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Catalog	name	Description	price
R-R-4402	Pramipexole-d5 dihydrochloride CAS No.1217601-58-5	Pramipexole-d5 (dihydrochloride)/CAS No.1217601-58-5 is deuterium labeled Pramipexole (dihydrochloride). Pramipexole dihydrochloride is a selective and blood-brain barrier (BBB) penetrant dopamine D2-type receptor agonist, with Kis of 2.2 nM, 3.9 nM, 0.5 nM and 1.3 nM for D2-type receptor, D2, D3 and D4 receptors, respectively.	price>
R-C-2703	Sephin1 CAS:951441-04-6	Sephin1 is a selective inhibitor of a holophosphatase.Sephin1 selectively bound and inhibited the stress-induced PPP1R15A,but not the related and constitutive PPP1R15B,to prolong the benefit of an adaptive phospho-signaling pathway, protecting cells from otherwise lethal protein misfolding stress.	price>
R-R-4403	Dopamine D2 receptor agonist-3 CAS No.1257326-24-1	Dopamine D2 receptor agonist-3 (compound 3)/CAS No.1257326-24-1 is a selective D2 receptor partial agonist and Dopamine D3 receptor antagonist (with pEC50 of 8.3 and <5.5 respectively).	price>
R-C-2704	Cercosporamide CAS：131436-22-1	Cercosporamide,an usnic amide,was originally identified in Cercosporidium henningsii as a host-selective phytotoxin and broad-spectrum antifungal agent and is a potent inhibitor of MAP-kinase interacting kinase-2(Mnk2;IC50=11 nM),JAK3(IC50=31),and Mnk1(IC50=116nM).	price>
R-R-4404	Ropinirole-d7 hydrochloride CAS No.1261396-31-9	Ropinirole-d7 (hydrochloride)/CAS No.1261396-31-9 is the deuterium labeled Ropinirole hydrochloride[1]. Ropinirole (SKF 101468) hydrochloride is an orally active, potent D3/D2 receptor agonist with a Ki of 29 nM for D2 receptor. Ropinirole hydrochloride has pEC50s of 7.4, 8.4 and 6.8 for hD2, hD3 and hD4 receptors, respectively. Ropinirole hydrochloride has no affinity for the D1 receptors.	price>
R-C-2705	EPZ004777 CAS：1338466-77-5	EPZ004777 is a potent,selective DOT1L inhibitor with IC50 of 0.4nM in a cell-free assay and demonstrates>1,200-fold selectivity for DOT1L over all other tested PMTs.EPZ004777 induces apoptosis.	price>
R-R-4405	(E/Z)-Chlorprothixene-d6 hydrochloride CAS No.1246832-91-6	(E/Z)-Chlorprothixene-d6 hydrochloride/CAS No.1246832-91-6 is the deuterium labeled (E/Z)-Chlorprothixene hydrochloride.	price>
R-C-2706	ML 228 CAS：1357171-62-0	ML228(CID-46742353)is a potent the Hypoxia Inducible Factor(HIF)pathway activator with EC50 of 1μM.ML228 potently activates HIF in vitro as well as its downstream target VEGF.	price>
R-R-4406	Fluphenazine-d8 dihydrochloride	Fluphenazine-d8 (dihydrochloride) is the deuterium labeled Fluphenazine dihydrochloride. Fluphenazine dihydrochloride is a phenothiazine-class D1DR and D2DR inhibitor; used to deliver Fluphenazine to biological systems in studies probing the effects and metabolic fates of this commonly used dopamine antagonist.	price>
R-C-2707	OG-L002 CAS:1357302-64-7	OG-L002 is a potent and highly selective LSD1 inhibitor with an IC50 of 0.02 μM.OG-L002 is a potent monoamine oxidases(MAO)inhibitor with IC50s of 1.38μM and 0.72μM for MAO-A and MAO-B,respectively.OG-L002 potently inhibits the expression of HSV IE genes.	price>
R-R-4407	Bromperidol hydrochloride CAS No.59453-24-6	Bromperidol (R-11333) hydrochloride/CAS No.59453-24-6 possesses antipsychotic activity, with a high affinity for central dopamine receptors D2. Bromperidol hydrochloride can kill Mycobacteria in a synergistic manner with Spectinomycin.	price>
R-C-2708	CBB1003 CAS:1379573-88-2	CBB1003 is a novel histone demethylase LSD1 inhibitor with IC50 of 10.54uM.	price>
R-R-4408	PG01037 dihydrochloride CAS No.675599-62-9	PG01037 (dihydrochloride)/CAS No.675599-62-9 is a potent and selective dopamine D3 receptor antagonist with a Ki of 0.7 nM.	price>
R-C-2709	CBB1007 CAS:1379573-92-8	CBB1007 is a cell-permeable amidino-guanidinium compound that acts as a potent,reversible and substrate competitive LSD1 selective inhibitor (IC50=5.27μM for hLSD1).	price>
R-R-4409	Cabergoline-d6 CAS No.2738376-76-4	Cabergoline-d6 is deuterium labeled Cabergoline. Cabergoline is an ergot derived-dopamine D2-like receptor agonist that has high affinity for D2, D3, and 5-HT2B receptors (Ki=0.7, 1.5, and 1.2, respectively).	price>
R-C-2710	YM 750 CAS:138046-43-2	YM-750 is a potent acyl-CoA:cholesterol acyltransferase(ACAT)inhibitor(IC50=0.18 μM).ACAT catalyzes the formation of cholesteryl esters from cholesterol and long-chain fatty-acyl-coenzyme A.	price>
R-R-4410	OS-3-106 CAS No.1580000-17-4	OS-3-106/CAS No.1580000-17-4 is a potent, BBB-penetrated and selective dopamine D3 receptor (D3R) agonist. OS-3-106 binds with high affinity (Ki = 0.2 nM) at the D3R. OS-3-106 can be used for psychoactivator addiction research.	price>
R-C-2711	GSK J5 CAS:1394854-51-3	Inactive isomer of GSK J4;also cell permeable ester derivative of the inactive control,GSK J2.	price>
R-R-4411	Clomipramine-d3 hydrochloride CAS No.1398065-86-5	Clomipramine-d3 (hydrochloride)/CAS No.1398065-86-5 is a deuterium labeled Clomipramine hydrochloride. Clomipramine hydrochloride is a serotonin transporter (SERT), norepinephrine transporter (NET) dopamine transporter (DAT) blocker with Ki of 0.14, 54 and 3 nM, respectively.	price>
R-C-2712	WZ4002 CAS:1213269-23-8	WZ4002 is a mutant selective EGFR inhibitor with IC50s of 2,8,3 and 2nM for EGFRL858R,EGFRL858R/T790M,EGFRE746-A750 and EGFRE746-A750/T790M,respectively.	price>

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