2-Imino-4-methylpiperidine (acetate)potent, general NOS inhibitor |
Sample solution is provided at 25 µL, 10mM.
Quality Control & MSDS
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- Purity = 98.00%
- COA (Certificate Of Analysis)
- MSDS (Material Safety Data Sheet)
Chemical structure
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Cas No. | 165383-72-2 | SDF | Download SDF |
Chemical Name | 3,4,5,6-tetrahydro-4-methyl-2-pyridinamine, acetate | ||
Canonical SMILES | CC1CCN=C(N)C1.CC([O-])=O | ||
Formula | C6H12N2 · C2H3O2 | M.Wt | 171.2 |
Solubility | ≤5mg/ml in ethanol;5mg/ml in DMSO;5mg/ml in dimethyl formamide | Storage | Store at -20°C |
Physical Appearance | A crystalline solid | Shipping Condition | Evaluation sample solution : ship with blue ice.All other available size:ship with RT , or blue ice upon request |
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. |
2-Imino-4-methylpiperidine (acetate) is a potent NOS inhibitor [1]
Nitric oxide (NO) is an endogenously produced inorganic free radical gas which has been implicated in endothelium-dependent vascular relaxation, cell-to-cell communication, and cytotoxicity associated with phagocytic cells. NO is synthesized by three isoforms of nitric oxide synthase (NOS): nNOS, eNOS and iNOS [1].
2-Imino-4-methylpiperidine (acetate) is a 2-iminopiperidine class of NOS inhibitor. In the presence of a final L-arginine concentration of 30 μM, 2-Imino-4-methylpiperidine inhibited human iNOS, eNOS, and nNOS with IC50 values of 0.1, 1.1, and 0.2 μM, respectively. 2-Imino-4-methylpiperidine exhibited 9-fold and 1-fold selectivity for iNOS compared to eNOS and nNOS, respectively [1].
In LPS-treated rats, 2-Imino-4-methylpiperidine (10 mg/kg, po) inhibited plasma nitrite levels by 87%.
Reference:[1]. Webber RK, Metz S, Moore WM, et al. Substituted 2-iminopiperidines as inhibitors of human nitric oxide synthase isoforms. J Med Chem. 1998 Jan 1;41(1):96-101.
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没有这8种氨基酸就会发生由于缺乏营养所引起的疾病;氨基酸在医药上也有很大的用途,现在手术中输液都加有各种氨基酸,使患者的抵抗力增强,同时也增加营养。随着人民生活水平的提高,人们对摄入的营养物质的要求越来越高,尤其是幼儿、青少年的健康成长,疾病患者的康复,都迫切需要高质量的营养物质,所以有效开发氨基酸食品是很有必要的。
只有9个氨基酸,分子量1KD左右,想免疫小鼠制备单抗,有没有前辈做过这方面的东西?想了一些方法,但价值不大,请前辈们指教,不甚感激。
采用OPA柱前衍生,波长是338nm
流动相A:20mmol/LNaH2PO4(用10mol/LNaOH溶液调pH至7.8±0.2);
流动相B:甲醇:乙腈:水=(45:45:10,V/V/V);
柱温:40℃;
然后进其他单标氨基酸的时候都没有问题,但是进单标胱氨酸的时候,HPLC色谱图中出了两峰,为什么会有两峰?这两峰分别是什么峰?其中一个是半胱氨酸的峰吗?用何种方法可以确定这两个分别是什么峰?
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