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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- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
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- 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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| 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)
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| JP2005505595A true JP2005505595A (ja) | 2005-02-24 |
| JP2005505595A5 JP2005505595A5 (https=) | 2006-01-05 |
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| US (1) | US6903131B2 (https=) |
| EP (1) | EP1434775A1 (https=) |
| JP (1) | JP2005505595A (https=) |
| CN (1) | CN1599734A (https=) |
| CA (1) | CA2462862A1 (https=) |
| MX (1) | MXPA04003439A (https=) |
| WO (1) | WO2003031440A1 (https=) |
Cited By (2)
| 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 |
| JP2024025430A (ja) * | 2022-08-12 | 2024-02-26 | 富士フイルム株式会社 | 化合物又はその塩、タンパク質間相互作用阻害剤、医薬組成物、及び抗腫瘍剤 |
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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 |
| JP2005505595A (ja) | 2001-10-12 | 2005-02-24 | シェーリング コーポレイション | 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 |
| US20040053953A1 (en) * | 2002-03-18 | 2004-03-18 | Schering Corporation | Treatment of chemokine mediated diseases |
| CN100355423C (zh) | 2002-06-28 | 2007-12-19 | 诺瓦提斯公司 | 用于治疗肿瘤的包含血管抑制化合物和烷化剂的组合 |
| MY139601A (en) * | 2002-10-09 | 2009-10-30 | Schering Corp | Thiadiazoledioxides and thiadiazoleoxides as cxc-and cc-chemokine receptor ligands |
| PL2256106T3 (pl) | 2003-07-22 | 2015-08-31 | Astex Therapeutics Ltd | Związki 3,4-pochodne 1h-pirazolu i ich zastosowanie jako kinazy zależne od cyklin (cdk) i modulatory kinazy syntazy glikogenu-3 (gsk-3) |
| MXPA06007076A (es) * | 2003-12-19 | 2006-08-31 | Pharmacopeia Drug Discovery | Tiadiazoles como ligandos del receptor cxc y cc-quimiocina. |
| CA2550540A1 (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 |
| SE0500055D0 (sv) | 2005-01-10 | 2005-01-10 | Astrazeneca Ab | Therapeutic agents 3 |
| CA2592771A1 (en) | 2005-01-10 | 2006-07-13 | Astrazeneca Ab | Derivatives of isothiazol-3(2h)-one 1,1-dioxides as liver x receptor modulators |
| SE0500058D0 (sv) * | 2005-01-10 | 2005-01-10 | Astrazeneca Ab | Therapeutic agents 5 |
| 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 |
| MX2008000366A (es) * | 2005-06-29 | 2008-03-07 | Schering Corp | Oxadiazoles di-sustituidos como ligandos del receptor cxc-quimiocina. |
| JP2009500328A (ja) * | 2005-06-29 | 2009-01-08 | シェーリング コーポレイション | Cxc−ケモカインレセプターリガンドとしての5,6−ジ−置換オキサジアゾロピラジンおよびチアジアゾロピラジン |
| AR061829A1 (es) * | 2006-07-07 | 2008-09-24 | Schering Corp | Ciclobuten-1, 2-dionas 3,4-di sustituidas como ligandos de receptores de quimiocinas cxc |
| 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 |
| KR20140138293A (ko) | 2012-03-16 | 2014-12-03 | 액시킨 파마수티컬스 인코포레이티드 | 3,5-다이아미노피라졸 키나아제 억제제 |
| 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 |
| JP6064062B2 (ja) | 2013-03-15 | 2017-01-18 | ファイザー・インク | Ampkを活性化させるインダゾール化合物 |
| NZ631142A (en) | 2013-09-18 | 2016-03-31 | Axikin Pharmaceuticals Inc | Pharmaceutically acceptable salts of 3,5-diaminopyrazole kinase inhibitors |
| US9546163B2 (en) | 2014-12-23 | 2017-01-17 | Axikin Pharmaceuticals, Inc. | 3,5-diaminopyrazole kinase inhibitors |
| US10610104B2 (en) | 2016-12-07 | 2020-04-07 | 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 |
| US20220249814A1 (en) | 2018-11-19 | 2022-08-11 | Progenity, Inc. | Methods and devices for treating a disease with biotherapeutics |
| CN121197633A (zh) | 2019-12-13 | 2025-12-26 | 比特比德科有限责任公司 | 用于将治疗剂递送至胃肠道的可摄取装置 |
| 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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| US5206252A (en) | 1992-05-08 | 1993-04-27 | American Home Products Corporation | Thiadiazolyl-amino derivatives of benzopyrans and indanes |
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| ATE224358T1 (de) | 1998-10-02 | 2002-10-15 | Neurosearch As | Diaminocyclobuten-3,4-dionderivate, deren herstellung und deren verwendung |
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| CZ20012185A3 (cs) | 1998-12-16 | 2001-10-17 | Bayer Aktiengesellschaft | Nové bifenylové sloučeniny a sloučeniny analogické bifenylovým sloučeninám, způsob jejich přípravy, farmaceutické prostředky a pouľití těchto sloučenin a prostředků jako antagonistů integrinu |
| US6420396B1 (en) | 1998-12-16 | 2002-07-16 | Beiersdorf Ag | Biphenyl and biphenyl-analogous compounds as integrin antagonists |
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| EP1265905A4 (en) | 2000-03-01 | 2003-03-12 | Smithkline Beecham Corp | IL-2 RECEPTOR ANTAGONISTS |
| JP2003527360A (ja) | 2000-03-14 | 2003-09-16 | スミスクライン・ビーチャム・コーポレイション | Il−8受容体アンタゴニスト |
| MXPA02011868A (es) | 2000-05-30 | 2003-04-10 | Smithkline Beecham Corp | Antagonistas de receptor de interleucina 8. |
| US20040048897A1 (en) | 2001-01-16 | 2004-03-11 | Mccleland Brent | Il-8 receptor antagonists |
| DE60230722D1 (de) | 2001-01-16 | 2009-02-26 | Smithkline Beecham Corp | Il-8-rezeptor-antagonisten |
| US20030204085A1 (en) | 2001-02-02 | 2003-10-30 | Taveras Arthur G. | 3, 4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor antagonists |
| RU2003126913A (ru) | 2001-02-02 | 2005-03-10 | Шеринг Корпорейшн (US) | 3,4-дизамещенные циклобутен-1,2-дионы, как антагонисты хемокинового рецептора схс |
| PL208928B1 (pl) | 2001-04-16 | 2011-06-30 | Pharmacopeia | 3, 4-di-podstawione cyklobuten-1, 2-diony jako ligandy receptora CXC chemokiny |
| JP2005505595A (ja) | 2001-10-12 | 2005-02-24 | シェーリング コーポレイション | 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 |
| US6878709B2 (en) | 2002-01-04 | 2005-04-12 | Schering Corporation | 3,4-di-substituted pyridazinediones as CXC chemokine receptor antagonists |
| US20040053953A1 (en) | 2002-03-18 | 2004-03-18 | Schering Corporation | Treatment of chemokine mediated diseases |
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Cited By (2)
| 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 |
| JP2024025430A (ja) * | 2022-08-12 | 2024-02-26 | 富士フイルム株式会社 | 化合物又はその塩、タンパク質間相互作用阻害剤、医薬組成物、及び抗腫瘍剤 |
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| US20040034229A1 (en) | 2004-02-19 |
| WO2003031440A1 (en) | 2003-04-17 |
| CN1599734A (zh) | 2005-03-23 |
| US6903131B2 (en) | 2005-06-07 |
| MXPA04003439A (es) | 2004-07-08 |
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