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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
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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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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DCC4197 Pmed-1
Novel inhibitor of β-catenin signaling, significantly reduced β-catenin activity in hepatoblastoma and several HCC cells
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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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DCC4195 Plx647(ome)
Slightly less potent inhibitor of FMS than PLX647 but has better aqueous solubility
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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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