To enhance service speed and avoid tariff delays, we've opened a US warehouse. All US orders ship directly from our US facility.
| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC5533 | Wp-871 Monohydrate |
Main active metabolite of tazanolast, inhibiting dose-dependently compound 48/80-induced histamine release from rat peritoneal mast cells
More description
|
|
| DCC5532 | Wp1193 |
Novel inhibitor of the JAK2/STAT3 pathway
More description
|
|
| DCC5531 | Wo-459 |
Novel GPR52 agonist, dose-dependently inducing elevation of intracellular cAMP in HEK293/GPR52 cells
More description
|
|
| DCC5530 | Wny0824 |
Novel dual BRD4 and PLK1 inhibitor (IC 50 values of 109 and 22 nM, respectively), showing strong antiproliferative activity against cancer cells
More description
|
|
| DCC5529 | Wnt/hh-in-1 |
Novel potent dual inhibitor of Wnt and hedgehog signalings, blocking porcupine and smoothened
More description
|
|
| DCC5528 | Wnk-in-3 |
Novel Allosteric WNK Kinase Inhibitor
More description
|
|
| DCC5527 | Wn1316 |
Unique neuroprotectant against oxidative injury, being a highly promising remedy for the treatment of amyotrophic lateral sclerosis (ALS)
More description
|
|
| DCC5526 | Wms-2539 |
Potent uncompetitive NMDA receptor antagonist
More description
|
|
| 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
More description
|
|
| 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
More description
|
|
| DCC5523 | Wj35435 |
Novel dual inhibitor of histone deacetylase and topoisomerase I
More description
|
|
| DCC5522 | Withangulatin A |
Natural potent antitumoragent, targeting sarco/endoplasmic reticulum calcium-ATPase (SERCA)2
More description
|
|
| DCC5521 | Win-64338 |
B2 bradykinin receptor antagonist
More description
|
|
| DCC5520 | Win-35428 |
Dopamine reuptake inhibitor, also having some SERT affinity
More description
|
|
| DCC5519 | Whz-04 |
Novel Anti-malarial Plasmodium-Selective Proteasome Inhibitor
More description
|
|
| 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
More description
|
|
| DCC5517 | Wen05-03 |
Novel inhibitor of type III secretion system ATPase EscN from enteropathogenic Eecherichia coli
More description
|
|
| DCC5516 | Web2347 |
Novel very potent and long acting hetrazepinoic PAF-antagonist
More description
|
|
| DCC5515 | We-14 Tfa Salt |
Highly conserved neuropeptide derived from Chromogranin A (Parathyroid Secretory Protein 1)
More description
|
|
| 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
More description
|
|
| DCC5513 | Wb4-24 |
Non-peptide GLP-1 receptor agonist, blocking inflammatory nociception by stimulating β-endorphin release from spinal microglia
More description
|
|
| 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.
More description
|
|
| DCC5511 | Way-316606 Hydrochloride |
Secreted frizzled-related protein-1 (sFRP-1) modulaitor
More description
|
|
| DCC5510 | Way-260022 |
Potent and Selective Inhibitor of the Norepinephrine Transporter
More description
|
|
| DCC5509 | Way-171230 |
Inhibitor of matrix metalloproteinase-1 (MMP-1)
More description
|
|
| DCC5508 | Way-170523 |
Potent and selective inhibitor of matrix metalloprotease MMP-13 (Collagenase-3)
More description
|
|
| DCC5507 | Way-151693 |
Inhibitor of human collagenase-3 (MMP-13)
More description
|
|
| DCC5506 | way-133537 |
ATP-sensitive potassium channel opener
More description
|
|
| DCC5505 | Way-123783 |
SGLT2 inhibitor
More description
|
|
| 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
More description
|
|