实验名称:In vivo inhibition of SCoR2 in ischemia/reperfusion induced acute kidney injury mouse...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL5340497
实验名称:Inhibition of C-terminal 6His-tagged human recombinant SCoR2 AKR1A1 expressed in Esch...
来源:ChEMBL
靶标:Aldo-keto reductase family 1 member A1
External Id:CHEMBL5340495
实验名称:Inhibition of C-terminal 6His-tagged human recombinant AKR1B1 expressed in Escherichi...
来源:ChEMBL
靶标:Aldo-keto reductase family 1 member B1
External Id:CHEMBL5340493
实验名称:Selectivity index, ratio of IC50 for inhibition of human recombinant AKR1B1 expressed...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL5340491
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 咪瑞司他英文别名

Imirestatum [INN-Latin]
Alcon 1576
2,7-Difluorospiro(fluorene-9,4'-imidazolidine)-2',5'-dione
2,7-di-fluoro-spiro(9H-fluorene-9,4'-imidazolidine)-2',5'-dione
Imirestat
spiro-[2,7-difluorofluoren-9,4'-imidazolidine]-2',5'-dione
Spiro(9H-fluorene-9,4'-imidazolidine)-2',5'-dione,2,7-difluoro
[14C]-Imirestat
Spiro-(2,7-difluoro-9H-fluoren-9,4'-imidazolidine)-2',5'-dione
HOE 843
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