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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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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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| 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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