http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2374449-T3

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filingDate 2006-08-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2012-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2374449-T3
titleOfInvention IMIDAZOL COMPOUNDS REPLACED AS KSP INHIBITORS.
abstract A compound of formula I: wherein: R 1 is selected from the group consisting of aminoacyl, acylamino, carboxyl, carboxyl ester, alkyl, and substituted alkyl, with the proviso that the substituted alkyl is not substituted with substituted aryl or aryl; R2 is selected from the group consisting of hydrogen alkyl, and aryl; R3 and R4 are independently selected from the group consisting of hydrogen hydroxy, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic, since only 1 of R3 or R4 is hydroxy; or R3 and R4 together with the nitrogen atom attached thereto join to form a substituted heterocyclic or heterocyclic; R5 is selected from the group consisting of hydrogen alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, heterocyclic, substituted heterocyclic, aryl, substituted aryl, heteroaryl, and substituted heteroaryl; or R1 and R5, together with the carbon and nitrogen atoms bonded respectively thereto join to form a substituted heterocyclic or heterocyclic group; or when R1 and R5, together with the carbon and nitrogen atoms bonded thereto respectively, do not form a heterocyclic group, and then R4 and R5, together with the atoms attached thereto, form a substituted heterocyclic or heterocyclic group; R8 is selected from the group consisting of L-A1, where L is selected from the group consisting of -S (O) q where q is one or two, and C1 to C5 alkylene optionally substituted with hydroxy, halo, or acylamino; and A1 is selected from the group consisting of aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, substituted heterocyclic, cycloalkyl, and substituted cycloalkyl; and one or both of R6 or R7 is selected from the group consisting of cycloalkyl, heterocyclic, aryl and heteroaryl, all of which may be optionally substituted with - (R9) m where R9 is as defined herein and m is an integer from 1 to 4 , and the other or R6 or R7 is selected from the group consisting of halo hydrogen, and alkyl; R9 is selected from the group consisting of cyano, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, -CF3, alkoxy, substituted alkoxy, halo, and hydroxy; and when m is an integer from 2 to 4, and then each R9 can be the same or different; or pharmaceutically acceptable salts or esters thereof.
priorityDate 2005-08-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 655.