CB-103
CAS No. 218457-67-1
CB-103( —— )
Catalog No. M22609 CAS No. 218457-67-1
CB-103 is a orally active inhibitor of notch signaling pathway, with anti-tumor activity. CB-103 has shown the ability to block NOTCH signaling in human T cell acute lymphoblastic leukemia cancer cell lines, and exhibits anti-tumor efficacy in GSI resistant T-ALL cell lines.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 35 | In Stock |
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| 50MG | 41 | In Stock |
|
| 100MG | 50 | In Stock |
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| 200MG | 72 | In Stock |
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| 500MG | 120 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameCB-103
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NoteResearch use only, not for human use.
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Brief DescriptionCB-103 is a orally active inhibitor of notch signaling pathway, with anti-tumor activity. CB-103 has shown the ability to block NOTCH signaling in human T cell acute lymphoblastic leukemia cancer cell lines, and exhibits anti-tumor efficacy in GSI resistant T-ALL cell lines.
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DescriptionCB-103 is a orally active inhibitor of notch signaling pathway, with anti-tumor activity. CB-103 has shown the ability to block NOTCH signaling in human T cell acute lymphoblastic leukemia cancer cell lines, and exhibits anti-tumor efficacy in GSI resistant T-ALL cell lines.CB-103 inhibits growth of GSI/Mab resistant triple negative breast cancer, and exhibits anti-tumor activity in xenograft models of human T-ALL and mouse mammary tumors.(In Vitro):CB-103 acts as a pan-NOTCH inhibitor by targeting NOTCH transcriptional activation complex.CB-103 can block NOTCH signaling in human T cell acute lymphoblastic leukemia cancer cell lines.CB-103 exhibits anti-tumor efficacy in GSI resistant T-ALL cell lines.(In Vivo):CB-103 inhibits NOTCH dependent cellular processes in mice.CB-103 blocks in vivo growth of PDX models of T-ALL.CB-103 (25 mg/kg; i.p./p.o.; 2x daily; for 2 weeks) inhibits growth of GSI/Mab resistant triple negative breast cancer.CB-103 exhibits anti-tumor activity in xenograft models of human T-ALL and mouse mammary tumors.
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In VitroLimantrafin acts as a pan-NOTCH inhibitor by targeting NOTCH transcriptional activation complex.Limantrafin can block NOTCH signaling in human T cell acute lymphoblastic leukemia cancer cell lines.Limantrafin exhibits anti-tumor efficacy in GSI resistant T-ALL cell lines. Cell Viability Assay Cell Line:RPMI 8402, KOPTK1, PANC1, nRas driven melanoma cells Concentration:10 μM Incubation Time:4 days, 6 days Result:Caused a significant reduction in their growth potential.
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In VivoLimantrafin inhibits NOTCH dependent cellular processes in mice.Limantrafin blocks in vivo growth of PDX models of T-ALL.Limantrafin (25 mg/kg; i.p./p.o.; 2x daily; for 2 weeks) inhibits growth of GSI/Mab resistant triple negative breast cancer.Limantrafin exhibits anti-tumor activity in xenograft models of human T-ALL and mouse mammary tumors. Animal Model:NSG mice, triple negative breast cancer mouse xenograft model Dosage:25 mg/kg Administration:Oral administration/Intraperitoneal injection; 2x daily; for 2 weeks Result:Inhibited growth of GSI/Mab resistant triple negative breast cancer.
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Synonyms——
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PathwayNeuroscience
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TargetGamma-secretase
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Recptornotch
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Research AreaCancer
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IndicationBreast Cancer;Colorectal Cancer;Cholangiocellular Carcinoma;Sarcoma;Desmoid Tumour;Adenoid Cystic Carcinoma;Non-hodgkin Lymphoma;Glomus Tumor, Malignant
Chemical Information
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CAS Number218457-67-1
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Formula Weight242.32
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Molecular FormulaC15H18N2O
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Purity>98% (HPLC)
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SolubilityDMSO:230 mg/mL (949.16 mM; Need ultrasonic)
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SMILESCC(C)(C)c1ccc(Oc2ccc(N)cn2)cc1
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Chemical Name——
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. Freddy Radtke, et al. Inhibitors of notch signalling pathway and use thereof in treatment of cancers. US9296682B2.
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