http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CS-227301-B2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D203-06
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-443
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D203-08
filingDate 1979-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_13af9a2fde660f7813a072eea5d70028
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9ce78c027fdf983c6613c53d74341465
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b4005750abafc65d112e251d2f7906f3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5f05d34d728ff650fd7828760d86b20c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d52b5b4b83b4597abdc3ff1f7eeee68b
publicationDate 1984-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CS-227301-B2
titleOfInvention Method of preparing n-substituted aziridine-2-carboxylic acid derivatives
abstract Aziridine-2-carboxylic acid derivatives of the formula <IMAGE> wherein X is a carboxyl, nitrile, alkoxycarbonyl or carbamoyl group, and R and R1 are various organic radicals, or pharmacologically acceptable salts thereof, exhibit marked immunostimulant activity, especially in conjunction with added chemotherapeutic agents such as a penicillin, a cephalosporin, a nitrofuran or chloramphenicol. Those compounds are new where X is a cyano group or an alkoxycarbonyl radical and R1 is a hydrogen atom, but R' is not an unsubstituted alkyl radical or an alkyl radical substituted by hydroxyl, alkoxy, dialkylamino, phenyl, 4-chlorophenyl or 4-methoxyphenyl or a vinyl radical substituted by a phenyl or methyl radical, or a cycloalkyl radical, a phenyl a 4-chlorophenyl, a 4-methoxyphenyl, an s-triazinyl or a pyridinyl radical; or where X is a carbamoyl group and R1 is a hydrogen atom, R' is not an unsubstituted cyclohexyl, alkyl or benzyl radical; or where X is a cyano group or an alkoxycarbonyl radical and R1 is a phenyl radical, R' is not an isopropyl, cyclohexyl, phenyl, benzyl or p-chlorobenzyl radical; or where R1 is a methyl radical, R1 is not a benzyl, p-chloro- or p- methoxybenzyl radical.
priorityDate 1978-08-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21880519
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450201584
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456412732
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12432039
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421123838
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421069432
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420312335
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458427722
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421123875
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20483636
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID297
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID86738798
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421123889
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20483637
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20483647
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70197
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412216270
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421123822
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421124245
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20483551
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457560897
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20483552
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421123824
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413744147
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID260

Total number of triples: 319.