CBL0137
CAS No. 1197996-80-7
CBL0137( CBL-0137 | CBL 0137 | Curaxin CBL0137 | CBLC 137 )
Catalog No. M10708 CAS No. 1197996-80-7
CBL0137 (Curaxin CBL0137) is a histone chaperone FACT (facilitates chromatin transcription) and MYC signal inhibitor that markedly reduced tumor initiation and progression in vivo.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 339 | In Stock |
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| 10MG | 498 | In Stock |
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| 25MG | 780 | In Stock |
|
| 50MG | 1071 | In Stock |
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| 100MG | 1431 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameCBL0137
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NoteResearch use only, not for human use.
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Brief DescriptionCBL0137 (Curaxin CBL0137) is a histone chaperone FACT (facilitates chromatin transcription) and MYC signal inhibitor that markedly reduced tumor initiation and progression in vivo.
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DescriptionCBL0137 (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.
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In VitroTreatment 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.
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In VivoThe 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.
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SynonymsCBL-0137 | CBL 0137 | Curaxin CBL0137 | CBLC 137
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PathwayCell Cycle/DNA Damage
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Targetc-Myc
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Recptorp53|NF-κB
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Research AreaCancer
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IndicationBrain Cancer
Chemical Information
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CAS Number1197996-80-7
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Formula Weight336.435
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Molecular FormulaC21H24N2O2
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Purity>98% (HPLC)
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Solubility——
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SMILESCC(NCCN1C2=C(C3=C1C=CC(C(C)=O)=C3)C=C(C(C)=O)C=C2)C
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Chemical Name1,1'-(9-(2-(isopropylamino)ethyl)-9H-carbazole-3,6-diyl)bis(ethan-1-one)
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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.
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