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
1 mL x 10 mM in DMSO 28 In Stock
100MG 31 In Stock
200MG 45 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    CB-103
  • Note
    Research use only, not for human use.
  • Brief Description
    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.
  • Description
    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.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.
  • In Vitro
    Limantrafin 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.
  • In Vivo
    Limantrafin 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.
  • Synonyms
    ——
  • Pathway
    Neuroscience
  • Target
    Gamma-secretase
  • Recptor
    notch
  • Research Area
    Cancer
  • Indication
    Breast Cancer;Colorectal Cancer;Cholangiocellular Carcinoma;Sarcoma;Desmoid Tumour;Adenoid Cystic Carcinoma;Non-hodgkin Lymphoma;Glomus Tumor, Malignant

Chemical Information

  • CAS Number
    218457-67-1
  • Formula Weight
    242.32
  • Molecular Formula
    C15H18N2O
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:230 mg/mL (949.16 mM; Need ultrasonic)
  • SMILES
    CC(C)(C)c1ccc(Oc2ccc(N)cn2)cc1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Freddy Radtke, et al. Inhibitors of notch signalling pathway and use thereof in treatment of cancers. US9296682B2.
molnova catalog
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