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