36 Results for "

NMDA NR2B

" in MedChemExpress (MCE) Product Catalog:
Products (36)

36 Results for "NMDA NR2B" in MCE Product Catalog:

11
11 Publications Verification
Cat. No.: HY-12882A
CAS No.: 23210-58-4
Purity:  99.95%
Synonyms: NP-120 tartrate; RC-61-91 tartrate
Ifenprodil (NP-120) tartrate, a cerebral vasodilator, is a noncompetitive NMDA receptor antagonist. Ifenprodil tartrate exerts high affinity at NR1A/NR2B receptors (IC50=0.34 μM) over 400-fold than at NR1A/NR2A receptors (IC50=146 μM) . Ifenprodil tartrate is an α1 adrenergic receptor antagonist. Ifenprodil tartrate inhibits GIRK (Kir3), reduces inward currents through the basal GIRK activity. Ifenprodil tartrate has reliable inhibitory effects against A/H1N1 strains (EC50 of 6.6 µM). Ifenprodil tartrate has neuroprotective, anticonvulsant and antinociceptive effects. Ifenprodil tartrate can be used for the study of cerebrovascular diseases and peripheral arterial obliterative disease .
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11
11 Publications Verification
Cat. No.: HY-12882
CAS No.: 23210-56-2
Purity:  99.94%
Synonyms: NP-120; RC-61-91
Ifenprodil (NP-120), a cerebral vasodilator, is a noncompetitive NMDA receptor antagonist. Ifenprodil exerts high affinity at NR1A/NR2B receptors (IC50=0.34 μM) over 400-fold than at NR1A/NR2A receptors (IC50=146 μM) . Ifenprodil is an α1 adrenergic receptor antagonist. Ifenprodil inhibits GIRK (Kir3), reduces inward currents through the basal GIRK activity. Ifenprodil has reliable inhibitory effects against A/H1N1 strains (EC50 of 6.6 µM). Ifenprodil has neuroprotective, anticonvulsant and antinociceptive effects. Ifenprodil can be used for the study of cerebrovascular diseases and peripheral arterial obliterative disease .
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9
9 Cited Publications
Cat. No.: HY-13993
CAS No.: 169274-78-6
Purity:  99.55%
Target:  

iGluR

Research Areas:  

Neurological Disease

Ro 25-6981 is a potent, selective and activity-dependent NR2B subunit specific NMDA receptor antagonist. Ro 25-6981 shows anticonvulsant and anti-parkinsonian activity. Ro 25-6981 has the potential for the research of parkinson's disease (PD) .
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9
9 Cited Publications
Cat. No.: HY-13993A
CAS No.: 1312991-76-6
Purity:  99.25%
Target:  

iGluR

Research Areas:  

Neurological Disease

Ro 25-6981 Maleate is a potent, selective and activity-dependent NR2B subunit specific NMDA receptor antagonist. Ro 25-6981 Maleat shows anticonvulsant and anti-parkinsonian activity. Ro 25-6981 Maleate has the potential for the research of parkinson's disease (PD) .
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Cat. No.: HY-14777
CAS No.: 496054-87-6
Purity:  99.16%
Synonyms: RGH-896
Target:  

iGluR

Research Areas:  

Neurological Disease

Radiprodil (RGH-896) is an orally active and selective NMDA NR2B antagonist. A potential therapeutic agent in treatment of neuropathic pain and possibly other chronic pain conditions .
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Cat. No.: HY-145585
CAS No.: 1892581-29-1
Synonyms: MIJ-821
Target:  

iGluR

Research Areas:  

Neurological Disease

Onfasprodil (MIJ-821) is a selective intravenous NMDA receptor NR2B subunit negative allosteric modulator (NAM). Onfasprodil inhibits the activity of NR2B-NMDA receptors. Onfasprodil has a rapid antidepressant effect. Onfasprodil can be used for the research of treatment-resistant depression (TRD) .
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Cat. No.: HY-107706
CAS No.: 193356-17-1
Purity:  99.80%
Synonyms: PD 174494 hydrochloride
Target:  

iGluR

Research Areas:  

Neurological Disease

Co 101244 (PD 174494) hydrochloride is a NR2B-containing NMDA receptor antagonist .
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Cat. No.: HY-12881
CAS No.: 119431-25-3
Purity:  99.43%
Synonyms: SL-820715
Target:  

iGluR

Research Areas:  

Neurological Disease

Eliprodil(SL-820715) is a non-competitive NR2B-NMDA receptor antagonist(IC50=1 uM), less potent for NR2A- and NR2C-containing receptors(IC50> 100 uM).
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Cat. No.: HY-W747599
CAS No.: 68652-37-9
Synonyms: ​Tetrasialoganglioside GQ1b sodium
Ganglioside GQ1b (​Tetrasialoganglioside GQ1b) (bovine) sodium is a central and peripheral nervous system ganglioside and an immunostimulator. Ganglioside GQ1b (bovine) sodium modulates NMDA receptor signaling via ERK1/2, PKA, CREB, NR2A, NR2B, and GSK3β, and increases BDNF expression. Ganglioside GQ1b (bovine) sodium reduces pathology, tau phosphorylation, and APP levels. Ganglioside GQ1b (bovine) sodium can be used for the research of Alzheimer’s disease .
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Cat. No.: HY-106408
CAS No.: 640290-67-1
Purity:  99.84%
Synonyms: Salfaprodil free base; Neu2000
Research Areas:  

Neurological Disease

Nelonemdaz (Salfaprodil free base) is an NR2B-selective and uncompetitive antagonist of N-methyl-D-aspartate (NMDA). Nelonemdaz is also a free radical scavenger. Nelonemdaz has excellent neuroprotection against NMDA- and free radical-induced cell death .
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Cat. No.: HY-177127
CAS No.: 2416269-15-1
Target:  

iGluR

Research Areas:  

Neurological Disease

Satoprodil (example 2) is a potent N-methyl-D-aspartate (NMDA) receptor negative allosteric modulator with an IC50 value of 123 nM for NR2B .
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Cat. No.: HY-12962
CAS No.: 700878-19-9
Purity:  98.98%
Target:  

iGluR

Research Areas:  

Neurological Disease

NMDA-IN-1 is a potent and NR2B-selective NMDA antagonist with Ki of 0.85 nM; NR2B Ca2+ influx IC50 is 9.7 nM; no activities on NR2A, NR2C, NR2D, hERG-channel and α1-adrenergic receptor.
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Cat. No.: HY-126123
CAS No.: 457897-92-6
Target:  

iGluR Potassium Channel

Research Areas:  

Neurological Disease

NR2B-selective NMDA receptor antagonist 1 (compound 29) is a potent antagonist of NR1/NR2B receptors, with IC50s of 0.05 μM, 0.73 μM, 2.4 μM to NR1/NR2B NMDA receptor, hERG, α1-AdR, respectivity. NR2B-selective NMDA receptor antagonist 1 exhibites efficient permeability across the blood–brain barrier .
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Cat. No.: HY-106408A
CAS No.: 916214-57-8
Purity:  99.86%
Synonyms: Salfaprodil; Neu2000 potassium
Research Areas:  

Neurological Disease

Nelonemdaz (Salfaprodil) potassium is an NR2B-selective and uncompetitive antagonist of N-methyl-D-aspartate (NMDA). Nelonemdaz potassium is also a free radical scavenger. Nelonemdaz potassium has excellent neuroprotection against NMDA- and free radical-induced cell death .
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Cat. No.: HY-121100
CAS No.: 305339-41-7
Purity:  99.81%
Target:  

iGluR

Research Areas:  

Neurological Disease

BZAD-01 is a potent, selective and orally active inhibitor of NMDA NR2B subunit, with a Ki of 72 nM. BZAD-01 can improve postural asymmetry as well as Apomorphine-induced rotation .
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Cat. No.: HY-137049
CAS No.: 193359-26-1
Synonyms: PD 174494
Target:  

iGluR

Research Areas:  

Others

Co-101244 (PD 174494) is an NMDA receptor blocker that specifically targets the NR2B subunit.
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Cat. No.: HY-136659
CAS No.: 194089-07-1
Target:  

iGluR

Research Areas:  

Others

Ro 04-5595 is a selective antagonist with specific activity against the NR2B subunit of the NMDA receptor. Ro 04-5595 exhibits favorable pharmacokinetic properties in in vitro and in vivo studies, with rapid uptake and clearance. Ro 04-5595 exhibits strong binding in NR2B receptor-enriched regions and low binding in the cerebellum. Ro 04-5595 is able to effectively inhibit specific binding, showing high affinity for the NR2B receptor and a clear ranking of binding affinity with a variety of other compounds .
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Cat. No.: HY-107716
CAS No.: 1312991-77-7
Target:  

iGluR

Research Areas:  

Neurological Disease

Ro 8-4304 hydrochloride is a potent NMDA receptor antagonist. Ro 8-4304 hydrochloride is a NR2B selective, non-competitive, voltage-independent antagonist .
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Cat. No.: HY-170410
CAS No.: 178165-43-0
Target:  

iGluR

Research Areas:  

Neurological Disease

EMD-95885 is a selective NR2B-containing NMDA receptors antagonist with an IC50 of 3.9 nM. EMD-95885 does not interact with other sites on the NMDA receptor .
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Cat. No.: HY-12882AR
CAS No.: 23210-58-4
Synonyms: NP-120 tartrate (Standard); RC-61-91 tartrate (Standard)
Ifenprodil (tartrate) (Standard) is the analytical standard of Ifenprodil (tartrate). This product is intended for research and analytical applications. Ifenprodil tartrate is a typical noncompetitive NMDA receptor antagonist. Ifenprodil tartrate exerts high affinity at NR1A/NR2B receptors (IC50=0.34 μM) over 400-fold than at NR1A/NR2A receptors (IC50=146 μM) . Ifenprodil tartrate inhibits GIRK (Kir3), reduces inward currents through the basal GIRK activity. Ifenprodil tartrate has the potential to be a cerebral vasodilator .
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