T26520 |
ABP688
|
924298-51-1
|
97.85%
|
|
ABP688 is a non-competitive and selective mGluR5 antagonist(Ki = 1.7 nM). ABP688 can be used as a PET tracer for clinical imaging.
|
T21935L |
AMN082 free base
|
83027-13-8
|
97.76%
|
|
AMN082 free base is a metabotropic glutamate receptor 7 allosteric agonist.
|
TP1943L1 |
Pep2-EVKI acetate(1315378-67-6 free base)
|
TP1943L1
|
97.63%
|
|
Pep2-EVKI acetate is a cell-permeable peptide. Pep2-EVKI acetate interferes the interaction between protein interacting with C-kinase (PICK1) and GluR2 AMPA rece...
|
T14389 |
AZD 9272
|
327056-26-8
|
97.53%
|
|
AZD 9272 is a brain-permeable mGluR5 antagonist for the study of gastroesophageal reflux.
|
T19698 |
CX614
|
191744-13-5
|
97.43%
|
|
CX614 is a positive allosteric modulator of the AMPA receptor with respect to AMPA.
|
T35028 |
Valiglurax
|
1976050-09-5
|
97.38%
|
|
Valiglurax (VU2957), also known as VU0652957 and VU2957, is a potent, selective, CNS penetrant, and orally bioavailable mGlu4 PAM. VU2957 possessed attractive in...
|
T29118 |
VU 0469650
|
1443748-47-7
|
97.27%
|
|
VU 0469650 is a potent and selective negative allosteric modulator of mGluR1 (IC50 = 99 nM).
|
T3482 |
CFMTI
|
864864-17-5
|
97.23%
|
|
CFMTI is a potent and selective metabotropic glutamate receptor (mGluR) 1 allosteric antagonist (IC50: 2.6 nM). The selectivity of CFMTI to mGluR1 is higher 2000...
|
T23010 |
MNI 137
|
946619-21-2
|
97.21%
|
|
MNI 137 is a negative allosteric modulator of mGlu2. MNI 137 inhibits glutamate-induced calcium mobilization with IC50s of 8.3 and 12.6 nM for human and rat.
|
TP1944L1 |
Pep2-SVKI acetate
|
TP1944L1
|
97.14%
|
|
Pep2-SVKI acetate(pep2-SVKI acetate (328944-75-8 free base)) is a synthetic peptide salt that prevents internalization of AMPA-type glutamate receptor.
|
T21747 |
VU0483605
|
1623101-11-0
|
97.03%
|
|
VU0483605 is an effective and selective positive allosteric modulator of mGluR1 with EC50s of 390 and 356 nM for human and rat, respectively.
|
T27748L |
KRP-199 sodium
|
|
96.85%
|
|
KRP-199 sodium sodium is highly potent and selective for AMPA-R in vitro and exhibits good neuroprotection in vivo.
|
T16977 |
Talampanel
|
161832-65-1
|
95.54%
|
|
Talampanel (LY-300164) is an orally and selective α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate receptor antagonist with anti-seizure activity. Talampanel (IV...
|
T29135 |
VU0422288
|
1630936-95-6
|
95.48%
|
|
VU0422288 (ML396) is a potent orthosteric modulator of type III mGlu receptors (mGlus).VU0422288 shows inhibition of mGluR4, mGluR7, and mGluR8 in a calcium mobi...
|
T22730 |
DL-AP3
|
20263-06-3
|
95%
|
|
DL-AP3 is a competitive group I metabotropic glutamate receptor antagonist and inhibitor of phosphoserine phosphatase.
|
T3483 |
FTIDC
|
873551-53-2
|
94.58%
|
|
FTIDC is a highly potent and selective allosteric antagonist of mGluR1 receptors and shows very weak potency against human and rat mGluR5 receptors. The inhibiti...
|
T2194 |
Direct Blue 1
|
2610-05-1
|
50%
|
|
Direct Blue 1 (Pontamine sky blue), a counterstain for background autofluorescence in immunofluorescence histochemistry, structurally resembles glutamate and ope...
|
T15812 |
LY2979165
|
1311385-32-6
|
100.00%
|
|
LY2979165 (mGlu2 agonist) is an orthosteric agonist of mGluR2 and can be used in studies about serving as an anti-depressant.
|
T3565 |
VU0155041
|
1093757-42-6
|
100%
|
|
VU0155041 is an effective and positive allosteric modulator/allosteric agonist at mGlu4 receptors (EC50: 798/693 nM, at human/rat).
|
T7823 |
IDRA-21
|
22503-72-6
|
100%
|
|
IDRA-21 is a positive AMPA receptor modulator.
|