JP2005505595A - Cxc−ケモカインレセプターアンタゴニストとしての3,4−二置換マレイミド化合物 - Google Patents
Cxc−ケモカインレセプターアンタゴニストとしての3,4−二置換マレイミド化合物 Download PDFInfo
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- JP2005505595A JP2005505595A JP2003534423A JP2003534423A JP2005505595A JP 2005505595 A JP2005505595 A JP 2005505595A JP 2003534423 A JP2003534423 A JP 2003534423A JP 2003534423 A JP2003534423 A JP 2003534423A JP 2005505595 A JP2005505595 A JP 2005505595A
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- 0 *S(C1=NCCCN1)S Chemical compound *S(C1=NCCCN1)S 0.000 description 35
- JQGLAVJLNNXURG-CQSZACIVSA-N CC[C@H](c1ccc(C)[o]1)NC(C(N(C)C1=O)=O)=C1Nc(cccc1C(N(C)C)=O)c1O Chemical compound CC[C@H](c1ccc(C)[o]1)NC(C(N(C)C1=O)=O)=C1Nc(cccc1C(N(C)C)=O)c1O JQGLAVJLNNXURG-CQSZACIVSA-N 0.000 description 4
- HBAAQPJMGQLSEC-NSHDSACASA-N C[C@@H](C(C)(C)C)NC(C(N(C)C1=O)=O)=C1Nc(cccc1C(N(C)C)=O)c1O Chemical compound C[C@@H](C(C)(C)C)NC(C(N(C)C1=O)=O)=C1Nc(cccc1C(N(C)C)=O)c1O HBAAQPJMGQLSEC-NSHDSACASA-N 0.000 description 3
- LPJXKYONEDECSY-OAHLLOKOSA-N CC[C@H](c1ccc2OCOc2c1)NC(C(N(C)C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O Chemical compound CC[C@H](c1ccc2OCOc2c1)NC(C(N(C)C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O LPJXKYONEDECSY-OAHLLOKOSA-N 0.000 description 2
- PICDYHDLKUUWEH-AAEUAGOBSA-N C[C@@H](CCC1)[C@H]1NC(C(N(C)C1=O)=O)=C1Nc(cccc1C(N(C)C)=O)c1O Chemical compound C[C@@H](CCC1)[C@H]1NC(C(N(C)C1=O)=O)=C1Nc(cccc1C(N(C)C)=O)c1O PICDYHDLKUUWEH-AAEUAGOBSA-N 0.000 description 2
- MRBFGEHILMYPTF-UHFFFAOYSA-N C(C1)NCCN1c1ncccn1 Chemical compound C(C1)NCCN1c1ncccn1 MRBFGEHILMYPTF-UHFFFAOYSA-N 0.000 description 1
- HQVOCUUMNJZXKD-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCN1C(c1ccc[s]1)=O)=O Chemical compound CC(C)(C)OC(N(CC1)CCN1C(c1ccc[s]1)=O)=O HQVOCUUMNJZXKD-UHFFFAOYSA-N 0.000 description 1
- CWXPZXBSDSIRCS-UHFFFAOYSA-N CC(C)(C)OC(N1CCNCC1)=O Chemical compound CC(C)(C)OC(N1CCNCC1)=O CWXPZXBSDSIRCS-UHFFFAOYSA-N 0.000 description 1
- XPZNSCFAWCDNPR-SECBINFHSA-N CC(C)[C@H](c1ccc(C)[o]1)N Chemical compound CC(C)[C@H](c1ccc(C)[o]1)N XPZNSCFAWCDNPR-SECBINFHSA-N 0.000 description 1
- DMBGBAJZGAJGLD-UHFFFAOYSA-N CC(C)c1c2OCOc2ccc1 Chemical compound CC(C)c1c2OCOc2ccc1 DMBGBAJZGAJGLD-UHFFFAOYSA-N 0.000 description 1
- YRIIJKXKOPMHPD-UHFFFAOYSA-N CC(C1=CC=CC1)N(C(C(N(C)C1O)=O)=C1NC1=CCCC(C(N(C)C)=O)=C1O)N Chemical compound CC(C1=CC=CC1)N(C(C(N(C)C1O)=O)=C1NC1=CCCC(C(N(C)C)=O)=C1O)N YRIIJKXKOPMHPD-UHFFFAOYSA-N 0.000 description 1
- ADXMPPPHMODQCK-OAHLLOKOSA-N CC([C@H](c1ccc[o]1)NC1=C2Nc(cccc3C(N(C)C)=O)c3O)=[O]=C1N(C)C2=O Chemical compound CC([C@H](c1ccc[o]1)NC1=C2Nc(cccc3C(N(C)C)=O)c3O)=[O]=C1N(C)C2=O ADXMPPPHMODQCK-OAHLLOKOSA-N 0.000 description 1
- ANICIXGVIBXLNI-YMBWGVAGSA-N CC/C(/C(N(C)C)=O)=C(\C(\[N+]([O-])=O)=C/N)/O Chemical compound CC/C(/C(N(C)C)=O)=C(\C(\[N+]([O-])=O)=C/N)/O ANICIXGVIBXLNI-YMBWGVAGSA-N 0.000 description 1
- NIMOSJDYEALZSN-GXHLCREISA-N CCC([HH]C(C(/C(/N1C)=C/C)Nc2cccc(C(N(C)C)=O)c2O)C1=O)C1=CC=C(C)CCO1 Chemical compound CCC([HH]C(C(/C(/N1C)=C/C)Nc2cccc(C(N(C)C)=O)c2O)C1=O)C1=CC=C(C)CCO1 NIMOSJDYEALZSN-GXHLCREISA-N 0.000 description 1
- BMLJQTLWWZAALI-UHFFFAOYSA-N CCC(c1ccc2OCOc2c1)NC(C(C(N1C)=O)Nc2cccc(C(N(C)C)=O)c2O)C1O Chemical compound CCC(c1ccc2OCOc2c1)NC(C(C(N1C)=O)Nc2cccc(C(N(C)C)=O)c2O)C1O BMLJQTLWWZAALI-UHFFFAOYSA-N 0.000 description 1
- JQGLAVJLNNXURG-AWEZNQCLSA-N CC[C@@H](c1ccc(C)[o]1)NC(C(N(C)C1=O)=O)=C1Nc(cccc1C(N(C)C)=O)c1O Chemical compound CC[C@@H](c1ccc(C)[o]1)NC(C(N(C)C1=O)=O)=C1Nc(cccc1C(N(C)C)=O)c1O JQGLAVJLNNXURG-AWEZNQCLSA-N 0.000 description 1
- IZQQXOCNJLZJLF-XLEXHMCLSA-N CC[C@@H](c1ccc(C)[o]1)NC(C(N(C)C1O)=O)=C1N(c1cccc(C(N(C)C)=O)c1O)N Chemical compound CC[C@@H](c1ccc(C)[o]1)NC(C(N(C)C1O)=O)=C1N(c1cccc(C(N(C)C)=O)c1O)N IZQQXOCNJLZJLF-XLEXHMCLSA-N 0.000 description 1
- DPESCTHZSBBJOT-AFYYWNPRSA-N CC[C@H](C1OC=CC1)NC(C(N(C)C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O Chemical compound CC[C@H](C1OC=CC1)NC(C(N(C)C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O DPESCTHZSBBJOT-AFYYWNPRSA-N 0.000 description 1
- OFDWCYVKINWUCJ-SECBINFHSA-N CC[C@H](c1cc(cccc2)c2[o]1)N Chemical compound CC[C@H](c1cc(cccc2)c2[o]1)N OFDWCYVKINWUCJ-SECBINFHSA-N 0.000 description 1
- PUNIFPSSSKUDOI-MRXNPFEDSA-N CC[C@H](c1ccc[o]1)N(C(C(N(C)CCC1)=O)=C1N(c1cccc(C(N(C)C)=O)c1O)N)N Chemical compound CC[C@H](c1ccc[o]1)N(C(C(N(C)CCC1)=O)=C1N(c1cccc(C(N(C)C)=O)c1O)N)N PUNIFPSSSKUDOI-MRXNPFEDSA-N 0.000 description 1
- SHSZSWUCWCFLEH-KWCCSABGSA-N CC[C@H](c1ccc[o]1)NC(C(N(C)C1=O)=O)=C1NC(CC=C1)C(O)=C1C(N(C)C)=O Chemical compound CC[C@H](c1ccc[o]1)NC(C(N(C)C1=O)=O)=C1NC(CC=C1)C(O)=C1C(N(C)C)=O SHSZSWUCWCFLEH-KWCCSABGSA-N 0.000 description 1
- FHFLDWFPDQGCNJ-CYBMUJFWSA-N CC[C@H](c1ccc[o]1)NC(C(N(C)C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O Chemical compound CC[C@H](c1ccc[o]1)NC(C(N(C)C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O FHFLDWFPDQGCNJ-CYBMUJFWSA-N 0.000 description 1
- IIFPQTXGPPBIEA-CYBMUJFWSA-N CC[C@H](c1ccc[s]1)NC(C(N(C)C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O Chemical compound CC[C@H](c1ccc[s]1)NC(C(N(C)C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O IIFPQTXGPPBIEA-CYBMUJFWSA-N 0.000 description 1
- BFFNNPDKZDZGHV-KPMSDPLLSA-N CC[C@H](c1ccccc1)N(C(C(N(C)C1C)=O)=C1N(c1cccc(C(N(C)C)=O)c1O)N)N Chemical compound CC[C@H](c1ccccc1)N(C(C(N(C)C1C)=O)=C1N(c1cccc(C(N(C)C)=O)c1O)N)N BFFNNPDKZDZGHV-KPMSDPLLSA-N 0.000 description 1
- SDCOVLHXQJJAOD-MRXNPFEDSA-N CC[C@H](c1ccccc1)NC(C(N(C)C1=O)=O)=C1Nc(cccc1C(N(C)C)=O)c1O Chemical compound CC[C@H](c1ccccc1)NC(C(N(C)C1=O)=O)=C1Nc(cccc1C(N(C)C)=O)c1O SDCOVLHXQJJAOD-MRXNPFEDSA-N 0.000 description 1
- KBSIOHJHIQMTKN-ADRQNKRLSA-N CC[C@H](c1ccccc1)NC(C(N(C)C1O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O Chemical compound CC[C@H](c1ccccc1)NC(C(N(C)C1O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O KBSIOHJHIQMTKN-ADRQNKRLSA-N 0.000 description 1
- YVXNHAJJZKXKCR-UHFFFAOYSA-N CN(C(C=C1O)O)C=C1N Chemical compound CN(C(C=C1O)O)C=C1N YVXNHAJJZKXKCR-UHFFFAOYSA-N 0.000 description 1
- GWAPDOXKAXSEBQ-CYBMUJFWSA-N CN(C)C(c(cccc1NC(C(N(C)C2=O)=O)=C2N[C@H](CC(F)(F)F)c2ccc[s]2)c1O)=O Chemical compound CN(C)C(c(cccc1NC(C(N(C)C2=O)=O)=C2N[C@H](CC(F)(F)F)c2ccc[s]2)c1O)=O GWAPDOXKAXSEBQ-CYBMUJFWSA-N 0.000 description 1
- IYDREKOJGZDBHU-UHFFFAOYSA-N CN(C)C(c1cncc(N)c1O)=O Chemical compound CN(C)C(c1cncc(N)c1O)=O IYDREKOJGZDBHU-UHFFFAOYSA-N 0.000 description 1
- RIOMXOUJKIOQLL-UHFFFAOYSA-N CN(C)C(c1cnccc1O)=O Chemical compound CN(C)C(c1cnccc1O)=O RIOMXOUJKIOQLL-UHFFFAOYSA-N 0.000 description 1
- ISFRSMMUUQWJCU-UHFFFAOYSA-N CN(C=CC(O)=C1)C1=O Chemical compound CN(C=CC(O)=C1)C1=O ISFRSMMUUQWJCU-UHFFFAOYSA-N 0.000 description 1
- CMTDMIYJXVBUDX-SECBINFHSA-N COC[C@H](c1ccccc1)N Chemical compound COC[C@H](c1ccccc1)N CMTDMIYJXVBUDX-SECBINFHSA-N 0.000 description 1
- HHHUBZYZOFCOGD-OWSBYEOFSA-N C[C@@H](CCC1)C1NC(C(N1C)=O)=C(C2N=C2c(cccc2C(N(C)C)=O)c2O)C1O Chemical compound C[C@@H](CCC1)C1NC(C(N1C)=O)=C(C2N=C2c(cccc2C(N(C)C)=O)c2O)C1O HHHUBZYZOFCOGD-OWSBYEOFSA-N 0.000 description 1
- SQCDNHGBRRAQRW-AAEUAGOBSA-N C[C@@H](CCC1)[C@H]1NC(C(N(C)C1=O)=O)=C1N(c(cccc1C(N(C)C)=O)c1O)N Chemical compound C[C@@H](CCC1)[C@H]1NC(C(N(C)C1=O)=O)=C1N(c(cccc1C(N(C)C)=O)c1O)N SQCDNHGBRRAQRW-AAEUAGOBSA-N 0.000 description 1
- MGZRUNZPPPMWJX-CYBMUJFWSA-N C[C@H](c1ccccc1)NC(C(N(C)C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O Chemical compound C[C@H](c1ccccc1)NC(C(N(C)C1=O)=O)=C1Nc1cccc(C(N(C)C)=O)c1O MGZRUNZPPPMWJX-CYBMUJFWSA-N 0.000 description 1
- LKMBMMQMAVRFMP-UHFFFAOYSA-N Cc1c(CCOC2)c2ccc1 Chemical compound Cc1c(CCOC2)c2ccc1 LKMBMMQMAVRFMP-UHFFFAOYSA-N 0.000 description 1
- KRGXPXGVOCUKRS-MRVPVSSYSA-N Nc(c(C(N1[C@@H](CO)CCC1)=O)ccc1)c1[N+]([O-])=O Chemical compound Nc(c(C(N1[C@@H](CO)CCC1)=O)ccc1)c1[N+]([O-])=O KRGXPXGVOCUKRS-MRVPVSSYSA-N 0.000 description 1
- HFZKYLQVHNTIIY-UHFFFAOYSA-N Nc(cccc1C(N(CC2)CCN2C(c2ccc[s]2)=O)=O)c1O Chemical compound Nc(cccc1C(N(CC2)CCN2C(c2ccc[s]2)=O)=O)c1O HFZKYLQVHNTIIY-UHFFFAOYSA-N 0.000 description 1
- PDKLCBXKPBRMMK-UHFFFAOYSA-N Nc(cccc1C(N(CC2)CCN2c2ncccn2)=O)c1O Chemical compound Nc(cccc1C(N(CC2)CCN2c2ncccn2)=O)c1O PDKLCBXKPBRMMK-UHFFFAOYSA-N 0.000 description 1
- KVBAKSQRUXXHCK-UHFFFAOYSA-N O=C(C(Cl)=C1Cl)NC1=O Chemical compound O=C(C(Cl)=C1Cl)NC1=O KVBAKSQRUXXHCK-UHFFFAOYSA-N 0.000 description 1
- QIQITDHWZYEEPA-UHFFFAOYSA-N O=C(c1ccc[s]1)Cl Chemical compound O=C(c1ccc[s]1)Cl QIQITDHWZYEEPA-UHFFFAOYSA-N 0.000 description 1
- KUKGMDPEGDZCTL-UHFFFAOYSA-N O=C(c1ccc[s]1)N1CCNCC1 Chemical compound O=C(c1ccc[s]1)N1CCNCC1 KUKGMDPEGDZCTL-UHFFFAOYSA-N 0.000 description 1
- CHCUBGPSZDGABM-UHFFFAOYSA-N OC(c1cnccc1O)=O Chemical compound OC(c1cnccc1O)=O CHCUBGPSZDGABM-UHFFFAOYSA-N 0.000 description 1
- UDCSPPCIXFPUSU-UHFFFAOYSA-N [O-][N+](c(cccc1C(N(CC2)CCN2C(c2ccc[s]2)=O)=O)c1O)=O Chemical compound [O-][N+](c(cccc1C(N(CC2)CCN2C(c2ccc[s]2)=O)=O)c1O)=O UDCSPPCIXFPUSU-UHFFFAOYSA-N 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N c1cncnc1 Chemical compound c1cncnc1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- KYQCOXFCLRTKLS-UHFFFAOYSA-N c1nccnc1 Chemical compound c1nccnc1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/44—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members
- C07D207/444—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5
- C07D207/456—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5 with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to other ring carbon atoms
-
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- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
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| US32900501P | 2001-10-12 | 2001-10-12 | |
| PCT/US2002/032628 WO2003031440A1 (en) | 2001-10-12 | 2002-10-11 | 3,4-di-substituted maleimide compounds as cxc-chemokine receptor antagonists |
Publications (2)
| Publication Number | Publication Date |
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| JP2005505595A true JP2005505595A (ja) | 2005-02-24 |
| JP2005505595A5 JP2005505595A5 (enExample) | 2006-01-05 |
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| JP2003534423A Pending JP2005505595A (ja) | 2001-10-12 | 2002-10-11 | Cxc−ケモカインレセプターアンタゴニストとしての3,4−二置換マレイミド化合物 |
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| Country | Link |
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| US (1) | US6903131B2 (enExample) |
| EP (1) | EP1434775A1 (enExample) |
| JP (1) | JP2005505595A (enExample) |
| CN (1) | CN1599734A (enExample) |
| CA (1) | CA2462862A1 (enExample) |
| MX (1) | MXPA04003439A (enExample) |
| WO (1) | WO2003031440A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013173743A (ja) * | 2005-11-24 | 2013-09-05 | Dompe Pha R Ma Spa | (r)−アリールアルキルアミノ誘導体類と、それらを含有する薬剤組成物 |
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| US20040106794A1 (en) | 2001-04-16 | 2004-06-03 | Schering Corporation | 3,4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands |
| US7132445B2 (en) | 2001-04-16 | 2006-11-07 | Schering Corporation | 3,4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands |
| CN1599734A (zh) | 2001-10-12 | 2005-03-23 | 先灵公司 | 作为cxc趋化因子受体拮抗剂的3,4-二取代的马来酰亚胺化合物 |
| WO2003080053A1 (en) * | 2002-03-18 | 2003-10-02 | Schering Corporation | Combination treatments for chemokine-mediated diseases |
| BR0312283A (pt) | 2002-06-28 | 2005-04-12 | Novartis Ag | Combinação compreendendo um agente de alquilação e um agente redutor da atividade de vegf |
| EP1551818B1 (en) * | 2002-10-09 | 2009-02-04 | Schering Corporation | Thiadiazoledioxides and thiadiazoleoxides as cxc- and cc-chemokine receptor ligands |
| BRPI0412259B1 (pt) | 2003-07-22 | 2019-08-20 | Astex Therapeutics Limited | Compostos de 1H-pirazol 3,4-dissubstituídos como moduladores de quinases dependentes de ciclina (CDK), seus usos, processo para a preparação dos mesmos e composição farmacêutica |
| DE602004016211D1 (en) * | 2003-12-19 | 2008-10-09 | Schering Corp | Thiadiazole als cxc- und cc-chemokinrezeptorliganden |
| WO2005068460A1 (en) | 2003-12-22 | 2005-07-28 | Schering Corporation | Isothiazole dioxides as cxc- and cc- chemokine receptor ligands |
| WO2005103711A2 (en) * | 2004-04-20 | 2005-11-03 | Bayer Healthcare Ag | Diagnostics and therapeutics for diseases associated with cxc chemokine receptor 1 (cxcr1) |
| WO2005113534A2 (en) * | 2004-05-12 | 2005-12-01 | Schering Corporation | Cxcr1 and cxcr2 chemokine antagonists |
| SE0500058D0 (sv) * | 2005-01-10 | 2005-01-10 | Astrazeneca Ab | Therapeutic agents 5 |
| SE0500055D0 (sv) | 2005-01-10 | 2005-01-10 | Astrazeneca Ab | Therapeutic agents 3 |
| US7582629B2 (en) | 2005-01-10 | 2009-09-01 | Astrazeneca Ab | Derivatives of isothiazol-3(2H)-one 1,1-dioxides as liver X receptor modulators |
| US8440217B1 (en) | 2005-06-15 | 2013-05-14 | Mawaheb M. EL-Naggar | Method and system with contact lens product for treating and preventing adverse eye conditions |
| US7718678B2 (en) | 2005-06-29 | 2010-05-18 | Schering Corporation | Di-substituted oxadiazoles as CXC-chemokine receptor ligands |
| DE602006017849D1 (de) * | 2005-06-29 | 2010-12-09 | Schering Corp | 5,6-disubstituierte oxadiazolopyrazine und thiadiazolopyrazine als liganden des cxc-chemokinrezeptors |
| TW200813033A (en) * | 2006-07-07 | 2008-03-16 | Schering Corp | 3, 4-di-substituted cyclobutene-1, 2-diones as CXC-chemokine receptor ligands |
| FR2927075A1 (fr) * | 2008-02-04 | 2009-08-07 | Centre Nat Rech Scient | Molecules comprenant un squelette bis-(heteroaryl)maleimide, et leur utilisation dans l'inhibition d'enzymes |
| US7943527B2 (en) * | 2008-05-30 | 2011-05-17 | The Board Of Trustees Of The University Of Illinois | Surface preparation for thin film growth by enhanced nucleation |
| CA2799154A1 (en) | 2010-05-12 | 2011-11-17 | Abbvie Inc. | Indazole inhibitors of kinase |
| MX2014011115A (es) | 2012-03-16 | 2015-03-13 | Axikin Pharmaceuticals Inc | Inhibidores de 3,5-diaminopirazol cinasa. |
| US8889730B2 (en) | 2012-04-10 | 2014-11-18 | Pfizer Inc. | Indole and indazole compounds that activate AMPK |
| KR101556276B1 (ko) * | 2012-12-28 | 2015-09-30 | 제일모직 주식회사 | 하드마스크 조성물용 모노머, 상기 모노머를 포함하는 하드마스크 조성물 및 상기 하드마스크 조성물을 사용하는 패턴형성방법 |
| CA2905242C (en) | 2013-03-15 | 2016-11-29 | Pfizer Inc. | Indole compounds that activate ampk |
| NZ631142A (en) | 2013-09-18 | 2016-03-31 | Axikin Pharmaceuticals Inc | Pharmaceutically acceptable salts of 3,5-diaminopyrazole kinase inhibitors |
| MY191736A (en) | 2014-12-23 | 2022-07-13 | Axikin Pharmaceuticals Inc | 3,5-diaminopyrazole kinase inhibitors |
| WO2018106931A1 (en) | 2016-12-07 | 2018-06-14 | Progenity Inc. | Gastrointestinal tract detection methods, devices and systems |
| CA3045310A1 (en) | 2016-12-14 | 2018-06-21 | Progenity, Inc. | Treatment of a disease of the gastrointestinal tract with a chemokine/chemokine receptor inhibitor |
| JP7161219B2 (ja) * | 2017-08-31 | 2022-10-26 | 国立大学法人京都工芸繊維大学 | 蛍光体及びその利用 |
| CN116726361A (zh) | 2018-11-19 | 2023-09-12 | 比奥拉治疗股份有限公司 | 用生物治疗剂治疗疾病的方法和装置 |
| US11707610B2 (en) | 2019-12-13 | 2023-07-25 | Biora Therapeutics, Inc. | Ingestible device for delivery of therapeutic agent to the gastrointestinal tract |
| WO2022193187A1 (en) * | 2021-03-17 | 2022-09-22 | Biofront Ltd. (Cayman) | Modulators of fpr1 and methods of using same |
| CN115433115A (zh) * | 2022-10-17 | 2022-12-06 | 聊城大学 | 一种3,4-二取代马来酰亚胺类化合物及其合成方法 |
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| DE1669798A1 (de) | 1966-07-28 | 1971-08-26 | Huels Chemische Werke Ag | Verfahren zum Stabilisieren markomolekularer Polyacetale |
| CS214745B2 (en) * | 1976-08-28 | 1982-05-28 | Huels Chemische Werke Ag | Shaped and non-shaped products from plastic materials |
| FI832519A7 (fi) | 1982-07-12 | 1984-01-13 | Bristol Myers Co | Farmaseuttisia menetelmiä ja koostumuksia. |
| DE3309655A1 (de) | 1983-03-17 | 1984-09-20 | Bayer Ag, 5090 Leverkusen | 1,2,5-thiadiazol-1-oxide und 1,1-dioxide, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel |
| JPS60255756A (ja) * | 1984-06-01 | 1985-12-17 | Ikeda Mohandou:Kk | アミノアルキルフエノキシ誘導体 |
| US4978665A (en) | 1987-01-20 | 1990-12-18 | Nissan Chemical Industries Ltd. | 3(2H)pyridazinone, and antagonistic agent against SRS-A containing it |
| JPH02256668A (ja) | 1988-12-20 | 1990-10-17 | Nissan Chem Ind Ltd | ピリダジノン誘導体 |
| US5206252A (en) * | 1992-05-08 | 1993-04-27 | American Home Products Corporation | Thiadiazolyl-amino derivatives of benzopyrans and indanes |
| GB9312210D0 (en) | 1993-06-14 | 1993-07-28 | Smithkline Beecham Plc | Chemical compounds |
| US5506252A (en) * | 1993-11-17 | 1996-04-09 | American Home Products Corporation | Substituted N-heteroaryl and N-aryl-1,2-diaminocyclobutene-3,4-diones |
| US5354763A (en) | 1993-11-17 | 1994-10-11 | American Home Products Corporation | Substituted N-heteroaryl and N-aryl-1,2-diaminocyclobutene-3,4-diones |
| US5466712A (en) * | 1994-11-04 | 1995-11-14 | American Home Products Corporation | Substituted n-aryl-1,2-diaminocyclobutene-3,4-diones |
| DK0796243T3 (da) | 1994-11-16 | 1999-09-13 | American Home Prod | Diaminocyclobuten-3,4-dioner |
| US6300325B1 (en) * | 1997-01-23 | 2001-10-09 | Smithkline Beecham Corporation | IL-8 receptor antagonists |
| AU6250298A (en) | 1997-01-30 | 1998-08-25 | American Home Products Corporation | Substituted hydroxy-anilino derivatives of cyclobutene-3,4-diones |
| US5840764A (en) * | 1997-01-30 | 1998-11-24 | American Home Products Corporation | Substituted hydroxy-anilino derivatives of cyclobutene-3,4-diones |
| AR015425A1 (es) * | 1997-09-05 | 2001-05-02 | Smithkline Beecham Corp | Compuestos de benzotiazol, composicion farmaceutica que los contiene, su uso en la manufactura de un medicamento, procedimiento para su preparacion,compuestos intermediarios y procedimiento para su preparacion |
| ATE224358T1 (de) | 1998-10-02 | 2002-10-15 | Neurosearch As | Diaminocyclobuten-3,4-dionderivate, deren herstellung und deren verwendung |
| DE69922526T2 (de) | 1998-10-08 | 2005-06-02 | Smithkline Beecham Plc, Brentford | 3-(3-chloro-4-hydroxyphenylamino)-4-(2-nitrophenyl)-1h-pyrrol-2,5-dion als glykogen synthase kinase-3 inhibitor (gsk-3) |
| US6376555B1 (en) * | 1998-12-04 | 2002-04-23 | American Home Products Corporation | 4-substituted-3-substituted-amino-cyclobut-3-ene-1,2-diones and analogs thereof as novel potassium channel openers |
| AU2357600A (en) | 1998-12-14 | 2000-07-03 | American Home Products Corporation | 3,4-diamino-3-cyclobutene-1,2-dione derivatives which inhibit leukocyte adhesionmediated by vla-4 |
| US6420396B1 (en) * | 1998-12-16 | 2002-07-16 | Beiersdorf Ag | Biphenyl and biphenyl-analogous compounds as integrin antagonists |
| ID30235A (id) | 1998-12-16 | 2001-11-15 | Bayer Ag | Senyawa bifenil dan analognya sebagai antagonis-antagonis integrin |
| US6518283B1 (en) | 1999-05-28 | 2003-02-11 | Celltech R&D Limited | Squaric acid derivatives |
| CA2386049A1 (en) | 1999-10-15 | 2001-04-26 | Daniel S. Gardner | Bicyclic and tricyclic amines as modulators of chemokine receptor activity |
| EP1265905A4 (en) | 2000-03-01 | 2003-03-12 | Smithkline Beecham Corp | IL-2 RECEPTOR ANTAGONISTS |
| AR033803A1 (es) * | 2000-03-01 | 2004-01-07 | Smithkline Beecham Corp | Compuestos de dianilino escuarano, composiciones farmaceuticas que los comprenden, y el uso de los mismos en la fabricacion de medicamentos para tratar enfermedades mediadas por quimioquinas |
| WO2001068569A2 (en) | 2000-03-14 | 2001-09-20 | Smithkline Beecham Corporation | Il-8 receptor antagonists |
| CN1454204A (zh) | 2000-05-30 | 2003-11-05 | 史密丝克莱恩比彻姆公司 | Il-8受体拮抗剂 |
| WO2002067919A1 (en) | 2001-01-16 | 2002-09-06 | Smithkline Beecham Corporation | Il-8 receptor antagonists |
| ATE346043T1 (de) | 2001-01-16 | 2006-12-15 | Smithkline Beecham Corp | Il-8-rezeptorantagonisten |
| IL156793A0 (en) | 2001-02-02 | 2004-02-08 | Schering Corp | 3,4-di-substituted cyclobutene-1,2-diones as cxc chemokine receptor antagonists |
| US20030204085A1 (en) | 2001-02-02 | 2003-10-30 | Taveras Arthur G. | 3, 4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor antagonists |
| CA2444031C (en) | 2001-04-16 | 2012-02-21 | Schering Corporation | 3,4-di-substituted cyclobutene-1,2-diones as cxc-chemokine receptor ligands |
| CN1599734A (zh) | 2001-10-12 | 2005-03-23 | 先灵公司 | 作为cxc趋化因子受体拮抗剂的3,4-二取代的马来酰亚胺化合物 |
| US6878709B2 (en) | 2002-01-04 | 2005-04-12 | Schering Corporation | 3,4-di-substituted pyridazinediones as CXC chemokine receptor antagonists |
| WO2003080053A1 (en) | 2002-03-18 | 2003-10-02 | Schering Corporation | Combination treatments for chemokine-mediated diseases |
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- 2002-10-11 EP EP02786395A patent/EP1434775A1/en not_active Withdrawn
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013173743A (ja) * | 2005-11-24 | 2013-09-05 | Dompe Pha R Ma Spa | (r)−アリールアルキルアミノ誘導体類と、それらを含有する薬剤組成物 |
Also Published As
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| WO2003031440A1 (en) | 2003-04-17 |
| US20040034229A1 (en) | 2004-02-19 |
| US6903131B2 (en) | 2005-06-07 |
| CA2462862A1 (en) | 2003-04-17 |
| CN1599734A (zh) | 2005-03-23 |
| MXPA04003439A (es) | 2004-07-08 |
| EP1434775A1 (en) | 2004-07-07 |
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