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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC3974 | P97-in-23 |
Novel potent inhibitor of the AAA+ ATPase p97
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| DCC3973 | P97-in-17 |
Novel potent inhibitor of the AAA+ ATPase p97
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| DCC3972 | P7c3a20 |
Neuroprotective agent, protecting ventral horn spinal cord motor neurons from cell death
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| DCC3971 | P7 Peptide |
Novel bFGF antagonist peptide, inhibiting breast cancer cell growth
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| DCC3970 | P5-peptide |
Novel inhibitor of atherogenesis and diabetes, significantly and specifically inhibiting αD-CEP binding
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| DCC3969 | P53 Reactivator C85 |
Novel reactivator of mutant p53, fuctioning as a zinc metallochaperone (ZMC) with diminished copper binding that functions as a chemotherapy and radiation sensitizer
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| DCC3968 | p53 Modulator 10d |
Novel modulator of p53 activity, arresting at G2/M phase inducing delay of cell cycle progression
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| DCC3967 | P505-15 Acetate |
Selective spleen tyrosine kinase (SYK) inhibitor, suppressing leukocyte immune function and inflammation, and leading to a reduction in arthritis score and attenuated histological damage
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| DCC3966 | P2y1-in-16 |
Novel P2Y1 Antagonist
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| DCC3964 | P217564 |
Second-generation active site-targeted covalent irreversible inhibitor of USP7
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| DCC3963 | P18smi-41 |
Novel INK4C inhibitor, specifically blocking the bioactivity of p18 protein
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| DCC3962 | P18smi-22 |
Novel INK4C inhibitor, specifically blocking the bioactivity of p18 protein
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| DCC3961 | P18smi-21 |
Novel INK4C inhibitor, specifically blocking the bioactivity of p18 protein
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| DCC3960 | P18in005 Hydrochloride |
Novel p18(INK4C) inhibitor
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| DCC3959 | Oxymorphindole |
δ-Opioid receptor agonist
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| DCC3958 | Oxymetholone |
Synthetic hormone with anabolic and androgenic properties
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| DCC3957 | Oxyl Surfen |
Antagonist of cell-surface heparan sulfate and heparin-protein interactions, reducing tau hyperphosphorylation and mitigating or delaying neuronal defects in tauopathies, including Alzheimer's disease
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| DCC3956 | Oxyfedrine Hydrochloride |
Vasodilator and β-adrenoreceptor agonist
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| DCC3955 | Oxt-328 |
Novel sulindac derivative; anti-inflammatory and anti-cancer agent
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| DCC3954 | Oxs000675 |
Novel inducer of differentiation in all six AML cell lines
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| DCC3953 | Oxocarbazate |
Novel inhibitor of human cathepsin L
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| DCC3951 | Oxfbd03 |
Novel inhibitor of the bromodomain and extra terminal domain (BET) bromodomain family member BRD4(1)
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| DCC3950 | Oxendolone |
Novel potent inhibitor of GVIA iPLA2 with little or no inhibition against GIVA cPLA2 (XI(50) = 0.0073 and >0.91, respectively)
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| DCC3949 | Oxeglitazar |
PPARalpha/gamma agonist
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| DCC3948 | Oxaz-1 |
Novel dual inhibitor of the p53 interaction with MDM2 and MDMX
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| DCC3947 | Oxa-06 Dihydrochloride |
Potent inhibitor of PANC-1 cell migration and MYPT1 phosphorylation
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| DCC3946 | Ox2r-in-f7.3 |
Novel selective Ligand for the Orexin 2 Receptor (OX2R)
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| DCC3945 | Ox1r Antagonist 56 |
Brain penetrant, selective and high affinity OX1R antagonist
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| DCC3944 | Ox03699 |
Novel anthelmintic agent
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| DCC3943 | Ox02983 |
Novel anthelmintic agent, immobilising whipworm and reducing the ability of embryonated T. muris eggs to establish infection in the mouse host in vivo
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