http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-074061-A1

Outgoing Links

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filingDate 2009-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_288143d893f12895f2402a9073424f40
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publicationDate 2010-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AR-074061-A1
titleOfInvention S1P LIASA INHIBITORS FOR THE TREATMENT OF CEREBRAL MALARIA AND PHARMACEUTICAL FORMULATION
abstract Claim 1: Use of an S1P lyase inhibitor in the preparation of a medicament for treating, managing and / or preventing cerebral malaria. Claim 4: The use of any one of claims 1-3 wherein the S1P lyase inhibitor is a compound of the formula: 1 or a pharmaceutically acceptable salt thereof, wherein: R1 is hydrogen, alkyl or aryl; R3 is OR3a, NHC (O) R3a, NHSO2R3a or hydrogen; each R3a is independently hydrogen or alkyl, aryl, alkylaryl, arylalkyl, heteroalkyl, heterocycle, alkylheterocycle or heterocycloalkyl, optionally substituted with halo: R6 is OR6a or OC (O) R6a; R7 is OR7a or OC (O) R7a; R8 is OR8a or OC (O) R8a; R9 is hydrogen, CH2OR9a or CH2OC (O) R9a; and each R6a, R7a, R8a and R9a is, independently, hydrogen or lower alkyl. Claim 7: The use of any one of claims 1-3, wherein the S1P lyase inhibitor is a compound of the formula: 2 or a pharmaceutically acceptable salt thereof, wherein: A is an optionally substituted heterocycle; R5 is OR5a or OC (O) R5a; R6 is OR6a, or OC (O) R6a; R7 is OR7a or OC (O) R7a; R8 is hydrogen, CH2OR8a or CH2OC (O) R8a; and each of R5a, R6a, R7a and R8a is, independently, hydrogen or lower alkyl.
priorityDate 2008-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
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Total number of triples: 29.