|   Butyzamide structure | Common Name | Butyzamide | ||
|---|---|---|---|---|
| CAS Number | 1110767-45-7 | Molecular Weight | 591.55 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C29H32Cl2N2O5S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
| Use of ButyzamideButyzamide is an orally active activator of Mpl, a thrombopoietin (TPO) receptor. Butyzamide increases the phosphorylation level of JAK2, STAT3, STAT5 and MAPK. Butyzamide increases the level of human platelets in mouse xenotransplantation assay[1]. | 
| Name | Butyzamide | 
|---|
| Description | Butyzamide is an orally active activator of Mpl, a thrombopoietin (TPO) receptor. Butyzamide increases the phosphorylation level of JAK2, STAT3, STAT5 and MAPK. Butyzamide increases the level of human platelets in mouse xenotransplantation assay[1]. | 
|---|---|
| Related Catalog | |
| Target | JAK2 STAT3 STAT5 | 
| In Vitro | Butyzamide (3 μM;15 分钟) 诱导 Ba/F3-hMpl 细胞中 JAK2、STAT3、STAT5 和 MAPK 的磷酸化[1]。 Butyzamide (3 μM; 48 小时) 诱导人 CD34+ 造血祖细胞产生集落形成单位-巨核细胞和多倍体巨核细胞[1]。 | 
| In Vivo | Butyzamide (10 mg/kg、50 mg/kg;口服;每天一次,持续 20 天) 在移植了人胎肝来源的 CD34+ 细胞的 NOG 小鼠内增加人血小板水平[1]。< br/> | 
| References | 
| Molecular Formula | C29H32Cl2N2O5S | 
|---|---|
| Molecular Weight | 591.55 |