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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC4252 | Procaspase-8 Inhibitor 63-r |
Novel selective procaspase-8 (Pro-C8) Inhibitor covalently binding the zymogen, or inactive precursor (pro-form), of caspase-8, but not other caspases
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| DCC4251 | Probimane |
Potent inhibitor of tumor metastasis, inhibiting calmodulin, sialic acid, lipoperoxidation, fibrinogen, cell-movement and the cell-cycle arrest
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| DCC4250 | pr-nhp5g |
Antagonist at the NR1/NR2A subtype but an agonist at the NR1/NR2D subtype
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| DCC4249 | Prn1126 |
Novel reversible covalent selective LMP7 inhibitor
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| DCC4248 | Prn1008 |
Novel, Reversible Covalent BTK Inhibitor for Rheumatoid Arthritis
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| DCC4247 | Prmts Inhibitor A9 |
Potent inhibitor of protein arginine methyltransferases (PRMTs)
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| DCC4244 | Prmt5-in-4b14 |
Novel potent PRMT5 inhibitor, exhibiting potent anti-proliferative activity against a panel of leukemia and lymphoma cells
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| DCC4243 | Prmt4-in-1 |
Novel potent and selective inhibitor of PRMT4 (also known as CARM1)
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| DCC4242 | prmt3 Inhibitor 14u |
Potent and selective inhibitor of protein arginine methyltransferase 3 (PRMT3)
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| DCC4241 | prmt3 Inhibitor 1 |
Allosteric inhibitor of protein arginine methyltransferase 3 (PRMT3)
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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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