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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC2135 | Flufenacet |
Herbicide, inhibiting very-long-chain fatty acid elongase (VLCFAE) synthesis
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| DCC2134 | flu-dnb |
Novel photolabile NO donor
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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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| DCC2132 | fluacrypyrim |
Novel STAT3 activation inhibitor, induces cell cycle arrest and apoptosis in cancer cells harboring constitutively-active STAT3
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| DCC2131 | Flt3-in-50 |
Novel selective and efficacious inhibitor of FLT3 mutations
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| DCC2130 | Flt3 Inhibitor Iv |
Novel potent ATP-competitive inhibitor of Flt3
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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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| DCC2128 | Flortanidazole |
Tumour hypoxia probe
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| DCC2127 | flll62 |
Inhibitor of STAT3 phosphorylation and apoptotic promoter of human renal cell carcinoma and melanoma cell lines
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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
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| 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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| DCC2124 | fli-28 |
Novel inhibitor of general secretion in early stage; FLI-06 analogue twice as active as FLI-06
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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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| DCC2122 | Flemingin A |
Natural anticancer and antioxidant
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| DCC2121 | Flaviviruses-inhibitor-i |
Specific inhibitor of several viruses belonging to the family of flaviviridae
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| DCC2120 | Fkbp12-in-q2 |
Novel Inhibitor of FKBP12
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| DCC2119 | Fk-3657 |
Novel non-peptide bradykinin (BK)-B2 receptor antagonist
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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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| DCC2117 | Fitc-sulfono-γ-aa Peptide |
Fluorescent protein-protein interaction (PPI) inhibitor
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| DCC2116 | Fischerin |
Natural potent cytotoxic agent
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| DCC2115 | Finafloxacin Hydrochloride |
Antibacterial agent, expressing enhanced activity at acidic pH
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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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| 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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| DCC2112 | Fibroblast Growth Factor (1-10) |
Fibroblast growth factor fragment
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| DCC2111 | Fhu-779 |
Novel light-regulated diltiazem derivative, photoswitching LTCC in pancreatic β cells, cardiomyocytes and mouse hearts
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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
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| 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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| DCC2108 | Fgfr-in-21 |
Novel potentl and selective covalent FGFR inhibitor, inhibiting proliferation of FGFR-amplified cancer cell lines with low nM IC50 values
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| DCC2107 | Fgfr4 Inhibitor F-30 |
Novel potent and selective FGFR4 inhibitor, covalently binding to FGFR4 protein
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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
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