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Catalog	name	Description	price
R-C-1713	SGC 707 CAS:1687736-54-4	SGC 707 is a potent allosteric inhibitor of PRMT3(IC50=50 nM)with >100-fold selectivity over other methyltransferases and other non-epigenetic targets.	price>
R-R-3413	Vortioxetine-d8 CAS No.2140316-62-5	Vortioxetine-d8/CAS No.2140316-62-5 is a deuterium labeled Vortioxetine. Vortioxetine is an inhibitor of 5-HT1A, 5-HT1B, 5-HT3A, 5-HT7 receptor and SERT, with Ki values of 15 nM, 33 nM, 3.7 nM, 19 nM and 1.6 nM, respectively.	price>
R-C-1714	BGP-15 CAS:66611-37-8	BGP-15 is a PARP inhibitor,that can protect against heart failure and atrial fibrillation in mice.	price>
R-R-3414	Isopteropodine CAS No.5171-37-9	Isopteropodine/CAS No.5171-37-9 is heteroyohimbine-type oxindole alkaloid components of Uncaria tomentosa (Willd.) DC. Isopteropodine acts as positive modulators of muscarinic M1 and 5-HT2 receptors.	price>
R-C-1715	CNX774 CAS:1202759-32-7	CNX-774 is an orally active,irreversible and selective BTK inhibitor,with an IC50 of <1nM.CNX-774 specifically targets Cysteine 481 of Btk for covalent modification.	price>
R-R-3415	Anpirtoline hydrochloride CAS No.99201-87-3	Anpirtoline hydrochloride/CAS No.99201-87-3 is a hydrochloride of anpirtoline. Anpirtoline is a agonist of 5-HT1B.	price>
R-C-1716	Telaglenastat (CB-839) CAS:1439399-58-2	Telaglenastat(CB-839)is a potent,selective,and orally bioavailable glutaminase inhibitor with IC50 of 24nM for recombinant human GAC.CB-839(Telaglenastat)inudces autophagy and has antitumor activity.	price>
R-R-3416	Lurasidone-d8 CAS No.1132654-54-6	Lurasidone-d8/CAS No.1132654-54-6 is deuterium labeled Lurasidone. Lurasidone (SM-13496) is an antagonist of both dopamine D2 and 5-HT7 with IC50s of 1.68 and 0.495 nM, respectively. Lurasidone (SM-13496) is also a partial agonist of 5-HT1A receptor with an IC50 of 6.75 nM.	price>
R-C-1717	DDR1-IN-1 CAS:1449685-96-4	DDR1-IN-1 is a potent and selective discoidin domain receptor 1(DDR1)receptor tyrosine kinase inhibitor with IC50 of 105 nM,about 3-fold selectivity over DDR2.	price>
R-R-3417	Loxapine-d8 CAS No.1189455-63-7	Loxapine-d8/CAS No.1189455-63-7 is the deuterium labeled Loxapine.	price>
R-C-1718	Remodelin CAS:949912-58-7	Remodelin is an inhibitor of N-acetyltransferase 10(NAT10),which acetylates both histones and microtubules.Remodelin improves nuclear architecture,chromatin organization,and survival of both cells lacking lamin A and cells from patients with progeria.	price>
R-R-3418	(S)-Renzapride	(S)-Renzapride ((S)-BRL 24924) is the isomer of HY-14147 Renzapride. Renzapride is a 5-HT4 receptor agonist with a Ki value of 115 nM. Renzapride also is a 5HT2b and 5HT3 receptor antagonist. Renzapride can be used for constipation predominant irritable bowel syndrome (C-IBS) study.	price>
R-C-1719	AZD5153 6-Hydroxy-2-naphthoic acid CAS:1869912-40-2	AZD-5153 6-hydroxy-2-naphthoic acid (HNT salt)is a potent,selective,and orally available BET/BRD4 bromodomain inhibitor with pKi of 8.3 for BRD4.AZD-5153 inhibits the expression of Nuclear receptor binding SET domain protein 3 (NSD3)target genes.NSD3,via H3K36me2, acts as an epigenetic deregulator to facilitate the expression of oncogenesis-promoting genes.	price>
R-R-3419	Cyclobenzaprine-d3 hydrochloride CAS No.1184983-42-3	Cyclobenzaprine-d3 (hydrochloride)/CAS No.1184983-42-3 is the deuterium labeled Cyclobenzaprine hydrochloride. Cyclobenzaprine hydrochloride (MK130 hydrochloride) is a skeletal muscle relaxant and a central nervous system (CNS) depressant.	price>
R-C-1720	AZD0156 CAS:1821428-35-6	AZD0156 is a potent and selective inhibitors of ATM kinase,with potential chemo-/radio-snsitizing and antineoplastic activities.AZD0156 prevents DNA damage checkpoint activation,disrupts DNA damage repair,induces tumor cell apoptosis,and leads to cell death of ATM-overexpressing tumor cells.	price>
R-R-3420	LY 344864 S-enantiomer CAS No.186544-27-4	LY 344864 S-enantiomer/CAS No.186544-27-4 is the S-enantiomer of LY344864. LY344864 is a 5-HT1F receptor agonist.	price>
R-C-1721	ISCK03 CAS:945526-43-2	ISCK03(N-(4-imidazol-1-yl phenyl)sulfonamide)is a cell-permeable inhibitor of stem-cell factor(SCF)/c-kit signaling.ISCK03 inhibits SCF-induced c-c-kit phosphorylation and downstream ERK phosphorylation.	price>
R-R-3421	Perphenazine-d4 CAS No.155593-75-2	Perphenazine-d4/CAS No.155593-75-2 is the deuterium labeled Perphenazine. Perphenazine is a typical antipsychotic agent, inhibits 5-HT2Areceptor, Alpha-1A adrenergic receptor, Dopamine receptor D2/D3, D2L receptor, and Histamine H1 receptor, with Ki values of 5.6, 10, 0.765/0.13, 3.4, and 8 nM, respectively.	price>
R-C-1722	PD-166866 CAS:192705-79-6	PD166866 is a FGFR1 inhibitor with IC50 value of 55 nM,and no effect on c-Src, PDGFR-b,EGFR or insulin receptor tyrosine kinases or MEK,PKC,and CDK4.	price>
R-R-3422	3-Hydroxy agomelatine-d3 CAS No.1079774-23-4	3-Hydroxy agomelatine-d3/CAS No.1079774-23-4 is a deuterium labeled 3-Hydroxy agomelatine. 3-Hydroxy agomelatine is a 5-HT2C receptor antagonist with an IC50 of 3.2 μM and a Ki of 1.8 μM.	price>

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