
Bosutinib
CAS No. 380843-75-4
Bosutinib( SKI 606 )
Catalog No. M14314 CAS No. 380843-75-4
Bosutinib is a Bcr-Abl kinase inhibitor for the treatment of Philadelphia chromosome-positive (Ph+) chronic myelogenous leukemia (CML).
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
10MG | 45 | In Stock |
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25MG | 57 | In Stock |
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50MG | 88 | In Stock |
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100MG | 133 | In Stock |
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200MG | 158 | 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 NameBosutinib
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NoteResearch use only, not for human use.
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Brief DescriptionBosutinib is a Bcr-Abl kinase inhibitor for the treatment of Philadelphia chromosome-positive (Ph+) chronic myelogenous leukemia (CML).
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DescriptionBosutinib is a Bcr-Abl kinase inhibitor for the treatment of Philadelphia chromosome-positive (Ph+) chronic myelogenous leukemia (CML). Compared to other tyrosine kinase inhibitors, it has a more favourable hematologic toxicity profile. FDA approved on September 4, 2012. (In Vitro):Bosutinib (SKI-606) is an active inhibitor of Bcr-Abl in several chronic myelogenous leukemia cell lines, with IC50 values in the low nanomolar range.(In Vivo):Bosutinib (oral gavage; 75 mg/kg twice daily or 150 mg/kg once daily) has activity against human KU812 xenografts in nude mice. Bosutinib (150 mg/kg; once daily, 5 days weekly) has activity against syngeneic Bcr-Abl WT and mutant Ba/F3 xenografts.
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In VitroBosutinib (SKI-606) is an active inhibitor of Bcr-Abl in several chronic myelogenous leukemia cell lines, with IC50 values in the low nanomolar range. Cell Proliferation Assay Cell Line:The leukemic Bcr-Abl+ cell lines (KCL22, K562, KU812, and Lama84)Concentration:0.1 μmol/L Incubation Time:72 h Result:Inhibited several human CML derived cell lines with IC50 values ranging from 1 to 20 nmol/L
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In VivoBosutinib (oral gavage; 75 mg/kg twice daily or 150 mg/kg once daily) has activity against human KU812 xenografts in nude mice. Bosutinib (150 mg/kg; once daily, 5 days weekly) has activity against syngeneic Bcr-Abl WT and mutant Ba/F3 xenografts. Animal Model:KU812CM L xenograft modelDosage:75 mg/kg twice daily or 150 mg/kg once daily Administration:Bosutinib (oral gavage; 75 mg/kg twice daily or 150 mg/kg once daily) Result:Had the therapeutic activity and produced a dose- and schedule-dependent weight loss.Animal Model:Syngeneic Bcr-Abl WT and mutant Ba/F3 xenografts Dosage:150 mg/kg Administration:Bosutinib (150 mg/kg; once daily, 5 days weekly)Result:Decreased the rate of tumor growth and prolonged event-free survival of mice.
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SynonymsSKI 606
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PathwayTyrosine Kinase
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TargetBcr-Abl
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RecptorAbl| MAPK| c-Src
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Research AreaCancer
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Indication——
Chemical Information
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CAS Number380843-75-4
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Formula Weight530.45
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Molecular FormulaC26H29Cl2N5O3
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Purity>98% (HPLC)
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SolubilityEthanol: 2 mg/mL (3.77 mM); DMSO: 100 mg/mL (188.51 mM)
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SMILESN#CC1=C(NC2=CC(OC)=C(Cl)C=C2Cl)C3=CC(OC)=C(OCCCN4CCN(C)CC4)C=C3N=C1
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Chemical Name4-(2,4-dichloro-5-methoxyphenylamino)-6-methoxy-7-(3-(4-methylpiperazin-1-yl)propoxy)quinoline-3-carbonitrile
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.Remsing Rix LL, et al. Leukemia. 2009 Mar;23(3):477-85. .
molnova catalog



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