About 6 results found for searched term "63-74-1" (0.128 seconds)
Cat.No. | Name | Target |
---|---|---|
M3319 | Sulfanilamide | Antibiotic |
Sulphanilamide | ||
Sulfanilamide (Sulphanilamide) is a competitive inhibitor for bacterial enzyme dihydropteroate synthetase with IC50 of 320 μM. | ||
M24757 | Denintuzumab | Others |
hBU 12 | ||
Denintuzumab (hBU 12) is a recombinant humanized anti-CD19 monoclonal antibody. Denintuzumab can be used as the antibody moiety (ADC antibody) of antibody-drug conjugates to synthesize ADC, Denintuzumab Mafodotin (SGN-CD19A). Denintuzumab Mafodotin can be used in the research of acute lymphoblastic leukemia. | ||
M28740 | Cipepofol | GABA Receptor |
Ciprofol; HSK3486 | ||
Cipepofol (HSK3486), a psychomotor stabilizing agent, is a gamma-aminobutyric acid (GABA) receptor potentiator. | ||
M42585 | Lp-PLA2-IN-12 | Phospholipase |
Lp-PLA2-IN-12 is an Lp-PLA2 inhibitor. | ||
M6876 | L-161982 | Prostaglandin Receptor |
L161982 | ||
L-161982 is a EP4 receptor antagonist that is selective over all other members of the prostanoid receptor family (Ki values are 0.024, 0.71, 1.90, 5.10, 5.63, 6.74, 19 and 23 μM for human EP4, TP, EP3, DP, FP, IP, EP1 and EP2 receptors respectively). L-161982 completely blocks PGE2-induced ERK phosphorylation and cell proliferation of HCA-7 cells. | ||
M41198 | Neuraminidase-IN-16 | Anti-infection |
Neuraminidase-IN-16 is a potent neuraminidase inhibitor with IC50s of 0.031, 0.15, 0.25, 0.60, 0.63 and 10.08 μM against neuraminidase of H5N1, H5N8, H1N1, H3N2, H5N1-H274Y and H1N1-H274Y, respectively. |
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