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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC1775 | Dibromo-morin |
Morin derivative, enhancing neural glyoxalase pathway (GP) activity and preventing methylglyoxal-mediated oxidative stress (OS) in an AD model
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| DCC1774 | Diazoline |
Histamine H1-receptor antagonist
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| DCC1773 | Diazaborine |
Novel Inhibitor of the AAA-ATPase Drg1, blocking ribosome biogenesis
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| DCC1772 | Dianicline |
Selective alpha4beta2 nAChR partial agonist for the treatment of nicotine dependence to assist in smoking cessation
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| DCC1771 | Diafluo |
Novel probe for protein S-sulfinylation from cells
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| DCC1770 | Diabzi Sting Agonist-3 |
Novel potent and selective STING agonist, activating secretion of IFNβ, IL-6, TNF, and KC/GROα, exhibiting durable anti-tumour effects
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| DCC1769 | Diabzi Sting Agonist |
Novel STING agonist with enhanced binding to STING and cellular function, displaying strong anti-tumour activity
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| DCC1768 | Di-1859 |
Novel potent, selective and covalent inhibitor of DCN1, selectively inhibiting neddylation of cullin 3 in cells
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| DCC1767 | Dhpm-93 |
The most potent inhibitor of sodium iodide symporter (NIS) reported to date
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| DCC1766 | Dhpcc-9 |
Novel Pim kinase inhibitor
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| DCC1765 | Dha-37 |
Novel inducer of autophagic cell death through upregulation of HMGB1 in A549 cells
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| DCC1764 | Dh20931 |
Novel growth inhibitor of both triple-positive and triple-negative human breast cancer cell lines
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| DCC1763 | Dgy-08-097 |
Novel HCV NS3 degrader, reducing susceptibility to resistance mutations, potently inhibiting HCV in a cellular infection model, exhibiting the most potent degradation (DC50 of 50nM at 4h) of HCV NS3,
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| DCC1762 | Dgts(16:0/16:0) |
Abundant lipid in the membranes of many algae, lower plants, and fungi, showing an inverse concentration relationship with phosphatidylcholine, being capable of replacing phosphatidylcholine
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| DCC1761 | Dgj-pfpht |
Novel human α-galactosidase A ligand, capable of stabilizing α-Gal A and restoring trafficking
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| DCC1760 | Dg-c8-phip |
The major adduct formed by the food-borne carcinogen, PhIP with DNA
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| DCC1759 | dgat2 Inhibitor 122 |
Selective inhibitor of diacylglycerol acyltransferase 2 (DGAT2)
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| DCC1758 | Dg-051 |
Novel potent, orally active inhibitor of LTA4H
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| DCC1757 | Dfkbp-2 |
Proteolysis targeting chimeras (PROTAC), potently decreasing FKBP12 abundance in MV4;11 cells, leading to over 80% reduction of FKBP12 at 0.1 μM and 50% reduction at 0.01 μM
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| DCC1756 | Dfk167 |
Cell-permeable, reversible and selective inhibitor of ɣ-secretase
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| DCC1755 | Df-461 |
Potent Squalene Synthase Inhibitor
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| DCC1754 | Df-1012 |
5-HT3 Receptor antagonist; Antitussive; Anti-inflammatory; Antiasthmatic
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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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