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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC2089 | Fcpr16 |
Novel phosphodiesterase 4 (PDE4) inhibitor with little emetic potential, blocking MPP+ induced oxidative damage in SH-SY5Y cells and neurons via AMPK-dependent autophagy
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| DCC2088 | Fc11a-2 |
Specific inhibitor of inflammasome assembly, targeting the NLRP3 inflammasome by interfering with the proximity-induced autocleavage of procaspase-1
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| DCC2087 | Fc11409b |
Novel CAIX inhibitor, inhibiting breast cancer invasion and metastasis
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| DCC2086 | Fb-pmt |
Novel potent αvβ3 antagonist. reducing GBM tumor growth and viability by up to 98%
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| DCC2085 | Fba Inhibitor 2a11 |
First-in-class covalent allosteric inhibitor of fructose-1,6-bisphosphate aldolase (FBA) from Candida albicans (CaFBA)
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| DCC2084 | Fauc-346 |
Potent and selective dopamine D3 receptor partial agonist
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| DCC2083 | Fauc-312 |
Highly potent and selective dopamine D4 receptor agonist
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| DCC2082 | Fauc-3019 |
Dopamine D4 receptor antagonist
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| DCC2081 | Fauc150 |
Novel irreversible dopamine D2 receptor ligand, covalently binding the L94C mutant of the dopamine D2 receptor
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| DCC2080 | Fauc-113 |
Dopamine D4 receptor antagonist
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| DCC2079 | Fa-tlr7-54 |
Novel folate-targeted TLR7 agonist, selectively accumulating in profibrotic macrophages and suppressing fibrosis-inducing cytokine production, reprograming M2-like fibrosis-inducing macrophages into fibrosis-suppressing macrophages, resulting in dramatic
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| DCC2078 | Fasn-in-56 |
Novel fatty acid synthase (FASN)
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| DCC2077 | Fasn-in-41 |
Novel potent and specific fatty acid synthase (FASN) inhibitor
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| DCC2076 | Fasii-in-1 |
Novel inhibitor of C. difficile's FASII pathway
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| DCC2075 | Fa-s2-ms4048 |
Novel folate-caged pomalidomide-based anaplastic lymphoma kinase (ALK) PROTAC, effectively degrading ALK fusion proteins in cancer cells in a FOLR1-dependent manner
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| DCC2074 | Farnesylthiotriazole |
Stable and persistent PKC activator
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| DCC2073 | Farnesiferol C |
Inducer of apoptosis via regulation of L11 and c-Myc with combinational potential with anticancer drugs in non-small-cell lung cancers
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| DCC2072 | Fapl-s0456 |
Novel FAP-targeted NIR dye conjugate
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| DCC2071 | Fapl-fluorescein |
Novel FAP-targeted Fluorescein dye conjugate
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| DCC2070 | Fanetizole Mesylate |
Inhibitor of neutrophil superoxide production
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| DCC2069 | Famprofazone |
Nonsteroidal anti-inflammatory drug (NSAID)
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| DCC2068 | F-amidine |
Potent and bioavailable irreversible inactivator of PAD4
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| DCC2067 | Fam-deala-hyp-yipd |
Novel Fluorescent HIF-1α peptide
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| DCC2066 | Fak Degrader Fc-11 |
Novel highly potent FAK-targeting PROTAC degrader, showing a rapid and reversible FAK degradation
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| DCC2065 | Fak Blocker A18 |
Novel blocker of focal adhesion kinase (FAK) autophosphorylation
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| DCC2064 | Fai-40 |
Novel inhibitor of fungal fatty acid biosynthesis, demonstrating broad-spectrum activity against Candida auris and mucormycetes and retained the activity against azole-resistant candida isolates
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| DCC2063 | Fa-hp-ß-cyd |
Novel folate-appended 2-hydroxypropyl-ß-cyclodextrin (HP-ß-CyD), showing strong anti-leukemia and cell-binding activities, inhibiting the growth of FR-expressing cells, enterjng CML cells through endocytosis and inducing both apoptosis and autophagy via m
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| DCC2062 | Fa-gflg-sn38 |
Novel Folate Receptor Targeting and Cathepsin B-Sensitive Drug Delivery System for Selective Cancer Cell Death and Imaging, exhibited strong cytotoxicity against FR-overexpressing SK-Hep-1, HeLa, and Siha cells, with IC50 values of 2-3 μM, but had no effe
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| DCC2061 | Fagaronine Chloride |
Novel antileukaemic alkaloid; Inhibitor of reverse transcriptase activity of RNA-tumor viruses; Inhibitor of topoisomerase I
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| DCC2060 | Factor Viia Inhibitor 2 |
Novel factor VIIa inhibitor
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