http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-049558-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0597f9c318d2aeca86db94711c516383
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-10
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-28
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-519
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-91
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P37-06
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P19-02
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P17-06
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P37-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P37-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P17-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P17-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P13-12
filingDate 2005-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ab48c608017d41e29b9eafa8edad6464
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a159e26bd03170ae1267aa45593a5f64
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b545918c016183bc7119a14c3d196f61
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_285d9bd8928b1f89293e0512a143e03f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e1ba24996bfa78d58e72feb100824980
publicationDate 2006-08-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AR-049558-A1
titleOfInvention COMPOUNDS DERIVED FROM FUSED PYRIMIDINS AND THEIR COMPOSITIONS, FOR THE TREATMENT OF INFLAMMATORY AND IMMUNOREGULATORY DISORDERS.
abstract The compounds are useful for the treatment of inflammatory and autoimmune diseases and conditions. Compositions and treatment methods used by the object compounds. For example, the methods are useful for the treatment of inflammatory and immune disorders and diseases such as multiple sclerosis, rheumatoid arthritis, psoriasis and inflammatory bowel disease. Claim 1: A compound having the formula (1), or a pharmaceutically acceptable salt or pro-drug, wherein: A1 and A4 are independently C (Rb) or N; Q is a member selected from the group consisting of a bond, C1-8 alkylene, C2-8 heteroalkylene, -C (O) -, OC (O) -, -CH2CO-, CH2SO and CH2SO2-; L is a C1-5 bond or alkylene; X is -CH2-, SO2 or - C (O) -; Ra is selected from the group consisting of halogen, -OR ', = O, = NR', = N-OR ', -NR'R' ', -SR', -halogen, -SiR'R''R '' ', -OC (O) R', -C (O) R ', -CO2R', -CONR'R '', -OC (O) NR'R '', -NR''C (O) R ' , -NR'-C (O) NR''R '' ', -NR''C (O) 2R', NH-C (NH2) = NH, - NR'C (NH2) = NH, -NH- C (NH2) = NR ', -S (O) R', -S (O) 2R ', -S (O) 2NR'R' ', -CN and -NO2; Rb is selected from the group consisting of halogen, -OR ', = O, = NR', = N-OR ', -NR'R' ', -SR', -halogen, -SiR'R''R '' ', -OC (O) R', -C (O) R ', -CO2R', -CONR'R '', -OC (O) NR'R '', - NR''C (O) R ' , -NR'-C (O) NR''R '' ', -NR''C (O) 2R', NH-C (NH2) = NH, -NR'C (NH2) = NH, -NH- C (NH2) = NR ', -R', -S (O) R ', -S (O) 2R', -S (O) 2NR'R '', -CN and -NO2; the subscript n is 0, 1.2 or 3; each R ', R' ', R' '' is independently H, unsubstituted C1-8 alkyl, heteroalkyl, unsubstituted aryl, or substituted aryl; R1 is heteroaryl or aryl; R2 is a member selected from the group consisting of hydrogen, halogen, C1-10 alkyl, C2-10 heteroalkyl, C1-10 heterocycloalkyl, C1-10 alkylaryl and C2-10 heteroalkylaryl or optionally R2 may be combined with L to form a ring 5-, 6-, 7- or 8- members containing 1 to 3 heteroatoms selected from the group consisting of N, O and S; R3 is absent or is a member selected from the group consisting of -H, -CHR6R7, -S (O) mR5, -S (O) mN (R8) R9, -S (O) mN (R8) CH2R6, -N (R8) SO2R5, -N (R8) CH2R10, or a group of formulas (2), or optionally R3 can be combined with R2 to form a 4-, 5-, 6-, 7-, or 8-membered ring containing 1 to 3 heteroatoms selected from the group consisting of N, O, and S; R4 is a member selected from the group consisting of C1-20 alkyl, C2-20 heteroalkyl, heteroaryl, aryl, C1-6 heteroarylalkyl, C2-6 heteroarylheteroalkyl, C1-6 arylalkyl and C2-6 arylheteroalkyl; R5 is selected from the group consisting of C1-8 alkyl, C2-8 heteroalkyl, aryl and heteroaryl; R6 and R7 are independently hydrogen, C1-8 alkyl or C2-8 heteroalkyl; R8 is hydrogen, C1-8 alkyl, C2-8 heteroalkyl, heteroaryl or aryl; R9 is C1-8 alkyl; R10 is aryl; Z is CH or N; X1 is a bond, C1-6 alkylene or C1-6 heteroalkylene; Y1 is C1-6 alkylene; and the subscript m is 0, 1 or 2.
priorityDate 2004-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458392451

Total number of triples: 45.