CC-930

CC-930 (订货以英文为准)

编号:C126262
CAS号:899805-25-5
分子式:C21H23F3N6O2
分子量:448.44
货号 品牌 包装 目录价 您的价格 库存 数量 购买
C126262-100mg 阿拉丁 100mg ¥9886.90
C126262-5mg 阿拉丁 5mg ¥1031.90
C126262-10mg 阿拉丁 10mg ¥1544.90
C126262-50mg 阿拉丁 50mg ¥6179.90
C126262-25mg 阿拉丁 25mg ¥3295.90
产品名称 CC-930
中文名称 CC-930
CAS号 899805-25-5
分子式(M.F.) C21H23F3N6O2
分子量(M.W.) 448.44
储存条件 -20°C储存
溶解性25°C: DMSO
存贮条件储存温度-20°C
生化机理Description:IC50 Value: 61nM (JNK1); 7nM (JNK2); 6nM (JNK3) [1]CC-930 is a selective c-Jun amino-terminal kinase (JNK) inhibitor and is currently under clinical development for fibrotic and infammatory indications.in vitro: Compound 1 (CC-930) showed remarkable selectivity in a panel of 240 kinases, EGFR being the only non-MAP kinase inhibited more than 50% at 3 lM (IC50 = 0.38 lM). It inhibited no receptor at greater than 50% at 10 lM concentration in a panel of 75 receptors, ion channels and neurotransmitter transporters. Finally, when tested against 22 diverse non-kinase enzymes at 10 lM, no inhibition greater than 50% was observed [1]. Incubation with CC-930 prevented the phosphorylation of c-Jun and reduced the stimulatory levels of these cytokines on the release of collagen [2].in vivo: Inhibition of JNK by CC-930 prevented dermal thickening, myofibroblast differentiation and the accumulation of collagen in a dose-dependent manner in mice challenged with bleomycin and in TSK1 mice. In addition to the prevention of fibrosis, treatment with pharmacologically relevant doses of CC-930 also induced regression of established experimental fibrosis [2].  CC-930 did not affect blood pressure, kidney hypertrophy, glomerular hyperfiltration, podocyte loss, glomerular fibrosis or tubulointerstitial injury in diabetic SHR (spontaneously hypertensive rats). However, CC-930 reduced macrophages and ccl2 mRNA levels in diabetic kidneys [3].Toxicity: There were no deaths or AEs that led to withdrawal during the study. Fifteen (33%) subjects reported a total of 22 treatment-emergent adverse events (TEAEs). Subject 207 (25-mg CC-930 group) was involved in a road traffic accident 6 days after the dose and was hospitalized. This adverse event was considered as a serious adverse event but not related to the study drug. The severity of all other adverse events was rated as mild [4].Clinical trial: N/A
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