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Cat. No.	Product Name	Field of Application
DC23501	Finazine	Finazine is a high-affinity, brain penetrant sigma-1 and sigma 2 receptor ligand with Ki of 2.6 nM and 46 nM, respectively.
DC12637	Finerenone Featured	Finerenone (BAY 94-8862) is a third-generation, selective, and orally available nonsteroidal mineralocorticoid receptor (MR) antagonist (IC50=18 nM). Finerenone displays excellent selectivity versus glucocorticoid receptor (GR), androgen receptor (AR), and progesterone receptor (>500-fold). Finerenone has the potential for cardiorenal diseases research, such as type 2 diabetes mellitus and chronic kidney disease.
DC8936	Fingolimod	Fingolimod(FTY720 free base) is a S1P antagonist with IC50 of 0.033 nM.
DC11309	Fipronil	Fipronil is an insecticide that acts as a selective antagonist of insect GABA receptors (IC50s = 30 and 1,600 nM for cockroach and rat receptors, respectively).
DC8200	Firategrast(SB-683699) Featured	Firategrast is an orally bioavailable alpha4 beta1/alpha4 beta7 integrin antagonist designed to reduce trafficking of lymphocytes into the central nervous system (CNS).
DC8917	Firocoxib	Firocoxib(ML 1785713) is a potent and selective cyclooxygenase (COX)-2 inhibitor with IC50 of 0.13 uM, 58 fold sensitivity for COX2 VSCOX1.
DC21015	FIT-039 Featured	FIT-039 is a potent, selective CDK9 inhibitor with IC50 of 5.8 uM for CKD9/cyclin T1, suppresses the replication of HSV-1 (IC50=0.69 uM).
DC9845	FITM Featured	FITM is a nove mGlu1 inhibitor. FITM shows high affinity (Ki = 2.5 nM, fig. S2) and selectivity for mGlu1 over mGlu5.
DC20386	Pioglitazone Featured	Pioglitazone is a potent and selective PPARγ agonist with high affinity binding to the PPARγ ligand-binding domain with EC50 of 0.93 and 0.99 μM for human and mouse PPARγ, respectively.
DC21016	FJ 5002	FJ 5002 is a potent telomerase inhibitor with IC50 of 2 uM, a close derivative of MKT077.
DC7112	FK 3311 Featured	FK 3311 is a selective inhibitor of COX-2; antiinflammatory agent.
DC22093	FKGK18	FKGK18 (FKGK18) is a potent, selective inhibitor of iPLA2 (group VIA Ca2+-independent phospholipase A2) with IC50 of 50 nM.
DC10845	FL-411 Featured	FL-411 is a selective BRD4 inhibitor.
DC20019	Flagelin 22(TFA) (Flagellin 22(TFA))	Flagelin 22 TFA, a fragment of bacterial flagellin, is an effective elicitor in both plants and algae.
DC10972	Flavokawain B	Flavokawain B is a natural chalcone that can induce apoptosis in androgen receptor-negative, hormone-refractory prostate cancer cell lines (IC50=3-50 uM), via up-regulation of death-receptor 5 and Bim expression.
DC2014	Flavopiridol Featured	Flavopiridol competes with ATP to inhibit CDKs including CDK1, CDK2, CDK4 and CDK6 with IC50 of ~ 40 nM, and CDK7 with IC50 of 300 nM.
DC8780	Flavopiridol Hydrochloride Featured	Flavopiridol hydrochloride competes with ATP to inhibit CDKs including CDK1, CDK2, CDK4 and CDK6 with IC50 of ~ 40 nM. It is 7.5-fold more selective for CDK1/2/4/6 than CDK7. Flavopiridol is initially found to inhibit EGFR and PKA.
DC11414	Flavoxate Hydrochloride Featured	Flavoxate Hydrochloride(DW-61 Hydrochloride) is a muscarinic AChR antagonist used in various urinary syndromes and as an antispasmodic.
DC9623	Flecainide (acetate) Featured	Flecainide(Tambocor) is a class 1C antiarrhythmic drug especially used for the management of supraventricular arrhythmia; works by blocking the Nav1.5 sodium channel in the heart, causing prolongation of the cardiac action potential.
DCAPI1347	Fleroxacin (Quinodis)	Fleroxacin (Quinodis)
DC7415	FLI-06 Featured	FLI-06 is a novel potent and selective small molecule intercepting Notch signaling and the early secretory pathway (EC50 ~2.3 μM).
DC9321	Flibanserin Featured	Flibanserin is a novel multifunctional serotonin agonist and antagonist (MSAA) that improves sexual functioning in premenopausal women who suffer from reduced sexual interest and desire.
DC8726	FLLL31 Featured	FLLK31 is a potent and selective inhibitor of the STAT3 signaling pathway.
DC7751	FLLL32 Featured	FLLL32, a novel curcumin analogue, is a potent STAT3 inhibitor.
DC8164	Gilteritinib(ASP2215) Featured	FLT3/AXL inhibitor
DC8230	FLT3-IN-1(SKLB4771) Featured	FLT3-IN-1(SKLB4771) is a novel potent and selective Flt3 inhibitor with IC50 of 10 nM; against FLT3-ITD-expressing MV4-11 cells with IC50 of 6 nM.
DC11780	FLT3-IN-5e	FLT3-IN-5e is a nove potent, selective FLT3 inhibitor with Kd of 3.6 nM, IC50 of <6 nM.
DC9060	Flubendazole	Flubendazole is a potent broad spectrum anthelmintic.
DCAPI1375	Fluconazole	Fluconazole
DCAPI1108	Flucytosine (Ancobon)	Flucytosine (5-Fluorocytosine, 5-FC, Ancobon) is an antifungal drug with IC50 of 0.12 μg/mL in C.albicans.

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