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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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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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| DCC3942 | Ov-potentiator-28 |
First-in-class small molecule potentiator of cancer virotherapy, significantly enhancing virus replication-associated luciferase expression specifically in the tumor
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| DCC3941 | Ovatodiolide |
Narural broad anticancer agent, upregulating hsa-miR-155, suppressing the BCR-ABL fusion gene and dysregulating the PI3K/AKT/mTOR pathway
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| DCC3940 | Ova323-339 Peptide |
Ovalbumin fragment peptide for study class II MHC-peptide binding and T-cell activation, binding to I-A(d) MHC class II protein, encompassing an allergenic and antigenic epitope of the ovalbumin protein
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| DCC3939 | Ova257-264 Peptide |
Ovalbumin fragment peptide as a class I (Kb)-restricted peptide epitope, triggering T cell activation in immunology studies
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| DCC3938 | oup-186 |
High affinity and human/rat species-selective histamine H3 receptor antagonist
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| DCC3937 | Ouabain |
Natural inhibitor of the Na+/K+-ATPase sodium-potassium ion pump
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| DCC3936 | Ota-5781 |
Novel potent inhibitor of the natural function of FDX1, promoting a unique form of copper-dependent cell death
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| DCC3935 | Osu-53 |
Novel AMPK activator, inhibiting mTOR signaling and autophagy stimulation, activating mutations in RAS or BRAF
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| DCC3934 | Osteosarcoma-in-d15 |
Novel Inhibitor of Migration and Invasion of Osteosarcoma Cells Mediated by p53, Regulating EMT-Related Genes
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| DCC3933 | Osteosarcoma-in-d14 |
Novel Inhibitor of Migration and Invasion of Osteosarcoma Cells Mediated by p53, Regulating EMT-Related Genes
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| DCC3932 | Osteoprotegerin |
Soluble secreted member of the tumor necrosis factor receptor superfamily, inhibiting osteoclastogenesis by interrupting the signaling between stromal cells and osteoclastic progenitor cells, leading to excess accumulation of bone and cartilage
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| DCC3931 | Osteoclast Differentiation Inhibitor T63 |
Novel inhibitor of osteoclast differentiation through regulating MAPKs and Akt signaling pathways
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| DCC3930 | Osl-95ii |
Inhibitor of the glycan-processing enzyme endoplasmic-reticular glucosidase
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| DCC3929 | Osi-461 |
Novel cGMP phosphodiesterase (cGMP-PDE) inhibitor
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| DCC3928 | Osi-296 |
Novel potent, orally efficacious, dual inhibitor of cMET and RON kinases
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| DCC3927 | Oseltamivir Hydrochloride |
Inhibitor of the influenza neuramidase enzyme, blocking neuraminidases on the surfaces of influenza viruses, interfering with host cell release of complete viral particles
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| DCC3926 | Ortataxel |
Second-generation taxane derivative with potential antineoplastic activity, binding to and stabilizing tubulin molecules, inhibiting cell division and cellular proliferation
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| DCC3925 | Orp-101 |
Peripheral weak partial mu-opioid receptor agonist and a weak kappa-opioid receptor antagonist, preventing from being absorbed and entering the central nervous system
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| DCC3924 | Oroidin Hydrochloride |
Inhibitor of an enzyme responsible for the multidrug resistance phenotype in the yeast Saccharomyces cerevisiae.
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| DCC3923 | Orn0829 |
Novel potent dual orexin 1/2 receptor (OX1/2R) antagonist for the treatment of insomnia
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| DCC3922 | orm-10103 |
Novel sodium/calcium exchanger (NCX) inhibitor
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| DCC3921 | Oritavancin |
Lipoglycopeptide Antibacterial, acting as a inhibitor of Cytochrome P450 2C19/2C9, and a inducer of Cytochrome P450 3A4/2D6
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| DCC3920 | Org48762-0 |
Selective p38alpha and p38beta kinase inhibitor
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| DCC3919 | Org-29647 |
CB1 allosteric modulator
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| DCC3918 | Org-27759 |
Negative allosteric modulator at the CB1 receptor
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| DCC3917 | Orex-1019 |
Novel mixed κ/μ receptor antagonist. having therapeutic potential for the treatment of depression and other stress-induced conditions
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| DCC3916 | Orcein |
Collagen immunostain
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