Cat.No. | Name | Information |
---|---|---|
M25422 | Glypromate | Glypromate (Gly-Pro-Glu) is a neuroactive peptide with a potent action on acetylcholine release. Glypromate (Gly-Pro-Glu) is a weak NMDA receptor agonist binds to N-methyl-D-aspartate (NMDA) receptor with an IC50 value of 14.7 μM. |
M10606 | Radiprodil (RGH-896) | Radiprodil (also known as RGH-896) is an orally active and selective NMDA receptors antagonist which was evaluated as potential treatment of neuropathic pain associated with diabetic peripheral neuropathy (DPNP). |
M10581 | Trans-crocetin | Trans-crocetin (Croceic Acid) is a blood-brain barrier-permeable NMDA receptor antagonist with high affinity, extracted from saffron (Crocus sativus L.). *The compound is unstable in solutions, freshly prepared is recommended |
M9529 | L-Glutamic acid monosodium salt hydrate | L-Glutamic acid monosodium salt hydrate is also a Kainate receptor, NMDA receptor and quisqualate receptor agonist; an excitatory amino acid neurotransmitter. |
M8022 | Putrescine dihydrochloride | Binds to the polyamine modulatory site of the NMDA receptor and potentiates NMDA-induced currents; precursor of spermidine. |
M7587 | Arcaine sulfate salt | Potent antagonist at the polyamine site of the NMDA glutamate receptor. |
M7178 | Quinolinic acid | Quinolinic acid is a endogenous NMDA agonist and transmitter candidate. |
M6805 | Ibotenic acid | Ibotenic acid is a non-selective NMDA agonist. Ibotenic acid has agonist activity at both the N-methyl-D-aspartate (NMDA) and trans-ACPD or metabolotropic quisqualate (Qm) receptor sites. |
M6798 | Homoquinolinic acid | Homoquinolinic acid is a selective, potent NMDA agonist. |
M6012 | Tiletamine HCl | Tiletamine hydrochloride is a dissociative anesthetic and pharmacologically classified as an NMDA receptor antagonist. |
M5566 | Dextromethorphan hydrobromide monohydrate | Dextromethorphan hydrobromide hydrate is an antitussive drug. |
M5554 | D-Cycloserine | D-Cycloserine is an analog of the amino acid D-alanine. |
M4726 | Linalool | Linalool is a natural monoterpenoid compound, which exists in coriander and other plants. As a competitive NMDA receptor antagonist, Linalool has anti-tumor and anti-cardiotoxicity effects. Linalool is a PPARα ligand that reduces plasma thyroglobulin (TG) levels and alters liver transcriptome structure and plasma metabolites. |
M2646 | Dizocilpine | Dizocilpine (MK-801) is a potent N-methyl-D-aspartate (NMDA) receptor antagonist with Ki of 30.5 nM. |
M25469 | Esketamine | Esketamine (ESK) is an NMDA-receptor antagonist. |
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