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Cat. No. Product Name Field of Application Chemical Structure
DCC4319 Pu-29f
Hsp90α- and Hsp90ß-selective inhibitor
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DCC4318 Pu24fcl
Novel specific inhibitor of tumor Hsp90
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DCC4317 Pu-20f
Hsp90α- and Hsp90ß-selective inhibitor
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DCC4316 Ptzmes2b
Novel thermally activated delayed fluorescence (TADF) molecule that exhibits high external quantum efficiency (EQE) in non-doped organic light-emitting diodes (OLEDs) at high luminescence
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DCC4315 Ptpmt1-in-1
Novel PTEN-like mitochondrial phosphatase PTPMT1 inhibitor
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DCC4314 Ptp1b-in-18k
Novel non-competitive potent and selective inhibitor of protein tyrosine phosphatase 1B (PTP1B)
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DCC4313 Pto-41
Novel NIR fluorescent probe for the detection of Aβ oligomers
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DCC4312 Ptk-sma1
Unique promoter of SMN2 exon 7 splicing, acting by directly stimulating splicing of exon 7
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DCC4311 Ptk-in-6a
Novel Potent Multi-target PTK Inhibitor for the Treatment of Idiopathic Pulmonary Fibrosis (IPF)
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DCC4310 Ptk7/ß-catenin Inhibitor 03653
Novel Inhibitor of the PTK7/β-Catenin Interaction Targeting the Wnt Signaling Pathway in Colorectal Cancer
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DCC4309 Ptk7/ß-catenin Inhibitor 01065
Novel Inhibitor of the PTK7/β-Catenin Interaction Targeting the Wnt Signaling Pathway in Colorectal Cancer
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DCC4308 Ptk6-in-21b
Novel Brk/PTK6 kinase inhibitor
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DCC4307 Pti-cv
Novel CFTR modulator, binding to the poly-r(C) binding protein 1 (PCBP1), showing an affinity for RNA-bound PCBP1 higher than that of free PCBP1
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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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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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