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filingDate 2019-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_94705411bfa030dfb8940c7cbc409ed5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5964597ce6e212e8ad838377e4eb843f
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publicationDate 2021-09-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BR-112021012682-A2
titleOfInvention FAK INHIBITOR AND DRUG COMBINATION THEREOF
abstract FAK INHIBITOR AND DRUG COMBINATION THEREOF.nThe invention relates to a deuterated compound as represented by formula (I)nnor an optical isomer, a tautomer, a pharmaceutically acceptable salt, a prodrug, a hydrate or a solvate thereof. Compared with a compound before deuteration, the deuterated compound shows better pharmacokinetics, higher peak plasma drug concentration, higher exposure and longer half-life, and has more excellent metabolic performance. In addition, the deuterated compound can effectively inhibit FAK activity, and it has good expectation of application in the preparation of FAK inhibitors and/or drugs for cancer treatment. Furthermore, the use of the deuterated compound in combination with an anticancer drug (such as a PD-1 inhibitor) can achieve a synergistic effect, thereby significantly improving the tumor suppression effect, and providing a better choice for clinical treatment. of cancer.
priorityDate 2018-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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