产品
编 号:F613482
分子式:C24H21N5O2S
分子量:443.52
产品类型
结构图
CAS No: 306959-01-3
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产品详情
生物活性:
MYLS22 is a selective optic atrophy 1OPA1 inhibitor. MYLS22 reduces tumor vascularization and associated lymphatic angiogenesis by inhibiting OPA1, thereby limiting tumor growth and metastasis and effectively normalizing tumor vascular morphology. MYLS22 has anticancer activity.
体内研究:
MYLS22 (30 mg/kg, 腹腔注射, 每天一次连续7天) 显著降低了白血病小鼠的总瘤负荷。MYLS22 (10 mg/kg, 瘤旁注射, 两天一次持续六天) 通过靶向 OPA1 来抑制皮下 B16F10 黑色素肿瘤小鼠的肿瘤生长。MYLS22 (12.5 mg/kg, 腹腔注射, 1 次) 会加重 LPS 诱导的 ALI 小鼠肺部的病理损伤和炎症反应,同时也会加重 AEC 的坏死。Animal Model:LPS‐induced ALI mice
Dosage:12.5 mg/kg
Administration:i.p., 2 days
Result:Increased lung inflammatory score, Tnf‐α and pro‐Il‐1β mRNA expression, and total IL‐1β or IL‐1β p17 protein expression.Increased the levels of RIPK3, MLKL protein, and their phosphorylation.Decreased the levels of SPC protein.
体外研究:
MYLS22 (10-30 μM; 7-10 天) 能够抑制急性髓系白血病 (AML) 细胞的克隆生长 IC50 为 12.5 μM。MYLS22 (10-30 μM; 7-10 天) 能显著抑制 AML 细胞线粒体的融合从而降低 ROS 含量,将细胞周期抑制在 G0/G1 的过度阶段。MYLS22 (10 nM,30 分钟) 在 MLE12 细胞中 LPS 体外刺激下会加剧 AEC 的坏死。