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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
DCC4306 Pti-ch
Novel CFTR modulator, increasing CFTR protein expression across different mutations, including F508del, by increasing CFTR mRNA levels by ~1.5 to ~2-fold in HBE cells
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DCC4305 Pterophyllin 2
Natural antifungal agent, against postharvest fruit pathogenic fungi
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DCC4304 Ptc-510 Tfa Salt
Novel inhibitor of hypoxia-induced VEGF expression
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DCC4303 Ptc-12
Novel Bovine Viral Diarrhea (BVD) Inhibitor, specifically blocking BVDV cell entry
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DCC4302 Pst2774 Oxalate
Na-K ATPase inhibitor, stimulating SERCA2a and accelerating calcium cycling in heart failure by relieving phospholamban inhibition
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DCC4301 Psma-sulfocy7
Novel PSMA ligand conjugated with fluorescent dye SulfoCy7, demonstrating good visualization of PSMA-expressing tumors and the absence of any explicit toxicity up to 87.9 mg/kg
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DCC4300 Psma-1092
Novel Highly Sensitive PSMA Probe for NIR-II Imaging and Intraoperative Tumor Resection, Visualizing Tumors in Real Time
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DCC4299 psb-sb-489
Novel Selective, competitive GPR55 antagonist
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DCC4298 psb-sb-1203
Potent GPR55 antagonist
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DCC4297 Psb-kd477
Novel Agonist of the Cannabinoid-Activated Orphan G-Protein-Coupled Receptor GPR18, being selective versus the CB-sensitive receptors CB1, CB2, and GPR55
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DCC4296 Psb-kd107
Novel Agonist of the Cannabinoid-Activated Orphan G-Protein-Coupled Receptor GPR18, being selective versus the CB-sensitive receptors CB1, CB2, and GPR55
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DCC4295 Psb-6426
The first potent and selective inhibitor of human nucleoside triphosphate diphosphohydrolase-2 (NTPDase2)
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DCC4294 Psb-19416
Fluorescent Probe for Ecto-5'--nucleotidase (CD73)
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DCC4293 Psb-18484
Novel Potent Agonist of the Orphan G Protein-Coupled Receptor GPR17 (EC 50 32.1 nM)
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DCC4292 Psb-18422
Novel Potent Agonist of the Orphan G Protein-Coupled Receptor GPR17 (EC 50 27.9 nM)
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DCC4291 Psb-18332
Fluorescent Probe for Ecto-5'--nucleotidase (CD73)
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DCC4290 Psb-16434
Novel potent and selective agonist of the orphan G protein-coupled receptor 84 (GPR84)
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DCC4289 Psb-16282
Novel Potent Agonist of the Orphan G Protein-Coupled Receptor GPR17 (EC 50 12 nM)
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DCC4288 Psb-16133
Novel Potent and Selective Antagonist for the UTP-Activated P2Y4 Receptor
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DCC4287 Psb-16131
Novel potent Lp1NTPDase inhibitor
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DCC4284 Psb-1410
Highly potent, selective, competitive, and reversible inhibitor of monoamine oxidase B (MAO-B)
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DCC4283 Psb-12105
Novel fluorescent-labeled selective adenosine A2B receptor antagonist
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DCC4282 Psb-10211
Potent competitive antagonist and positive modulator of the P2X2 receptor
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DCC4281 Psb-10129
Positive modulator of ATP effects at P2X2 receptors
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DCC4280 Psb-1011
Potent competitive antagonist and positive modulator of the P2X2 receptor with >100-fold selectivity versus P2X4, P2X7, and several investigated P2Y receptor subtypes (P2Y(2,4,6,12))
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DCC4279 Psammaplysin F
Unique inhibitor of bacterial chromosomal partitioning, increasing the efficacy of bortezomib and sorafenib through regulation of stress granule formation
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DCC4278 Psammaplysene B
Naturally occurring inhibitor of FOXO1a nuclear export
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DCC4277 Ps121912
Highly potent and selective VDR-coactivator inhibitor
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DCC4276 Ps1145 Dihydrochloride
Novel inhibitor of upstream IκB kinase (IKK), specifically inhibiting the IκB phosphorylation and degradation and the subsequent nuclear translocation of NF-κB
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DCC4274 Prx-07034
Novel selective 5-HT6 receptor antagonist, enhancing cognition and memory and potently decreasing food intake and body weight in rodents
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