Cas No.: | 208110-64-9 |
Chemical Name: | Befiradol |
Synonyms: | Befiradol;1-(3-Chloro-4-fluorobenzoyl)-4-fluoro-N-[(5-methyl-2-pyridinyl)methyl]-4-piperidinemethanamine;(3-CHLORO-4-FLUORO-PHENYL)-(4-FLUORO-4-{[(5-METHYL-PYRIDIN-2-YLMETHYL)-AMINO]-METHYL}-PIPERIDIN-1-YL)-METHANONE;(3-chloro-4-fluorophenyl)-[4-fluoro-4-[[(5-methylpyridin-2-yl)methylamino]methyl]piperidin-1-yl]methanone;UNII-RAT9OHA1YH;(3-Chloro-4-fluoro-phenyl)-(4-fluoro-4-{[(5-methyl-pyridin-2-ylmethyl)-amino]-methyl}-piperidin-1-yl)-methanone;F13640;F 13640;[3H]F13640;[3H]NLX-112;HY-14785;Befiradol [INN];(3-chloro-4-fluorophenyl)(4-fluoro-4-(((5-methylpyridin-2-yl)methylamino)methyl)piperidin-1-yl)methanone;SCHEMBL678174;Q4880242;GLXC-15037;F-13640; F13640; F 13640; NLX-112; NLX112; NLX 112;F-13640;NLX-112; F13640;DTXSID90943058;BEFIRADOL [WHO-DD];NLX-112;NLX-112 hydrochloride;208110-64-9;CHEMBL45305;CS-0003559;(3-CHLORO-4-FLUOROPHENYL)(4-FLUORO-4-((((5-METHYLPYRIDIN-2-YL)METHYL)AMINO)METHYL)PIPERIDIN-1-YL)METHANONE;BCP31302;GTPL3925;BDBM50328639;L001676;Befiradol (free base);AKOS032954037;RAT9OHA1YH;((3-chloro-4-fluoro-phenyl)-(4-fluoro-4-((5-methyl-pyridin-2-ylmethyl)-amino)-methyl)piperidin-1-yl)-methadone |
SMILES: | O=C(C1=CC=C(F)C(Cl)=C1)N2CCC(CNCC3=NC=C(C)C=C3)(F)CC2 |
Formula: | C20H22N3OF2Cl |
M.Wt: | 393.85798 |
Purity: | >98% |
Sotrage: | 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
Description: | Befiradol (F13640, NLX 112) is a highly potent, selective 5-HT1A receptor agonist with Ki of 2.7 nM; exhibits agonist efficacy greater than for (±)8-OH-DPAT or buspirone; stimulates 'total G-proteins', but unlike (±)8-OH-DPAT and buspirone, more potent for Gαo activation, in rat hippocampal membranes; dose-dependently decreases extracellular 5-HT in the hippocampus and mPFC in rats, activates both 5-HT(1A) autoreceptors and postsynaptic 5-HT(1A) receptors in prefrontal cortex with a similar potency. Pain Discontinued |