硝普酸钠

更新时间：2025-08-24 22:18:55

硝普酸钠结构式	常用名	硝普酸钠	英文名	sodium nitroprusside
	CAS号	14402-89-2	分子量	261.91800
	密度	1.72	沸点	N/A
	分子式	C₅FeN₆Na₂O	熔点	N/A
	MSDS	N/A	闪点	N/A

硝普酸钠用途

Sodium Nitroprusside是血管舒张剂,能促使NO释放于血液中。

中文名	硝普酸钠
英文名	sodium nitroprusside
英文别名	更多

描述	Sodium Nitroprusside是血管舒张剂,能促使NO释放于血液中。
相关类别	信号通路 >> 其他 >> 其他研究领域 >> 心血管疾病
参考文献	[1]. Wink, D.A., et al., The effect of various nitric oxide-donor agents on hydrogen peroxide-mediated toxicity: a direct correlation between nitric oxide formation and protection. Arch Biochem Biophys, 1996. 331(2): p. 241-8. [2]. Garg, U.C. and A. Hassid, Nitric oxide-generating vasodilators and 8-bromo-cyclic guanosine monophosphate inhibit mitogenesis and proliferation of cultured rat vascular smooth muscle cells. J Clin Invest, 1989. 83(5): p. 1774-7. [3]. Namazi, H., Sodium nitroprusside as a nitric oxide donor in a rat intestinal ischemia reperfusion model: a novel molecular mechanism. Clinics (Sao Paulo), 2008. 63(3): p. 405.

描述

Sodium Nitroprusside是血管舒张剂,能促使NO释放于血液中。

相关类别

信号通路 >> 其他 >> 其他

研究领域 >> 心血管疾病

参考文献

[1]. Wink, D.A., et al., The effect of various nitric oxide-donor agents on hydrogen peroxide-mediated toxicity: a direct correlation between nitric oxide formation and protection. Arch Biochem Biophys, 1996. 331(2): p. 241-8.

[2]. Garg, U.C. and A. Hassid, Nitric oxide-generating vasodilators and 8-bromo-cyclic guanosine monophosphate inhibit mitogenesis and proliferation of cultured rat vascular smooth muscle cells. J Clin Invest, 1989. 83(5): p. 1774-7.

[3]. Namazi, H., Sodium nitroprusside as a nitric oxide donor in a rat intestinal ischemia reperfusion model: a novel molecular mechanism. Clinics (Sao Paulo), 2008. 63(3): p. 405.

密度	1.72
分子式	C₅FeN₆Na₂O
分子量	261.91800
精确质量	261.92800
PSA	148.38000
LogP	0.29850
InChIKey	PECOKVKJVPMJBN-UHFFFAOYSA-N
SMILES	[C-]#N.[C-]#N.[C-]#N.[C-]#N.[C-]#N.[Fe+4].[N-]=O.[Na+].[Na+]
外观性状	Liquid \| Clear tan-gold
储存条件	室温

硝普酸钠MSDS英文版

硝普酸钠毒性英文版

危害码 (欧洲)	T: Toxic;
风险声明 (欧洲)	25
安全声明 (欧洲)	45
危险品运输编码	UN 3288 6.1/PG 3
WGK德国	3
RTECS号	LJ8925000
包装等级	III
危险类别	6.1(b)

实验名称：Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident pro...
来源：NCGC
靶标：N/A
External Id：SERCaMPGLuc-p1-antagonist

实验名称：qHTS Assay for Inhibitors of the Phosphatase Activity of Eya2
来源：NCGC
靶标：eyes absent homolog 2 isoform a [Homo sapiens]
External Id：EYA2477

实验名称：qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1)
来源：NCGC
靶标：thioredoxin reductase [Rattus norvegicus]
External Id：TRXR193

实验名称：Primary qHTS assay for inhibitors of alpha-synuclein gene (SNCA) expression
来源：NCGC
External Id：SNCA-p-activity-luciferase

实验名称：qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1)
来源：NCGC
靶标：thioredoxin reductase [Rattus norvegicus]
External Id：TRXR188

实验名称：qHTS Validation Assay for Inhibitors of Ubiquitin-specific Protease USP2a Using CHOP2...
来源：NCGC
靶标：ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens]
External Id：UBCH001

实验名称：qHTS Assay for Identifying Gametocytocidal Compounds
来源：NCGC
靶标：N/A
External Id：MALG0567

实验名称：qHTS assay to identify small molecule inhibitors of chordoma cells - UCH-1
来源：NCGC
靶标：N/A
External Id：UCH01

实验名称：qHTS assay for measurement of the activity of small molecule inhibitors on Zika virus...
来源：NCGC
靶标：N/A
External Id：ZIK159

实验名称：Small-molecule inhibitors of ST2 (IL1RL1)
来源：20881
靶标：interleukin-1 receptor-like 1 isoform [homo sapiens]
External Id：ST2_IL33_Inhibitors_Primary_Screening_77700

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