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Cat. No. Product Name Field of Application Chemical Structure
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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