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GluR

GluR

GluR related products

Structure Cat No. Product Name CAS No. Product Description
ADX-47273 (BA 94673139) V1087 ADX-47273 (BA 94673139) 851881-60-2 ADX47273 (ADX-47273;BA-94673139;BA94673139)is a potent, selectiveand specific mGlu5 positive allosteric modulator(PAM) with important biological activity.
BTS 72664 V130729 BTS 72664 165383-52-8 BTS 72664 is a broad-spectrum, non-sedating, orally effective antiepileptic drug.
CNQX V33762 CNQX 115066-14-3 CNQX (FG9065; FG-9065; 6-cyano-7-nitroquinoxaline-2,3-dione)is an AMPA/kainate antagonist that inhibits AMPA and kainate receptors with IC50values of 0.3 μM, 1.5 μM, respectively.
CTEP (RO4956371) V1084 CTEP (RO4956371) 871362-31-1 CTEP (also called RO4956371; RO 4956371;RO-4956371) is a long-acting and orally bioavailable allosteric antagonist of metabotropic glutamate receptor 5 (mGlu5) receptor with important biological activity.
D-谷氨酰胺 V1982 D-glutamine 5959-95-5 D-glutamine (also known as H-D-Gln-OH), an unnatural isomer of glutamine, is a D type stereoisomer of glutamine which is one of the 20 amino acids encoded by the standard genetic code.
DL-2-氨基-5-膦酰基缬草酸 V11432 DL-AP-5 76326-31-3 AP-5 (AP5) is a novel, selective and potent NMDA (N-methyl-D-aspartate) receptor antagonist with anticonvulsant activity.
Evans Blue V2710 Evans Blue 314-13-6 Evans Blue (Direct Blue 53)is a potent inhibitor of the uptake of L-glutamate into synaptic vesicles, it is also an AMPA/kainate receptor antagonist.
IEM 1754 2HBr V1088 IEM 1754 2HBr 162831-31-4 IEM 1754 2HBr (IEM-1754; IEM 1754; IEM1754), the dihydrobromide salt ofIEM-1754, is a selective voltage-dependent open-channel blocker of AMPA/kainate receptorswith important biological activity.
JNJ-54082730 V138267 JNJ-54082730 2097493-39-3 JNJ-54082730 is an orally effective phosphodiesterase (PDE) inhibitor that inhibits PDE2A, PDE3B, and PDE10A2, with IC50 values of 0.95 nM, 6.17 μM (pIC50=5.21), and 87.1 nM (pIC50=7.06), respectively.
L-Glutamic acid ammonium V138829 L-Glutamic acid ammonium 7558-63-6 L-Glutamic acid ammonium is an excitatory amino acid neurotransmitter that can act as an agonist for all subtypes of glutamate receptors (metaboloid theophylline receptor, NMDA receptor, and AMPA receptor).
MDAR-IN-1 V139543 MDAR-IN-1 MDAR-IN-1 is an acetylcholinesterase (AChE) inhibitor that can cross the blood-brain barrier, and also an antagonist of the NMDAR receptor GluN1/GluN2B subtype.
mGluR1 activator-1 V139915 mGluR1 activator-1 mGluR1 activator-1 is a stable vitamin K analog and an mGluR1 activator that can cross the blood-brain barrier.
N-甲基-D-天冬氨酸 V1086 NMDA (N-Methyl-D-aspartic acid) 6384-92-5 NMDA (N-Methyl-D-aspartic acid; LC488A; LC488 A;LC488-A; LC 488A; LC-488A) is an aspartic acid analog withan N-methyl substituent and D-configuration and a glutamate-like excitatory chemical substance.
Pomaglumetad (LY404039) V1079 Pomaglumetad (LY404039) 635318-11-5 Pomaglumetad (LY404039; LY-404039; LY-404,039; LY404,039) is a novel and potent agonist of recombinant human mGlu2/mGlu3 receptors with the potential for the treatment of Schizophrenia.
Ro 25-6981 free base V23963 Ro 25-6981 free base 169274-78-6 Ro 25-6981 is a highly potent and selective blocker of N-methyl-D-aspartate receptors containing the NR2B subunit.
Tezampanel etibutil V145946 Tezampanel etibutil 620113-98-6 Tezampanel etibutil is an orally effective AMPA/GluR antagonist.
VU 0357121 V1090 VU 0357121 433967-28-3 VU0357121 (VU-0357121, VU 0357121) is a positive allosteric modulator (PAM) of mGlu5 (metabotropic glutamate receptor 4) with antiparkinsonian-like effects.
VU 0361737 V1092 VU 0361737 1161205-04-4 VU 0361737 (VU0361737; VU-0361737) is a novel, brain-penetrable and selective positive allosteric modulator (PAM) for mGlu4 receptor with important biological activity.
VU 0364439 V1085 VU 0364439 1246086-78-1 VU 0364439 (VU0364439; VU-0364439) is a mGlu4 (metabotropic glutamate receptor 4) positive allosteric modulator (PAM) with important biological activity.
VU 0364770 V1091 VU 0364770 61350-00-3 VU 0364770 (VU-0364770, VU0364770) is a potent positive allosteric modulator (PAM) of mGlu4 (metabotropic glutamate receptor 4) with anti-parkinsonian-likeactivity.
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