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filingDate 1997-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_028699d20006bf51b609b15d01db457c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_95ff6ff9b6eabb7c2719e8a9ba350459
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publicationDate 2000-02-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NZ-333903-A
titleOfInvention Substituted 2(2,6-dioxopiperidin-3-yl)phthalimides and -1oxoisoindolines and method of reducing TNF-alpha levels in a mammal
abstract A 2,6-dioxopiperidine also known as 2-Phthalimidoglutarimide from the formula 1 where one X and Y is C=O and the other of X and Y is C=O or CH2; i) each of R1, R2, R3 and R4 independently of the others, is halo, alkyl of 1-4 carbon atoms or alkoxy of 1-4 carbon atoms ii) one of R1, R2, R3, and R4 is NHR5 and the remaining R1, R2, R3, and R4 are hydrogen R5 is hydrogen or alkyl of C1-8 carbon atoms R6 is hydrogen or alkyl of C1-8 carbon atoms, benzyl, or halo provided that R6 is other than hydrogen if X and Y are C=O and (I) each of R1 , R2, R3, and R4 is fluoro or (ii) one of R1, R2m R3 and R4 is amino and (b) the acid addition salts of the compound which contains a nitrogen atoms capable of being protonated. Also claimed is the use of the compound for reducing levels of TNFa in a mammal.
priorityDate 1996-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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