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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC4336 | Pyrithione Zinc |
Novel KMD5A inhibitor
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| DCC4335 | Pyridinone-14 |
Novel highly potent agonist of the apelin receptor (APJ) receptor (APJ cAMP EC50: human 0.023nM; rat 0.024nM; dog 0.030nM; monkey 0.080nM)
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| DCC4334 | Pyrenocine A |
Natural phytotoxin, inducing monopolar spindle formation and suppressing proliferation of cancer cells
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| DCC4333 | Pyrd-in-14 |
Novel inhibitor of the PyrD protein (a dihydroorotate dehydrogenase (DHODase) involved in pyrimidine biosynthesis), suppressing bacterial cytotoxicity, biofilm formation and antibiotic resistance
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| DCC4332 | pyranoxanthone 1 |
Novel inhibitor of p53-MDM2 interaction
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| DCC4331 | Pyochelin |
Bacterial siderophore, acting as an iron-chelating growth promoter for Pseudomonas aeruginosa
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| DCC4330 | Py-itc |
Novel suppressor of cancerous cell growth and proliferation
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| DCC4329 | Pyimdc |
Novel potent inhibitor of collagen prolyl-4-hydroxylases (CP4H)
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| DCC4328 | Pyclen |
Inhibitor of cell death induced by oxidative stress and inhibitor of AB1-40 aggregation induced by Cu2+ ion
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| DCC4327 | Pw0564 |
Novel selective FGF14:Nav1.6 PPI modulator
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| DCC4326 | Pvhgprt Inhibitor |
Novel Plasmodium vivax Hypoxanthine-Guanine Phosphoribosyltransferase Inhibitor
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| DCC4325 | Pvhd303 |
Novel potent anticancer agent, disturbing microtubule formation at the centrosomes and inhibiting the growth of tumors dose-dependently in the HCT116 human colon cancer xenograft model in vivo
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| DCC4324 | Pv1019 |
Novel potent and selective CHEK2>Chk2 inhibitor
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| DCC4323 | Pu-ws13b |
Novel Grp94-selective inhibitor PU-WS13 biotin probe
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| DCC4322 | Puupehenone |
Natural heat shock protein 90 (Hsp90) inhibitor, potentiating the echinocandin drug caspofungin in caspofungin-resistant fungal pathogens, blocking the induction of caspofungin-responding genes required for the adaptation to cell wall stress through the c
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| DCC4321 | Pumafentrine |
Dual inhibitor of PDE3 and PDE4
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| DCC4320 | Pu-h39 |
Novel specific Hsp90b1 inhibitor
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| DCC4319 | Pu-29f |
Hsp90α- and Hsp90ß-selective inhibitor
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| DCC4318 | Pu24fcl |
Novel specific inhibitor of tumor Hsp90
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| DCC4317 | Pu-20f |
Hsp90α- and Hsp90ß-selective inhibitor
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| DCC4316 | Ptzmes2b |
Novel thermally activated delayed fluorescence (TADF) molecule that exhibits high external quantum efficiency (EQE) in non-doped organic light-emitting diodes (OLEDs) at high luminescence
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| DCC4315 | Ptpmt1-in-1 |
Novel PTEN-like mitochondrial phosphatase PTPMT1 inhibitor
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| DCC4314 | Ptp1b-in-18k |
Novel non-competitive potent and selective inhibitor of protein tyrosine phosphatase 1B (PTP1B)
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| DCC4313 | Pto-41 |
Novel NIR fluorescent probe for the detection of Aβ oligomers
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| DCC4312 | Ptk-sma1 |
Unique promoter of SMN2 exon 7 splicing, acting by directly stimulating splicing of exon 7
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| DCC4311 | Ptk-in-6a |
Novel Potent Multi-target PTK Inhibitor for the Treatment of Idiopathic Pulmonary Fibrosis (IPF)
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| DCC4310 | Ptk7/ß-catenin Inhibitor 03653 |
Novel Inhibitor of the PTK7/β-Catenin Interaction Targeting the Wnt Signaling Pathway in Colorectal Cancer
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| DCC4309 | Ptk7/ß-catenin Inhibitor 01065 |
Novel Inhibitor of the PTK7/β-Catenin Interaction Targeting the Wnt Signaling Pathway in Colorectal Cancer
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| DCC4308 | Ptk6-in-21b |
Novel Brk/PTK6 kinase inhibitor
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| DCC4307 | Pti-cv |
Novel CFTR modulator, binding to the poly-r(C) binding protein 1 (PCBP1), showing an affinity for RNA-bound PCBP1 higher than that of free PCBP1
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