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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
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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