http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4317821-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5929f2d6f4dba84be8dd3a8ba633db12
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D498-18
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-535
filingDate 1980-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1982-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b92f2b95300101f155294eb099c73496
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_677f50cc6f93a13d2023f4b560100bad
publicationDate 1982-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4317821-A
titleOfInvention Maytansinoids, their use and pharmaceutical compositions thereof
abstract Novel maytansinoids of the formula: <IMAGE> wherein Y is H or Cl, and R is C2-15alkyl, phenyl-C1-4alkyl, pyridyl-C1-4alkyl, imidazolyl-C1-4alkyl, indolyl-C1-4alkyl, furyl-C1-4alkyl or thienyl-C1-4alkyl, said R group being substituted by hydroxyl, halogen or C1-5alkanoyloxy at its alpha - and/or beta -position, have antimitotic, antitumor and antimicrobial activities.
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Total number of triples: 713.