OICR-9429
CAS No. 1801787-56-3
OICR-9429 ( OICR9429 | OICR 9429 )
产品货号. M12746 CAS No. 1801787-56-3
一种有效的、选择性的 WDR5-MLL 相互作用小分子拮抗剂,与 WDR5 结合,Kd 为 93±28 nM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥356 | 有现货 |
|
| 5MG | ¥551 | 有现货 |
|
| 10MG | ¥915 | 有现货 |
|
| 25MG | ¥1596 | 有现货 |
|
| 50MG | ¥2657 | 有现货 |
|
| 100MG | ¥4277 | 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OICR-9429
-
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
-
产品简述一种有效的、选择性的 WDR5-MLL 相互作用小分子拮抗剂,与 WDR5 结合,Kd 为 93±28 nM。
-
产品描述A potent, selective, small-molecule antagonist of WDR5-MLL interaction that binds to WDR5 with Kd of 93±28 nM; competitively disrupts the interaction with a high-affinity Wdr5-INteracting (WIN) peptide of MLL (Kdisp=64 nM), shows no significant binding or inhibition for 22 human methyltransferases, 9 different WD40- and histone reader domains; selectively inhibits proliferation and induces differentiation in p30-expressing human AML cells.
-
体外实验Cell Proliferation Assay Cell Line:BCa cell lines (T24, UM-UC-3 and TCCSUP) Concentration:70 μM, 120 μM, 140 μM and 240 μM Incubation Time:5 days Result:Had a low proliferation rate and remarkably reduced the number of colonies formed by the three BCa cell lines in a dose-dependent manner.Cell Cytotoxicity Assay Cell Line:BCa cell lines (T24, UM-UC-3 and TCCSUP)Concentration:0-10 μM Incubation Time:48 h Result:Inhibited cell viability in a dose-dependent manner in BCa cell lines.Apoptosis Analysis Cell Line:BCa cell lines (T24, UM-UC-3 and TCCSUP)Concentration:70 μM, 120 μM, 140 μM and 240 μM Incubation Time:24 h Result:Showed no obvious apoptotic cells for 24 h but the apoptotic rate was significantly increased at 72 h and upregulated caspase 3/7 activity. Cell Migration Assay Cell Line:BCa cell lines (T24, UM-UC-3 and TCCSUP)Concentration:70 μM, 120 μM, 140 μM and 240 μM Incubation Time:24 h, 48 h Result:Reduced the migratory speed and decreased the migration of the three BCa cell lines.Cell Invasion Assay Cell Line:BCa cell lines (T24, UM-UC-3 and TCCSUP) Concentration:70 μM, 120 μM, 140 μM and 240 μM Incubation Time:24 h, 48 h Result:Decreased the invasion of the three BCa cell lines.Western Blot Analysis Cell Line:BCa cell lines (T24, UM-UC-3 and TCCSUP)Concentration:70 μM, 120 μM, 140 μM and 240 μMIncubation Time:48 h Result:Showed significant downregulation of H3K4me3 in treated cells but not WDR5 or total H3.Reduced the expression of PD-L1 induced by IFN-γ in a dose-dependent manner at both the RNA and protein levels.RT-PCRCell Line:BCa cell lines (T24, UM-UC-3 and TCCSUP)Concentration:70 μM, 120 μM, 140 μM and 240 μM Incubation Time:48 h Result: Downregulated some genes related to the cell cycle, such as CDK1, PLK1, CCNE2, CCNB1, CCNA2, AURKA, and E2F1, genes related to apoptosis and DNA repair, such as BIRC5, XRCC2, AURKA, E2F1, and MCM2, and genes related to metastasis, such as AURKA and FOXM1.Cell Cycle Analysis Cell Line:BCa cell lines (T24, UM-UC-3 and TCCSUP)Concentration:70 μM, 120 μM, 140 μM and 240 μM Incubation Time:48 h Result:Increased the cell population in the G0/G1 phase of three BCa cells and reduced cell population in the S and G2/M phases.
-
体内实验Animal Model:xenograft mouse model Dosage:30 mg/kg, 60 mg/kg Administration:30 mg/kg, 60 mg/kg, i.p.Result:Suppressed tumour growth, small tumours and enhanced tumour sensitivity.
-
同义词OICR9429 | OICR 9429
-
通路Chromatin/Epigenetic
-
靶点HMTase
-
受体WDR5
-
研究领域Cancer
-
适应症——
化学信息
-
CAS Number1801787-56-3
-
分子量555.5913
-
分子式C29H32F3N5O3
-
纯度>98% (HPLC)
-
溶解度DMSO: ≥ 32 mg/mL
-
SMILESO=C(C(C(C(F)(F)F)=C1)=CNC1=O)NC2=CC(C3=CC=CC(CN4CCOCC4)=C3)=CC=C2N5CCN(C)CC5
-
化学全称3-Pyridinecarboxamide, 1,6-dihydro-N-[4-(4-methyl-1-piperazinyl)-3'-(4-morpholinylmethyl)[1,1'-biphenyl]-3-yl]-6-oxo-4-(trifluoromethyl)-
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. Grebien F, et al. Nat Chem Biol. 2015 Aug;11(8):571-578.
2. Getlik M, et al. J Med Chem. 2016 Mar 24;59(6):2478-96.
产品手册
关联产品
-
CARM1 inhibitor 9
CARM1抑制剂9是一种有效的、选择性的精氨酸甲基转移酶1(CARM1、PRMT4)抑制剂,IC50为94 nM。
-
PF-06726304
PF-06726304 是 zeste 同源物 2 (EZH2) 抑制剂的新型强效增强剂。
-
UNC0224
一种有效的选择性 G9a/GLP 抑制剂,CLOT 生化测定的 IC50 为 57 nM 和 58 nM。
021-51111890
购物车()
sales@molnova.cn

