http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111867577-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e0cc60606ee0bd56d23541c30c977c77
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K2300-00
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B59-002
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-473
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filingDate 2019-03-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_265ecb44b3e502f520569bfe760d91ce
publicationDate 2020-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-111867577-A
titleOfInvention Deuterated analogs of Ikrita
abstract The present invention relates to efflux inhibitor compounds, compositions and methods of use thereof. More specifically, the present invention includes deuterated analogs of Ikrita that have excellent pharmacokinetic properties such that it is now possible to promote therapeutic agents in patients with diseases such as breast cancer. Efflux transporters such as drug resistance protein (BCRP) and P-glycoprotein (P-GP) accumulate and distribute to effective levels in cells or compartments protected by efflux transporters. The transporter-protected compartments include brain, spinal cord, nerve, cerebrospinal fluid, testis, eyeball, retina, inner ear, placenta, breast, liver, biliary tract, kidney, intestine, lung, adrenal cortex, endometrium, hematopoietic cells, Stem cells and solid tumors. In other embodiments, the invention includes methods of using the deuterated analogs of the invention.
priorityDate 2018-03-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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