Cat. No. | Product Name | Field of Application | Chemical Structure |
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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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