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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC0207 | 3,4-dcqame |
Natural inhibitor of respiratory syncytial virus entry and infection by blocking the interaction of the viral fusion protein with the cell membrane.
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| DCC0206 | 3,4,5-tri-cqa |
Inhibitor of Beta_amyloid>amyloid β-mediated cellular toxicity
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| DCC0205 | 3',3'-c-di(2'f,2'damp) |
Novel STING Agonist
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| DCC0204 | 3,3'-biplumbagin |
Novel, active, and less toxic anti-tuberculosis (anti-TB) agent
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| DCC0203 | 3,3',4,4',5,5'-hms |
Novel pro-angiogenic agent, potently promoting proliferation, migration, invasion and tube formation of human umbilical vein VECs (HUVECs) in vitro
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| DCC0202 | 2r,4r-apdc |
Highly selective and relatively potent group II metabotropic glutamate receptor agonist
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| DCC0201 | 2ppg-fk-acrha |
Novel double photocaged cathepsin B activity-based probe for monitoring the light-activation by the blue fluorescence of 7-diethylamino-4-hydroxymethyl-coumarin (DEACM) and simultaneously probe the activity of cathepsin B through the green fluorescence of
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| DCC0200 | 2-oxaadamantane 22 |
Novel inhibitor of soluble epoxide hydrolase (sEH), showing good solubility, microsomal stability, and selectivity for sEH
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| DCC0199 | 2-oh-5-f-dppro |
Novel inhibitor of thioredoxin reductase (TrxR)
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| DCC0198 | 2-o-acetylcorosolic Acid |
Antiatherosclerotic, antihyperlipidemic, antiinflammatory, antifungal, antiviral and antineoplastic
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| DCC0197 | 2-mc-1,4-nhq |
Inhibitor of the Cdc42-PBD interaction, blocking the association of Cdc42 with the PBD
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| DCC0196 | 2-iodoestradiol |
Potent human sex hormone binding globulin (SHBG) ligand
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| DCC0195 | 2-hydroxyethyl-sp600125 |
Potent and selective JNK inhibitor; Analogue of SP600125 with improved potency and selectivity
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| DCC0194 | 2-hexylthio-β,γ-ch2-atp |
Non-hydrolyzable ATP analog, acting as an effective and selective NTPDase2 inhibitor
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| DCC0192 | 2-ethoxystypandrone |
Novel potent natural STAT3 signaling inhibitor from Polygonum cuspidatum, inhibiting cell growth and inducing apoptosis of HCC cells and HCC Cancer stem cells.
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| DCC0191 | 2'-deoxy-adpr |
Endogenous superagonist of transient receptor potential melastatin 2 (TRPM2)
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| DCC0190 | 2-cldg |
Inhibitor of cellular glycosylation; Analytical standard
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| DCC0189 | 2-cl-8-ma-camp |
Site BI- selective synergistic activator of PKA I
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| DCC0188 | 2ccpa Sodium |
Lipid mediator, regulates neuronal apoptosis in traumatic brain injury (TBI)
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| DCC0187 | 2-bispeb |
Metabotropic Glutamate Receptor 5-selective Negative Allosteric Modulator
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| DCC0186 | 2b182c |
Novel potent activator of both human and mouse TLR4-NF-κB reporter cells and primary cells, inducing serum anti-HA and anti-NA IgG1 levels
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| DCC0185 | 2-ampp |
Novel GPR88 Agonist
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| DCC0184 | 27-caua |
Novel selective inhibitor of EGFR kinase, leading to inactivation of PI3K/AKT/mTOR and Ras-Raf-MEK-ERK signal pathways
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| DCC0183 | 24(s)-saringosterol |
Novel Selective LXRβ Agonist
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| DCC0182 | 24(s),25-epoxycholesterol |
Oxysterol agonist of the liver X receptor
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| DCC0181 | 2,5-2f-kbz |
Novel Versatile Probe for Interrogating Histone Benzoylation and Interactions in Living Cells
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| DCC0180 | 2,4-dichloroamphetamine Hcl |
Stimulator of the central nervous system, decreasing the 5-hydroxytryptamine (5-HT) and 5-hydroxyindoleacetic acid (5-HIAA) levels in brain
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| DCC0179 | 2,4-bis(p-hydroxyphenyl)-2-butenal |
Concentration- and time-dependent inhibitor of the growth of NSCLC cells inducing apoptosis
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| DCC0178 | 2,3-dmb-pp1 |
Inhibitor of SykM442A S505A ASKA- (analog-sensitive kinase alleles) mediated cellular calcium flux
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| DCC0177 | 2',3'-dihydroxypuberulin |
Natural Inhibitor for FcεRI expression on mast cell from Verbasucum thapsus L
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