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Ranirestat

COA

级别和纯度:

≥96%

CAS编号: 147254-64-6
分子式: C₁₇H₁₁BrFN₃O₄
分子量: 420.19
PubChem编号: 153948

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货号 (SKU)	包装规格	是否现货
R651726-5mg	5mg	期货
R651726-10mg	10mg	期货
R651726-25mg	25mg	期货
R651726-50mg	50mg	期货

查看相关系列

Aldose Reductase (31) Glucose Metabolism (3713) Metabolic Enzyme/Protease (4889)

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基本描述

别名	雷尼司他
英文别名	2-(4-bromo-2-fluorobenzyl)-1,2,3,4-tetrahydropyrrolo(1,2-a)pyrazine-4-spiro-3'-pyrrolidine-1.2',3,5'-tetrone \| Spiro(pyrrolidine-3,4'(1'H)-pyrrolo(1,2-a)pyrazine)-1',2,3',5(2'H)-tetrone, 2'-((4-bromo-2-fluorophenyl)methyl)-, (3'R)- \| Q7293074 \| (3R)-2'-[(
规格或纯度	≥96%
英文名称	Ranirestat
生化机理	雷尼司他（AS-3201）是一种有效的口服活性醛糖还原酶（AR）抑制剂，对大鼠晶状体 AR 和重组人 AR 的 IC 50 s 分别为 11 nM 和 15 nM，对重组人 AR 的 K i 为 0.38 nM。雷尼司他具有治疗糖尿病的潜力。
储存温度	-20°C储存
运输条件	超低温冰袋运输
产品介绍	Ranirestat (AS-3201) potent and orally active aldose reductase (AR) inhibitor with IC 50 s of 11 nM and 15 nM for rat lens AR and recombinant human AR , respectively, and a K i of 0.38 nM for recombinant human AR . Ranirestat has the potential for diabetic sensorimotor polyneuropathy treatment. Ranirestat also has a neuroprotective effect on diabetic retinas In Vitro Ranirestat concentration-dependently inhibits sorbitol accumulation in rat erythrocytes and sciatic nerves incubated in the high concentration (500 mg/dl) of glucose. The potency of Ranirestat inhibition of sorbitol accumulation is similar between rat erythrocytes and sciatic nerves with IC 50 values of 0.010 μM and 0.041 μM, respectively. MCE has not independently confirmed the accuracy of these methods. They are for reference only. In Vivo Ranirestat (0.03-1.0 mg/kg; oral administration; once daily; for 3 weeks; male STD-Wistar rats) treatment dose-dependently decreases the elevated sorbitol and fructose levels in the rat sciatic nerves without affecting blood glucose level. Ranirestat also improves the STZ-induced decrease in motor nerve conduction velocity (MNCV) in a dose-dependent manner . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Male STD-Wistar rats aged about (12-week-old; 260-290 g) injected with Streptozotocin (STZ) Dosage: 0.03 mg/kg, 0.1 mg/kg, 0.3 mg/kg, 1 mg/kg Administration: Oral administration; once daily; for 3 weeks Result: Dose-dependently decreased the elevated sorbitol and fructose levels in the rat sciatic nerves without affecting blood glucose level. Form:Solid IC50& Target:IC50: 11 nM (Rat lens aldose reductase) and 15 nM (Recombinant humanaldose reductase), Ki: 0.38 nM (Recombinant humanaldose reductase)
纯度	≥96%

关联靶点（人）

AKR1B1 Tclin 醛糖还原酶(Aldose reductase) (1 活性数据)

点击查看靶蛋白信息： AKR1B1

活性类型	活性值-log(M)	作用机制	期刊	参考文献(PubMed IDs)

AKR1B1 Tclin Aldose reductase (1404 活性数据)

点击查看靶蛋白信息： AKR1B1

活性类型	Relation	Activity value	Units	Action Type	期刊	PubMed Id	doi	Assay Aladdin ID

关联靶点（其它种属）

Hdac6 Histone deacetylase 6 (222 活性数据)

点击查看靶蛋白信息： Hdac6

活性类型	Relation	Activity value	Units	Action Type	期刊	PubMed Id	doi	Assay Aladdin ID

Rattus norvegicus (775804 活性数据)

点击查看此靶标相关信息

活性类型	Relation	Activity value	Units	Action Type	期刊	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 活性数据)

点击查看靶蛋白信息： rep

活性类型	Relation	Activity value	Units	Action Type	期刊	PubMed Id	doi	Assay Aladdin ID

SARS-CoV-2 (38078 活性数据)

点击查看此靶标相关信息

活性类型	Relation	Activity value	Units	Action Type	期刊	PubMed Id	doi	Assay Aladdin ID

作用机制

作用机制	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	参考文献

名称和识别符

分子类型	小分子
IIUPAC Name	(3R)-2'-[(4-bromo-2-fluorophenyl)methyl]spiro[pyrrolidine-3,4'-pyrrolo[1,2-a]pyrazine]-1',2,3',5-tetrone
INCHI	1S/C17H11BrFN3O4/c18-10-4-3-9(11(19)6-10)8-21-14(24)12-2-1-5-22(12)17(16(21)26)7-13(23)20-15(17)25/h1-6H,7-8H2,(H,20,23,25)/t17-/m1/s1
InChi Key	QCVNMNYRNIMDKV-QGZVFWFLSA-N
Smiles	C1C(=O)NC(=O)C12C(=O)N(C(=O)C3=CC=CN23)CC4=C(C=C(C=C4)Br)F
Isomeric SMILES	C1C(=O)NC(=O)[C@@]12C(=O)N(C(=O)C3=CC=CN23)CC4=C(C=C(C=C4)Br)F
关联CAS	147254-64-6
PubChem CID	153948
MeSH Entry Terms	2-(4-bromo-2-fluorobenzyl)-1,2,3,4-tetrahydropyrrolo(1,2-a)pyrazine-4-spiro-3'-pyrrolidine-1.2',3,5'-tetrone;AS 3201;AS-3201;ranirestat;SX 3030;SX 3202;SX-3030;SX-3202
分子量	420.19

化学和物理性质

溶解性	DMSO : ≥ 50 mg/mL (118.99 mM)
分子量	420.200 g/mol
XLogP3	1.300
氢键供体数Hydrogen Bond Donor Count	1
氢键受体数Hydrogen Bond Acceptor Count	5
可旋转键计数Rotatable Bond Count	2
精确质量Exact Mass	418.992 Da
单同位素质量Monoisotopic Mass	418.992 Da
拓扑极表面积Topological Polar Surface Area	88.500 Å²
重原子数Heavy Atom Count	26
形式电荷Formal Charge	0
复杂度Complexity	689.000
同位素原子数Isotope Atom Count	0
定义的原子立体中心计数Defined Atom Stereocenter Count	1
未定义的原子立体中心计数Undefined Atom Stereocenter Count	0
定义的键立体中心计数Defined Bond Stereocenter Count	0
未定义的键立体中心计数Undefined Bond Stereocenter Count	0
所有立体化学键的总数The total count of all stereochemical bonds	0
共价键合单元计数Covalently-Bonded Unit Count	1