Catalog |
name |
Description |
price |
R-C-1967 |
PF-06869206 CAS:2227425-05-8 |
PF-06869206 is an orally bioavailable selective inhibitor of the sodium-phosphate cotransporter NaPi2(SLC34A1)with an IC50 of 380nM. |
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R-C-1971 |
GNE-131 CAS:1629063-81-5 |
GNE-131 is a Potent and Selective hNaV1.7 Inhibitor(Na V1.7 IC50 =3nM)for the Treatment of Pain.GNE-131 showed excellent potency,good in vitro metabolic stability,and low in vivo clearance in mouse,rat and,dog.GNE-131 also displayed excellent efficacy in a transgenic mouse model of induced pain. |
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R-C-2020 |
Zuranolone(sage217) CAS:1632051-40-1 |
Zuranolone is an orally active and potent neuroactive steroid positive allosteric modulator of GABAA receptor,with EC50s of 296 and 163nM for α1β2γ2 and α4β3δ GABAA receptors,respectively. |
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R-C-2024 |
IC-87201 CAS:866927-10-8 |
IC87201,an inhibitor of PSD95-nNOS protein-protein interactions, suppresses NMDAR-dependent NO and cGMP formation. |
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R-C-2047 |
Org 25543 hydrochloride cas:495076-64-7 |
Org 25543 hydrochloride is a potent and selective glycine transporter type 2 (GlyT2)inhibitor for hGlyT2.Two major subtypes of glycine transporter are type 1(GlyT-1)and type 2(GlyT-2)revealed by molecular cloning.The GlyT-2 transporter has a similar distribution to ssGlyR with being confined to the spinal cord and brain stem,whereas the GlyT-1 transporter has a wide distribution throughout the CNS. |
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R-C-2058 |
Nelonicline CAS:1026134-63-3 |
Nelonicline(ABT-126)is an Alpha7 nicotinic acetylcholine receptor agonist and Nicotinic acetylcholine receptor agonist.Nelonicline is potentially useful for the treatment of Alzheimer is diseases.ABT-126 may be useful to reduce dyskinesias in both early-and later-stage Parkinson is disease.Accumulating evidence suggests that the α7 subtype of nicotinic acetylcholine receptors (nAChRs)plays a key role in inflammatory processes,thought to be involved in the pathophysiology of neuropsychiatric diseases,such as schizophrenia and Alzheimer is disease. |
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R-C-2094 |
PF06869206 CAS:2227425-05-8 |
PF-06869206 is an orally bioavailable selective inhibitor of the sodium-phosphate cotransporter NaPi2a(SLC34A1)with an IC50 of 380nM. |
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R-C-2096 |
ONO-8590580 CAS:1802661-73-9 |
ONO-8590580 is a GABAAα5 negative allosteric modulator which enhances long-term potentiation and improves cognitive deficits in preclinical models. |
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R-C-2099 |
(-)-(S)-B973B CAS:2244989-34-0 |
(-)-(S)-B-973B is a potent allosteric agonist and positive allosteric modulator of α7 nAChR,with antinociceptive activity. |
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R-C-2297 |
Cilnidipine (FRC-8653) CAS:132203-70-4 |
Cilnidipine(FRC-8653)is a calcium channel blocker.Cilnidipine is the novel calcium antagonist accompanied with L-type and N-type calcium channel blocking function.It was approved in 1995.Compared with other calcium antagonists,cilnidipine can act on the N-type calcium channel that existing sympathetic nerve end besides acting on L-type calcium channel that similar to most of the calcium antagonists. |
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