http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2002156113-A1

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filingDate 2002-01-16^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_22cdc4f8f2fb0f3b581a1172971b4fd2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_75bb4afc467fe2522b6fbe9b9aae3424
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_417210c6d7f30a67a600926ab5753f22
publicationDate 2002-10-24^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2002156113-A1
titleOfInvention Cycloheptene compounds
abstract Compound of formula (I): n n n wherein: n X represents a bond or alkylene, CO, S(O) n , —S(O) n —A 1 —, —CO—A 1 —, —A—S(O) n —A′ 1 — or —A 1 —CO—A′ 1 —, n Y represents aryl, heteroaryl, cycloalkyl or heterocycloalkyl, each unsubstituted or substituted, n R 1 , R 2 , R 3 and R 4 each independently of the others represent hydrogen or aryl, heteroaryl, cycloalkyl or heterocycloalkyl, each unsubstituted or substituted, n  or R 1 , R 2 , R 3 and R 4 , taken in pairs, together form a bond, or form a fused benzene ring or a fused aromatic or partially unsaturated heterocycle, n T represents —CH(R 5 )—, —N(R 5 )— or —N(R 5 )CO—, n V represents hydrogen or unsubstituted or substituted aryl or heteroaryl, n A 2 represents [C(R 6 )(R′ 6 )] p , n R 7 and R 8 are as defined in the description, n their isomers and addition salts thereof with a pharmaceutically acceptable acid or base and medicinal products containing the same are useful as farnesyl transferase inhibitors.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114573501-A
priorityDate 2001-01-18^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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