5-Hydroxy-1-methylhydantoin
CAS No. 84210-26-4
5-Hydroxy-1-methylhydantoin ( NZ-419 | HD-003 )
产品货号. M27907 CAS No. 84210-26-4
NZ-419 是一种抗氧化剂,有可能用于治疗肾衰竭。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥283 | 有现货 |
|
| 10MG | ¥448 | 有现货 |
|
| 25MG | ¥876 | 有现货 |
|
| 50MG | ¥1376 | 有现货 |
|
| 100MG | ¥2007 | 有现货 |
|
| 200MG | ¥2871 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥238 | 有现货 |
|
生物学信息
-
产品名称5-Hydroxy-1-methylhydantoin
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述NZ-419 是一种抗氧化剂,有可能用于治疗肾衰竭。
-
产品描述NZ-419 is an antioxidant potentially for the treatment of renal failure. A creatinine metabolite, NZ-419, a hydroxyl radical scavenger, has previously been shown to confer renoprotection by inhibiting the progression of chronic kidney disease in rats. NZ-419 a novel anti-oxidant drug completely suppressed the expression of B2-kinin receptors (B2KR) in response to high glucose (25 mM) stimulation in VSMC and was also shown to attenuate the effects of BK on VSMC remodeling. NZ-419 inhibited the BK-induced increase in MAPK phosphorylation and attenuated the increase in connective tissue growth factor (CTGF) protein levels in VSMC. These findings suggest that NZ-419 may confer vascular protection against high glucose concentrations and BK-stimulation to ameliorate vascular injury and remodeling through its anti-oxidant properties.
-
体外实验——
-
体内实验——
-
同义词NZ-419 | HD-003
-
通路GPCR/G Protein
-
靶点Bradykinin Receptor
-
受体——
-
研究领域——
-
适应症——
化学信息
-
CAS Number84210-26-4
-
分子量114.1
-
分子式C4H6N2O2
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESO=C1NC(CN1C)=O
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.Dana M, et al. Synthesis of homoveratric acid-imprinted polymers and their evaluation as selective separation materials. Molecules. 2011 May 5;16(5):3826-44.
产品手册
关联产品
-
MEN 11270
Peptide antagonist of the B2 bradykinin receptor (pKi = 10.3); conformationally constrained cyclized analog of HOE 140. Blocks hypotension and bronchoconstriction in vivo. Displays selectivity for B2 over 29 other receptors and ion channels (pIC50 < 5.5).
-
MK-0686
MK-0686 is an orally available bradykinin B1 receptor antagonist with potential anti-inflammatory activity.
-
Sar-[D-Phe8]-des-Arg...
Potent and selective bradykinin B1 receptor agonist (EC50 = 9.02 nM in rabbit aorta) that is resistant to aminopeptidase, kininase I and II (ACE) and neutral endopeptidase cleavage. Exhibits hypotensive and angiogenic activity in vivo.
021-51111890
购物车()
sales@molnova.cn

