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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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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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| DCC2159 | Folate-ms99 |
Novel ALK PROTAC, being capable of degrading ALK in a folate receptor-dependent manner in cancer cells
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| DCC2158 | Folate-arv-771 |
Novel BRD PROTAC, being capable of degrading BRDs in a folate receptor-dependent manner in cancer cells
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| DCC2157 | Fol7185 |
Inhibitor of IspD and IspE enzymes isolated from bacteria
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| DCC2156 | Fnir-tag-co2h |
Novel fluorescent near-infrared (NIR) linker for building brighter labeled biomolecules, exhibiting no evidence of H-aggregation even at high labeling density when appended to monoclonal antibodies or virus-like particles
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| DCC2155 | Fndr-20081 |
First in class anti-tubercular agent against sensitive and drug-resistant Mycobacterium tuberculosis (Mtb)
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| DCC2154 | Fnd-4b |
Novel AMPK activator, inhibiting growth and induces apoptosis in colon cancer and increasing apoptosis in triple negative and estrogen-receptor positive breast cancers
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| DCC2153 | Fmp-401319-3 |
Novel concentration-dependent inhibitor of CRF1R-pPL cotranslational translocation at the level of the Sec61 complex
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| DCC2152 | Fmf-04-159-r |
Novel potent dual CDK14 and CDK16 inhibitor
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| DCC2151 | Fmf-02-063-1 |
Novel potent and selective Dual inhibitor of PI3K-δ and PI3K-γ
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| DCC2150 | Fmf-01-086-2 |
Novel highly selective inhibitor of Aurora kinases A, B and C, with potent cellular activity and minimal off-target activity (PLK4)
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| DCC2149 | Fm-743 |
Negative control for Skepinone-L
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| DCC2148 | Fm-476 |
Negative control for FM-381
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| DCC2147 | Fm4-64 |
Fluorescent probe for monitoring synaptic activity at neuromuscular junctions
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| DCC2146 | Flutonidine |
alpha2-Adrenergic receptor agonist
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| DCC2145 | Flutazolam |
Benzodiazepine with sedative, muscle relaxant, anticonvulsant, and anxiolytic activities
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