About 9 results found for searched term "56-86-0" (0.094 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M7843 | 5HPP-33 | Others |
| 5HPP-33 is a thalidomide derivative which was reported to be active as anticancer agent through stabilization of the microtubules. | ||
| M8975 | CWHM-12 | Integrin |
| CWHM-12 is a potent inhibitor of αV integrins with IC50 values of 0.2, 0.8, 1.5, and 1.8 nM for αvβ8, αvβ3, αvβ6, and αvβ1, respectively. | ||
| M10346 | Glutamic acid (L-Glutamic acid) | Metabolite/Endogenous Metabolite |
| L-Glutamic acid acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). | ||
| M17612 | 6α-Hydroxystigmast-4-en-3-one | Steroids |
| 6α-Hydroxystigmast-4-en-3-one | ||
| M24716 | Cedelizumab | Others |
| RWJ 49004 | ||
| Cedelizumab (RWJ 49004) is a IgG4 monoclonal antibody targeting CD4. Cedelizumab has immunosuppressant properties. | ||
| M38813 | Indinavir sulfate ethanolate | Apoptosis |
| Indinavir sulfate ethanolate (MK-639 ethanolate) is an orally active and selective HIV-1 protease inhibitor with a Ki of 0.54 nM for PR. Indinavir sulfate ethanolate exhibits anticancer activity by inhibiting the activation of MMPs-2 hydrolysis, anti-angiogenesis and inducing apoptosis. | ||
| M43110 | KHK-IN-3 | Ketohexokinase |
| LY3522348 | ||
| KHK-IN-3 is a ketohexokinase (KHK) inhibitor. | ||
| M43440 | PROTAC BTK Degrader-3 | PROTAC |
| PROTAC BTK Degrader-3 is a potent BTK degrader with a DC50 value of 10.9 nM of BTK degradation in Mino cells. | ||
| M50204 | Tulmimetostat | EZH2 |
| CPI-0209 | ||
| Tulmimetostat is an orally active dual EZH1/EZH2 protein inhibitor with antitumor activity for use in a variety of solid tumor studies. | ||
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