About 10 results found for searched term "87-78-5" (0.075 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M2314 | TW-37 | Bcl-2 |
| TW-37 is a novel nonpeptide inhibitor to recombinant Bcl-2, Bcl-xL and Mcl-1 with Ki of 0.29 μM, 1.11 μM and 0.26 μM, respectively. | ||
| M4871 | CL-387785 | EGFR/HER2 |
| EKI-785 | ||
| CL-387785 (EKI-785) is an irreversible, and selective EGFR inhibitor with IC50 of 370 pM. | ||
| M4955 | PLX647 | CSF-1R (c-Fms) |
| PLX-647 | ||
| PLX647 is a highly specific dual FMS/KIT kinase inhibitor with IC50 of 28/16 nM respectively. | ||
| M16897 | erythro-Guaiacylglycerol β-sinapyl ether | Lignans |
| erythro-Guaiacylglycerol β-sinapyl ether | ||
| M19355 | Mannitol | Others |
| DL-Mannitol is obtained by combining D-mannitol with a sample of Lmannitol obtained by reduction of L-mannono-1, Clactone. | ||
| M20884 | RG3039 | DNA/RNA Synthesis |
| PF-06687859, PF 6687859, Quinazoline 495 | ||
| RG3039 (PF-06687859, PF 6687859, Quinazoline 495) is an orally bioavailable and brain-penetrant inhibitor of the mRNA decapping enzyme DcpS with IC50 of 4.2 nM and IC90 of 40 nM, respectively. | ||
| M30788 | KG5 | Raf |
| KG5 is an orally active dual PDGFRβ and B-Raf allosteric inhibitor. KG5 also inhibits Flt3, KIT and c-Raf. KG5 has anticancer, antiangiogenic activities. | ||
| M44311 | Glucobarbarin | Others |
| Glucobarbarin | ||
| M44444 | 10-O-trans-p-coumaroylscandoside | Others |
| 10-O-trans-p-coumaroylscandoside | ||
| M56409 | Rabeximod | TLR |
| Rabeximod (ROB-803), an anti-rheumatic compound, impairs the differentiation and function of human pro-inflammatory dendritic cells and macrophages via downregulating TLR2 and TLR4 stimulation. | ||
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