S150
精胺-一氧化氮复合物
source of nitric oxide
别名:
N-[4-[1-（3-氨丙基）-2-羟基-2-亚硝基肼] 丁基]-1,3-丙二胺, SPER/NO, 壬酸精胺
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关于此项目
经验公式（希尔记法）:
C10H26N6O2
化学文摘社编号:
分子量:
262.35
UNSPSC Code:
12352204
PubChem Substance ID:
MDL number:
Form:
powder
InChI
1S/C10H26N6O2/c11-5-3-8-13-7-1-2-9-15(10-4-6-12)16(18)14-17/h13,18H,1-12H2
SMILES string
NCCCN(N(N=O)O)CCCCNCCCN
InChI key
QPIOUFBAROSIAN-UHFFFAOYSA-N
form
powder
storage condition
desiccated
color
white
solubility
methanol: ≥1 mg/mL, H2O: ≥2 mg/mL
εmax
8500 at 252 nm
shipped in
dry ice
storage temp.
−20°C
Quality Level
Application
用于产生溶液中一氧化氮的控制释放。
Other Notes
空气敏感
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Thais de Castro Barbosa et al.
Metabolism: clinical and experimental, 62(1), 79-89 (2012-08-15)
The amino acid Arginine (Arg) is the main biological precursor of nitric oxide (NO) and has been described to improve insulin sensitivity in diabetes and obesity. We investigated the molecular mechanisms involved in the long-term effects of Arg on glucose
A S Deshmukh et al.
Diabetologia, 53(6), 1142-1150 (2010-03-30)
We investigated the direct effect of a nitric oxide donor (spermine NONOate) on glucose transport in isolated human skeletal muscle and L6 skeletal muscle cells. We hypothesised that pharmacological treatment of human skeletal muscle with N-(2-aminoethyl)-N-(2-hydroxy-2-nitrosohydrazino)-1,2-ethylenediamine (spermine NONOate) would increase
Payam Dibaj et al.
Glia, 58(9), 1133-1144 (2010-05-15)
To understand the pathomechanisms of spinal cord injuries will be a prerequisite to develop efficient therapies. By investigating acute lesions of spinal cord white matter in anesthetized mice with fluorescently labeled microglia and axons using in vivo two-photon laser-scanning microscopy
Travis J Bourret et al.
Scientific reports, 7(1), 15083-15083 (2017-11-10)
The PhoPQ two-component regulatory system coordinates the response of Salmonella enterica serovar Typhimurium to diverse environmental challenges encountered during infection of hosts, including changes in Mg
Fang Cheng et al.
Cancer letters, 273(1), 148-154 (2008-09-12)
Here we demonstrate a synergistic and tumor selective cytotoxic effect by combined treatment with naphthoxylosides, polyamine synthesis inhibitor, and polyamine based nitric oxide (NO) donor, using in vitro human tumor models. We have earlier reported that heparan sulfate priming naphthoxyloside
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