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BOSUTINIB

  • Bosutinib
  • Chemical compound

    Bosutinib, sold under the brand name Bosulif, is a small molecule BCR-ABL and src tyrosine kinase inhibitor used for the treatment of chronic myelogenous

    Bosutinib

    Bosutinib

    Bosutinib

  • Bcr-Abl tyrosine-kinase inhibitor
  • Pharmaceutical drug class

    Bosutinib's activity was first described in 2001 and it was disclosed as an Abl kinase inhibitor in 2003. At first it was believed that bosutinib was

    Bcr-Abl tyrosine-kinase inhibitor

    Bcr-Abl_tyrosine-kinase_inhibitor

  • Chronic myelogenous leukemia
  • Type of blood cancer

    approved in South Korea for people resistant to or intolerant of imatinib. Bosutinib received US FDA and EU European Medicines Agency approval on 4 September

    Chronic myelogenous leukemia

    Chronic myelogenous leukemia

    Chronic_myelogenous_leukemia

  • Philadelphia chromosome
  • Genetic abnormality in leukemia cancer cells

    generation BCR::ABL1 TKI Generation Imatinib First-generation Dasatinib, Nilotinib, Bosutinib Second-generation Ponatinib, Asciminib Third-generation

    Philadelphia chromosome

    Philadelphia chromosome

    Philadelphia_chromosome

  • Pfizer
  • American multinational pharmaceutical and biotechnology corporation

    injectables such as the EpiPen. On September 4, 2012, the FDA approved bosutinib (Bosulif) for chronic myelogenous leukemia (CML), a rare type of leukemia

    Pfizer

    Pfizer

    Pfizer

  • Elranatamab
  • Medication

    (ALK) Non-receptor bcr-abl Asciminib Bosutinib Dasatinib Imatinib Nilotinib Ponatinib Radotinib Src (Bosutinib Dasatinib) Janus kinase (JAK) Baricitinib

    Elranatamab

    Elranatamab

  • Protein kinase inhibitor
  • Enzymes that block actions of protein kinases

    VEGFR1/VEGFR2/VEGFR3/PDGFRB/c-KIT Pfizer Small molecule 2012 Renal cell carcinoma Bosutinib Bcr-Abl / SRC Pfizer Small molecule 2012 Chronic myelogenous leukemia

    Protein kinase inhibitor

    Protein_kinase_inhibitor

  • Asciminib
  • Chemical compound

    tyrosine kinase inhibitors (IS-TKIs) (imatinib, nilotinib, dasatinib, or bosutinib). The main efficacy outcome measure was major molecular response rate

    Asciminib

    Asciminib

    Asciminib

  • Mosunetuzumab
  • Monoclonal antibody

    (ALK) Non-receptor bcr-abl Asciminib Bosutinib Dasatinib Imatinib Nilotinib Ponatinib Radotinib Src (Bosutinib Dasatinib) Janus kinase (JAK) Baricitinib

    Mosunetuzumab

    Mosunetuzumab

  • List of antineoplastic agents
  • posterior leucoencephalopathy syndrome (rare) and polycythaemia (uncommon). Bosutinib PO Bcr-Abl and SRc kinase inhibitor. Chronic myeloid leukaemia Diarrhoea

    List of antineoplastic agents

    List_of_antineoplastic_agents

  • Clonal hypereosinophilia
  • Group of blood-based disorders

    of FIP1L1-PDGFRA. Second generation tyrosine kinase inhibitors, e.g. bosutinib, sorafenib, and nilotinib, show little success in treating T674I FIP1L-PDGFRA

    Clonal hypereosinophilia

    Clonal_hypereosinophilia

  • Proto-oncogene tyrosine-protein kinase Src
  • Mammalian protein found in humans

    Other tyrosine kinase inhibitor drugs that are in clinical trials include bosutinib, bafetinib, Saracatinib(AZD-0530), XLl-999, KX01 and XL228. HSP90 inhibitor

    Proto-oncogene tyrosine-protein kinase Src

    Proto-oncogene tyrosine-protein kinase Src

    Proto-oncogene_tyrosine-protein_kinase_Src

  • Targeted therapy
  • Type of therapy

    Sunitinib (Sutent) Dasatinib (Sprycel) Lapatinib (Tykerb) Nilotinib (Tasigna) Bosutinib (Bosulif) Ponatinib (Iclusig) Asciminib (Scemblix) Afatinib (Giotrif)

    Targeted therapy

    Targeted therapy

    Targeted_therapy

  • ATC code L01
  • Pharmaceutical drug classification

    Utidelone L01EA01 Imatinib L01EA02 Dasatinib L01EA03 Nilotinib L01EA04 Bosutinib L01EA05 Ponatinib L01EA06 Asciminib L01EB01 Gefitinib L01EB02 Erlotinib

    ATC code L01

    ATC_code_L01

  • Nitrile
  • Organic compound with a –C≡N functional group

    tyrosine kinase inhibitor bosutinib, which is used in chronic myeloid leukemia. Crystal structures have been reported in which bosutinib is complexed with various

    Nitrile

    Nitrile

  • Tyrosine kinase
  • Enzyme

    available inhibitors to treat CML are imatinib, dasatinib, nilotinib, bosutinib and ponatinib. Gastrointestinal stromal tumors (GIST) are known to withstand

    Tyrosine kinase

    Tyrosine kinase

    Tyrosine_kinase

  • Antineoplastic
  • Class of drugs used to treat malignant tumors

    toxicity Liver toxicity Hypertension Dasatinib (Sprycel) Nilotinib (Tasigna) Bosutinib Ponatinib Gefitinib (Iressa) Second-line treatment for advanced or metastatic

    Antineoplastic

    Antineoplastic

    Antineoplastic

  • Src inhibitor
  • the first clinical inhibitor with GI50 of 9–60 nM in cancer cell lines. Bosutinib has been developed for the treatment of chronic myelogenous leukemia by

    Src inhibitor

    Src inhibitor

    Src_inhibitor

  • Saracatinib
  • Chemical compound

    the LCK tyrosine kinase in cells displaying high level of lipid rafts. Bosutinib Dasatinib Hennequin LF, Allen J, Breed J, Curwen J, Fennell M, Green TP

    Saracatinib

    Saracatinib

    Saracatinib

  • List of drugs: Bi–Bo
  • (INN) Borofax bortezomib (USAN) Boruzu Bosatria bosentan (INN) Bosulif bosutinib (USAN, INN) botiacrine (INN) Botox Boudreaux's Butt Paste boxidine (INN)

    List of drugs: Bi–Bo

    List_of_drugs:_Bi–Bo

  • Hagop Kantarjian
  • tyrosine kinase inhibitors such as imatinib, dasatinib, nilotinib, and bosutinib, which have increased 10-year survival rates for CML from 20% to 90%.

    Hagop Kantarjian

    Hagop_Kantarjian

  • Carlo Gambacorti-Passerini
  • Italian oncologist and hematologist

    develop at preclinical and clinical level another drug for CML named bosutinib. He is also the first researcher who (in June 2010) successfully treated

    Carlo Gambacorti-Passerini

    Carlo Gambacorti-Passerini

    Carlo_Gambacorti-Passerini

  • Autosomal dominant polycystic kidney disease
  • Medical condition

    mechanism, antiproliferative agents such as tyrosine kinase inhibitor bosutinib. However, results in clinical trials have shown mixed results, with studies

    Autosomal dominant polycystic kidney disease

    Autosomal dominant polycystic kidney disease

    Autosomal_dominant_polycystic_kidney_disease

  • Cancer pharmacogenomics
  • address new, mutated forms of BCR-ABL. These include dasatinib, nilotinib, bosutinib, and ponatinib. Cancer pharmacogenomics has also contributed to the understanding

    Cancer pharmacogenomics

    Cancer pharmacogenomics

    Cancer_pharmacogenomics

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