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Cat. No. Product Name Field of Application Chemical Structure
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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DCC0176 2,3-acbt 1p
Novel potent antiangiogenic agent, binding to VEGFR2, significantly reducing neovascularization in both ex vivo and in vivo angiogenic assays without affecting the proliferation of endothelial cells
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DCC0175 2,2'-dioh-5,5'-dif-dppen
Novel inhibitor of thioredoxin reductase (TrxR)
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DCC0174 1ß-hydroxy Vitamin D3
inactive isomeric impurity of Alphacalcidol
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DCC0173 1-nitro-2-phenylethane
The first organic NO2-containing molecule isolated from plants, stimulating the soluble guanylate cyclase-cGMP pathway
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DCC0172 1h-thieno[3,4-d]pyrimidine-2,4-dione
Building Block
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DCC0171 1h-thieno[3,2-d]pyrimidine-2,4-dione
Building Block
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DCC0170 1h-thieno[2,3-d]pyrimidine-2,4-dione
Building Block
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DCC0169 1-hex-glcnalk
Reporter molecule functionalized at the anomeric position, exhibiting robust labeling over background with negligible amounts of nonspecific chemical labeling in cell lysates
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DCC0168 1-hex-6azglcnac
Reporter molecule functionalized at the anomeric position, exhibiting robust labeling over background with negligible amounts of nonspecific chemical labeling in cell lysates
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DCC0167 1-deoxy-d-allulose
Strong growth inhibitor as an antimetabolite
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DCC0166 1-benzyl-i3c
Highly potent inhibitor of Wnt/βcatenin signaling in melanoma cells, coordinately inhibiting cell proliferation and disrupts expression of Microphthalmia Associated Transcription Factor isoform M, also inhibiting NEDD4-1
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DCC0165 18bioder
Novel Neuroprotective GSK-3β Inhibitor, highly selectively inhibiting HIV-1; The second generation derivative of 6BIO
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DCC0164 17β-hsd1 Inhibitor 1
Novel inhibitor of 17β-hydroxysteroid dehydrogenase type 1 (17β-HSD1), being highly selective over 17β-HSD2
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DCC0163 17ß-hsd2-in-24
Novel potent inhibitor of 17ß-hydroxysteroid dehydrogenase type 2 (17ß-HSD2)
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