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D-NAME (hydrochloride)

D-NAME (hydrochloride)

产品编号 T36719   CAS 50912-92-0

N(G)-Nitro-D-arginine methyl ester (D-NAME) is the less active enantiomer of the nitric oxide (NO) synthase inhibitor N(G)-nitro-L-arginine methyl ester . D-NAME was initially thought to be inactive and was often used as a negative control for L-NAME. Later studies showed that D-NAME (40 mg/kg/day in rats) can have similar but less pronounced effects as L-NAME (40 mg/kg/day in rats) in the cardiovascular system, particularly at long-term timepoints. D-NAME (3-10 µg/mouse) had no effect on nociception in mice assessed using the tail flick test.

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D-NAME (hydrochloride) Chemical Structure
D-NAME (hydrochloride), CAS 50912-92-0
规格 价格/CNY 货期 数量
250 mg ¥ 542 35日内发货
500 mg ¥ 987 35日内发货
1 g ¥ 1,870 35日内发货
5 g ¥ 8,190 35日内发货
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产品目录号及名称: D-NAME (hydrochloride) (T36719)
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参考文献
产品描述 N(G)-Nitro-D-arginine methyl ester (D-NAME) is the less active enantiomer of the nitric oxide (NO) synthase inhibitor N(G)-nitro-L-arginine methyl ester . D-NAME was initially thought to be inactive and was often used as a negative control for L-NAME. Later studies showed that D-NAME (40 mg/kg/day in rats) can have similar but less pronounced effects as L-NAME (40 mg/kg/day in rats) in the cardiovascular system, particularly at long-term timepoints. D-NAME (3-10 &#181g/mouse) had no effect on nociception in mice assessed using the tail flick test.
分子量 269.69
分子式 C7H16ClN5O4
CAS No. 50912-92-0

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

PBS (pH 7.2): 10 mg/mL

DMF: 20 mg/mL

DMSO: 20 mg/mL

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TargetMol Library Books参考文献

1. Palmer, R.M.J., Rees, D.D., Ashton, D.S., et al. L-arginine is the physiological precursor for the formation of nitric oxide in endothelium-dependent relaxation Biochem. Biophys. Res. Commun. 153(3), 1251-1256 (1988). 2. Chinellato, A., Froldi, G., Caparrota, L., et al. Pharmacological characterization of endothelial cell nitric oxide synthase inhibitors in isolated rabbit aorta Life Sci. 62(6), 479-490 (1998). 3. Babál, P., Pechánová, O., and Bernátová, I. Long-term administration of D-NAME induces hemodynamic and structural changes in the cardiovascular system Physiol. Res. 49(1), 47-54 (2000). 4. Kawabata, A., Umeda, N., and Takagaki, H. L-arginine exerts a dual role in nociceptive processing in the brain: Involvement of the kyotorphin-Met-enkephalin pathway and NO-cyclic GMP pathway Br. J. Pharmacol. 109(1), 73-79 (1993).

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Keywords

D-NAME (hydrochloride) 50912-92-0 D NAME (hydrochloride) DNAME (hydrochloride) D-NAME Inhibitor inhibitor inhibit

 

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