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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC2189 | Furaltadone Hydrochloride |
Anti-bacterial metabolite of Nitrofuran
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| DCC2188 | Fur-2-oyl-leu-gly-nh2 |
Highly potent dopamine D2 modulator
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| DCC2187 | Fumitremorgin C |
Chemosensitizing agent, selectively reversing BCRP-mediated multidrug resistance to mitoxantrone, doxorubicin, and topotecan
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| DCC2186 | Fumarprotocetraric Acid |
Natural antimicrobial agent, showing neuroprotective, expectorant, and antioxidant activities
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| DCC2185 | Fumaropimaric Acid |
Direct inhibitor of the p53 transactivation domain from binding to replication protein A
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| DCC2184 | Fty720-mitoxy |
FTY720 analog as novel stimulator of the activity of the protein phosphatase 2A (PP2A), targeting mitochondria
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| DCC2183 | Fty720-c2 |
FTY720 analog as novel potent stimulator of the activity of the protein phosphatase 2A (PP2A)
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| DCC2182 | Ftsz Probe (r)-5 |
Novel specific high-affinity fluorescent probe for FtsZ antibacterial inhibitor
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| DCC2181 | Fto-04 |
Novel fat mass- and obesity-associated protein (FTO) inhibitor, preventing neurosphere formation in patient-derived glioblastoma stem cells (GSCs) without inhibiting the growth of healthy neural stem cell-derived neurospheres
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| DCC2180 | Fti-277 Tfa Salt |
Farnesyltransferase inhibitor, inhibiting both H- and K-Ras oncogenic signaling
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| DCC2179 | Fti-2628 |
Novel inhibitor of protein farnesyltransferase (FT), inhibiting the growth of P. falciparum in red blood cells and suppressing parasitemia
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| DCC2178 | Ftbu-1 |
Novel Anabolic Selective Androgen Receptor Modulator (SARM)
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| DCC2177 | Fs-694 |
Novel highly potent and selective inhibitor (type 1.5 binding mode) of MAPK14 [IC50 = 0.2 nM (ELISA, cell free); KD = 1.5 nM (DiscoverX)]
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| DCC2176 | Fs2921 |
Novel N-Methyl-d-aspartate receptor (NMDAR) positive allosteric modulator (PAM) with potential antidepressant effects
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| DCC2175 | Fropofol |
Potent ligand for a protein site governed largely by van der Waals interactions, producing excitatory activity in tadpoles and mice; also antagonizing propofol-induced hypnosis
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| DCC2174 | Frf-01-116 |
Novel Potent and Selective Covalent Inhibitor of KRAS G12C
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| DCC2173 | Fr194921 |
Potent, selective, and orally active antagonist for central adenosine A1 receptors
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| DCC2172 | Fr-190997 |
Novel Nonpeptide Bradykinin B2-Receptor Partial Agonist
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| DCC2171 | Fr-190809 |
Potent and nonadrenotoxic ACAT inhibitor
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| DCC2170 | Fr181877 |
Nonprostanoid PGI2 agonist
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| DCC2169 | Fr171456 |
Natural specific inhibitor of mammalian NSDHL and yeast Erg26p, inhibiting an artificial Hepatitis C viral replicon, and showung broad antifungal activity
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| DCC2168 | Fr-139317 |
Selective ET(A) receptor antagonist
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| DCC2167 | Fpr-agonist-17b |
Novel agonist of the formyl peptide receptor (FPR), protecting against myocardial ischaemia-reperfusion injury in mice
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| DCC2166 | Fotyr-amp |
Novel NO-donating antimicrobial peptide, exhibiting Staphylococcus aureus and Escherichia coli biofilm dispersion and eradication, and potent antibacterial activities in vitro
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| DCC2165 | Fotocaine |
Novel Photochromic Ion Channel Blocker
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| DCC2164 | Fotagliptin Benzoate |
Novel Dipeptidyl Peptidase-4 (DPP-4) Inhibitor
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| DCC2163 | Fotagliptin |
Novel dipeptidyl peptidase IV (DPP4) inhibitor
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| DCC2162 | Fosmidomycin |
Natural antibiotic, acting as an inhibitor of DOXP reductoisomerase
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| DCC2161 | Formyl Lenalidomide |
Impurity of Lenalidomide
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| DCC2160 | Fomocaine |
Local anaesthetic agent, blocking voltage-gated Na(+) currents in neurons
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