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Cat No. | Product Name | Synonyms | Targets |
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T8458 | CNQX disodium | iGluR | |
CNQX disodium is a competitive non-NMDA receptor antagonist and competitive AMPA/kainate receptor antagonist in neuronal cultures. | |||
T8459 | DNQX disodium salt | DNQX Disodium | NMDAR , iGluR |
DNQX disodium salt is a water-soluble form of selective antagonist of non-NMDA receptor | |||
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) | |||
T7178 | CNQX | FG9065 | GluR , iGluR |
CNQX (FG9065) is a competitive, non-NMDA glutamate receptor antagonist (IC50s = 0.3 and 1.5 μM for AMPA and kainate receptors, respectively) | |||
T2362 | QNZ46 | NMDAR , iGluR | |
QNZ46 is a NR2C/NR2D-selective NMDA receptor non-competitive antagonist. | |||
T26645 | Aptiganel | CNS 1102,CNS-1102,CNS1102 | NMDAR |
Aptiganel (CNS-1102) is a non-competitive NMDA antagonist, a peptide that may be used to study acute ischemic stroke. | |||
T23048 | N20C hydrochloride | 2-((3,3-diphenylpropyl)amino)acetamide hydrochloride | NMDAR |
N20C hydrochloride (2-((3,3-diphenylpropyl)amino)acetamide hydrochloride) is a non-competitive NMDA receptor open-channel blocker. | |||
T22798 | Gavestinel | GV 150526,Gavestinel sodium salt | NMDAR , iGluR |
Gavestinel (GV 150526) is a non-competitive NMDA receptor antagonist that is potent, selective and orally active.Gavestinel binds to the glycine site of the NMDA receptor with a binding affinity (pKi value) of 8.5.Gavest... | |||
T6352 | (-)-Dizocilpine maleate | C13737,(-)-MK 801 (Maleate),(-)-MK 801 Maleate | NMDAR , iGluR |
(-)-Dizocilpine maleate ((-)-MK 801 (Maleate)) is a potent, selective and non-competitive NMDA receptor antagonist with Kd of 37.2 nM in rat brain membranes. | |||
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... | |||
T22513 | 4-PPBP maleate | Sigma receptor , NMDAR | |
4-PPBP maleate is a potent σ1 receptor (ligand) agonist. 4-PPBP maleate can be considered a selective, non-competitive NR1a/2B NMDA receptor antagonist in the context of Xenopus oocytes expression. 4-PPBP maleate has neu... | |||
T6504 | Flupirtine maleate | Katadolon maleate | Potassium Channel , NMDAR , iGluR |
Flupirtine maleate (Katadolon maleate), a centrally acting non-opioid analgesia, is the salt form of Flupirtine. It is an NMDA receptor antagonist , and also a specific neuronal potassium channel opener. | |||
T22640 | CCMQ | Others | |
inhibits [3H]-homoquinolinic acid binding to non-NMDA sensitive sites | |||
T61470 | NMDA receptor antagonist 5 | ||
NMDA receptor antagonist 5 (Compound 10e), a potent and non-toxic NMDA receptor antagonist, exhibits brain permeability. It is of significance in studying neurological disorders [1]. | |||
TP2235 | Conantokin-T | Others | |
Non-competitive NMDA receptor antagonist | |||
T21449 | GYKI-52466 | GYKI 52,466,GYKI-5,2466,GYKI52,466 | |
GYKI-52466 is a selective non-competitive AMPA receptor antagonist (IC50 values are 10-20, ~ 450 and >50 μM for AMPA-, kainate- and NMDA-induced responses, respectively) used as a Skeletal muscle relaxant, orally active ... | |||
T11522 | GYKI 52466 dihydrochloride | Others | |
GYKI 52466 dihydrochloride is orally active and non-competitive kainate- and AMPA-activated currents antagonist (IC50s: 7.5 μM and 11 μM). It is inactive against NMDA or γ-aminobutyric acid responses. It is a muscle rela... | |||
T69422 | Flupirtine HCl | ||
Flupirtine HCl is the salt form of Flupirtine, also known as W-2964, an aminopyridine that functions as a centrally acting non-opioid analgesic. It first became available in Europe in 1984, and is sold mainly under the n... | |||
T37671 | CAY10608 | CAY10608 | |
N-Methyl-D-aspartate (NMDA) receptors are Ca2+ permeable ligand-gated channels of the central nervous system that are activated after binding of the co-agonists glutamate and glycine. CAY10608 is a propanolamine that pot... |
Cat No. | Product Name | Synonyms | Targets |
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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. | |||
T6S0659 | Rhynchophylline | Rhynchophyllin,Rhyncophylline,Mitrinermine,Mitrinermin | Calcium Channel , NF-κB |
1. Rhynchophylline (Mitrinermine) can protect against ischemic damage, probably via regulating the Akt/mTOR pathway. 2. Rhynchophylline can protect against glutamate-induced neuronal death, can inhibit MA impairment in c... | |||
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. |
Cat No. | Product Name | Species | Expression System |
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TMPY-04384 | Src Protein, Human, Recombinant (His & GST) | Human | Baculovirus-Insect Cells |
Proto-oncogene tyrosine-protein kinase SRC is a hydrophobic protein belonging to the SRC family kinase including nine members that is a family of non-receptor tyrosine kinases. SRC protein may exist in different forms: C... | |||
TMPY-04434 | Src Protein, Mouse, Recombinant (His & GST) | Mouse | Baculovirus-Insect Cells |
Proto-oncogene tyrosine-protein kinase SRC is a hydrophobic protein belonging to the SRC family kinase including nine members that is a family of non-receptor tyrosine kinases. SRC protein may exist in different forms: C... |