| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| 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 |
|
| DCC4346 | Qs Inhibitor 1 | Novel potent inhibitor of quorum sensing (QS) pathways, strongly blocking agr-type QS in S. aureus |
|
| DCC4347 | Qs Inhibitor 2 | Novel potent inhibitor of quorum sensing (QS) pathways, strongly blocking agr-type QS in S. aureus |
|
| DCC4348 | Qtc-4-meobne | Novel multitarget anti-AD agent, significantly increasing in adult neurogenesis and remyelination through Prox1/NeuroD1 and Wnt/β-catenin pathways, demonstrating beneficial effects in preclinical models of AD |
|
| DCC4349 | Quatcy-i2 | Novel photodynamic antitumor agent |
|
| DCC4350 | Quazepam | Modulator of specific GABAA receptors via the benzodiazepine site on the GABAA receptor |
|
| DCC4351 | Quilseconazole Besylate | Potent, orally active fungal Cyp51 (lanosterol 14-α-demethylase) inhibitor |
|
| DCC4352 | Quinine Sulfate | Natural disrupter of DNA replication and transcription via DNA intercalation, reducing oxygen intake and carbohydrate metabolism and the excitability of muscle fibers, inhibiting the drug efflux pump P-glycoprotein |
|
| DCC4353 | Quoromycin | Novel antivirulence agent against Vibrio vulnificus, inhibiting the quorum-sensing signaling pathway by controlling the DNA-binding affinity of SmcR and thus effectively alleviating the virulence of V. vulnificus in vitro and in vivo |
|
| DCC4354 | Qw-296 | Novel microtubule destabilizer |
|
| DCC4355 | R-(+)-eu-1180-453 | Second-Generation GluN2C- and GluN2D-selective positive allosteric modulator (PAM) of the N-methyl-d-aspartate (NMDA) receptor |
|
| DCC4356 | R(ccug) Ligand 63 | Novel Potent and Specific Ligand of r(CCUG)exp, Targeting r(CCUG) Repeats in Myotonic Dystrophy Type 2, Facilitating Degradation by RNA Quality Control Pathways |
|
| DCC4357 | r-138329 | Novel scavenger receptor class B type I blocker |
|
| DCC4358 | r-154716 | Novel inhibitor of HDL uptake induced by overexpression of scavenger receptor BI (SR-BI) |
|
| DCC4359 | R523062 | Novel Antiviral agent for Enterovirus D68 |
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