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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC0878 | Bam Complex Inhibitor 2 |
Novel BAM complex inhibitor, interferring with BamA-related processes and affect folding and insertion of OMPs
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| DCC0877 | Bam Complex Inhibitor 14 |
Novel BAM complex inhibitor, interferring with BamA-related processes and affect folding and insertion of OMPs
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| DCC0876 | Balofloxacin Hydrate |
Antibacterial; Antimicrobial; Inhibitor of DNA gyrase and intracellular accumulation of quinolones
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| DCC0875 | Balanol |
Potent ATP-competitive inhibitor of Protein Kinase C (PKC) and Protein Kinase A (PKA)
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| DCC0874 | Bal101553 Dihydrochloride |
Novel microtubule inhibitor as the prodrug of BAL27862, activating spindle assembly checkpoint, exerting antiproliferative effects and dose-dependent vascular disruption
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| DCC0873 | Bak2-66 |
Selective Dopamine D3 Receptor Antagonist
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| DCC0872 | Bag-1 Inhibitor Thio-2 |
Novel inhibitor of BAG-1-mediated protein interactions, targeting the RAF-MEK-ERK signaling pathway, transformed cells
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| DCC0871 | Baclmk |
Allosteric Inhibitor of the NS2B-NS3 Protease from Dengue Virus
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| DCC0870 | Bace1-in-cpd C |
Novel potent nonbrain-penetrant BACE1 inhibitor
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| DCC0869 | Baa485 |
Novel activator of Pyrin inflammasome
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| DCC0868 | Ba-53038b |
Novel HBV core protein allosteric modulator (CpAM), bing to the HAP pocket and modulating HBV capsid assembly in a distinct manner
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| DCC0867 | B07 Hydrochloride |
Novel CCR5 antagonist-based HIV-1 entry inhibitor
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| DCC0866 | Az-vem |
Novel chimeric inhibitor of dimeric RAF, inhibiting B-Raf V600E mutan
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| DCC0865 | Azumamide E |
Natural potent HDAC inhibitor
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| DCC0864 | Az-pfkfb3-26 |
Potent and selective PFKFB3 inhibitor
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| DCC0863 | Azorosi-4 |
Novel photoswitchable agonist for peroxisome proliferator-activated receptor γ (PPARγ)
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| DCC0862 | Azolig 9 |
Novel photoswitchable ligand for the cannabinoid receptor 2 (CB2)
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| DCC0861 | Azogw1929 |
Novel photoswitchable agonist for peroxisome proliferator-activated receptor γ (PPARγ)
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| DCC0860 | Azocholine |
Excellent photoswitchable agonist for neuronal α7 nAChRs
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| DCC0859 | Azithromycin Monohydrate |
Macrolide antibiotic, binding to the 50S subunit of the bacterial ribosome and thus inhibiting translation of mRNA
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| DCC0858 | Azido-tpp1 |
Mitochondria-luciferin releasing agent, reacting with mitochondria-activatable luciferin (MAL-Probe), such as TPP-CL2, to release luciferin
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| DCC0856 | Az-ghs-38 |
Novel CNS penetrant potent inverse agonist of GHS-R1a (IC 50 (affinity) = 0.77 nM)
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| DCC0855 | Azelastine |
Potent, second-generation, selective histamine-H1-receptor antagonist and mast cell stabilizer
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| DCC0854 | Az-dyrk1b-33 |
Potent and selective ATP-competitive Dyrk1B kinase inhibitor
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| DCC0853 | Azd9742 |
Antimicrobials, active against methicillin resistant S. aureus (MRSA)
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| DCC0852 | Azd7254 |
Novel potent smoothened inhibitor, demonstrating in vivo activity in abrogating the Hh paracrine pathway as well as anti- tumor effects
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| DCC0851 | Azd6703 |
Novel, potent and selective inhibitor of p38α MAP kinase
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| DCC0850 | Azd6642 |
Novel selective inhibitor of 5-Lipoxygenase Activating Protein (FLAP) for the treatment of inflammatory diseases
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| DCC0849 | Azd6564 |
Novel Fibrinolysis Inhibitor, Acting via Interference of a Protein-Protein Interaction
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| DCC0848 | Azd6370 |
Glucokinase activator, decreasing fasting and postprandial glucose in type 2 diabetes mellitus patients
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