DCAPI1591 |
FEBUXOSTAT
Featured
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FEBUXOSTAT is an inhibitor xanthine oxidase and xanthine dehydrogenase |
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DC5099 |
Felbamate
Featured
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Felbamate (Felbatol) is an anticonvulsant drug used in the treatment of epilepsy. |
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DC9105 |
Felodipine |
Felodipine is a long-acting 1,4-dihydropyridine calcium channel blocker. |
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DC20382 |
FEN1-IN-1 |
FEN1-IN-1 is a potent, selective Flap Endonuclease-1 (FEN1) inhibitor with IC50 of 11 nM. |
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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. |
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DCAPI1181 |
Fenbendazole (Panacur) |
Fenbendazole (Panacur) |
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DC9065 |
Fenofibric acid |
Fenofibric acid is a lipid regulating agent available as delayed release capsules for oral administration. |
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DC9424 |
Fenoldopam (mesylate)
Featured
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Fenoldopam(SKF 82526) mesylate is a drug and synthetic benzazepine derivative which acts as a selective D1 receptor partial agonist.
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DCAPI1157 |
Fenoprofen calcium |
Fenoprofen calcium |
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DC8684 |
Fenoxaprop-P-ethyl
Featured
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Fenoxaprop-P-ethyl is a post-emergent phenoxy herbicide of the aryloxyphenoxy propionate group. |
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DCAPI1326 |
Fenticonazole nitrate |
Fenticonazole nitrate |
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DC12246 |
Feretoside |
Feretoside, a phenolic compound extracted from the barks of E. ulmoides, is a HSP inducer which act as cytoprotective agent. |
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DC20102 |
Ferulic acid methyl ester
Featured
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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 |
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DC23516 |
Fesoterodine |
Fesoterodine (PF-00695838) is a competitive muscarinic receptor antagonist with muscle relaxant and urinary antispasmodic properties. |
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DC23515 |
Fesoterodine maleate |
Fesoterodine (PF-00695838) is a competitive muscarinic receptor antagonist with muscle relaxant and urinary antispasmodic properties. |
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DC7811 |
Fexinidazole
Featured
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Fexinidazole is a new Oral Nitroimidazole Drug Candidate Entering Clinical Development for the Treatment of Sleeping Sickness |
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DC21010 |
FF-10501-01 |
FF-10501-01 is a potent, selective and orally available IMPDH inhibitor. |
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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. |
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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 |
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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). |
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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). |
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DC7637 |
FH1(BRD-K4477)
Featured
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FH1 (BRD-K4477) is a small molecule, which promotes differentiation of iPS-derived hepatocytes. |
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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.. |
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DC20385 |
FICZ
Featured
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FICZ is a high affinity aryl hydrocarbon receptor (AhR) agonist with Kd of 70 pM. |
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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.. |
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DC21817 |
Filaminast |
Filaminast (WAY-PDA-641. |
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DC21482 |
Filibuvir |
Filibuvir (PF-00868554. |
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DC9349 |
Fimasartan
Featured
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Fimasartan(BR-A-657) is a non-peptide angiotensin II receptor antagonist used for the treatment of hypertension and heart failure.
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DC11432 |
FimH inhibitor 5h |
FimH inhibitor 5h is a potent and orally active FimH inhibitor. |
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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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