Chemical Structure : Nebicapone
CAS No.: 274925-86-9
货号: PC-35791Not For Human Use, Lab Use Only.
Nebicapone (BIA 3-202, BIA3-202) is a potent, long-acting, reversible and competitive peripheral inhibitor of catechol-O-methyltransferase (COMT) with IC50 of 3.7 nM for rat brain COMT, much less potent for liver COMT with IC50 of 696 nM.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | ¥1980 | In stock | |
25 mg | ¥3280 | In stock | |
100 mg | Get quote | ||
200 mg | Get quote | ||
1 g | Get quote |
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Nebicapone (BIA 3-202, BIA3-202) is a potent, long-acting, reversible and competitive peripheral inhibitor of catechol-O-methyltransferase (COMT) with IC50 of 3.7 nM for rat brain COMT, much less potent for liver COMT with IC50 of 696 nM.
Nebicapone (BIA 3-202, BIA3-202) enhances the availability of L-DOPA to the brain and reduces its O-methylation.
Nebicapone (BIA 3-202, BIA3-202) is an adjunct to levodopa/carbidopa or levodopa/benserazide in the treatment of Parkinson's disease.
分子量 | 273.244 | |
分子式 | C14H11NO5 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
1-(3,4-dihydroxy-5-nitrophenyl)-2-phenylethan-1-one |
1. Parada A, et al. Pharmacology. 2003 May;68(1):29-37.
2. Bonifácio MJ, et al. Eur J Pharmacol. 2003 Jan 24;460(2-3):163-70.
3. Learmonth DA, et al. J Med Chem. 2002 Jan 31;45(3):685-95.
4. Parada A, et al. Eur J Pharmacol. 2001 May 18;420(1):27-32.
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