TJ08
CAS No. 2924274-19-9
TJ08 ( —— )
产品货号. M36545 CAS No. 2924274-19-9
TJ08 是一种 1,2,5-三取代苯并咪唑衍生物,可有效诱导 G1/S 期阻滞并促进多种癌细胞凋亡。TJ08 是一种抗癌剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥5129 | 有现货 |
|
| 5MG | ¥7833 | 有现货 |
|
| 10MG | ¥9529 | 有现货 |
|
| 25MG | ¥12356 | 有现货 |
|
| 50MG | ¥15484 | 有现货 |
|
| 100MG | ¥19125 | 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TJ08
-
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TJ08 是一种 1,2,5-三取代苯并咪唑衍生物,可有效诱导 G1/S 期阻滞并促进多种癌细胞凋亡。TJ08 是一种抗癌剂。
-
产品描述TJ08, a 1,2,5-trisubstituted benzimidazole derivative, efficiently induces G1/S phase arrest and promotes apoptosis in various cancer cells. TJ08 is an anticancer agent.
-
体外实验Cell Proliferation Assay Cell Line:Human leukemic cancer cells (Jurkat, K562, and Molt4), human cervical cancer cells (HeLa), human colorectal carcinoma cells (HCT116), and human pancreatic ductal adenocarcinoma (MIAPaCa-2)Concentration:0-20 μM Incubation Time:48 and 72 h Result:Showed effective against various cells with IC50s of 1.88 μM, 1.89 μM, 2.05 μM, 2.11 μM, 3.04 μM, and 3.82 μM against Jurkat, K562, MOLT-4, HeLa, HCT116, and MIA PaCa-2 cancer cell lines, respectively. Apoptosis Analysis Cell Line:Jurkat cells Concentration:1, 5, 10 μM Incubation Time:24 h Result:Induced cell death by apoptosis, not by necrosis, in a concentration-dependent manner.Cell Cycle AnalysisCell Line:Jurkat cells Concentration:1, 5, 10 μM Incubation Time:24 h Result:Cauesd the accumulation of cells at the S phase in a concentration-dependent manner followed by increased accumulation of a sub-G1 population of cells.Western Blot Analysis Cell Line:Jurkat cells Concentration:1, 5, 10 μM Incubation Time:24 h Result:Caused the upregulation of cleaved caspase and downregulation of antiapoptotic BCl2 proteins.
-
体内实验——
-
同义词——
-
通路Apoptosis
-
靶点Apoptosis
-
受体Apoptosis
-
研究领域——
-
适应症——
化学信息
-
CAS Number2924274-19-9
-
分子量405.38
-
分子式C22H16FN3O4
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESO=C(C1=CC=C2C(N=C(N2CC3=CC=CC=C3)C4=CC([N+]([O-])=O)=C(F)C=C4)=C1)OC
-
化学全称——
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. Jagadeesha Gullahalli Swathantraiah, et al. Novel 1,2,5-Trisubstituted Benzimidazoles Potentiate Apoptosis by Mitochondrial Dysfunction in Panel of Cancer Cells. ACS Omega. 2022 Dec 6;7(50):46955-46971.?
产品手册
关联产品
-
Ac-DEVD-CHO
Ac-DEVD-CHO 是一种特异性 Caspase-3 抑制剂,Ki 值为 230 pM。
-
AZD-4877
AZD4877是 Ispinesib (HY-50759)的另一种构型,是纺锤体驱动蛋白 (kinesin) (Eg5) 抑制剂,对其 IC50 值为 2 nM。 AZD4877 能够阻止细胞有丝分裂,并导致形成单极纺锤体表型,介导细胞凋亡(Apoptosis)。 AZD4877 能够抑制循环外周血单核细胞 (PBMC),具有抗肿瘤活性。
-
Voreloxin hydrochlor...
Voreloxin Hydrochloride 是一种有效的拓扑异构酶 II 抑制剂,具有广谱抗肿瘤活性。
021-51111890
购物车()
sales@molnova.cn

