http://rdf.ncbi.nlm.nih.gov/pubchem/patent/NZ-620933-A

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filingDate 2012-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_32f9b11c26bfd69b1e0327c6ffe626d8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aed11ddb48c62379cdbe4020d5504f1e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_60f284482ae8180f93e180691bb27bc4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aa367b19938a6f43087e8702b9e49106
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9e7172713d539bddbe9cfbd9e08d7dce
publicationDate 2016-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NZ-620933-A
titleOfInvention Pharmaceutical compositions of hydrophobic camptothecin derivatives
abstract Disclosed herein are pharmaceutical compositions comprising at least one hydrophobic camptothecin derivative, such as the compounds of formula I, or a pharmaceutically acceptable salt of said derivative and a polyethylene glycol (PEG) conjugated phospholipid. Also disclosed are methods for inhibiting cancer cells in a subject in need thereof by administering the pharmaceutical composition of the present invention. An example of the camptothecin derivatives of formula I is the compound (S)-10-[(dimethylamino)methyl]-4-ethyl-9-hydroxy-4-O-[(±)-2-(2”,4”,5”,7”-tetranitro-9”-fluorenylideneaminooxy)propionyl]-1H-pyrano[3’,4’:6,7]indolizino[1,2-b]quinoline-3,14-(4H,12H)-dione.
priorityDate 2011-11-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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