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ONX-0801
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    ONX-0801

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    ONX-0801
    ONX-0801 structure.png
    Clinical data
    ATC code
    • none
    Identifiers
    • N-[4-[2-propyn-1-yl[(6S)-4,6,7,8-tetrahydro-2-(hydroxymethyl)-4-oxo-3H-cyclopenta[g]quinazolin-6-yl]amino]benzoyl]-l-γ-glutamyl-D-glutamic acid
    CAS Number
    PubChem CID
    UNII
    Chemical and physical data
    Formula C33H31N5O10
    Molar mass 657.636 g·mol−1
    3D model (JSmol)
    • C#CCN(c1ccc(C(=O)N[C@@H](CCC(=O)N[C@H](CCC(=O)O)C(=O)O)C(=O)O)cc1)[C@H]4CCc3cc2nc(CO)[nH]c(=O)c2cc34

    ONX-0801 (BGC 945) is an experimental drug that has been developed to target ovarian cancer. It is a folate receptor alpha mediated thymidylate synthase inhibitor.

    ONX-0801 was originally developed by BTG and the Institute of Cancer Research in the UK, and subsequently licensed to Onyx Pharmaceuticals for clinical development. It is designed to selectively target tumour tissues of certain kinds of cancer. It is poorly absorbed into most cells, but is actively transported by folate receptor alpha (FRα), which is usually only expressed at low levels in the apical membrane of some specialised tissues, but is expressed at much higher levels in some subtypes of ovarian cancer. This causes the drug to accumulate selectively in tumour tissues, while healthy tissues are only exposed to a much lower concentration.

    In 2017, it received press coverage following the successful completion of a Phase I clinical trial.



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