CBL0137
CAS No. 1197996-80-7
CBL0137 ( CBL-0137 | CBL 0137 | Curaxin CBL0137 | CBLC 137 )
产品货号. M10708 CAS No. 1197996-80-7
CBL0137 (Curaxin CBL0137) 是一种组蛋白伴侣 FACT(促进染色质转录)和 MYC 信号抑制剂,可显着减少体内肿瘤的发生和进展。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥943 | 有现货 |
|
| 10MG | ¥1492 | 有现货 |
|
| 25MG | ¥2632 | 有现货 |
|
| 50MG | ¥3953 | 有现货 |
|
| 100MG | ¥5319 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥873 | 有现货 |
|
生物学信息
-
产品名称CBL0137
-
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CBL0137 (Curaxin CBL0137) 是一种组蛋白伴侣 FACT(促进染色质转录)和 MYC 信号抑制剂,可显着减少体内肿瘤的发生和进展。
-
产品描述CBL0137 (Curaxin CBL0137) is a histone chaperone FACT (facilitates chromatin transcription) and MYC signal inhibitor that markedly reduced tumor initiation and progression in vivo; simultaneously activates p53 and inhibits NF-κB without causing detectable genotoxicity, causes phosphorylation of p53 Ser(392) by CK2 and inhibition of NF-κB-dependent transcription in neuroblastoma cells; eradicates drug resistant cancer stem cells and potentiates efficacy of gemcitabine in preclinical models of pancreatic cancer.Brain Cancer Phase 1 Clinical.
-
体外实验Treatment with CBL-0137 leads to complete absence of living cells at concentrations above 2.5 μM. CBL-0137 causes a greater reduction in the number of colonies formed of not only MiaPaCa-2 cells when combined with gemcitabine, but also gemcitabine-resistant PANC-1 cells. Treatment of human pancreatic cancer cells with CBL-0137 results in a dose dependent reduction of protein and mRNA levels of RRM1 and RRM2. CBL-0137 is able to prevent gemcitabine induced expression of RRM1 and RRM2 on mRNA and protein levels.
-
体内实验The CBL-0137 monotherapy group and the CBL-0137-gemcitabine combination group samples show large necrotic fields, numerous apoptotic bodies and loss of tumor cells. Sub-optimal doses of 50 to 60 mg/kg CBL-0137 causes similar enhancement of gemcitabine antitumor activity as that produced by the maximum tolerated dose (MTD) of 90 mg/kg as indicated by the lack of statistically significant differences among the combination groups. CBL0137 hydrochloride inhibits FACT function through depletion of the pool of active FACT involved in transcription elongation. CBL-0137, given by oral gavage at a nontoxic dose of 30 mg/kg per day on a 5 days on/2 days off schedule, suppresses tumor growth in xenografts of colon (DLD-1), renal cell carcinoma (Caki-1), and melanoma (Mel-7) tumor cell lines and transplanted surgical samples from patients with pancreatic ductal adenocarcinoma.
-
同义词CBL-0137 | CBL 0137 | Curaxin CBL0137 | CBLC 137
-
通路Cell Cycle/DNA Damage
-
靶点c-Myc
-
受体p53|NF-κB
-
研究领域Cancer
-
适应症Brain Cancer
化学信息
-
CAS Number1197996-80-7
-
分子量336.435
-
分子式C21H24N2O2
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESCC(NCCN1C2=C(C3=C1C=CC(C(C)=O)=C3)C=C(C(C)=O)C=C2)C
-
化学全称1,1'-(9-(2-(isopropylamino)ethyl)-9H-carbazole-3,6-diyl)bis(ethan-1-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
1. Carter DR, et al. Sci Transl Med. 2015 Nov 4;7(312):312ra176.
2. Gasparian AV, et al. Sci Transl Med. 2011 Aug 10;3(95):95ra74.
3. Burkhart C, et al. Oncotarget. 2014 Nov 30;5(22):11038-53.
4. Barone TA, et al. Neuro Oncol. 2017 Feb 1;19(2):186-196.
产品手册
关联产品
-
MYCMI-6
MYCMI-6 (NSC354961) 是一种选择性、高亲和力的 MYC-MAX 相互作用抑制剂。
-
MYCi361
MYCi361 是 MYC 的抑制剂(与 MYC 结合,Kd 为 3.2 μM)。 MYCi361 是一种小分子 MYC 抑制剂,可抑制 MYC 依赖性癌细胞的活力,包括前列腺癌(MycCaP、LNCaP 和 PC3)、白血病(MV4-11)、淋巴瘤(HL-60 和 P493-6)和神经母细胞瘤(SK-N-B2) 具有低微摩尔 IC50 值。
-
APTO-253 hydrochlori...
APTO-253 是 KLF4 的小分子诱导剂,可稳定 G-四链体 DNA 并降低 MYC mRNA 表达和蛋白质水平。
021-51111890
购物车()
sales@molnova.cn

