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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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