
KO-947
CAS No. 1695533-89-1
KO-947 ( KO 947 | KO947 )
产品货号. M12583 CAS No. 1695533-89-1
KO-947 是一种在生化、细胞和体内抗肿瘤活性测定中有效的选择性 ERK1/2 激酶抑制剂。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1037 | 有现货 |
![]() ![]() |
10MG | ¥1709 | 有现货 |
![]() ![]() |
25MG | ¥3208 | 有现货 |
![]() ![]() |
50MG | ¥4820 | 有现货 |
![]() ![]() |
100MG | ¥6877 | 有现货 |
![]() ![]() |
200MG | 获取报价 | 有现货 |
![]() ![]() |
500MG | 获取报价 | 有现货 |
![]() ![]() |
1G | 获取报价 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称KO-947
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述KO-947 是一种在生化、细胞和体内抗肿瘤活性测定中有效的选择性 ERK1/2 激酶抑制剂。
-
产品描述KO-947 is a potent and selective inhibitor of ERK1/2 kinase in biochemical, cellular and in vivo antitumor activity assays; blocks ERK signaling and proliferation of tumor cells exhibiting dysregulation of MAPK pathway signaling, including mutations in BRAF, NRAS or KRAS, at low nanomolar concentrations.Solid Tumors Phase 1 Clinical(In Vitro):KO-947 is a 10 nM inhibitor of ERK with at least 50-fold selectivity against a panel of 450 kinases. KO-947 blocks ERK signaling and proliferation of tumor cells exhibiting dysregulation of MAPK pathway signaling, including mutations in BRAF, NRAS or KRAS, at low nanomolar concentrations.(In Vivo):In cell-line derived xenograft studies, KO-947 profoundly suppresses ERK signaling for up to five days after a single dose and induces regressions in RAS- and RAF-mutant melanoma, NSCLC and pancreatic cancer models on administration schedules ranging from daily to weekly. Intermittent dosing enables comparable antitumor activity at reduced dose-intensity.
-
体外实验KO-947 is a 10 nM inhibitor of ERK with at least 50-fold selectivity against a panel of 450 kinases. KO-947 blocks ERK signaling and proliferation of tumor cells exhibiting dysregulation of MAPK pathway signaling, including mutations in BRAF, NRAS or KRAS, at low nanomolar concentrations.
-
体内实验In cell-line derived xenograft studies, KO-947 profoundly suppresses ERK signaling for up to five days after a single dose and induces regressions in RAS- and RAF-mutant melanoma, NSCLC and pancreatic cancer models on administration schedules ranging from daily to weekly. Intermittent dosing enables comparable antitumor activity at reduced dose-intensity.
-
同义词KO 947 | KO947
-
通路MAPK/ERK Signaling
-
靶点ERK
-
受体ERK
-
研究领域Cancer
-
适应症Solid Tumors
化学信息
-
CAS Number1695533-89-1
-
分子量355.401
-
分子式C21H17N5O
-
纯度>98% (HPLC)
-
溶解度DMSO : 62.5 mg/mL 175.86 mM
-
SMILESO=C1NC2=CC(NN=C3C4=CC=NC=C4)=C3C=C2CN1CC5=CC=CC=C5
-
化学全称6-benzyl-3-(pyridin-4-yl)-1,5,6,8-tetrahydro-7H-pyrazolo[4,3-g]quinazolin-7-one
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
产品手册




关联产品
-
1-Butanol
1-丁醇具有抗氧化作用,可降低高血糖。 1-丁醇通过抑制肥大细胞脱颗粒和炎症细胞因子的表达而具有抗过敏炎症作用。
-
ISRIB (trans-isomer)
ISRIB(反式异构体),ISRIB 的反式异构体,是一种有效的选择性 PERK 抑制剂,IC50 为 5 nM。
-
Tussilagone
Tussilagone 通过诱导血红素加氧酶-1 抑制树突状细胞功能。