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Cat. No. Product Name Field of Application Chemical Structure
DCC5527 Wn1316
Unique neuroprotectant against oxidative injury, being a highly promising remedy for the treatment of amyotrophic lateral sclerosis (ALS)
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DCC5526 Wms-2539
Potent uncompetitive NMDA receptor antagonist
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DCC5525 Wms-1410
Novel GluN2B-specific NMDAR antagonist, completely preventing the decrease in insulin secretion of about 32 % provoked by a 24-h-treatment with NMDA/glycine, eliminating NMDA-induced changes in the oxidation status of the islet cells and elevating the sen
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DCC5524 Wjd008
Novel potent dual inhibitor of phosphatidylinositol 3-kinase (PI3K)/mammalian target of rapamycin (mTOR), preventing PI3K signaling and inhibiting the proliferation of transformed cells with oncogenic PI3K mutant
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DCC5523 Wj35435
Novel dual inhibitor of histone deacetylase and topoisomerase I
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DCC5522 Withangulatin A
Natural potent antitumoragent, targeting sarco/endoplasmic reticulum calcium-ATPase (SERCA)2
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DCC5521 Win-64338
B2 bradykinin receptor antagonist
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DCC5520 Win-35428
Dopamine reuptake inhibitor, also having some SERT affinity
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DCC5519 Whz-04
Novel Anti-malarial Plasmodium-Selective Proteasome Inhibitor
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DCC5518 Wfq-228
Novel fluoroquinolone antibiotic with potent antimicrobial activity, showing the potential to overcome major drug resistance; its antimicrobial activity was less affected by both pump-mediated efflux and QRDR mutations in P. aeruginosa compared with LVX a
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DCC5517 Wen05-03
Novel inhibitor of type III secretion system ATPase EscN from enteropathogenic Eecherichia coli
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DCC5516 Web2347
Novel very potent and long acting hetrazepinoic PAF-antagonist
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DCC5515 We-14 Tfa Salt
Highly conserved neuropeptide derived from Chromogranin A (Parathyroid Secretory Protein 1)
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DCC5514 Wck5153
Novel Inhibitor of PBP2, Showing Potent β-Lactam Enhancer Activity against Pseudomonas aeruginosa, Including Multidrug-Resistant Metallo-β-Lactamase-Producing High-Risk Clones
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DCC5513 Wb4-24
Non-peptide GLP-1 receptor agonist, blocking inflammatory nociception by stimulating β-endorphin release from spinal microglia
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DCC5512 Wb-308
Novel inhibitor of The epidermal growth factor receptor (EGFR), decreasing NSCLC cell proliferation and colony formation, by causing G2/M arrest and apoptosis.
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DCC5511 Way-316606 Hydrochloride
Secreted frizzled-related protein-1 (sFRP-1) modulaitor
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DCC5510 Way-260022
Potent and Selective Inhibitor of the Norepinephrine Transporter
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DCC5509 Way-171230
Inhibitor of matrix metalloproteinase-1 (MMP-1)
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DCC5508 Way-170523
Potent and selective inhibitor of matrix metalloprotease MMP-13 (Collagenase-3)
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DCC5507 Way-151693
Inhibitor of human collagenase-3 (MMP-13)
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DCC5506 way-133537
ATP-sensitive potassium channel opener
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DCC5505 Way-123783
SGLT2 inhibitor
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DCC5504 Way103
Very late adhesion molecule 4 (VLA-4) antagonist, inhibiting VLA-4/VCAM-1 ligation as a means of modulating eosinophil functions beyond its action on cell adhesion and migration
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DCC5503 Wallichoside
Nocel inhibitor of BMI1 promoter activity, decreasing BMI1 protein levels in HCT116 human colon carcinoma cells, significantly reducing levels of the CSC biomarker epithelial cell adhesion molecule and diminishing the self-renewal capability of CSCs
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DCC5502 waladin1
Mixed competitive/noncompetitive inhibitor of
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DCC5501 w-5 Hydrochloride
Calmodulin antagonist, inhibiting Ca2+/calmodulin-regulated enzyme activities
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DCC5499 Vzmc013
Novel Probe of Putative MOR-CCR5 Heterodimers to Inhibit Opioid Exacerbated HIV-1 Infectivity
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DCC5497 Vuf8504
Allosteric modulator of A3 adenosine receptors
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DCC5496 Vuf-8430
Potent histamine H4 receptor full agonist
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