Mivebresib
CAS No. 1445993-26-9
Mivebresib ( ABBV-075;ABBV075 )
产品货号. M11890 CAS No. 1445993-26-9
Mivebresib (ABBV-075) is a potent and orally available BET bromodomain inhibitor with Ki of 1.0, 12.2, 1.5, and 2.2 nM for BRD2, BRD3, BRD4 and BRDT, respectively.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥608 | 有现货 |
|
5MG | ¥794 | 有现货 |
|
10MG | ¥1312 | 有现货 |
|
25MG | ¥2187 | 有现货 |
|
50MG | ¥3937 | 有现货 |
|
100MG | ¥5630 | 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Mivebresib
-
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Mivebresib (ABBV-075) is a potent and orally available BET bromodomain inhibitor with Ki of 1.0, 12.2, 1.5, and 2.2 nM for BRD2, BRD3, BRD4 and BRDT, respectively.
-
产品描述Mivebresib (ABBV-075) is a potent and orally available BET bromodomain inhibitor with Ki of 1.0, 12.2, 1.5, and 2.2 nM for BRD2, BRD3, BRD4 and BRDT, respectively; displays 54-fold selectivity over EP300, has potential weak activity against SMARCA4 (70% inhibition at 1 uM), Kd >1 uM for 18 other bromodomains; exhibits inhibition of c-Myc expression and displacing BRD4 from the Myc promoter; dose-dependently inhibits IL-6 concentration in a murine model of LPS-induced endotoxic shock, shows vivo antitumor efficacy in a Kasumi-1 AML mouse xenograft model.Breast Cancer Phase 1 Clinical
-
同义词ABBV-075;ABBV075
-
通路Chromatin/Epigenetic
-
靶点Bromodomain
-
受体BET
-
研究领域Cancer
-
适应症Breast Cancer
化学信息
-
CAS Number1445993-26-9
-
分子量459.47
-
分子式C22H19F2N3O4S
-
纯度>98% (HPLC)
-
溶解度DMSO: ≥ 37 mg/mL
-
SMILESCCS(=O)(NC1=CC=C(OC2=CC=C(F)C=C2F)C(C3=CN(C)C(C4=C3C=CN4)=O)=C1)=O
-
化学全称Ethanesulfonamide, N-[4-(2,4-difluorophenoxy)-3-(6,7-dihydro-6-methyl-7-oxo-1H-pyrrolo[2,3-c]pyridin-4-yl)phenyl]-
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
1. McDaniel KF, et al. J Med Chem. 2017 Oct 26;60(20):8369-8384.