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草酸苄唑啉盐

更新时间:2025-08-27 20:05:28

草酸苄唑啉盐结构式
草酸苄唑啉盐结构式
品牌特惠专场
常用名 草酸苄唑啉盐 英文名 Benazoline oxalate salt
CAS号 1021868-82-5 分子量 196.259003
密度 N/A 沸点 N/A
分子式 C13H12N2•(C2H2O4) 熔点 N/A
MSDS 中文版 美版 闪点 N/A
符号 GHS07
GHS07
信号词 Warning

 草酸苄唑啉盐用途


I2咪唑啉受体激动剂;对I2咪唑啉受体具有比α-肾上腺素受体高的亲和力和选择性。 I2 imidazoline receptor agonist; has high affinity and selectivity for I2 imidazoline receptors over α-adrenoceptors.

 草酸苄唑啉盐名称

中文名 草酸苄唑啉盐
英文名 Benazoline oxalate salt
英文别名 更多

 草酸苄唑啉盐物理化学性质

分子式 C13H12N2•(C2H2O4)
分子量 196.259003
精确质量 284.079712
水溶解性 Soluble in water: ≤8 mg/mL'}

 草酸苄唑啉盐安全信息

符号 GHS07
GHS07
信号词 Warning
危害声明 H315-H319-H335
警示性声明 P261-P305 + P351 + P338
个人防护装备 dust mask type N95 (US);Eyeshields;Gloves
危险品运输编码 NONH for all modes of transport

 草酸苄唑啉盐文献2

更多文献
Coupling of I(1) imidazoline receptors to the cAMP pathway: studies with a highly selective ligand, benazoline.

Mol. Pharmacol. 57 , 1142-51, (2000)

Clonidine and benazoline are two structurally related imidazolines. Whereas clonidine binds both to alpha(2)-adrenoceptors (alpha(2)R) and to I(1) imidazoline receptors (I(1)R), benazoline showed a hi...

Imidazoline receptors: qualitative structure-activity relationships and discovery of tracizoline and benazoline. Two ligands with high affinity and unprecedented selectivity.

Bioorg. Med. Chem. 5(5) , 833-841, (1997)

The observation that all the attempts to characterize imidazoline (I) receptors have been carried out with non-selective or poorly selective ligands prompted us to undertaken research aimed at develop...

 草酸苄唑啉盐靶点实验

查看更多实验

实验名称:qHTS assay to identify small molecule antagonists of the androgen receptor (AR) signa...
来源:824
靶标:AR protein [Homo sapiens]
External Id:MDAN535
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
实验名称:qHTS assay to identify small molecule antagonists of the androgen receptor (AR) sign...
来源:824
靶标:N/A
External Id:MDAV150
实验名称:qHTS assay for small molecules that induce genotoxicity in human embryonic kidney cel...
来源:824
靶标:RecName: Full=ATPase family AAA domain-containing protein 5; AltName: Full=Chromosome fragility-associated gene 1 protein
External Id:ELG271
实验名称:qHTS assay to identify small molecule antagonists of the thyroid receptor (TR) signal...
来源:824
靶标:thyroid hormone receptor beta isoform 2 [Rattus norvegicus]
External Id:TRN186
实验名称:qHTS assay to identify small molecule antagonists of the thyroid receptor (TR) signal...
来源:824
靶标:N/A
External Id:TRV455
实验名称:Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screeni...
来源:NCGC
靶标:N/A
External Id:CPF001
实验名称:qHTS for Inhibitors of binding or entry into cells for Marburg Virus
来源:NCGC
靶标:gene 4 small orf - Marburg virus
External Id:VSVM-OFFLINE
实验名称:qHTS for Inhibitors of binding or entry into cells for Lassa Virus
来源:NCGC
靶标:N/A
External Id:VSVL-OFFLINE
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 草酸苄唑啉盐英文别名

4,5-Dihydro-2-(2-naphthalenyl)-1H-imidazole oxalate salt
2-(2-Naphthyl)-1H-imidazole ethanedioate (1:1)
1H-Imidazole, 2-(2-naphthalenyl)-, ethanedioate (1:1)
Benazoline oxalate salt
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