Synthetic organic

InformationJNJ-42153605 JNJ-42153605 is a potent and selective mGlu2 receptor positive allosteric modulator with an EC50 of 17 nM.TargetsmGlu2 receptor 17 nM(EC50)In vitroJNJ-42153605 is found to not have agonist or antagonist activity toward other

InformationJNJ-42153605 JNJ-42153605 is a potent and selective mGlu2 receptor positive allosteric modulator with an EC50 of 17 nM.TargetsmGlu2 receptor 17 nM(EC50)In vitroJNJ-42153605 is found to not have agonist or antagonist activity toward other

InformationJNJ-42153605 JNJ-42153605 is a potent and selective mGlu2 receptor positive allosteric modulator with an EC50 of 17 nM.TargetsmGlu2 receptor 17 nM(EC50)In vitroJNJ-42153605 is found to not have agonist or antagonist activity toward other

InformationJNJ-42153605 JNJ-42153605 is a potent and selective mGlu2 receptor positive allosteric modulator with an EC50 of 17 nM.TargetsmGlu2 receptor 17 nM(EC50)In vitroJNJ-42153605 is found to not have agonist or antagonist activity toward other

InformationJNJ-42165279 JNJ-42165279 (JNJ-5279) is an inhibitor of fatty acid amide hydrolase (FAAH) that inhibits recombinant human and rat FAAH with IC50 of 70 nM and 313 nM, respectively.Targetsrecombinant human FAAH (Cell-free assay):

InformationJNJ-42165279 JNJ-42165279 (JNJ-5279) is an inhibitor of fatty acid amide hydrolase (FAAH) that inhibits recombinant human and rat FAAH with IC50 of 70 nM and 313 nM, respectively.Targetsrecombinant human FAAH (Cell-free assay):

InformationJNJ-42165279 JNJ-42165279 (JNJ-5279) is an inhibitor of fatty acid amide hydrolase (FAAH) that inhibits recombinant human and rat FAAH with IC50 of 70 nM and 313 nM, respectively.Targetsrecombinant human FAAH (Cell-free assay):

InformationJNJ-42165279 JNJ-42165279 (JNJ-5279) is an inhibitor of fatty acid amide hydrolase (FAAH) that inhibits recombinant human and rat FAAH with IC50 of 70 nM and 313 nM, respectively.Targetsrecombinant human FAAH (Cell-free assay):

InformationJNJ-42165279 JNJ-42165279 (JNJ-5279) is an inhibitor of fatty acid amide hydrolase (FAAH) that inhibits recombinant human and rat FAAH with IC50 of 70 nM and 313 nM, respectively.Targetsrecombinant human FAAH (Cell-free assay):

InformationJNJ-42165279 JNJ-42165279 (JNJ-5279) is an inhibitor of fatty acid amide hydrolase (FAAH) that inhibits recombinant human and rat FAAH with IC50 of 70 nM and 313 nM, respectively.Targetsrecombinant human FAAH (Cell-free assay):

JNJ-42226314.

JNJ-42226314.