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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC4228 | Ppq-581 |
Novel anti-influenza agent, interrupting the crucial RNP trafficking, resulting in influenza replication inhibition, preventing virus-induced cytopathic effects
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| DCC4227 | pppone |
Potent and selective antagonist of melanocortin-4 receptor (MC4R)
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| DCC4226 | Ppk1-in-8 |
Novel PPK1 inhibitor, preventing UTI effectively through the disruption of the PPK1 function
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| DCC4225 | Ppk1-in-17 |
Novel PPK1 inhibitor, preventing UTI effectively through the disruption of the PPK1 function
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| DCC4224 | Ppi-in-3344 |
Novel pan-RAS-effector PPI inhibitor
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| DCC4223 | pp-ii-a03 |
Novel insulin mimetic
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| DCC4222 | Ppi Inhibitor-i |
Novel inhibitor of protein-protein interaction (PPI), blocking #212121; font-family: BlinkMacSystemFont, -apple-system, "Segoe UI", Roboto, Oxygen, Ubuntu, Cantarell, "Fira Sans", "Droid Sans", "Helvetica Neue", sans-serif; font-size: 14px; font-style: no
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| DCC4221 | Pparalpha/gamma Agonist N15 |
Novel dual PPARα/γ agonist, ameliorating insulin resistance and gluconeogenesis in vivo and vitro
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| DCC4220 | Pparalpha/delta-in-11 |
The first reported PPARα/δ dual antagonist
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| DCC4219 | Ppa250 |
Novel iNOS homodimerization inhibitor
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| DCC4218 | Poziotinib Hydrochloride |
Novel pan-human EGF receptor (HER) inhibitor
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| DCC4217 | Ponfibrate |
Hypobetalipoproteinemic and Lipid decreasing agent
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| DCC4216 | Pom2-c-hmbp |
Potent Activator of Vγ9Vδ2 T-Lymphocytes; HMBPP ananlog prodrug
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| DCC4215 | polyphenol 13b |
Novel pan-inhibitor of KCa3.1/KCa2 channels
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| DCC4214 | Polymyxin |
Antibiotic as a last-line therapy to treat infections caused by these life-threatening 'superbugs'
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| DCC4213 | polygonatone D |
Novel activator of Adenosine monophosphate (AMP)-activated protein kinase (AMPK)
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| DCC4212 | Poly(ethyleneimine) Solution |
Used for the transfection of a broad variety of cell lines; Antimicrobial; Novel binding agent of diffusive gradients in thin-films (DGT) technique (PEI-DGT)
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| DCC4211 | Poloxipan |
Pan-Specific Inhibitor of the Polo-Box Domains of Polo-like Kinases Arrests Cancer Cells in Mitosis
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| DCC4210 | Poloppin-ii |
Novel modulator of protein-protein interactions of the mitotic polo-like kinases, targeting KRAS mutant xenografts, indicate avenues, acting synergistically with Crizotinib, an inhibitor of the c-MET receptor, against mutant KRAS-expressing cancer cells
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| DCC4209 | Pol7001 |
Novel macrocycle antibiotic with selective and potent activity against P. aeruginosa
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| DCC4208 | Pol I Inhibitor T5 |
Novel RNA polymerase I inhibitor, targeting ribosomal DNA G-quadruplexes, potently and selectively inhibiting cell growth by high-affinity binding to G4s in ribosomal DNA, impairing RNA polymerase I (Pol I) elongation, inducing a rapid inhibition of Pol I
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| DCC4207 | Podoverine A |
Novel microtubule destabilizing natural product from the Podophyllum species
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| DCC4206 | Pnz-tmp |
The first small-molecule approach capable of detecting and controlling engineered cell-cell outputs
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| DCC4205 | Pnu-69176e |
Allosteric modulator of 5-HT(2C)R with no intrinsic agonist activity
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| DCC4204 | Pnu-292137 |
Potent inhibitor of CDK2/cyclin A
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| DCC4203 | Pnr-4-20 |
Novel G Protein-Biased Cannabinoid 1 (CB1) Receptor Agonist
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| DCC4202 | P-nitro-pifithrin-α |
Cell-permeable analog of pifithrin-α, potently blocking p53-mediated expression of p21/WAF1 and apoptosis
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| DCC4201 | P-mppf Dihydrochloride |
Selective 5-HT1A serotonin receptor antagonist
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| DCC4200 | Pmpmease-in L-28 |
Novel inhibitor of prenylated methylated protein methyl esterase (PMPMEase), a key enzyme in the reversible methylation/demethylation step in the protein prenylation pathway
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| DCC4199 | Pmpmease-in L-23 |
Novel inhibitor of prenylated methylated protein methyl esterase (PMPMEase), a key enzyme in the reversible methylation/demethylation step in the protein prenylation pathway
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