JP2009544618A5 - - Google Patents
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- Publication number
- JP2009544618A5 JP2009544618A5 JP2009520862A JP2009520862A JP2009544618A5 JP 2009544618 A5 JP2009544618 A5 JP 2009544618A5 JP 2009520862 A JP2009520862 A JP 2009520862A JP 2009520862 A JP2009520862 A JP 2009520862A JP 2009544618 A5 JP2009544618 A5 JP 2009544618A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- aliphatic
- ring
- optionally substituted
- compound according
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 0 CCC(CC1=C(C(C2)C2C2)C=C*(*C(C(*)(C=*=C)N3C4=CC=C*(*)C=C4**C(*)(*)C3=O)=O)C=C1)*C1=C2C=CC=CC=CC=C1 Chemical compound CCC(CC1=C(C(C2)C2C2)C=C*(*C(C(*)(C=*=C)N3C4=CC=C*(*)C=C4**C(*)(*)C3=O)=O)C=C1)*C1=C2C=CC=CC=CC=C1 0.000 description 73
- YMQLSSLCXRWKQA-UHFFFAOYSA-O CC(C(N1)=O)(NC1=O)[IH+] Chemical compound CC(C(N1)=O)(NC1=O)[IH+] YMQLSSLCXRWKQA-UHFFFAOYSA-O 0.000 description 3
- SWFZYGSTUWMTPI-UHFFFAOYSA-N CC(C)(C=CN1)C1=O Chemical compound CC(C)(C=CN1)C1=O SWFZYGSTUWMTPI-UHFFFAOYSA-N 0.000 description 3
- BTJMCRAWBQGQIK-UHFFFAOYSA-N CC(C)(c(ccnc1)c1N1)C1=O Chemical compound CC(C)(c(ccnc1)c1N1)C1=O BTJMCRAWBQGQIK-UHFFFAOYSA-N 0.000 description 3
- FWWMMGOPZBVMNB-UHFFFAOYSA-N CC(C)(c(nccc1)c1N1)/C1=[O]\C Chemical compound CC(C)(c(nccc1)c1N1)/C1=[O]\C FWWMMGOPZBVMNB-UHFFFAOYSA-N 0.000 description 3
- CZGJOXNVXIVFAV-UHFFFAOYSA-N CC(C)(c(ncnc1)c1N1)/C1=[O]\C Chemical compound CC(C)(c(ncnc1)c1N1)/C1=[O]\C CZGJOXNVXIVFAV-UHFFFAOYSA-N 0.000 description 3
- OISPDNWOHCABMC-UHFFFAOYSA-N CC(C)C(C)(C1C(N2)OCCC1)C2=O Chemical compound CC(C)C(C)(C1C(N2)OCCC1)C2=O OISPDNWOHCABMC-UHFFFAOYSA-N 0.000 description 3
- SHAYFAIWNAOVSE-UHFFFAOYSA-N CC(C)C(C)(c1c(N2)nc[s]1)C2=O Chemical compound CC(C)C(C)(c1c(N2)nc[s]1)C2=O SHAYFAIWNAOVSE-UHFFFAOYSA-N 0.000 description 3
- QGECDFDEEKEVJO-UHFFFAOYSA-N CC(C)C(C)(c1cccnc1N1)C1=O Chemical compound CC(C)C(C)(c1cccnc1N1)C1=O QGECDFDEEKEVJO-UHFFFAOYSA-N 0.000 description 3
- SXVJIQFQZNOJAX-UHFFFAOYSA-N CC(C)C(CC(N1)=O)(C1=O)[IH]C Chemical compound CC(C)C(CC(N1)=O)(C1=O)[IH]C SXVJIQFQZNOJAX-UHFFFAOYSA-N 0.000 description 3
- WWFBWCVOVMKUCZ-UHFFFAOYSA-O CC(C1=C(N2)OCC1)(C2=O)[IH+] Chemical compound CC(C1=C(N2)OCC1)(C2=O)[IH+] WWFBWCVOVMKUCZ-UHFFFAOYSA-O 0.000 description 3
- FHDPJMNNOTUEKT-UHFFFAOYSA-N CC(C1=C(N2)OCCC1)(C2=O)[IH]I Chemical compound CC(C1=C(N2)OCCC1)(C2=O)[IH]I FHDPJMNNOTUEKT-UHFFFAOYSA-N 0.000 description 3
- LVQDZEAOMZKSMI-UHFFFAOYSA-N CC(C1=C(N2)SCC1)(C2=O)I Chemical compound CC(C1=C(N2)SCC1)(C2=O)I LVQDZEAOMZKSMI-UHFFFAOYSA-N 0.000 description 3
- OYOMJOLPSFPIBL-UHFFFAOYSA-N CC(C1C(N2)SCC1)(C2=O)[IH]C Chemical compound CC(C1C(N2)SCC1)(C2=O)[IH]C OYOMJOLPSFPIBL-UHFFFAOYSA-N 0.000 description 3
- DQFMPTUTAAIXAN-UHFFFAOYSA-N CC1(C)N=CNC1=O Chemical compound CC1(C)N=CNC1=O DQFMPTUTAAIXAN-UHFFFAOYSA-N 0.000 description 3
- CEDXQSMKYRXVHU-UHFFFAOYSA-N C[I-]C(c1c(N2)[s]cc1)(C2=O)[IH]C Chemical compound C[I-]C(c1c(N2)[s]cc1)(C2=O)[IH]C CEDXQSMKYRXVHU-UHFFFAOYSA-N 0.000 description 3
- DFIMFVQCVXMERG-UHFFFAOYSA-N O=C(C1([IH]I)[IH]I)Nc2c1cc[o]2 Chemical compound O=C(C1([IH]I)[IH]I)Nc2c1cc[o]2 DFIMFVQCVXMERG-UHFFFAOYSA-N 0.000 description 3
- BDEDPOLWMVWPSK-UHFFFAOYSA-N CC(C)(c1c(N2)nc[nH]1)C2=O Chemical compound CC(C)(c1c(N2)nc[nH]1)C2=O BDEDPOLWMVWPSK-UHFFFAOYSA-N 0.000 description 2
- FRUIAUUIOLTTEA-UHFFFAOYSA-N CC(C)(c1c(N2)nc[o]1)C2=O Chemical compound CC(C)(c1c(N2)nc[o]1)C2=O FRUIAUUIOLTTEA-UHFFFAOYSA-N 0.000 description 2
- FMYHJHHHIIJHRN-UHFFFAOYSA-N CC(C)C(C)(c(nccc1)c1N1)C1=O Chemical compound CC(C)C(C)(c(nccc1)c1N1)C1=O FMYHJHHHIIJHRN-UHFFFAOYSA-N 0.000 description 2
- NSEAPTQEZZLMKF-UHFFFAOYSA-N CC(C)C(CC(N1)=O)(C1=O)[I](C)I Chemical compound CC(C)C(CC(N1)=O)(C1=O)[I](C)I NSEAPTQEZZLMKF-UHFFFAOYSA-N 0.000 description 2
- RNWFHTNSACTMTG-UHFFFAOYSA-N CC(C)C1(C(C)I)N=CNC1=O Chemical compound CC(C)C1(C(C)I)N=CNC1=O RNWFHTNSACTMTG-UHFFFAOYSA-N 0.000 description 2
- CYKTWUBYWZXJSX-UHFFFAOYSA-N CC(C1=C(N2)SCCC1)(C2=O)[IH]I Chemical compound CC(C1=C(N2)SCCC1)(C2=O)[IH]I CYKTWUBYWZXJSX-UHFFFAOYSA-N 0.000 description 2
- VHNASZIROAFYSA-UHFFFAOYSA-O CC(C1C(N2)OCC1)(C2=O)[IH+](C)C Chemical compound CC(C1C(N2)OCC1)(C2=O)[IH+](C)C VHNASZIROAFYSA-UHFFFAOYSA-O 0.000 description 2
- LBHWSNRLSIZGPI-UHFFFAOYSA-N CC(C1C(N2)OCCC1)(C2=O)[IH]C Chemical compound CC(C1C(N2)OCCC1)(C2=O)[IH]C LBHWSNRLSIZGPI-UHFFFAOYSA-N 0.000 description 2
- VFJSJACITUAVID-UHFFFAOYSA-N CC(C=CN1)(C1=O)[IH]I Chemical compound CC(C=CN1)(C1=O)[IH]I VFJSJACITUAVID-UHFFFAOYSA-N 0.000 description 2
- IJUNQHFGBLBXBB-UHFFFAOYSA-N CC(c1c(N2)nn[nH]1)(C2=O)[I](C)C Chemical compound CC(c1c(N2)nn[nH]1)(C2=O)[I](C)C IJUNQHFGBLBXBB-UHFFFAOYSA-N 0.000 description 2
- BNMHGYUQURKKHB-UHFFFAOYSA-N C[IH]C1=[O][IH]c(ccnc2)c2N1 Chemical compound C[IH]C1=[O][IH]c(ccnc2)c2N1 BNMHGYUQURKKHB-UHFFFAOYSA-N 0.000 description 2
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83239706P | 2006-07-21 | 2006-07-21 | |
| US60/832,397 | 2006-07-21 | ||
| PCT/US2007/016559 WO2008011190A1 (en) | 2006-07-21 | 2007-07-23 | Cgrp receptor antagonists |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009544618A JP2009544618A (ja) | 2009-12-17 |
| JP2009544618A5 true JP2009544618A5 (enExample) | 2011-08-18 |
| JP5511379B2 JP5511379B2 (ja) | 2014-06-04 |
Family
ID=38754729
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009520862A Expired - Fee Related JP5511379B2 (ja) | 2006-07-21 | 2007-07-23 | Ｃｇｒｐレセプターアンタゴニスト |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US7842686B2 (enExample) |
| EP (1) | EP2049532B1 (enExample) |
| JP (1) | JP5511379B2 (enExample) |
| CN (1) | CN101516875A (enExample) |
| AT (1) | ATE469895T1 (enExample) |
| AU (1) | AU2007275577A1 (enExample) |
| CA (1) | CA2658573A1 (enExample) |
| DE (1) | DE602007006961D1 (enExample) |
| ES (1) | ES2343481T3 (enExample) |
| WO (1) | WO2008011190A1 (enExample) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3045182B1 (en) | 2005-11-14 | 2018-03-07 | Teva Pharmaceuticals International GmbH | Antagonist antibodies directed against calcitonin gene-related peptide for treating cluster headache |
| GEP20115140B (en) | 2006-05-09 | 2011-01-10 | Merck Sharp And Dome Corp | Substituted spirocyclic cgrp receptor antagonists |
| US8608632B1 (en) | 2009-07-03 | 2013-12-17 | Salutaris Medical Devices, Inc. | Methods and devices for minimally-invasive extraocular delivery of radiation and/or pharmaceutics to the posterior portion of the eye |
| US9873001B2 (en) | 2008-01-07 | 2018-01-23 | Salutaris Medical Devices, Inc. | Methods and devices for minimally-invasive delivery of radiation to the eye |
| US10022558B1 (en) | 2008-01-07 | 2018-07-17 | Salutaris Medical Devices, Inc. | Methods and devices for minimally-invasive delivery of radiation to the eye |
| US8602959B1 (en) | 2010-05-21 | 2013-12-10 | Robert Park | Methods and devices for delivery of radiation to the posterior portion of the eye |
| WO2009089288A1 (en) | 2008-01-07 | 2009-07-16 | Salutaris Md | Methods and devices for minimally-invasive extraocular delivery of radiation to the posterior portion of the eye |
| US9056201B1 (en) | 2008-01-07 | 2015-06-16 | Salutaris Medical Devices, Inc. | Methods and devices for minimally-invasive delivery of radiation to the eye |
| RU2522493C2 (ru) * | 2008-03-04 | 2014-07-20 | Пфайзер Лимитед | Способы лечения хронической боли |
| EP2265288B1 (en) * | 2008-03-04 | 2016-05-11 | Labrys Biologics Inc. | Methods of treating inflammatory pain |
| EP2271346B1 (en) * | 2008-03-28 | 2014-01-01 | Merck Sharp & Dohme Corp. | Monocyclic cgrp receptor antagonists |
| US8362005B2 (en) * | 2008-09-08 | 2013-01-29 | Merk. Sharp & Dohme Corp. | Monocyclic amide CGRP receptor antagonists |
| USD691268S1 (en) | 2009-01-07 | 2013-10-08 | Salutaris Medical Devices, Inc. | Fixed-shape cannula for posterior delivery of radiation to eye |
| USD691267S1 (en) | 2009-01-07 | 2013-10-08 | Salutaris Medical Devices, Inc. | Fixed-shape cannula for posterior delivery of radiation to eye |
| USD691270S1 (en) | 2009-01-07 | 2013-10-08 | Salutaris Medical Devices, Inc. | Fixed-shape cannula for posterior delivery of radiation to an eye |
| USD691269S1 (en) | 2009-01-07 | 2013-10-08 | Salutaris Medical Devices, Inc. | Fixed-shape cannula for posterior delivery of radiation to an eye |
| RU2535074C2 (ru) | 2009-08-28 | 2014-12-10 | Лэйбрис Байолоджикс, Инк. | Способы лечения висцеральной боли путем введения антител-антагонистов, направленных против пептида, связанного с геном кальцитонина |
| CN103957935B (zh) | 2011-05-20 | 2018-04-03 | 奥尔德生物控股有限责任公司 | 抗cgrp或抗cgrp‑r抗体或抗体片段用于治疗或预防慢性和急性形式的腹泻的用途 |
| JP6374789B2 (ja) | 2011-05-20 | 2018-08-15 | アルダーバイオ・ホールディングズ・エルエルシー | 羞明または光嫌悪症を予防または抑制する抗ｃｇｒｐ抗体および抗体断片のそれを必要とする対象、特に片頭痛患者における使用 |
| CN107602700B (zh) | 2011-05-20 | 2021-12-17 | H.伦德贝克公司 | 抗cgrp组合物及其用途 |
| MX2015005428A (es) | 2012-11-01 | 2015-07-21 | Incyte Corp | Derivados triciclicos fusionados de tiofeno como inhibidores de la cinasa janus (jak). |
| US20170114122A1 (en) | 2015-10-23 | 2017-04-27 | Alderbio Holdings Llc | Regulation of glucose metabolism using anti-cgrp antibodies |
| CN103804367B (zh) * | 2014-02-28 | 2016-09-14 | 天津药物研究院 | 苯并氮杂卓衍生物、其制备方法和用途 |
| US10556945B2 (en) | 2014-03-21 | 2020-02-11 | Teva Pharmaceuticals International Gmbh | Antagonist antibodies directed against calcitonin gene-related peptide and methods using same |
| FI3119431T3 (fi) | 2014-03-21 | 2024-03-20 | Teva Pharmaceuticals Int Gmbh | Kalsitoniinigeeniin liittyvää peptidiä vastaan suunnattuja antagonisti-vasta-aineita ja menetelmiä niiden käyttämiseksi |
| JP2017514832A (ja) | 2014-04-30 | 2017-06-08 | インサイト・コーポレイションＩｎｃｙｔｅ Ｃｏｒｐｏｒａｔｉｏｎ | Ｊａｋ１抑制剤を調製する方法及びその新しい形態 |
| FR3030521B1 (fr) * | 2014-12-23 | 2019-07-26 | Galderma Research & Development | Nouveaux composes heterocycliques et leur utilisation en medecine ainsi qu'en cosmetique |
| MY192762A (en) | 2015-07-02 | 2022-09-07 | Hoffmann La Roche | Bicyclic lactams and methods of use thereof |
| EP3414239A2 (en) | 2016-02-05 | 2018-12-19 | Denali Therapeutics Inc. | Inhibitors of receptor-interacting protein kinase 1 |
| USD814637S1 (en) | 2016-05-11 | 2018-04-03 | Salutaris Medical Devices, Inc. | Brachytherapy device |
| USD814638S1 (en) | 2016-05-11 | 2018-04-03 | Salutaris Medical Devices, Inc. | Brachytherapy device |
| USD815285S1 (en) | 2016-05-11 | 2018-04-10 | Salutaris Medical Devices, Inc. | Brachytherapy device |
| USD808528S1 (en) | 2016-08-31 | 2018-01-23 | Salutaris Medical Devices, Inc. | Holder for a brachytherapy device |
| USD808529S1 (en) | 2016-08-31 | 2018-01-23 | Salutaris Medical Devices, Inc. | Holder for a brachytherapy device |
| KR20190066607A (ko) | 2016-09-23 | 2019-06-13 | 테바 파마슈티컬스 인터내셔널 게엠베하 | 불응성 편두통의 치료 |
| JP7349359B2 (ja) | 2016-10-17 | 2023-09-22 | エフ． ホフマン－ラ ロシュ アーゲー | 二環式ピリドンラクタム及びその使用方法。 |
| SI3552017T1 (sl) | 2016-12-09 | 2022-09-30 | Denali Therapeutics Inc. | Spojine uporabne kot zaviralci RIPK1 |
| US11072607B2 (en) | 2016-12-16 | 2021-07-27 | Genentech, Inc. | Inhibitors of RIP1 kinase and methods of use thereof |
| HUE067471T2 (hu) | 2018-03-30 | 2024-10-28 | Incyte Corp | Gennyes verejtékmirigy-gyulladás kezelése jak inhibitorok alkalmazásával |
| CN112074519B (zh) | 2018-04-20 | 2024-08-02 | 豪夫迈·罗氏有限公司 | 作为rip1激酶抑制剂用于治疗例如肠易激综合征(ibs)的化合物 |
| MX2021008267A (es) | 2019-01-08 | 2021-08-05 | H Lundbeck As | Tratamiento agudo y tratamiento rapido de la cefalea usando anticuerpos anti-cgrp. |
| BR102020007149A8 (pt) | 2020-04-06 | 2023-09-26 | H Lundbeck As | Usos de um anticorpo anti-cgrp ou anti-cgrp-r ou um fragmento dos mesmos para melhorar o sintoma mais incômodo (mbs) e a impressão global de mudança (pgic) associados com enxaqueca |
| EP4463229A1 (en) | 2022-01-12 | 2024-11-20 | Denali Therapeutics Inc. | Crystalline forms of (s)-5-benzyl-n-(5-methyl-4-oxo-2, 3,4,5- tetrahydropyrido [3,2-b] [l,4]oxazepin-3-yl)-4h-l,2,4-triazole-3-carboxamide |
| EP4462999A4 (en) * | 2022-01-14 | 2025-12-24 | Enko Chem Inc | PROTOPORPHYRINOGEN OXIDASE INHIBITORS |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7189722B2 (en) * | 2003-03-14 | 2007-03-13 | Merck & Co., Inc. | Aryl spirohydantoin CGRP receptor antagonists |
| ATE556060T1 (de) * | 2003-03-14 | 2012-05-15 | Merck Sharp & Dohme | Monocyclische anilidspirohydantoine als cgrp- rezeptorantagonisten |
| US7288559B2 (en) * | 2003-03-14 | 2007-10-30 | Merck + Co, Inc. | Carboxamide spirohydantoin CGRP receptor antagonists |
| AU2004222383B2 (en) * | 2003-03-14 | 2009-10-01 | Merck Sharp & Dohme Corp. | Bicyclic anilide spirohydantoin CGRP receptor antagonists |
| US7205293B2 (en) * | 2003-03-14 | 2007-04-17 | Merck & Co., Inc. | Benodiazepine spirohydantoin CGRP receptor antagonists |
| CN101076527B (zh) * | 2004-09-13 | 2011-11-30 | 默沙东公司 | 三环酰苯胺螺乙内酰脲cgrp受体拮抗剂 |
| US7390798B2 (en) * | 2004-09-13 | 2008-06-24 | Merck & Co., Inc. | Carboxamide spirolactam CGRP receptor antagonists |
| US8003792B2 (en) * | 2004-09-13 | 2011-08-23 | Merck Sharp & Dohme Corp. | Bicyclic anilide spirolactam CGRP receptor antagonists |
| CA2582593A1 (en) * | 2004-10-07 | 2006-04-20 | Merck & Co., Inc. | Cgrp receptor antagonists |
| US7384930B2 (en) * | 2004-11-03 | 2008-06-10 | Bristol-Myers Squibb Company | Constrained compounds as CGRP-receptor antagonists |
-
2007
- 2007-07-23 CN CNA2007800342187A patent/CN101516875A/zh active Pending
- 2007-07-23 DE DE602007006961T patent/DE602007006961D1/de active Active
- 2007-07-23 EP EP07796984A patent/EP2049532B1/en not_active Not-in-force
- 2007-07-23 JP JP2009520862A patent/JP5511379B2/ja not_active Expired - Fee Related
- 2007-07-23 AT AT07796984T patent/ATE469895T1/de not_active IP Right Cessation
- 2007-07-23 ES ES07796984T patent/ES2343481T3/es active Active
- 2007-07-23 CA CA002658573A patent/CA2658573A1/en not_active Abandoned
- 2007-07-23 WO PCT/US2007/016559 patent/WO2008011190A1/en not_active Ceased
- 2007-07-23 AU AU2007275577A patent/AU2007275577A1/en not_active Abandoned
-
2009
- 2009-01-21 US US12/356,745 patent/US7842686B2/en active Active
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