About 6 results found for searched term "58-18-4" (0.787 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M5621 | Erlotinib (CP-358774) | EGFR/HER2 |
| CP358774; NSC 718781; OSI-774 | ||
| Erlotinib (CP-358774) is an EGFR inhibitor with IC50 of 2 nM, >1000-fold more sensitive for EGFR than human c-Src or v-Abl. | ||
| M6106 | 17α-Methyltestosterone | Androgen Receptor |
| Methyltestosterone; 17-Methyltestosterone | ||
| 17α-Methyltestosterone has similar binding affinity to AR and similar androgenic and anabolic activities as testosterone. IC50 value: 17 nM (Ki) Target:Androgen Receptor. | ||
| M7551 | Solcitinib | JAK |
| GSK-2586184; GLPG-0778 | ||
| Solcitinib is an oral, competitive, potent, and selective JAK1 inhibitor with an IC50 value of 9.8 nM, which is 11,55, and 23 times more selective than JAK2, JAK3, and TYK2. Solcitinib can be used in studies of psoriasis. | ||
| M28620 | PRN694 | Itk |
| PRN694 is an irreversible, highly selective and potent covalent interleukin-2-inducible T-cell kinase (ITK) and resting lymphocyte kinase (RLK) dual inhibitor with IC50s of 0.3 nM and 1.4 nM, respectively. PRN694 exhibits extended target residence time on ITK and RLK, enabling durable attenuation of effector cells in vitro and in vivo. | ||
| M52903 | Relaxin H3 (human) | Others |
| Relaxin H3 (human) is a kind of relaxin peptide. | ||
| M53344 | Larazotide | Others |
| Larazotideis a peptide which is an orally active zonulin antagonist. | ||
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