| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC4315 | Ptpmt1-in-1 | Novel PTEN-like mitochondrial phosphatase PTPMT1 inhibitor |
|
| 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 |
|
| DCC4317 | Pu-20f | Hsp90α- and Hsp90ß-selective inhibitor |
|
| DCC4318 | Pu24fcl | Novel specific inhibitor of tumor Hsp90 |
|
| DCC4319 | Pu-29f | Hsp90α- and Hsp90ß-selective inhibitor |
|
| DCC4320 | Pu-h39 | Novel specific Hsp90b1 inhibitor |
|
| DCC4321 | Pumafentrine | Dual inhibitor of PDE3 and PDE4 |
|
| 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 |
|
| DCC4323 | Pu-ws13b | Novel Grp94-selective inhibitor PU-WS13 biotin probe |
|
| DCC4324 | Pv1019 | Novel potent and selective CHEK2>Chk2 inhibitor |
|
| 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 |
|
| DCC4326 | Pvhgprt Inhibitor | Novel Plasmodium vivax Hypoxanthine-Guanine Phosphoribosyltransferase Inhibitor |
|
| DCC4327 | Pw0564 | Novel selective FGF14:Nav1.6 PPI modulator |
|
| DCC4328 | Pyclen | Inhibitor of cell death induced by oxidative stress and inhibitor of AB1-40 aggregation induced by Cu2+ ion |
|
| DCC4329 | Pyimdc | Novel potent inhibitor of collagen prolyl-4-hydroxylases (CP4H) |
|
| DCC4330 | Py-itc | Novel suppressor of cancerous cell growth and proliferation |
|
| DCC4331 | Pyochelin | Bacterial siderophore, acting as an iron-chelating growth promoter for Pseudomonas aeruginosa |
|
| DCC4332 | pyranoxanthone 1 | Novel inhibitor of p53-MDM2 interaction |
|
| 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 |
|
| DCC4334 | Pyrenocine A | Natural phytotoxin, inducing monopolar spindle formation and suppressing proliferation of cancer cells |
|
| 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) |
|
| DCC4336 | Pyrithione Zinc | Novel KMD5A inhibitor |
|
| DCC4337 | Pysoca Substrate-1 | Novel BBB-permeable substrate of pyrilamine-sensitive proton-coupled organic cation antiporter (PYSOCA), acting as a selective class I HDAC inhibitor |
|
| DCC4338 | Pyy3-36 | Y2/Y5 Neuropeptide Y receptor agonist, reducing food intake in normal-weight and obese individuals and the plasma levels of the hunger-promoting hormone ghrelin |
|
| DCC4339 | Pz-1444 | Novel inverse agonist of 5-HT6 receptor |
|
| DCC4340 | Q8pnap | Novel class of bright near infrared window II (NIR-II, 1,000 - 1,700 nm) probe, being successfully used to achieve high spatial and temporal resolution imaging of hind limb vasculature, lymphatic system, and small tumor metastasis, as well as precise NIR- |
|
| DCC4341 | q94 Hydrochloride | Selective PAR1 negative allosteric modulator |
|
| DCC4342 | Qc-308 Hydrochloride | Novel Heme Oxygenase-1 Inhibitor (HO-1 IC 50 =0.27μM; HO-2 IC 50 =0.46μM) |
|
| DCC4343 | Qd394-me | Novel reactive oxygen species (ROS) inducer, showing significant cytotoxicity in pancreatic cancer cells |
|
| DCC4344 | Qls-81 | Novel Nav1.7 channel blocker (IC 50 at 3.5±1.5 μM). being efficacious on chronic pain in mice |
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