83
16
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T14971 | CIQ | NMDAR | |
CIQ is a subunit-selective potentiator of NMDA receptors containing the NR2C or NR2D subunit. EC50 value: 2.7 μM for NR2C and 2.8 μM for NR2D. | |||
T12406 | PEPA | iGluR | |
PEPA is an allosteric AMPA receptors modulator; binds to the GluA2o and GluA3o LBDs and can be utilized as an indicator of AMPA receptor heterogeneity. | |||
T16402 | Org-26576 | GluR , iGluR | |
Org-26576 is a positive allosteric modulator of the AMPA receptor. | |||
T12234 | NMDA-IN-1 | NMDAR | |
NMDA-IN-1 is a potent and NR2B-selective antagonist of NMDA(NMDA Ki of 0.85 nM; NR2B Ca2+ influx IC50 is 9.7 nM). | |||
T8920 | Sepimostat | iGluR | |
Sepimostat exhibits neuroprotective activity via NR2B N-methyl-D-aspartate receptor antagonism at the Ifenprodil-binding site of the NR2B subunit. Sepimostat dimethanesulfonate inhibits the Ifenprodil binding with a Ki v... | |||
T20993 | Memantine | Others | |
Memantine, an amantadine derivative with some dopaminergic effects, has been proposed as an antiparkinson agent and has may be used to treat moderate to severe Alzheimer's disease. It acts on the glutamatergic system by ... | |||
T2362 | QNZ46 | NMDAR , iGluR | |
QNZ46 is a NR2C/NR2D-selective NMDA receptor non-competitive antagonist. | |||
T15623 | JNJ-61432059 | iGluR | |
JNJ-61432059 is an oral active and selective negative modulator of AMPAR associated with trans-membrane AMPAR regulatory protein (TARP) γ-8 (pIC50: 9.7 for GluA1/γ-8). | |||
T17293 | ZL006 | NMDAR , iGluR | |
ZL006 is an effective inhibitor of nNOS/PSD-95 interaction. ZL006 also inhibits NMDA receptor-mediated NO synthesis. | |||
T9626 | Cycloleucine | NMDAR | |
Cycloleucine is an antagonist of NMDA receptor associated glycine receptor with a Ki of 600 μM. Cycloleucine is also a competitive inhibitor of S-adenosyl-methionine mediated methylation with anxiolytic and cytostatic ef... | |||
T7355 | IC87201 | Others , iGluR | |
IC87201 is a nNOS-PDZ/PSD-95-PDZ inhibitor. IC87201 showed great promise in cellular experiments and animal models of ischemic stroke and pain. | |||
T1897 | MDL-29951 | NMDAR , iGluR | |
MDL-29951 is a novel glycine antagonist of NMDA receptor activation. | |||
T4573 | Cyclothiazide | GluR | |
Cyclothiazide is a benzothiadiazide that acts as a potentiator of AMPA receptorsthat potently inhibits AMPA receptor desensitization, positively modulating its response to glutamic acid (EC50 = 3.8 M). | |||
T5522 | NMDAR antagonist 1 | Others , iGluR | |
NMDAR antagonist 1 is an orally active, NR2B-selective NMDAR antagonist. | |||
TQ0289 | LY450108 | iGluR | |
LY450108 is a potentiator of the AMPA receptor that can be used in Parkinson's disease studies. | |||
TQ0233 | Traxoprodil | CP101606 | NMDAR , iGluR |
Traxoprodil (CP101606) is a selective NMDA antagonist and protects hippocampal neurons (IC50: 10 nM). | |||
T8458 | CNQX disodium | iGluR | |
CNQX disodium is a competitive non-NMDA receptor antagonist and competitive AMPA/kainate receptor antagonist in neuronal cultures. | |||
T4171 | PEAQX | NVP-AAM077 | NMDAR , iGluR |
PEAQX (NVP-AAM077)(NVP-AAM 077) is an effective and orally available NMDA antagonist. It can inhibit human NMDA receptors for 1A/2A(IC50: 270 nM), rather than 1A/2B(29, 600 nM). | |||
T5385 | Radiprodil | RGH-896 | NMDAR , iGluR |
Radiprodil (RGH-896) (RGH-896) is an orally active and selective NMDA NR2B receptors antagonist. It was a potential treatment of neuropathic pain associated with diabetic peripheral neuropathy (DPNP). | |||
T22748 | DQP 1105 | NMDAR | |
DQP 1105 is a NMDA receptor antagonist. | |||
T7870 | TCN 201 | TCN-201 | NMDAR , iGluR |
TCN 201 is a selective antagonist of NMDA receptors containing the NR2A subunit. | |||
T9177 | BPAM344 | iGluR | |
BPAM344 is a potent positive allosteric modulator (PAM) of the KAR subunits GluK1b, GluK2a, and GluK3a. | |||
T25196 | BZAD01 | BZAD-01,BZAD 01 | NMDAR |
BZAD01 is a selective NMDA NR1A/2B receptor antagonist. | |||
T7579 | 1-BCP | Piperonylic acid piperidide | GluR , iGluR |
1-BCP (Piperonylic acid piperidide) is a centrally active drug that modulates AMPA receptor gated currents. | |||
T37734 | AMPA receptor modulator-2 | GluR | |
AMPA receptor modulator-2 (Example 134) is a AMPA receptor modulator, with a pIC50 of 10.1 for TARPγ2 dependent AMPA receptor[1]. pIC50 = -lgIC50. [1]. BERRY CYNTHIA G B (US), et al. AZABENZIMIDAZOLES AND THEIR USE AS AM... | |||
T9723 | GluR6 antagonist-1 | Src | |
GluR6 antagonist-1 inhibits the pY binding site of tyrosine kinase p56lck SH2 domain. | |||
T7591 | Coluracetam | MKC-231 | AChR , iGluR |
Coluracetam (MKC-231)(MKC-231) is a Choline Uptake Enhancer. | |||
T8450 | TCN 213 | TCN213 | NMDAR |
TCN 213 is an antagonist of NMDA receptor that has a selective for NR1/NR2A over NR1/NR2B | |||
T0015 | Mephenesin | Cresoxydiol,Memphenesin,Mephedan,Decontractyl | NMDAR , iGluR |
Mephenesin (Cresoxydiol) is a centrally acting muscle relaxant with a short duration of action. | |||
T8779 | HBT1 | GluR | |
HBT1 is an AMPA receptor potentiator that induces production of brain-derived neurotrophic factor (BDNF) and exhibits little agonistic effect in primary neurons. HBT1 binds to ligand-binding domain of AMPA-R in glutamate... | |||
T1751 | Eliprodil | SL-820715 | NMDAR , iGluR |
Eliprodil (SL-820715)(SL-820715), a non-competitive NR2B-NMDA receptor antagonist(IC50: 1 uM), less effective for NR2A- and NR2C-containing receptors(IC50> 100 uM). It has been used in trials studying the treatment of Pa... | |||
T0426 | Piracetam | UCB-6215 | GluR , iGluR |
Piracetam (UCB-6215), a cyclic derivative of the neurotransmitter gamma-aminobutyric acid (GABA), is used in therapy of the extensive cognitive disorders. | |||
T12187L | Naspm trihydrochloride | 1-Naphthylacetyl spermine trihydrochloride | iGluR |
Naspm trihydrochloride (1-Naphthylacetyl spermine trihydrochloride) is a synthetic analogue of Joro spider toxin and is an antagonist of calcium permeable AMPA (CP-AMPA) receptors. | |||
T9133 | Caroverine hydrochloride | Caroverine HCL | GluR , NMDAR , iGluR |
Caroverine hydrochloride (Caroverine HCL) is a potent, competitive and reversible antagonist of NMDA and AMPA glutamate receptor. It is also an antioxidant and calcium-blocking agent that exhibits vasorelaxant action, an... | |||
T8459 | DNQX disodium salt | DNQX Disodium | NMDAR , iGluR |
DNQX disodium salt is a water-soluble form of selective antagonist of non-NMDA receptor | |||
T3957 | Farampator | Org24448,CX-691 | GluR , iGluR |
Farampator (CX-691) (CX-691;Org24448) is a positive modulator of AMPA receptor. | |||
T17179 | Tulrampator | CX-1632,S-47445 | iGluR |
Tulrampator (S-47445) is an orally bioavailable positive AMPAR with antidepressant effects. | |||
T6259 | Dizocilpine | MK-801 | NMDAR , iGluR |
MK-801 (Dizocilpine (MK-801)) is a potent N-methyl-D-aspartate (NMDA) receptor antagonist with Ki of 30.5 nM. | |||
T7599 | Sunifiram | DM-235 | iGluR |
Sunifiram (DM-235) is a potent nootropic agent. | |||
T22542 | 1-Aminocyclobutanecarboxylic acid | ACBC | NMDAR , iGluR |
1-Aminocyclobutanecarboxylic acid (ACBC) is a NMDA receptor partial agonist. 1-Aminocyclobutanecarboxylic acid act at the glycine site, NR1[1]. | |||
T7580 | CX546 | Autophagy , iGluR | |
CX546 is an AMPA receptor modulator. CX546 enhances cognitive function in rats. It has also been proposed as a treatment for schizophrenia. | |||
T7304 | DNQX | FG 9041 | GluR , iGluR |
DNQX (FG 9041) is a competitive, non-NMDA glutamate receptor antagonist (IC50s = 0.5 and 0.1 μM for AMPA and kainate receptors, respectively) | |||
T16977 | Talampanel | GYKI-53773,LY-300164 | Apoptosis , GluR |
Talampanel (LY-300164) is an orally and selective α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate receptor antagonist with anti-seizure activity. Talampanel (IVAX) has neuroprotective effects in rodent stroke models. | |||
T4113 | NBQX | FG9202,NBQX disodium salt | GluR , iGluR |
NBQX (FG9202) is a potent, selective and competitive AMPA receptor antagonist. Neuroprotective and anticonvulsant; active in vivo. | |||
T0324 | Isoxsuprine hydrochloride | Duvadilan,Isolait | Adrenergic Receptor , iGluR |
Isoxsuprine hydrochloride (Isolait) is a beta-adrenergic agonist that causes direct relaxation of uterine and vascular smooth muscle. | |||
T13480 | (S)-(-)-5-Fluorowillardiine | (S)-5-Fluorowillardiine,(5S)-Fluorowillardiine | iGluR |
(S)-(-)-5-Fluorowillardiine ((S)-5-Fluorowillardiine) is an AMPA receptor-specific agonist | |||
T1308 | Orphenadrine hydrochloride | Mebedrol,Mephenamin | Sodium Channel , NMDAR , Norepinephrine , iGluR , Histamine Receptor |
Orphenadrine hydrochloride (Mephenamin) is a muscarinic antagonist used to treat drug-induced parkinsonism and to relieve pain from muscle spasm. | |||
T12110 | MRZ 2-514 | 8-bromo-4,5-dihydroxypyridazino[4,5-b]quinolin-1-one | NMDAR |
MRZ 2-514 (8-bromo-4,5-dihydroxypyridazino[4,5-b]quinolin-1-one) is a strychnine-insensitive modulatory site of the NMDA receptor (glycineB)antagonist with Ki of 33 μM. | |||
T22733 | DL-AP5 | NMDAR | |
DL-AP5 is a NMDA antagonist. | |||
T7108 | Omberacetam | SGS-111,Noopept,GVS-111 | Others , iGluR |
Omberacetam (Noopept) is a synthetic dipeptide that has been shown to produce positive nootropic and cognitive effects in animal models by a mechanism similar to other related racetam compounds. |
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T1186 | Ifenprodil Tartrate | Potassium Channel , NMDAR , iGluR | |
Ifenprodil is a selective NMDA receptor (glutamate) antagonist. | |||
T2S2264 | Linalool | Linalol,(±)-Linalool,Phantol | Apoptosis , IL Receptor , TNF , Endogenous Metabolite , iGluR |
1. Linalool (Linalol), a natural compound of the essential oils, has been shown to have antinociceptive, antimicrobial, and anti-inflammatory properties. 2. Linalool was protected against LPS/GalN-induced liver injury th... | |||
T8394 | D-Serine | (R)-Serine | Endogenous Metabolite , NMDAR , iGluR |
D-Serine ((R)-Serine) is an endogenous amino acid,is a potent co-agonist at the NMDA glutamate receptor. | |||
T3379 | Decanoic Acid | Decoic acid,CAPRIC ACID,Caprynic acid | GluR , iGluR |
Decanoic Acid (Caprynic acid) acts as a non-competitive AMPA receptor antagonist. | |||
TQ0027 | Transcrocetinate disodium | Disodium trans-crocetinate | NMDAR , iGluR |
Transcrocetinate disodium (Disodium trans-crocetinate), extracted from saffron (Crocus sativus L.), is a high-affinity antagonist of NMDA receptor. | |||
T4096 | Quinolinic acid | pyridine-2,3-dicarboxylic acid,QUIN | Endogenous Metabolite , NMDAR , iGluR |
Quinolinic acid (QUIN) is an endogenous N-methyl-D-aspartate (NMDA) receptor agonist synthesized from L-tryptophan via the kynurenine pathway. | |||
T6608 | NMDA | N-Methyl-D-aspartic acid | Endogenous Metabolite , NMDAR , iGluR |
N-Methyl-D-aspartic acid is an amino acid that, as the D-isomer, is the defining agonist for the NMDA (N-Methyl-D-aspartic acid) receptor subtype of glutamate receptors. | |||
T4S0171 | Transcrocetin | trans-Crocetin,8,8'-Diapocarotenedioic Acid,Crocetin | Others , Endogenous Metabolite , iGluR |
Transcrocetin (8,8'-Diapocarotenedioic Acid) is a singlet oxygen quencher. | |||
T1589 | D-Cycloserine | RO-1-9213 | Others , Antibacterial , Antibiotic , iGluR |
D-Cycloserine (RO-1-9213) is a broad spectrum antibiotic used as a second line agent for treatment of drug resistant tuberculosis, always in combination with other antituberculosis agents. | |||
T2O2728 | Glycine | 2-Aminoacetic acid,Glycolixir,Aminoacetic acid,Glycosthene,Glycocoll | MT Receptor , Endogenous Metabolite , iGluR |
glycine (2-Aminoacetic acid) is a non-essential amino acid. It is found primarily in gelatin and silk fibroin and used therapeutically as a nutrient. It is also a fast inhibitory neurotransmitter. | |||
T3026 | (-)-Huperzine A | HupA,Huperzine A | Apoptosis , AChR , AChE , iGluR |
(-)-Huperzine A (HupA) , an active Lycopodium alkaloid extracted from the traditional Chinese herb, is a potent, selective and reversible acetylcholinesterase (AChE) inhibitor and has been widely used in China for the tr... | |||
T2A2497 | L-Glutamic acid | (S)-Glutamic acid,glutamic acid,(+)-L-Glutamic acid,Aciglut,glutacid,Glutaminol | Apoptosis , Ferroptosis , Endogenous Metabolite , iGluR |
L-Glutamic acid (Glutaminol) acts as an excitatory transmitter, shows a direct activating effect on the release of DA from dopaminergic terminals. | |||
T4885 | (-)-Aspartic acid | (R)-Aspartic acid,Asp,D-(-)-Aspartic acid,Aminosuccinic acid,asparagic acid,L-Homoproline,D-Aspartic acid | Endogenous Metabolite , NMDAR , iGluR |
(-)-Aspartic acid (L-Homoproline) is an endogenous amino acid existing in invertebrates and vertebrates. It can regulate testosterone synthesis and is an agonist of NMDA receptor. | |||
T6871 | L-Glutamic acid monosodium salt | Monosodium glutamate,Glutacyl,Glutavene,Ajinomoto,MSG | Apoptosis , Ferroptosis , GluR , iGluR |
L-Glutamic acid monosodium salt (MSG) (Monosodium glutamate) is an activator of mGlu1 receptor. | |||
T0948L | Corticosterone | 17-Deoxycortisol,11β,21-Dihydroxyprogesterone,Kendall's compound B,Corticosterone (From plants) | Glucocorticoid Receptor , Endogenous Metabolite |
Corticosterone (Kendall's compound B) is an adrenocortical steroid with salocorticoid and glucocorticoid activity that is orally active. Corticosterone is involved in the regulation of energy, immune responses, and stres... | |||
T3377 | L-Phenylalanine | (S)-2-Amino-3-phenylpropionic acid,phenylalanine,3-Phenyl-L-alanine | Calcium Channel , Endogenous Metabolite , iGluR |
L-Phenylalanine (3-Phenyl-L-alanine) is an essential amino acid and the precursor of the amino acid tyrosine, acts as an antagonist at α2δ calcium channels. |