L-NIO (hydrochloride)
(Synonyms: L-N5-(1-亚胺乙基)-鸟氨酸盐酸盐) 目录号 : GC10281A non-selective inhibitor of all NOS isoforms
Cas No.:36889-13-1
Sample solution is provided at 25 µL, 10mM.
Quality Control & SDS
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- Purity: >95.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
IC50: 1.7, 3.9, and 3.9 μM for nNOS (rat), eNOS (bovine), and iNOS (mouse), respectively
L-NIO is a NOS inhibitor.
Nitric oxide synthases (NOSs) are enzymes that catalyze the production of nitric oxide (NO) from L-arginine. NO is an important cellular signaling molecule and helps modulate vascular tone, airway tone, insulin secretion, and peristalsis. NO is involved in angiogenesis and neural development.
In vitro: Three analogues of L-arginine were characterized as inhibitors of endothelial NO synthase by measuring their effect on the endothelial NO synthase from porcine aortae. It was found that L-NMMA, L-NIO and L-NAME could cause concentration-dependent inhibition of the Ca2+-dependent endothelial NO synthase [1].
In vivo: In rats, L-NMMA, L-NIO and L-NAME could induce a dose-dependent increase in mean systemic arterial blood pressure accompanied by bradycardia. Moreover, L-NMMA, L-NIO and L-NAME at i.v. 100 mg/kg significantly inhibited the hypotensive responses to ACh and bradykinin. The increase in blood pressure and bradycardia produced by these compounds were able to be reversed by L-arginine in a dose-dependent manner. Moreover, all of these effects were enantiomer specific [1].
Clinical trial: So far, no clinical study has been conducted.
Reference:
[1] D. D. Rees, R. M. J. Palmer, R. Schulz, et al. Characterization of three inhibitors of endothelial nitric oxide synthase in vitro and in vivo. British Journal of Pharmacology 101, 746-752 (1990).
制备储备液 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 4.0634 mL | 20.3169 mL | 40.6339 mL |
5 mM | 0.8127 mL | 4.0634 mL | 8.1268 mL |
10 mM | 0.4063 mL | 2.0317 mL | 4.0634 mL |
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工作液浓度: mg/ml;
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