| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC4179 | Pkcθ-in-41 | Novel selective inhibitor of protein kinase Cθ (PKCθ) |
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| DCC4180 | Pkm2-in-8 | Novel highly potent and selective PKM2 inhibitor, blocking PKM2 mitochondrial translocation under nutritional stress and inhibits tumor growth in vivo |
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| DCC4181 | Pks21272 | Novel potent and specific β5i inhibitor |
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| DCC4182 | Pkumdl-ltq-301 | Potent inhibitor of HipA toxin, inhibiting E. coli persistence |
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| DCC4183 | Pladienolide B | mRNA splicing inhibitor |
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| DCC4184 | Plafibride | Antilipidemic and antiplatelet agent |
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| DCC4185 | Plap Inhibitor 16 | Novel Potent and Specific Inhibitor of Placental Alkaline Phosphatase (PLAP; IC 50 = 32 nM), Targeting Tumor of the Female Reproductive Tract |
|
| DCC4186 | Plasiatine | Novel Potent Activator of the Nonreceptor Protein Tyrosine Phosphatase Shp2 |
|
| DCC4187 | Plaunotol | Gastroprotective agent, increasing the prostaglandin production in the gastric mucosa and accelerates ulcer healing |
|
| DCC4188 | Plazomicin | Broad spectrum aminoglycoside antibiotic typically used for moderate-to-severe urinary tract infections or pyelonephritis |
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| DCC4189 | Plc Inhibitor 3017 | Novel inhibitor of phospholipase C (PLC) isozyme |
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| DCC4190 | pl-dhn | Novel enhancer of Reactive Oxygen Species (ROS), depleting glutathione levels in analogy to piperlongumine but with reduced cell death |
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| DCC4191 | Plectranthoic Acid | Novel activator of AMPK, inducing apoptotic death in prostate cancer cells |
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| DCC4192 | Plhspt | Plk1 PBD-specific phosphopeptide inhibitor, effectively inhibiting mitotic progression and cell proliferation |
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| DCC4193 | Plk1 Pbd-in-143 | Novel Inhibitor of the Polo-Box Domain of Polo-like Kinase 1 (Plk1 PBD) |
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| DCC4194 | Plk1-in-7k | Novel polo-like kinase 1 (PLK1) inhibitor |
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| DCC4195 | Plx647(ome) | Slightly less potent inhibitor of FMS than PLX647 but has better aqueous solubility |
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| DCC4196 | Pm00104 | Potent anticancer tetrahydroisoquinoline alkaloid, being able to form a covalent bond with the amino group of a guanine in selected triplets of DNA duplexes and eventually give rise to double-strand breaks |
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| DCC4197 | Pmed-1 | Novel inhibitor of β-catenin signaling, significantly reduced β-catenin activity in hepatoblastoma and several HCC cells |
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| DCC4198 | Pmmb-317 | Novel potent irriversible dual inhibitor of tubulin and epidermal growth factor receptor (EGFR), inducing the apoptosis of A549 cells in a dose- and time-dependent manner, along with decrease in mitochondrial membrane potential (MMP), production of ROS an |
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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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| 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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| DCC4201 | P-mppf Dihydrochloride | Selective 5-HT1A serotonin receptor antagonist |
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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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| DCC4203 | Pnr-4-20 | Novel G Protein-Biased Cannabinoid 1 (CB1) Receptor Agonist |
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| DCC4204 | Pnu-292137 | Potent inhibitor of CDK2/cyclin A |
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| DCC4205 | Pnu-69176e | Allosteric modulator of 5-HT(2C)R with no intrinsic agonist activity |
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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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| DCC4207 | Podoverine A | Novel microtubule destabilizing natural product from the Podophyllum species |
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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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