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Other Targets

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Cat. No. Product Name Field of Application Chemical Structure
DCAPI1591 FEBUXOSTAT Featured FEBUXOSTAT is an inhibitor xanthine oxidase and xanthine dehydrogenase
DC5099 Felbamate Featured Felbamate (Felbatol) is an anticonvulsant drug used in the treatment of epilepsy.
DC9105 Felodipine Felodipine is a long-acting 1,4-dihydropyridine calcium channel blocker.
DC20382 FEN1-IN-1 FEN1-IN-1 is a potent, selective Flap Endonuclease-1 (FEN1) inhibitor with IC50 of 11 nM.
DC20383 FEN1-IN-C20 FEN1-IN-C20 is an N‐hydroxyl urea derivative that specifically inhibits flap endonuclease 1 (FEN1) activity with IC50 of 3 nM.
DCAPI1181 Fenbendazole (Panacur) Fenbendazole (Panacur)
DC9065 Fenofibric acid Fenofibric acid is a lipid regulating agent available as delayed release capsules for oral administration.
DC9424 Fenoldopam (mesylate) Featured Fenoldopam(SKF 82526) mesylate is a drug and synthetic benzazepine derivative which acts as a selective D1 receptor partial agonist.
DCAPI1157 Fenoprofen calcium Fenoprofen calcium
DC8684 Fenoxaprop-P-ethyl Featured Fenoxaprop-P-ethyl is a post-emergent phenoxy herbicide of the aryloxyphenoxy propionate group.
DCAPI1326 Fenticonazole nitrate Fenticonazole nitrate
DC12246 Feretoside Feretoside, a phenolic compound extracted from the barks of E. ulmoides, is a HSP inducer which act as cytoprotective agent.
DC20102 Ferulic acid methyl ester Featured Ferulic acid methyl ester (Methyl ferulate) is a derivative of ferulic acid, isolated from Stemona tuberosa, with anti-inflammatory and antioxidant properties. Ferulic acid methyl ester is a cell membrane and brain permeable compound, shows free radical s
DC23516 Fesoterodine Fesoterodine (PF-00695838) is a competitive muscarinic receptor antagonist with muscle relaxant and urinary antispasmodic properties.
DC23515 Fesoterodine maleate Fesoterodine (PF-00695838) is a competitive muscarinic receptor antagonist with muscle relaxant and urinary antispasmodic properties.
DC7811 Fexinidazole Featured Fexinidazole is a new Oral Nitroimidazole Drug Candidate Entering Clinical Development for the Treatment of Sleeping Sickness
DC21010 FF-10501-01 FF-10501-01 is a potent, selective and orally available IMPDH inhibitor.
DC10973 FF-10502 FF-10502 (FF-10502-01) is a pyrimidine nucleoside antimetabolite that shows growth inhibition of pancreatic cancer cell lines with IC50 of 60-330 nM.
DC23627 FFN-206 dihydrochloride FFN-206 is an excellent VMAT2 (vesicular monoamine transporter 2) substrate capable of detecting VMAT2 activity in intact cells using fluorescence microscopy, with subcellular localization to VMAT2-expressing acidic compartments without apparent labeling
DC21012 FGI-103 FGI-103 is a small-molecule inhibitor of filovirus that exhibits potent antiviral activity against of EBOV (EC90=330 nM, ZEBOV) and MARV (EC50=2.5 uM, MARV-Ci67).
DC21013 FGI-104 FGI-104 is a small-molecule inhibitor of filovirus that exhibits potent antiviral activity against of EBOV (EC90=330 nM, ZEBOV) and MARV (EC50=2.5 uM, MARV-Ci67).
DC7637 FH1(BRD-K4477) Featured FH1 (BRD-K4477) is a small molecule, which promotes differentiation of iPS-derived hepatocytes.
DC20384 Fhit-IN-15 Fhit-IN-15 is a potent, competitive, reversible inhibitor of the enzymatic activity of tumor suppressor Fhit with IC50 of 49 nM, shows cytotoxicity in HEK293T cells..
DC20385 FICZ Featured FICZ is a high affinity aryl hydrocarbon receptor (AhR) agonist with Kd of 70 pM.
DC21673 Fidarestat Fidarestat (SNK860) is a potent aldose reductase inhibitor, improves motor nerve conduction velocity (MNCV) and metabolic abnormalities in sciatic nerve were investigated in acute STZ-induced diabetic rats..
DC21817 Filaminast Filaminast (WAY-PDA-641.
DC21482 Filibuvir Filibuvir (PF-00868554.
DC9349 Fimasartan Featured Fimasartan(BR-A-657) is a non-peptide angiotensin II receptor antagonist used for the treatment of hypertension and heart failure.
DC11432 FimH inhibitor 5h FimH inhibitor 5h is a potent and orally active FimH inhibitor.
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.

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