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Inhibitors & Agonists

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Cat. No. Product Name Field of Application Chemical Structure
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
DCC4345 Qndesa Novel fluorescent molecular rotor for the selective detection of the hybrid-conformation 22AG G-Quadruplex

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