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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| 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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| DCC5495 | Vuf-6884 |
Full agonist of hH4R with ~300-fold selectivity over hH3R and hH2R, but showing potent inverse agonistic activity at hH1R
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| DCC5494 | Vuf5834 |
Novel full inverse agonist at CXCR3 N3.35A
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| DCC5493 | vuf5455 |
Adenosine A3 receptor (A3AR) allosteric modulator
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| DCC5492 | Vuf5391 |
H3R inverse agonist
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| DCC5491 | vuf5228 |
Histamine H3 receptor antagonist
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| DCC5490 | Vuf16620 |
Novel photoswitchable modulator of the CXCR3 chemokine receptor
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| DCC5489 | Vuf16216 |
Novel CXCR3 ligand, photoswitching from antagonism to agonism
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| DCC5488 | Vuf15888 |
Novel photoswitchable modulator of the CXCR3 chemokine receptor
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| DCC5487 | Vuf15259 |
Novel inhibitor of Hbp secretion, activating σE stress, impairing Hbp secretion and decreasing the abundance of OMPs, consistent with impaired BAM function
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| DCC5486 | Vuf14862 |
Novel robust and fatigue-resistant photoswitchable GPCR antagonist
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