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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC2099 | Ffa2-agonist-1 |
Selective orthosteric agonist of human FFA2
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| DCC2098 | Ferulin C |
Natural potent colchicine site binding microtubule-destabilizing agent with anti-proliferation and anti-metastasis activity via PAK1 and p21-mediated signaling in breast cancer cells
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| DCC2097 | Ferroxamine B |
Iron chelator, mediating iron transport in Streptomyces pilosus
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| DCC2096 | Ferroptosis Inducer |
Novel ferroptosis inducer, killing selected cancer cell lines by harnessing reactive oxygen species (ROS)
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| DCC2095 | Ferric Maltol |
Novel oral iron therapy agent, being effective in correcting iron deficiency anemia in patients with inflammatory bowel disease
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| DCC2094 | Fenspiride Hydrochloride |
Non-steroidal antiinflammatory agent
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| DCC2093 | Fenoprofen Calcium Dihydrate |
Non-steroidal anti-inflammatory drug, being used for symptomatic relief for rheumatoid arthritis, osteoarthritis, and mild to moderate pain
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| DCC2092 | Fenobam |
Potent, selective, noncompetitive glutamate mGluR5 receptor antagonist
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| DCC2091 | Feiii-ppix Ligand-18 |
Novel potent antimalarial agent, binding to ferriprotoporphyrin-IX (FeIII-PPIX) (Kd = 33 nM) against chloroquine-resistant and sensitive strains of Plasmodium falciparum
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| DCC2090 | Fc-rapa |
Novel rapamycin derivative, targeting polycystic kidneys due to the high expression of the folate receptor (FRα), lacking the extra-renal effects of unconjugated rapamycin, in particular immunosuppressive effects
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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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