Cas No.: | 460746-46-7 |
Chemical Name: | ABT-239 |
Synonyms: | (R)-4-(2-(2-(2-Methylpyrrolidin-1-yl)ethyl)benzofuran-5-yl)benzonitrile;(R)-4-(2-(2-(2-Methylpyrrolidin-1-yl)-ethyl)benzofuran-5-yl)benzonitrile;ABT-239;Benzonitrile, 4-[2-[2-[(2R)-2-methyl-1-pyrrolidinyl]ethyl]-5-benzofuranyl]-;4-(2-((tert-butyldimethylsilyl)oxy)ethoxy)benzaldehyde;4-(2-{[tert-butyl(dimethyl)silyl]oxy}ethoxy)benzaldehyde;4-(2-{2-[(2R)-2-methylpyrrolidinyl]ethyl}-1-benzofuran-5-yl)benzonitrile;4-{2-[2-((R)-2-methylpyrrolidin-1-yl)ethyl]benzofuran-5-yl}benzonitrile;4-{2-[2-((R)-2-methyl-pyrrolidin-1-yl)-ethyl]-benzofuran-5-yl}benzonitrile;ABT239;Benzaldehyde, 4-[2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]ethoxy]-;CTK1F4031;CHEMBL351231;Z1816526082;ABT 239;BDBM50139391;HY-12195;benzofuran-5-yl)benzonitrile;4-{2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzofuran-5-yl}-benzonitrile;4-(2-{2-[(2R)-2-Methylpyrrolidin-1-yl]ethyl}-;460746-46-7;4-(2-{2-[(2R)-2-methyl-1-pyrrolidinyl]ethyl}-1-benzofuran-5-yl)benzonitrile;4-[2-[2-[(2R)-2-methylpyrrolidin-1-yl]ethyl]-1-benzofuran-5-yl]benzonitrile;(R)-4-(2-(2-(2-methylpyrrolidinyl)ethyl)benzofuran-5-yl)benzonitrile;KFHYZKCRXNRKRC-MRXNPFEDSA-N;(R)-4-(2-(2-(2-methyl-1-pyrrolidinyl)ethyl)-1-benzofuran-5-yl)benzonitrile;AKOS015891396;D94991;benzonitrile, 4-(2-(2-((2r)-2-methyl-1-pyrrolidinyl)ethyl)-5-benzofuranyl)-;UNII-86H6B395PI;GTPL1218;ABT-239 (tartrate);Q4650421;NCGC00386570-01;DTXSID00196710;SCHEMBL118976;CS-5904;AS-76470;4-(2-(2-(2-Methyl-1-pyrrolidinyl)ethyl)-1-benzofuran-5-yl)benzonitrile;4-(2-{2-[(2R)-2-methylpyrrolidinyl]ethyl}-benzofuran-5-yl)benzonitrile;86H6B395PI;4-(2-{2-[(2R)-2-methylpyrrolidin-1-yl]ethyl}-1-benzofuran-5-yl)benzonitrile;GLXC-04792;BRD-K22749967-046-02-3 |
SMILES: | O1C2C=CC(C3C=CC(C#N)=CC=3)=CC=2C=C1CCN1CCC[C@H]1C |
Formula: | C22H22N2O |
M.Wt: | 330.422885417938 |
Purity: | >98% |
Sotrage: | 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
Description: | A potent and selective Histamine H3 receptor antagonist with Ki of 0.1-5.8 nM (human, rat H3); exhibits 1000-fold selectivity versus H1, H2 and H4; excellent pharmacokinetic and metabolic properties across species and good oral bioavailability.PainDiscontinued |