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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| 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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| DCC0847 | Azd5438-protac-8 |
First-in-class selective, partial CDK2 degrader against hearing loss and cancer, protecting against cisplatin ototoxicity and kainic acid excitotoxicity
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| DCC0846 | Azd4996 |
Novel potent and highly selective cathepsin K inhibitor for the treatment of osteoarthritis
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| DCC0845 | Azd4619 |
Novel peroxisome proliferator-activated receptor alpha (PPARalpha) agonist, inducing alanine aminotransferase-1 gene and protein expression in human, but not in rat hepatocytes
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| DCC0843 | Azd1386 |
Novel transient receptor potential vanilloid 1 (TRPV1) antagonist
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| DCC0842 | Azd0328 |
Selective alpha7 nicotinic receptor activator
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| DCC0841 | Azd Cxcr2 Antagonist |
Novel CXCR2 antagonist with 200 times improvement in solubility than AZD8309
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| DCC0840 | Aza-thip |
Novel selective GABA-C antagonist
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| DCC0839 | Azalanstat |
Inhibitor of hepatic cholesterol biosynthesis, inhibiting the cytochrome P450 enzyme lanosterol 14alpha-demethylase
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| DCC0838 | azadirone |
Inducer of Death Receptors and Sensitizer of Human Cancer Cells to TRAIL through a p53-Independent Mechanism
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| DCC0837 | aza-bodipy |
Near-IR probe for detecting conformational changes of Aβ1-42 soluble oligomers in vitro
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