Catalog |
name |
Description |
price |
R-R-2755 |
VU0155094 CAS No.731006-86-3 |
VU0155094/CAS No.731006-86-3 is a positive allosteric modulator with differential activity at the various group III mGluRs. |
price> |
R-R-2756 |
(rel)-Eglumegad CAS No.176027-90-0 |
(rel)-Eglumegad ((rel)-LY354740)/CAS No.176027-90-0 is a relative configuration of Eglumegad (HY-18941). Eglumegad is a highly potent and selective group II (mGlu2/3) receptor agonist with EC50s of 5 and 24 nM for transfected human mGlu2 and mGlu3 receptors, respectively. |
price> |
R-R-2757 |
rel-ACPT-I CAS No.194918-76-8 |
rel-ACPT-I/CAS No.194918-76-8 is an agonist of group III mGluRs with diverse biological activities including neuroprotective, anticonvulsant, and anxiolytic-like effects. |
price> |
R-R-2758 |
A-841720 CAS No.869802-58-4 |
A-841720/CAS No.869802-58-4 is a potent, non-competitive and selective mGlu1 receptor antagonist with an IC50 of 10 nM for human mGlu1 receptor. A-841720 displays 34-fold selectivity over mGlu5 (IC50 of 342 nM), and no significant activity at a range of other neurotransmitter receptors, ion channels, and transporters. A-841720 has the potential for chronic pain research. |
price> |
R-R-2759 |
XAP044 CAS No.196928-50-4 |
XAP044/CAS No.196928-50-4 is a potent and selective antagonist of mGlu7. The metabotropic glutamate receptor subtype 7 (mGlu7) is an important presynaptic regulator of neurotransmission in the mammalian CNS. XAP044 demonstrates good brain exposure and wide spectrum anti-stress and antidepressant- and anxiolytic-like efficacy in rodent behavioral paradigms. |
price> |
R-R-2760 |
(±)-LY367385 CAS No.198419-90-8 |
(±)-LY367385/CAS No.198419-90-8 is the racemate of LY367385. LY367385 is a highly potent and selective mGluR1a antagonist. LY367385 has an IC50 of 8.8 μM for inhibits of quisqualate-induced phosphoinositide (PI) hydrolysis, compared with > 100 μM for mGlu5a. |
price> |
R-C-1061 |
AC55541 CAS:916170-19-9 |
AC-55541 is a highly selective protease-activated receptor 2(PAR2)agonist (pEC50=6.7),displays no activity at other PAR subtypes or at over 30 other receptors involved in nociception and inflammation. |
price> |
R-R-2761 |
Ro 67-4853 CAS No.302841-89-0 |
Ro 67-4853/CAS No.302841-89-0 is a positive allosteric modulator (PAM) of mGluR1 (pEC50=7.16 for rmGlu1a receptor). Ro67-4853 exhibits activity at all group I mGlu receptors including hmGlu1, rmGlu1, and rmGlu5. Ro 67-4853 enhances the potency of L-Glu by interacting with the transmembrane domain (TMD) of the receptor. Ro 67-4853 potentiates sensory synaptic responses to repetitive vibrissa stimulation. |
price> |
R-C-1062 |
ZK-811752(BX-471) CAS:217645-70-0 |
BX471(ZK-811752)is an orally active, potent and selective non-peptide CCR1 antagonist with a Ki of 1 nM,and exhibits 250-fold selectivity for CCR1 over CCR2,CCR5 and CXCR4. |
price> |
R-R-2762 |
TC-N 22A CAS No.1314140-00-5 |
TC-N 22A/CAS No.1314140-00-5 is a potent, selective, orally active and brain-permeable mGlu4 PAM with an EC50 of 9 nM in human mGlu4-expressing BHK cells. TC-N 22A is less active (EC50>10 μM) in agonist and PAM model at mGlu 1, 2, 3, 5, and 7 receptors. TC-N 22A has the potential for research of CNS disease in vivo. |
price> |