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Novel inhibitors

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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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