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Cat. No.	Product Name	Field of Application
DC22963	Org-9935	A potent, selective PDE3 inhibitor with IC50 of 50 nM. More description
DC22577	Revizinone	A potent, selective PDE3 inhibitor with IC50 of 36 nM, displays >20,000-fold selectivity over PDE1.. More description
DC23213	SCIO-469	A potent, selective p38α MAPK inhibitor with IC50 of 9 nM. More description
DC11849	DSM421	A potent, selective P. falciparum dihydroorotate dehydrogenase (PfDHODH) with IC50 of 53 nM. More description
DC22951	RN-9893	A potent, selective orally-bioavailable TRPV4 antagonist with IC50 of 320, 420 and 660 nM for mouse, human and rat TRPV4 channels, respectively. More description
DC22947	RN-9893 hydrochloride	A potent, selective orally-bioavailable TRPV4 antagonist with IC50 of 320, 420 and 660 nM for mouse, human and rat TRPV4 channels, respectively. More description
DC22672	SB-612111 hydrochloride	A potent, selective opiate receptor-like orphan receptor (ORL-1, NOP) antagonist with Ki of 0.33 nM. More description
DC22726	SB 290157	A potent, selective nonpeptide antagonist of anaphylatoxin C3a receptor (C3aR) with IC50 of 200 nM. More description
DC20771	Faldaprevir	A potent, selective noncovalent competitive inhibitor of HCV NS3/4A protease with Ki of 2.6 and 2.0 nM for GT1a and 1b NS3-NS4A protease, respectively. More description
DC24163	XEN-907	A potent, selective NaV1.7 blocker with IC50 of 3 nM. More description
DC11630	ND-378	A potent, selective MMP-2 inhibitor with Ki of 230 nM. More description
DC22921	AMN 082	A potent, selective mGluR7 allosteric agonist that inhibits forskolin-stimulated cAMP accumulation in mGluR7b CHO cells with EC50 of 64±32 nM. More description
DC22710	LY3020371 hydrochloride	A potent, selective metabotropic glutamate 2/3 receptor (mGlu2/3) antagonist with Ki of 5.3 and 2.5 nM, respectively. More description
DC26072	BMS 819881	A potent, selective melanin concentrating hormone receptor 1 (MCHR1) inhibitor with Ki of 10.4 nM. More description
DC20722	AZD-1979	A potent, selective melanin concentrating hormone receptor 1 (MCH-R1) antagonist with binding Ki of 12.2 nM. More description
DC24026	LPA2-IN-1	A potent, selective LPA2 (EDG4) antagonist with IC50 of 17 nM. More description
DC22859	LIMK-IN-22j	A potent, selective LIMK inhibitor with IC50 of 3.2 nM and 1.2 nM for LIMK1 and LIMK2, respectively. More description
DC22858	LIMK-IN-14	A potent, selective LIMK inhibitor with IC50 of 0.9 nM and 0.5 nM and 1.2 nM for LIMK1 and LIMK2, respectively. More description
DC22677	(±)-U-50488 hydrochloride	A potent, selective kappa-opioid receptor agonist with no μ-opioid antagonist effects. More description
DC23550	PF-05387252	A potent, selective IRAK4 inhibitor with IC50 of 1.3 nM, 200-fold selectivity over IRAK1 (IC50=290 nM). More description
DC23551	PF-05388169	A potent, selective IRAK4 inhibitor with IC50 of 0.094 nM, >500-fold selectivity over IRAK1 (IC50=65 nM). More description
DC22754	SKA-111	A potent, selective intermediate-conductance KCa3.1 positive-gating modulator with EC50 of 111 nM. More description
DC11967	PF-06649298	A potent, selective inhibitor of the Na+/citrate transporter NaCT (SLC13A5) that shows inhibition of citrate uptake in the HEKNaCT cells with IC50 of 0.41 uM. More description
DC23910	Microcystin-LR	A potent, selective inhibitor of protein phosphatase 2A (PP2A) with IC50 of 0.04 nM. More description
DC22658	Windorphen	A potent, selective inhibitor of p300 histone acetyltransferase (IC50=4.2 uM). More description
DC22847	L-870810	A potent, selective inhibitor of HIV integrase (IC50=8-15 nM) with potent antiviral activity in cell culture and good pharmacokinetic properties. More description
DC22897	KRH-1636	A potent, selective inhibitor of CXCR4 with IC50 of 13 nM, has no effect on CXCR1, CCR3, CCR4, or CCR5. More description
DC11700	Chalcone 4 hydrate	A potent, selective inhibitor of CXCL12 binding to CXCR4 and CXCR7 with IC50 of 200 nM. More description
DC11644	Pitstop 1	A potent, selective inhibitor of clathrin-independent endocytosis with IC50 of 18 uM (inhibition of clathrin TD-amphiphysin B/C complex formation). More description
DC20345	CLK inhibitor 2	A potent, selective inhibitor of cdc2-like kinase CLK1 and CLK2 with IC50 of 1.1 and 2.4 nM, respectively. More description

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