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  2. Tyrosine kinase inhibitor - Wikipedia

    en.wikipedia.org/wiki/Tyrosine_kinase_inhibitor

    A tyrosine kinase inhibitor (TKI) is a pharmaceutical drug that inhibits tyrosine kinases. Tyrosine kinases are enzymes responsible for the activation of many proteins by signal transduction cascades. The proteins are activated by adding a phosphate group to the protein (phosphorylation), a step that TKIs inhibit. TKIs are typically used as ...

  3. Category:Tyrosine kinase inhibitors - Wikipedia

    en.wikipedia.org/wiki/Category:Tyrosine_kinase...

    Inhibitors of tyrosine kinase are mainly used against some specific forms of cancer. Subcategories. This category has the following 2 subcategories, out of 2 total. ...

  4. Bcr-Abl tyrosine-kinase inhibitor - Wikipedia

    en.wikipedia.org/wiki/Bcr-Abl_tyrosine-kinase...

    Nilotinib is a selective Bcr-Abl kinase inhibitor. [13] [18] Nilotinib is 10-30 fold more potent than imatinib in inhibiting activity of the Bcr-Abl tyrosine kinase and proliferation of Bcr-Abl expressing cells. [12] [18] [20] [21] The drug effectively inhibits the auto phosphorylation of Bcr-Abl on Tyr-177 that is involved in CML pathogenesis ...

  5. Tyrosine kinase - Wikipedia

    en.wikipedia.org/wiki/Tyrosine_kinase

    Tyrosine kinase activity in the nucleus involves cell-cycle control and properties of transcription factors. [3] In this way, in fact, tyrosine kinase activity is involved in mitogenesis, or the induction of mitosis in a cell; proteins in the cytosol and proteins in the nucleus are phosphorylated at tyrosine residues during this process. [3]

  6. Targeted covalent inhibitors - Wikipedia

    en.wikipedia.org/wiki/Targeted_covalent_inhibitors

    Targeted covalent inhibitors (TCIs) or Targeted covalent drugs are rationally designed inhibitors that bind and then bond to their target proteins.These inhibitors possess a bond-forming functional group of low chemical reactivity that, following binding to the target protein, is positioned to react rapidly with a proximate nucleophilic residue at the target site to form a bond.

  7. VEGFR-2 inhibitor - Wikipedia

    en.wikipedia.org/wiki/VEGFR-2_inhibitor

    Intedanib is a multiple tyrosine kinase inhibitor and is the first drug to treat idiopathic pulmonary fibrosis. [4] Indol derivatives with 1-NH of 2-indolinone motif that is an H-bond donor, and 2-carbonyl oxygen that acts as an H-bond acceptor, bind with Glu915 and Cys917, respectively.

  8. RET inhibitor - Wikipedia

    en.wikipedia.org/wiki/RET_inhibitor

    These inhibitors are used to treat cancers like non-small cell lung cancer, medullary thyroid carcinoma, and some types of colorectal and pancreatic cancer. RET inhibitors fall under the category of the tyrosine kinase inhibitors, which work by inhibiting proteins involved in the abnormal growth of cancer cells. Existing molecules fall in two ...

  9. Category:Receptor tyrosine kinase inhibitors - Wikipedia

    en.wikipedia.org/wiki/Category:Receptor_tyrosine...

    Pages in category "Receptor tyrosine kinase inhibitors" The following 41 pages are in this category, out of 41 total. This list may not reflect recent changes. A.