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Cat. No. Product Name Field of Application Chemical Structure
DCC5588 Yycg Inhibitor 62
Novel YycG inhibitor, significantly inhibited biofilm formation in static and dynamic conditions
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DCC5587 Yycg Inhibitor 16
Novel YycG inhibitor, inhibiting planktonic cells of E. faecalis, including the vancomycin- or linezolid-resistant strains
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DCC5586 Yw2065
Novel inhibitor of Wnt signaling by stabilizing Axin-1, a scaffolding protein that regulates proteasome degradation of β-catenin
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DCC5585 Yu2534342249
Novel γ-lactam pyrazolidinone, targeting penicillin-binding proteins (PBPs) and incorporating a siderophore moiety to facilitate uptake into the periplasm, being effective against multidrug-resistant gram-negative Bacilli
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DCC5584 Yt-146
Selective A 2A receptor agonist
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DCC5583 Ysy01a
Novel Proteasome Inhibitor, Enhancing Cisplatin Cytotoxicity in Cisplatin-Resistant Human Ovarian Cancer Cells, inducing cell cycle arrest on G2 phase in MCF-7 cells via ERα and PI3K/Akt pathways
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DCC5582 Yoyo-1
DNA-intercalating dye as sensitive amyloid probe
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DCC5581 Ynt-707
Novel potent orexin 1 receptor (OX1R) antagonist
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DCC5580 Ynt-1310
Water-soluble analog of YNT-707, acting as a potent orexin 1 receptor (OX1R) antagonist
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DCC5579 Yml220
Potent and selective microbicidal agent against wild type (wt) HIV-1, NNRTI-, NRTI-, PRI-resistant mutants
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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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