化合物PI-55 T60390

Product Introduction
Bioactivity


英文名: PI-55

描述: PI-55 (6-(2-hydroxy-3-methylbenzylamino)purine) is a cytokinin receptor inhibitor that exhibits structural similarity to 6-benzylaminopurine (BAP). It competitively inhibits BAP binding on the specific Arabidopsis receptors CRE1/AHK4 and AHK3. Furthermore, PI-55 effectively suppresses cytokinins-induced haustorium formation and enhances parasite aggressiveness [1].

体外活性: The high concentrations (10 μM and 100 μM) of PI-55 lead to an incomplete blocking of early haustorial structure development, especially when cytokinin activity promotes it. PI-55 treatment also reduces the overall aggressiveness of P. ramosa when applied with BAP in comparison with BAP alone, suggesting that the signaling pathway leading to early haustorial structure formation involves histidine kinase receptors homologous to CRE1/AHK4 and AHK3 [1].

存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度: DMSO : 11.7 mg/mL (45.8 mM)


关键字: PI-55 | PI55 | PI 55

相关库: Bioactive Compounds Library Max | Inhibitor Library | Anti-Parasitic Compound Library | Bioactive Compound Library

化合物PI-55 T60390信息由TargetMol中国为您提供，如您想了解更多关于化合物PI-55 T60390报价、型号、参数等信息，欢迎来电或留言咨询。

注：该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案，不可用于临床诊断或治疗等相关用途