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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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