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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC4240 | Pridopidine Hydrochloride |
Inducer of Functional Neurorestoration Via the Sigma-1 Receptor
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| DCC4239 | Prexasertib Monolactate Monohydrate |
Novel inhibitor of checkpoint kinase 1 (CHK1)
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| DCC4238 | Prazosin |
Inverse agonist at alpha-1 adrenergic receptors
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| DCC4237 | Pravadoline Maleate |
Inhibitor of prostaglandin (PG) synthesis
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| DCC4235 | Pqsr Antagonist M64 |
Quorum sensing modulator as a PqsR antagonist
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| DCC4234 | Pqq-tme |
Novel human double minute 2 (HDM2) inhibitor
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| DCC4233 | Pqc-078 |
Novel inhibitor of IMPDH enzyme
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| DCC4232 | Pqa-11 |
Novel potent neuroprotectant, inhibiting glutamate-induced cell death, caspase-3 activation, and amyloid β1-42-induced cell death, also suppressing mitogen-activated protein kinase kinase 4 (MKK4) and c-jun N-terminal kinase (JNK) signaling activated by n
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| DCC4231 | Ppxy Budding Inhibitor 5 |
Specific blocker of the MARV VP40 PPxY-host Nedd4 interaction and subsequent PPxY-dependent egress of MARV VP40 VLPs.
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| DCC4230 | Ppxy Budding Inhibitor 4 |
Novel inhibitor of budding of mVP40 and eVP40 VLPs, blocking mVP40-795 Nedd4 protein-protein interaction.
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| DCC4229 | Ppt (water-heme Modulator) |
Novel Modulator of Water-Heme Interactions in Low-Spin P450 Complexes of CYP2C9d and CYP125A1
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| DCC4228 | Ppq-581 |
Novel anti-influenza agent, interrupting the crucial RNP trafficking, resulting in influenza replication inhibition, preventing virus-induced cytopathic effects
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| DCC4227 | pppone |
Potent and selective antagonist of melanocortin-4 receptor (MC4R)
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| DCC4226 | Ppk1-in-8 |
Novel PPK1 inhibitor, preventing UTI effectively through the disruption of the PPK1 function
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| DCC4225 | Ppk1-in-17 |
Novel PPK1 inhibitor, preventing UTI effectively through the disruption of the PPK1 function
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| DCC4224 | Ppi-in-3344 |
Novel pan-RAS-effector PPI inhibitor
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| DCC4223 | pp-ii-a03 |
Novel insulin mimetic
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| DCC4222 | Ppi Inhibitor-i |
Novel inhibitor of protein-protein interaction (PPI), blocking #212121; font-family: BlinkMacSystemFont, -apple-system, "Segoe UI", Roboto, Oxygen, Ubuntu, Cantarell, "Fira Sans", "Droid Sans", "Helvetica Neue", sans-serif; font-size: 14px; font-style: no
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| DCC4221 | Pparalpha/gamma Agonist N15 |
Novel dual PPARα/γ agonist, ameliorating insulin resistance and gluconeogenesis in vivo and vitro
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| DCC4220 | Pparalpha/delta-in-11 |
The first reported PPARα/δ dual antagonist
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| DCC4219 | Ppa250 |
Novel iNOS homodimerization inhibitor
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| DCC4218 | Poziotinib Hydrochloride |
Novel pan-human EGF receptor (HER) inhibitor
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| DCC4217 | Ponfibrate |
Hypobetalipoproteinemic and Lipid decreasing agent
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| DCC4216 | Pom2-c-hmbp |
Potent Activator of Vγ9Vδ2 T-Lymphocytes; HMBPP ananlog prodrug
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| DCC4215 | polyphenol 13b |
Novel pan-inhibitor of KCa3.1/KCa2 channels
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| DCC4214 | Polymyxin |
Antibiotic as a last-line therapy to treat infections caused by these life-threatening 'superbugs'
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| DCC4213 | polygonatone D |
Novel activator of Adenosine monophosphate (AMP)-activated protein kinase (AMPK)
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| DCC4212 | Poly(ethyleneimine) Solution |
Used for the transfection of a broad variety of cell lines; Antimicrobial; Novel binding agent of diffusive gradients in thin-films (DGT) technique (PEI-DGT)
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| DCC4211 | Poloxipan |
Pan-Specific Inhibitor of the Polo-Box Domains of Polo-like Kinases Arrests Cancer Cells in Mitosis
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| DCC4210 | Poloppin-ii |
Novel modulator of protein-protein interactions of the mitotic polo-like kinases, targeting KRAS mutant xenografts, indicate avenues, acting synergistically with Crizotinib, an inhibitor of the c-MET receptor, against mutant KRAS-expressing cancer cells
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