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