欢迎来到CSNpharm!产品仅用于科研!

400-920-2911 sales@csnpharm.cn

0

Neurological Disease

货号 产品名 CAS号 信息
CSN22437 JNJ-46778212 1363281-27-9 JNJ-46778212 is an mGlu5 positive allosteric modulator with an EC50 of 260 nM.
CSN22348 AP521 151227-08-6 AP521 is an agonist of human 5-HT1A receptor with an IC50 of 94 nM.
CSN22374 CI-943 89239-35-0 CI-943 is a potential antipsychotic agent.
CSN22450 Lurasidone Metabolite 14283 HCl 186204-32-0 Lurasidone Metabolite 14283 HCl is a major active metabolite of Lurasidone. Lurasidone is a FDA approved drug for the treatment of schizophrenia.
CSN22415 Glutaminyl Cyclase Inhibitor 1 2110449-60-8 Glutaminyl Cyclase Inhibitor 1 is a glutaminyl cyclase inhibitor with an IC50 of 0.5 μM.
CSN22241 NBQX 118876-58-7 NBQX is a potent, selective and competitive AMPAR antagonist, which shows activity of neuroprotective and anticonvulsant.
CSN22445 L-APB 23052-81-5 L-APB is a potent and specific agonist for the group III mGluRs, with EC50s of 0.13±0.02, 0.29±0.07, 1.0±0.3, 249±107 μM for mGlu4, mGlu8, mGlu6 and mGlu7 receptors, respectively.
CSN22913 MMPEP 823198-78-3 MPEP HCl is both a selective non-competitive mGlu5 receptor antagonist with IC50 value of 36 nM, and a mGlu4 receptor positive allosteric modulator.
CSN22503 Saredutant 142001-63-6 Saredutant is a selective NK2 receptor antagonist.
CSN22190 5-HT4 Antagonist 1 261766-73-8 5-HT4 antagonist 1 is a 5-HT4 receptor antagonist with a pKi of 9.6.
CSN22192 AR-A 2 220051-79-6 AR-A 2 is a selective 5-HT1B receptor antagonist, with high affinity to guinea pig cortex 5HT1B/1D and recombinant guinea pig 5-HT1B receptors (Ki=0.24 and 0.47 nM) and with 10-fold lower affinity to guinea pig 5-HT1D receptor (Ki=5 nM), and shows an EC50 of 4.5 nM for the guinea pig 5-HT1B receptor; AR-A 2 can be used in the research of depression and anxiety.
CSN22197 CX157 205187-53-7 CX-157 is a reversible inhibitor of monoamine oxidase-A (MAO-A) with an EC50 of 19.3 ng/mL.
CSN22187 W-2429 37795-69-0 W-2429 is a non-narcotic analgesic agent.
CSN22242 Antihistamine-1 1186430-60-3 Antihistamine-1 is a H1-antihistamine (Ki=6.9 nM) with acceptable blood-brain barrier penetration and also an inhibitor of CYP2D6 and hERG channel with IC50s of 5.4 and 0.8 μM, respectively.
CSN22216 NS1652 1566-81-0 NS1652 is a reversible anion conductance inhibitor, blocks chloride channel, with an IC50 of 1.6 μM in human and mouse red blood cells.
CSN22325 (+)-Phenserine 116839-68-0 Posiphen is a selective cholinesterase noncompetitive inhibitor with an IC50 of 45.3 μM.
CSN22373 CGRP Antagonist 1 1123757-49-2 CGRP antagonist 1 is a highly potent CGRP receptor antagonist with a Ki and IC50 of 35 and 57 nM, respectively.
CSN22331 5-HT7 Agonist 1 334974-31-1 5-HT7 agonist 1 is a selective 5-HT7 receptor agonist, with an IC50 of 222.93 nM, can be used for the 5-HT7 receptor related disease, such as CNS disorders.
CSN22323 (+)-Dihydrexidine HCl 158704-02-0 (+)-Dihydrexidine HCl is a dopamine D1 receptor agonist with an EC50 of 72± 21 nM.
CSN22403 Fonadelpar 515138-06-4 Fonadelpar is a PPARδ agonist, used in the research of neuroparalytic keratopathy.
CSN22396 Eplivanserin 130579-75-8 Eplivanserin is a potent, selective and orally available 5-HT2 receptor antagonist, with an IC50 of 5.8 nM in rat cortical membrane, and a Kd of 1.14 nM.
CSN22475 ORL1 Antagonist 1 1174985-59-1 ORL1 antagonist 1 is an opioid receptor-like 1 (ORL1) antagonist with an IC50 of 61 nM.
CSN22469 MSOP 66515-29-5 MSOP is a selective group III metabotropic glutamate receptor antagonist with apparent KD of 51 μM for the L-AP4-sensitive presynaptic mGluR.
CSN22538 β-Secretase Inhibitor IV 797035-11-1 β-Secretase Inhibitor IV is a potent, cell-active BACE-1 inhibitor with IC50s of 15.6 and 16.3nM under BACE-1 concentrations of 2 nM and 100 pM, respectively.
CSN23242 Cyromazin 66215-27-8 Cyromazine is a triazine insecticide and an acaricide.
<< PREV 1 2 3 4 5 6 7 8 9 NEXT >>
联系
我们