| Bioactivity | JNJ-46281222 is an metabotropic glutamate (mGlu) 2-selective, highly potent PAM (positive allosteric modulator) with nanomolar affinity (Kd = 1.7 nM) and a high modulatory potency (pEC50 = 7.71)[1]. | ||||||||||||
| Invitro | JNJ‐4628122 binds to the selected mGlu2 receptor mutants is significantly decreased by approximately 10‐fold compared with WT, in transfected mGlu2 WT and mutant receptors in CHO‐K1 cells, mutations F643A and N735D are selected[1]. Western Blot Analysis[1] Cell Line: | ||||||||||||
| Name | JNJ-46281222 | ||||||||||||
| CAS | 1254980-38-5 | ||||||||||||
| Formula | C23H25F3N4 | ||||||||||||
| Molar Mass | 414.47 | ||||||||||||
| Appearance | Solid | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
| Storage |
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| Reference | [1]. Doornbos ML,et al. Molecular mechanism of positive allosteric modulation of the metabotropic glutamate receptor 2 by JNJ-46281222.Br J Pharmacol. 2016 Feb;173(3):588-600. |
JNJ-46281222
CAS: 1254980-38-5 F: C23H25F3N4 W: 414.47
JNJ-46281222 is an metabotropic glutamate (mGlu) 2-selective, highly potent PAM (positive allosteric modulator) with nan
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