http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5492951-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_eea080e03bbd9386a81a90c22aa8bf43
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-234
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-234
filingDate 1977-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_44c568e024775840702c690ec6ecafbd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a20a72d88ffce5b71ceea73ded20638f
publicationDate 1979-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5492951-A
titleOfInvention Novel aminoglycoside derivative
abstract NEW MATERIAL:Compounds of formula I (R is H, alkyl, aralkyl; R 1 is aminomethyl, hydroxymethyl; R 2 , R 3 and R 6 are H or OH; R 4 is OH or NH 2 ; R 5 is NH 2 or methylamino; R 7 is OH or methyl; R 8 is H or hydroxymethyl; n is 1, 2 or 3; broken line exhibits the presence or absence of double bond). n EXAMPLE: 1-N-[3-Hydroxyazetidine-3-yl)methyl]tobramycin sulfate salt. n USE: Medicines for man and animal, food additive as antibacterial agent, disinfectants, these compound has strong antibacterial activity against grampositive and -negative bacteria. n PREPARATION: The reduction of a compound of formula II is carried out using 1W2 equivalent amount of lithiumaluminum hydride per mole of the compound in an anhydrous solvent under an atmosphere of inert gas for 1W8 hr to produce the objective compound of formula I. n COPYRIGHT: (C)1979,JPO&Japio
priorityDate 1977-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 19.