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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC4194 | Plk1-in-7k |
Novel polo-like kinase 1 (PLK1) inhibitor
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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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| DCC4192 | Plhspt |
Plk1 PBD-specific phosphopeptide inhibitor, effectively inhibiting mitotic progression and cell proliferation
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| DCC4191 | Plectranthoic Acid |
Novel activator of AMPK, inducing apoptotic death in prostate cancer cells
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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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| DCC4189 | Plc Inhibitor 3017 |
Novel inhibitor of phospholipase C (PLC) isozyme
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| DCC4188 | Plazomicin |
Broad spectrum aminoglycoside antibiotic typically used for moderate-to-severe urinary tract infections or pyelonephritis
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| DCC4187 | Plaunotol |
Gastroprotective agent, increasing the prostaglandin production in the gastric mucosa and accelerates ulcer healing
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| DCC4186 | Plasiatine |
Novel Potent Activator of the Nonreceptor Protein Tyrosine Phosphatase Shp2
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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
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| DCC4184 | Plafibride |
Antilipidemic and antiplatelet agent
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| DCC4182 | Pkumdl-ltq-301 |
Potent inhibitor of HipA toxin, inhibiting E. coli persistence
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| DCC4181 | Pks21272 |
Novel potent and specific β5i inhibitor
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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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| DCC4179 | Pkcθ-in-41 |
Novel selective inhibitor of protein kinase Cθ (PKCθ)
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| DCC4178 | Pkc-iota-in-19 |
Novel Protein Kinase C-iota (PKC-ι) Inhibitor, Binding Post-kinase Domain Residues
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| DCC4177 | Pk5196 |
Potent ligand to target the Y220C pocket, stabilizing Y220C
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| DCC4176 | Pixantrone |
Inhibitor of topoisomerase II, intercalating into DNA and inducing topoisomerase II-mediated DNA strand crosslinks, resulting in inhibition of DNA replication and tumor cell cytotoxicity
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| DCC4175 | Pitofenone |
Inhibitor of the acetylcholinesterase activity from bovine erythrocytes and electric eel
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| DCC4174 | Piroxicam-ß-cyclodextrin |
NSAID with better gastrointestinal (GI) tolerability
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| DCC4173 | Piperneolignan A |
Natural nitric oxide (NO) production inhibitor
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| DCC4172 | Piperidol B2 |
Novel potent in vitro and in vivo antifungal agent against azole-resistant Candida albicans
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| DCC4171 | Piperazinomycin |
Antifungal antibiotic, showing inhibitory activity against fungi and yeasts, especially against Trichophyton
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| DCC4170 | Piperacetazine |
Antipsychotic prodrug, most notably used for schizophrenia
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| DCC4168 | Pip4k-in-a131 |
Inhibitor of PIP 4 Ks, efficiently killing transformed BJ cells, but not normal counterparts, displaying a strong selective lethality against Ras-activated or Ras-transformed cells
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| DCC4167 | Pinoxepin Hydrochloride |
Antipsychotic agent
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| DCC4166 | Pim-in-a47 |
Novel potent PIM inhibitor
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| DCC4165 | Pim-in-14j |
Potent, highly selective, and orally bioavailable inhibitor of PIM-1 kinases
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| DCC4164 | Piloquinone |
Natural activator of cryptic biosynthetic gene clusters (BGC), also acting as a potent inhibitor of monoamine oxidase B
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| DCC4163 | Pik-c98 |
Novel PI3K inhibitor, displaying potent preclinical activity against multiple myeloma
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