Identification | Back Directory | [Name]
(S)-3-fluoro-4-(4-((2-(3-fluorophenyl)pyrrolidin-1-yl)methyl)phenoxy)benzamide | [CAS]
1346133-11-6 | [Synonyms]
FP3FBZ LY2444296 (S)-3-fluoro-4-(4-((2-(3-fluorophenyl)pyrrolidin-1-yl)methyl)phenoxy)benzamide | [Molecular Formula]
C24H22F2N2O2 | [MDL Number]
MFCD32067413 | [MOL File]
1346133-11-6.mol | [Molecular Weight]
408.44 |
Chemical Properties | Back Directory | [Boiling point ]
491.6±45.0 °C(Predicted) | [density ]
1.276±0.06 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
Ethanol: 27.5 mg/mL (67.33 mM); Methanol: 5 mg/mL (12.24 mM) | [form ]
Solid | [pka]
15.61±0.50(Predicted) | [color ]
Light yellow to yellow |
Hazard Information | Back Directory | [Biological Activity]
LY2444296 is a brain-penetrantorally activeshort-actinghigh-affinitypotent and selective K (kappa) opioid receptor (KOR) antagonist (human K/μ/δ Ki = 0.565/35.8/211 nM against diprenorphine binding; GTP-γ-S binding IC50/agonist/subtype transfectant = 1.57 nM/300 nM U69593/K21.3 nM/1 μM DAMGO/μ 293 nM/30 nM DPDPE/d). LY2444296 reverses K agonist antinociceptive efficacy in vivo (ED50 = 0.24 mg/kg p.o. against 1 mg/kg U69593 sc. by r at formalin test)decreases immobility time (10 or 30 mg/kg sc.) and prevents enhanced alcohol consumption (5 mg/kg i.p.) among mice subjected to stress by forced swimming. | [storage]
Store at -20°C |
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DC Chemicals
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cjbscvictory
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