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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC1753 | Dezocine |
Natural modulator of mu-, delta-, and kappa-opioid receptors
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| DCC1752 | Dexmethylphenidate Hydrochloride |
Norepinephrine-dopamine reuptake inhibitor (NDRI)
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| DCC1751 | Dexloxiglumide |
Cholecystokinin antagonist, selective for the CCKA subtype
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| DCC1750 | Dexamethasone Beloxil |
Glucocorticoid, Anti-inflammatory Agent
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| DCC1749 | Dexamethasone 21-phosphate Disodium |
Pro-drug of dexamethasone, anti-inflammatory glucocorticoid, stimulating glutamine uptake in the cerebral cortex
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| DCC1748 | Desthiobiotin Polyethyleneoxide Iodoacetamide |
Cysteine reactive protein labeling agent
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| DCC1747 | Desmethyl-hd-800 |
PET precursor of preparing radiolabel [11C]HD-800, a high affinity brain penetrant PET tracer for imaging microtubules
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| DCC1746 | Desmethyldiazepam |
Primary metabolite of diazepam, binding to the GABA A receptor benzodiazepine modulatory site
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| DCC1745 | Desmethyl Mk-6884 |
Precursor for PET imaging 11C-radiolabeled MK-6884
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| DCC1744 | Desfluoro Ezetimibe |
Desfluoro impurity of Ezetimibe
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| DCC1743 | Deramciclane Fumarate |
Inhibitor of acetyl-CoA carboxylase (ACC), activating GPR40, inhibiting West Nile virus (WNV) infection and reducing the multiplication of Usutu virus (USUV), a WNV-related flavivirus
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| DCC1742 | Dequalinium Bromide |
HIV-1 fusion inhibitor, targeting the membrane-proximal external region of Env spikes, specifically inhibiting the HIV-1 envelope-mediated membrane fusion by blocking CD4-induced conformational changes
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| DCC1741 | Depmpo |
Most efficient spin trap for the in vitro and in vivo detection of O-, N-, S- and C-centered free radicals
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| DCC1740 | Deoxynybomycin |
Selective anti-tumor agent, inducing apoptosis and inhibiting topoisomerase I
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| DCC1739 | Deoxy-dalsir |
Novel selective and sensitive near-infrared fluorescent probe for visualization of endogenous nitric oxide in living cells and animals
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| DCC1738 | Deox B 7,4 |
Novel reversible microtubule inhibitor, increasing lysosomal V-ATPase activity and lysosome acidity
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| DCC1737 | Denv2-in-3 |
Novel selective inhibitor of the DENV2 protease, inhibiting flavivirus protease through targeted covalent modification of active site serine, contrary to an allosteric binding mechanism as previously described
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| DCC1736 | Denv2-in-2 |
Novel selective inhibitor of the DENV2 protease, inhibiting flavivirus protease through targeted covalent modification of active site serine, contrary to an allosteric binding mechanism as previously described
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| DCC1735 | Denv2-in-1 |
Novel selective inhibitor of the DENV2 protease, inhibiting flavivirus protease through targeted covalent modification of active site serine, contrary to an allosteric binding mechanism as previously described
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| DCC1734 | Denosomin |
Novel anti-Alzheimer's disease agent, ameliorates spinal cord injury via axonal growth associated with astrocyte-secreted vimentin
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| DCC1733 | Denaverine Hydrochloride |
Antispasmodic agent, improving the elasticity of the soft birth canal and regulating labor contractions
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| DCC1732 | Denagliptin Tosylate |
Selective DPP-IV Inhibitor
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| DCC1731 | Demethoxyviridin |
Potent inhibitor of PI3 kinases
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| DCC1730 | Delta-tocopherol |
Vitamin E variant, inhibiting prostate adenocarcinoma, lung tumorigenesis, promoting thermogenic gene expression via PGC-1α upregulation, preventing methylglyoxal-induced apoptosis by reducing ROS generation and inhibiting apoptotic signaling cascades
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| DCC1729 | Delcasertib |
Novel selective δ-protein kinase C inhibitor
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| DCC1728 | Dehydrorabelomycin |
Natural polyketide matabolite
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| DCC1727 | Degrader Bt1 |
Novel selective degrader of BCR-ABL over c-ABL in leukemia cancer cells
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| DCC1726 | Deferoxamine Hydrochloride |
Iron chelating agent, chelating iron from intra-lysosomal ferritin and hemosiderin forming ferrioxamine, a water-soluble chelate excreted by the kidneys and in the feces via the bile
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| DCC1725 | Deferasirox Ferrate(iii) Tripotassium Complex |
Deferasirox iron complex
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| DCC1724 | Debio-1452-nh3 |
Novel potent inhibitor of the enoyl-acyl carrier protein reductase FabI, reducing bacterial burden in mice and rescuing mice from lethal infections with clinical isolates of Acinetobacter baumannii, Klebsiella pneumoniae and E. coli
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