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Cat. No. Product Name Field of Application Chemical Structure
DCC5578 Ym-90k
Novel AMPA receptor antagonist
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DCC5577 ym-298198 Dihydrochloride
Potent and selective mGLu1 antagonist
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DCC5575 ym-201627
Selective growth inhibitor of endothelial cells
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DCC5574 Ym-17690
Novel non-analogous leukotriene agonist
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DCC5573 Ylt205
Novel Inducer of Apoptosis in Human Colorectal Cells via Mitochondrial Apoptosis Pathway, Inhibiting Tumor Growth
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DCC5572 Ylt192
Novel, Orally Active Bioavailable Inhibitor of VEGFR2 Signaling with Potent Antiangiogenic Activity and Antitumor Efficacy
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DCC5571 Ykl-05-093
Novel salt inducible kinase (SIK) inhibitor, increasing bone formation and bone mass
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DCC5570 Yk-5-252
Novel dual action combretastatin A-4 (CA-4) prodrug, releasing CA-4 through a disulfide bond cleavage mechanism and containing a near-infrared (NIR) fluorophore
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DCC5569 Yh-gka
Novel glucokinase activator, significantlt decreasing in blood glucose levels with no adverse effects on serum lipids or body weight
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DCC5568 Yh18968
Novel GPR119 Agonist, improving glucose tolerance and augmenting the glucose lowering effect as well as the plasma level of active GLP-1 in normal mice in combination treatment with a dipeptidyl peptidase 4 (DPP-4) inhibitor
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DCC5567 Ycw-e11
Novel Inhibitor of Antiapoptotic Bcl-2 Family Proteins
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DCC5566 Yak037
Tamoxifen-analog that Suppresses Glial L-Glutamate Transport Activity without Interaction with Estrogen_receptor>Estrogen Receptors
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DCC5565 Y-39983 Dihydrochloride
Selective Rho-associated kinase (ROCK) inhibitor
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DCC5564 Y2-antagonist-2
Novel, selective, soluble non-​peptidic NPY Y2 receptor antagonist with enhanced CNS exposure
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DCC5563 Y2 Antagonist 36
Novel non-peptidic highly potent, soluble and selective NPY Y2 antagonist
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DCC5562 Y08624
Novel TRIM24/BRPF1 dual inhibitor with IC 50 values of 0.98 and 1.16 μM, respectively
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DCC5561 Xylarianaphthol-1
Novel activator of p21 promoter in a p53-independent manner
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DCC5560 Xylariamide A
Carbonic anhydrase inhibitor; Fungal metabolite
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DCC5559 Xstax-vhll
Novel selective β-catenin degrader
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DCC5558 Xr9051 Hydrochloride
Potent modulator of P-glycoprotein-mediated multidrug resistance (MDR), inhibiting the binding of cytotoxics to P-glycoprotein
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DCC5557 Xl-418
Novel Akt1/2 inhibitor
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DCC5556 Xl-147
Novel Potent Pan-Filovirus Inhibitor, showing potent inhibition against infectious EBOV Zaire (0.09 μM) and MARV (0.64 μM)
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DCC5555 Xl-13n
Novel dual inhibitor of AF9 and ENL YEATS domains
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DCC5554 Xist Ligand X1
Novel non-coding RNA prototype Xist ligand, specifically binding the RepA motif of Xist, reducing the conformational space of RepA, displacing cognate interacting protein factors (PRC2 and SPEN), suppressing histone H3K27 trimethylation, and blocking init
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DCC5553 Xie18-6
Novel INK4C inhibitor, specifically blocking the bioactivity of p18 protein and promoting human and murine hematopoietic stem cell ex vivo expansion
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DCC5552 Xen103
Potent and Selective Stearoyl-CoA Desaturase-1 Inhibitor
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DCC5551 xc-409
Novel PKM2 activator
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DCC5550 XAX-162
Quantity (mg or Unit) Unit Price ($/mg or $/Unit) Final Price 100 $26.55 Total: $2,655.00 50 $30.68 Total: $1,534.00 25 $35.99 Total: $899.75 10 $42.48 Total: $424.80 5 $50.15 Total: $250.75
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DCC5549 Xantholipin B
Novel antibiotic, showing 3- to 10-fold greater cytotoxicity than Xantholipin against a select panel of human cancer cell lines, demonstrating powerful antimicrobial activity against both Gram-positive bacteria and fungi
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DCC5548 Xantholipin
Antibiotic, exhibiting strong antibacterial activities and showing potent cytotoxicity, inhibiting HSP47 gene expression produced by Streptomyces sp
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