| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC2105 | Fgfr4 Inhibitor 5a | Novel potent and selective covalent inhibitor of FGFR4 kinase |
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| DCC2106 | Fgfr4 Inhibitor 7v | Novel highly selective covalent inhibitor of wild-type and gatekeeper mutant FGFR4, exhibiting excellent potency against FGFR4, FGFR4V550L, and FGFR4V550M with nanomolar activity in both the biochemical and cellular assays while sparing FGFR1/2/3 |
|
| DCC2107 | Fgfr4 Inhibitor F-30 | Novel potent and selective FGFR4 inhibitor, covalently binding to FGFR4 protein |
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| DCC2108 | Fgfr-in-21 | Novel potentl and selective covalent FGFR inhibitor, inhibiting proliferation of FGFR-amplified cancer cell lines with low nM IC50 values |
|
| DCC2109 | Fh1024 Tfa Salt | Novel regulator of transcription factor PU.1-DNA binding interactions, acting as a weak agonist that recruits PU.1 to DNA |
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| DCC2110 | Fh535-n | Novel inhibitor of the Wnt/β-catenin transcriptional activity, demonstrating significant increased rate of apoptosis in Huh7 and PLC/PRF |
|
| DCC2111 | Fhu-779 | Novel light-regulated diltiazem derivative, photoswitching LTCC in pancreatic β cells, cardiomyocytes and mouse hearts |
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| DCC2112 | Fibroblast Growth Factor (1-10) | Fibroblast growth factor fragment |
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| DCC2113 | Fibronectin Adhesion-promoting Peptide | Potent macrophage activator, enhancing interleukin 12-dependent interferon gamma production by lipopolysaccharide-stimulated mouse splenocytes, exerting an antiviral action against HSV-1 with the independent pathways of IFN-alpha |
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| DCC2114 | Fibronectin Cs1 Peptide | Cell-adhesive octapeptide as the authentic sequence within intact fibronectin, mediating OSCC cell spreading, migration, and invasion, regulating IL-17A levels and mechanical allodynia after peripheral nerve injury |
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| DCC2115 | Finafloxacin Hydrochloride | Antibacterial agent, expressing enhanced activity at acidic pH |
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| DCC2116 | Fischerin | Natural potent cytotoxic agent |
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| DCC2117 | Fitc-sulfono-γ-aa Peptide | Fluorescent protein-protein interaction (PPI) inhibitor |
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| DCC2118 | Fk1012-a | Highly potent membrane-permeable ligand of the immunophilin FKBP12, creating a new composite FKBP12-FK506 surface and inactivating calcineurin, a Ca calmodulin-dependent protein phosphatase |
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| DCC2119 | Fk-3657 | Novel non-peptide bradykinin (BK)-B2 receptor antagonist |
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| DCC2120 | Fkbp12-in-q2 | Novel Inhibitor of FKBP12 |
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| DCC2121 | Flaviviruses-inhibitor-i | Specific inhibitor of several viruses belonging to the family of flaviviridae |
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| DCC2122 | Flemingin A | Natural anticancer and antioxidant |
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| DCC2123 | Flg249 | Novel, potent, orally active, and nonsteroidal farnesoid X receptor (FXR) antagonist with propensity for accumulation and responsiveness in ileum |
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| DCC2124 | fli-28 | Novel inhibitor of general secretion in early stage; FLI-06 analogue twice as active as FLI-06 |
|
| DCC2125 | Flll11 | Curcumin analogue, exhibiting enhanced growth-suppressive activity and inhibiting AKT and signal transducer and activator of transcription 3 phosphorylation in breast and prostate cancer cells |
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| DCC2126 | Flll12 | Curcumin analogue, exhibiting enhanced growth-suppressive activity and inhibiting AKT and signal transducer and activator of transcription 3 phosphorylation in breast and prostate cancer cells |
|
| DCC2127 | flll62 | Inhibitor of STAT3 phosphorylation and apoptotic promoter of human renal cell carcinoma and melanoma cell lines |
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| DCC2128 | Flortanidazole | Tumour hypoxia probe |
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| DCC2129 | Flt3 Inhibitor 17 | Novel FLT3 inhibitor, displaying potent inhibitory activity against the FLT3-ITD mutant (IC 50 = 0.8 nM) and good selectivity over c-KIT kinase (over 500-fold), selectively inhibiting the proliferation of FLT3-ITD-positive AML cell lines MV4-11 (IC 50 = 2 |
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| DCC2130 | Flt3 Inhibitor Iv | Novel potent ATP-competitive inhibitor of Flt3 |
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| DCC2131 | Flt3-in-50 | Novel selective and efficacious inhibitor of FLT3 mutations |
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| DCC2132 | fluacrypyrim | Novel STAT3 activation inhibitor, induces cell cycle arrest and apoptosis in cancer cells harboring constitutively-active STAT3 |
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| DCC2133 | Flubendiamide | The first phthalic acid diamide insecticide, impairs neuronal calcium signalling in the honey bees antennae |
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| DCC2134 | flu-dnb | Novel photolabile NO donor |
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