JP6387086B2 - 新規ソマトスタチン受容体亜型4(sstr4)作動薬 - Google Patents
新規ソマトスタチン受容体亜型4(sstr4)作動薬 Download PDFInfo
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- JP6387086B2 JP6387086B2 JP2016513359A JP2016513359A JP6387086B2 JP 6387086 B2 JP6387086 B2 JP 6387086B2 JP 2016513359 A JP2016513359 A JP 2016513359A JP 2016513359 A JP2016513359 A JP 2016513359A JP 6387086 B2 JP6387086 B2 JP 6387086B2
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- 0 C*C(C)(*)NC([C@]1[C@@]2[C@]1CN(*)C2)=O Chemical compound C*C(C)(*)NC([C@]1[C@@]2[C@]1CN(*)C2)=O 0.000 description 1
- BKIKNNIHPPZMBG-UHFFFAOYSA-N CC(C)(C(NCc1ncncc1)=O)NC(OCc1ccccc1)=O Chemical compound CC(C)(C(NCc1ncncc1)=O)NC(OCc1ccccc1)=O BKIKNNIHPPZMBG-UHFFFAOYSA-N 0.000 description 1
- YVWLKWYISKFPEJ-UHFFFAOYSA-N CC(C)(C(O)=O)c1n[o]c2c1cccc2 Chemical compound CC(C)(C(O)=O)c1n[o]c2c1cccc2 YVWLKWYISKFPEJ-UHFFFAOYSA-N 0.000 description 1
- KXYUCHYTEPOFKD-JHIQODARSA-N CC(C)(C)OC(N(C[C@H]12)CC1[C@H]2C(NC(C)(C)c1n[nH]c2c(C(F)(F)F)cccc12)=O)=O Chemical compound CC(C)(C)OC(N(C[C@H]12)CC1[C@H]2C(NC(C)(C)c1n[nH]c2c(C(F)(F)F)cccc12)=O)=O KXYUCHYTEPOFKD-JHIQODARSA-N 0.000 description 1
- IGDFPMOKEBBAHK-QLPKVWCKSA-N CC(C)(C)OC(N(C[C@H]12)C[C@@H]1[C@H]2C(NC(C)(C)c1c(C)nc2[n]1cccc2)=O)=O Chemical compound CC(C)(C)OC(N(C[C@H]12)C[C@@H]1[C@H]2C(NC(C)(C)c1c(C)nc2[n]1cccc2)=O)=O IGDFPMOKEBBAHK-QLPKVWCKSA-N 0.000 description 1
- QVESQRFZUMXKBE-FICVDOATSA-N CC(C)(C)OC(N(C[C@H]12)C[C@@H]1[C@H]2C(NC(C)(C)c1nnc2[n]1cccc2C)=O)=O Chemical compound CC(C)(C)OC(N(C[C@H]12)C[C@@H]1[C@H]2C(NC(C)(C)c1nnc2[n]1cccc2C)=O)=O QVESQRFZUMXKBE-FICVDOATSA-N 0.000 description 1
- HWQMZDLNMTXZLI-UHFFFAOYSA-N CC(C)(CCc1ncccc1C(F)(F)F)N Chemical compound CC(C)(CCc1ncccc1C(F)(F)F)N HWQMZDLNMTXZLI-UHFFFAOYSA-N 0.000 description 1
- BDNJUGSFFTVBLW-UHFFFAOYSA-N CC(C)(COc(c(C)c1)ncc1F)N Chemical compound CC(C)(COc(c(C)c1)ncc1F)N BDNJUGSFFTVBLW-UHFFFAOYSA-N 0.000 description 1
- VPRVQLWPUQEZBW-FOLVSLTJSA-N CC(C)(COc(c1c2cccc1)cnc2Cl)NC([C@@H]1[C@@H]2[C@H]1CNC2)=O Chemical compound CC(C)(COc(c1c2cccc1)cnc2Cl)NC([C@@H]1[C@@H]2[C@H]1CNC2)=O VPRVQLWPUQEZBW-FOLVSLTJSA-N 0.000 description 1
- UVQOAIKFJAHEPD-IWIIMEHWSA-N CC(C)(COc1c(C(F)(F)F)ccnc1)NC([C@@H]1[C@@H]2[C@H]1CNC2)=O Chemical compound CC(C)(COc1c(C(F)(F)F)ccnc1)NC([C@@H]1[C@@H]2[C@H]1CNC2)=O UVQOAIKFJAHEPD-IWIIMEHWSA-N 0.000 description 1
- UMDPIRYSPFJXOV-SSGZVVCFSA-N CC(C)(COc1c(C)cccc1)NC([C@@H]1[C@@H]2[C@H]1CN(C)C2)O Chemical compound CC(C)(COc1c(C)cccc1)NC([C@@H]1[C@@H]2[C@H]1CN(C)C2)O UMDPIRYSPFJXOV-SSGZVVCFSA-N 0.000 description 1
- RUCBXBGWWWYZDZ-FICVDOATSA-N CC(C)(COc1c(C2CC2)cccn1)NC([C@@H]1[C@@H]2[C@H]1CNC2)=O Chemical compound CC(C)(COc1c(C2CC2)cccn1)NC([C@@H]1[C@@H]2[C@H]1CNC2)=O RUCBXBGWWWYZDZ-FICVDOATSA-N 0.000 description 1
- FPHQHULGJFFCLZ-UHFFFAOYSA-N CC(C)(COc1ccccc1F)[N+]([O-])=O Chemical compound CC(C)(COc1ccccc1F)[N+]([O-])=O FPHQHULGJFFCLZ-UHFFFAOYSA-N 0.000 description 1
- JNZSKKKRJYZYAA-UHFFFAOYSA-N CC(C)(COc1nnccc1C)NC(C1C2C1CNC2)=O Chemical compound CC(C)(COc1nnccc1C)NC(C1C2C1CNC2)=O JNZSKKKRJYZYAA-UHFFFAOYSA-N 0.000 description 1
- JMLKTWMDMDGNQX-IWIIMEHWSA-N CC(C)(c([nH]c1c2)nc1ccc2Cl)NC([C@@H]1[C@@H]2[C@H]1CNC2)=O Chemical compound CC(C)(c([nH]c1c2)nc1ccc2Cl)NC([C@@H]1[C@@H]2[C@H]1CNC2)=O JMLKTWMDMDGNQX-IWIIMEHWSA-N 0.000 description 1
- LYLHALCVDIWLTO-ONXXMXGDSA-N CC(C)(c(cc1)c[n]2c1ncc2)NC(C1[C@@H]2[C@H]1CNC2)=O Chemical compound CC(C)(c(cc1)c[n]2c1ncc2)NC(C1[C@@H]2[C@H]1CNC2)=O LYLHALCVDIWLTO-ONXXMXGDSA-N 0.000 description 1
- WDYRPVHKYSFTPL-UHFFFAOYSA-N CC(C)(c1c(cccc2)c2ncn1)NC(C1C2(C)C1CNC2)=O Chemical compound CC(C)(c1c(cccc2)c2ncn1)NC(C1C2(C)C1CNC2)=O WDYRPVHKYSFTPL-UHFFFAOYSA-N 0.000 description 1
- ALLAHEPCHBRBAQ-UHFFFAOYSA-N CC(C)(c1c(ccnc2)c2ccc1)NC(C1C2C1CNC2)=O Chemical compound CC(C)(c1c(ccnc2)c2ccc1)NC(C1C2C1CNC2)=O ALLAHEPCHBRBAQ-UHFFFAOYSA-N 0.000 description 1
- WAFNGLHVCXJFKD-UHFFFAOYSA-N CC(C)(c1cc2ncc[n]2cc1)NC(C1C2C1CNC2)=O Chemical compound CC(C)(c1cc2ncc[n]2cc1)NC(C1C2C1CNC2)=O WAFNGLHVCXJFKD-UHFFFAOYSA-N 0.000 description 1
- ORXLKEOBMQETFX-UHFFFAOYSA-N CC(C)(c1cncc2c1cccc2)NC(C1C2C1CNC2)=O Chemical compound CC(C)(c1cncc2c1cccc2)NC(C1C2C1CNC2)=O ORXLKEOBMQETFX-UHFFFAOYSA-N 0.000 description 1
- BSWSUJIEKZHADN-UHFFFAOYSA-N CC(C)(c1n[nH]c2c(C)cccc12)NC(C1C2(C)C1CNC2)=O Chemical compound CC(C)(c1n[nH]c2c(C)cccc12)NC(C1C2(C)C1CNC2)=O BSWSUJIEKZHADN-UHFFFAOYSA-N 0.000 description 1
- DEWGUMCLXFSVQC-UHFFFAOYSA-N CC(C)(c1n[o]c2c1cccc2C)NC(C1C2C1CNC2)=O Chemical compound CC(C)(c1n[o]c2c1cccc2C)NC(C1C2C1CNC2)=O DEWGUMCLXFSVQC-UHFFFAOYSA-N 0.000 description 1
- WNWXLHSKHQGJRW-YIOYIWSBSA-N CC(C)(c1ncnc2c1cccc2C)NC([C@@H]1C2[C@H]1CNC2)=O Chemical compound CC(C)(c1ncnc2c1cccc2C)NC([C@@H]1C2[C@H]1CNC2)=O WNWXLHSKHQGJRW-YIOYIWSBSA-N 0.000 description 1
- XIFKMRFYKUCGFA-UHFFFAOYSA-N CC(C)(c1nnc2[n]1cccc2C)N Chemical compound CC(C)(c1nnc2[n]1cccc2C)N XIFKMRFYKUCGFA-UHFFFAOYSA-N 0.000 description 1
- JYTVMQSGYSVKOE-JYBDTMGZSA-N CC(COc1c(C)cccc1)NC([C@@H]1[C@@H]2[C@H]1CNC2)=O Chemical compound CC(COc1c(C)cccc1)NC([C@@H]1[C@@H]2[C@H]1CNC2)=O JYTVMQSGYSVKOE-JYBDTMGZSA-N 0.000 description 1
- CVVDMUYJTWFLAW-UHFFFAOYSA-N CC(c1cnc2[n]1nccc2)=O Chemical compound CC(c1cnc2[n]1nccc2)=O CVVDMUYJTWFLAW-UHFFFAOYSA-N 0.000 description 1
- PVROETJHCUDAFG-UHFFFAOYSA-N C[n]1nc(C(N)=O)c2ccccc12 Chemical compound C[n]1nc(C(N)=O)c2ccccc12 PVROETJHCUDAFG-UHFFFAOYSA-N 0.000 description 1
- JAORERSHXBOUHR-UHFFFAOYSA-N Cc1cc2cnccc2c(C#N)n1 Chemical compound Cc1cc2cnccc2c(C#N)n1 JAORERSHXBOUHR-UHFFFAOYSA-N 0.000 description 1
- LAGDDNBYYCFVNJ-UHFFFAOYSA-N Cc1ccc[n]2c(C#N)ccc12 Chemical compound Cc1ccc[n]2c(C#N)ccc12 LAGDDNBYYCFVNJ-UHFFFAOYSA-N 0.000 description 1
- PQLZCOPDSVJING-JLRAQOTISA-N O=C([C@@H]1[C@@H]2[C@H]1CNC2)NC1(COCC1)c1nc(ccc(Cl)c2)c2[nH]1 Chemical compound O=C([C@@H]1[C@@H]2[C@H]1CNC2)NC1(COCC1)c1nc(ccc(Cl)c2)c2[nH]1 PQLZCOPDSVJING-JLRAQOTISA-N 0.000 description 1
- SMWDFEZZVXVKRB-UHFFFAOYSA-N c(cc1)cc2c1nccc2 Chemical compound c(cc1)cc2c1nccc2 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 1
- JMANUKZDKDKBJP-UHFFFAOYSA-N c(nc1)c2[n]1cccc2 Chemical compound c(nc1)c2[n]1cccc2 JMANUKZDKDKBJP-UHFFFAOYSA-N 0.000 description 1
- DVUBDHRTVYLIPA-UHFFFAOYSA-N c1c(cccc2)[n]2nc1 Chemical compound c1c(cccc2)[n]2nc1 DVUBDHRTVYLIPA-UHFFFAOYSA-N 0.000 description 1
- HOBCFUWDNJPFHB-UHFFFAOYSA-N c1c[n](cccc2)c2c1 Chemical compound c1c[n](cccc2)c2c1 HOBCFUWDNJPFHB-UHFFFAOYSA-N 0.000 description 1
- LFSXCDWNBUNEEM-UHFFFAOYSA-N c1ccc(cnnc2)c2c1 Chemical compound c1ccc(cnnc2)c2c1 LFSXCDWNBUNEEM-UHFFFAOYSA-N 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N c1ccc2ncncc2c1 Chemical compound c1ccc2ncncc2c1 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N c1ccccc1 Chemical compound c1ccccc1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N c1ccncc1 Chemical compound c1ccncc1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- LTHXZJUAGBTZSE-UHFFFAOYSA-N c1cnc2[n]1c(-c1c(ccnc3)c3ncc1)ccc2-c1cncc2c1cccc2 Chemical compound c1cnc2[n]1c(-c1c(ccnc3)c3ncc1)ccc2-c1cncc2c1cccc2 LTHXZJUAGBTZSE-UHFFFAOYSA-N 0.000 description 1
- BAXOFTOLAUCFNW-UHFFFAOYSA-N c1n[nH]c2c1cccc2 Chemical compound c1n[nH]c2c1cccc2 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 description 1
- KTZQTRPPVKQPFO-UHFFFAOYSA-N c1n[o]c2ccccc12 Chemical compound c1n[o]c2ccccc12 KTZQTRPPVKQPFO-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—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
- 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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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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- A61K31/415—1,2-Diazoles
- A61K31/4155—1,2-Diazoles non condensed and containing further heterocyclic rings
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- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
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- A61K31/42—Oxazoles
- A61K31/423—Oxazoles condensed with carbocyclic rings
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- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/502—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
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| US9371282B2 (en) * | 2013-05-17 | 2016-06-21 | Centrexion Therapeutics Corporation | Somatostatin receptor subtype 4 (SSTR4) agonists |
| HUE033587T2 (hu) | 2013-05-17 | 2017-12-28 | Incyte Corp | Bipirazol-származékok mint JAK inhibitorok |
| JP2017526728A (ja) | 2014-09-15 | 2017-09-14 | インフラマトリー・レスポンス・リサーチ・インコーポレイテッド | 炎症介在性状態の治療におけるレボセチリジン及びモンテルカスト |
| WO2016075239A1 (en) * | 2014-11-14 | 2016-05-19 | Boehringer Ingelheim International Gmbh | Aryl and heteroaryl-fused tetrahydro-1,4-oxazepine amides as somatostatin receptor subtype 4 (sstr4) agonists |
| SI3397631T1 (sl) | 2015-12-29 | 2022-01-31 | Pfizer Inc. | Substituirani 3-azabiciklo(3.1.0)heksani kot zaviralci ketoheksokinaze |
| EP3634406B1 (en) | 2017-05-12 | 2023-09-06 | Board of Trustees of The Southern Illinois University on behalf of Southern Illinois University Edwardsville | 3,4,5-trisubstituted-1,2,4-triazoles and 3,4,5-trisubstituted-3-thio-1,2,4-triazoles and uses thereof |
| US11912687B2 (en) | 2017-05-12 | 2024-02-27 | Board of Trustees of the Southern Illinois University | 3,4,5-trisubstituted-1,2,4-triazoles and 3,4,5-trisubstituted-3-thio-1,2,4-triazoles and uses thereof |
| US10865163B2 (en) | 2017-12-20 | 2020-12-15 | The University Of Toledo | Carbon dioxide as a directing group for C—H functionalization reactions involving Lewis basic amines, alcohols, thiols, and phosphines for the synthesis of compounds |
| KR102925957B1 (ko) | 2018-02-16 | 2026-02-11 | 인사이트 코포레이션 | 사이토카인-관련 장애의 치료를 위한 jak1 경로 억제제 |
| TWI834637B (zh) | 2018-03-01 | 2024-03-11 | 日商武田藥品工業有限公司 | 六氫吡啶基-3-(芳氧基)丙醯胺及丙酸酯 |
| SMT202400306T1 (it) | 2018-03-30 | 2024-09-16 | Incyte Corp | Trattamento dell'idrosadenite suppurativa utilizzando inibitori di jak. |
| US11668295B2 (en) | 2018-12-28 | 2023-06-06 | Avent, Inc. | Pump head for a peristaltic pump |
| CN112979655A (zh) | 2019-12-16 | 2021-06-18 | 上海赛默罗生物科技有限公司 | 三唑并哒嗪类衍生物、其制备方法、药物组合物和用途 |
| AR121682A1 (es) * | 2020-03-31 | 2022-06-29 | Takeda Pharmaceuticals Co | Derivados de n-(heterociclil y heterociclilalquil)-3-bencilpiridin-2-amina como agonistas de sstr4 |
| EP4153178A4 (en) * | 2020-05-19 | 2024-06-05 | Irr, Inc. | Levocetirizine and montelukast in the treatment of sepsis and symptoms thereof |
| WO2021233428A1 (zh) * | 2020-05-21 | 2021-11-25 | 广州费米子科技有限责任公司 | 含氮饱和杂环化合物及其制备方法、药物组合物和应用 |
| JP7774312B2 (ja) * | 2020-05-21 | 2025-11-21 | クワンチョウ フェルミオン テクノロジー カンパニー リミテッド | 縮合環化合物、それらの製造方法、医薬組成物、およびそれらの使用 |
| MX2022015221A (es) | 2020-06-02 | 2023-03-08 | Incyte Corp | Procesos para preparar un inhibidor de cinasa jano 1 (jak1). |
| WO2022012534A1 (zh) * | 2020-07-13 | 2022-01-20 | 广州费米子科技有限责任公司 | 含氮杂环化合物、药物组合物和应用 |
| CN116601279A (zh) | 2020-07-28 | 2023-08-15 | 思进股份有限公司 | 用于生产多肽的方法和系统 |
| CA3193745A1 (en) * | 2020-10-02 | 2022-04-07 | Kang Le | Imidazopiperazine inhibitors of transcription activating proteins |
| CA3204374A1 (en) | 2020-12-08 | 2022-06-16 | Incyte Corporation | Jak1 pathway inhibitors for the treatment of vitiligo |
| UA129643C2 (uk) | 2021-05-03 | 2025-06-18 | Інсайт Корпорейшн | Інгібітори шляху jak1 для лікування вузлуватого свербця |
| TWI860849B (zh) | 2021-09-14 | 2024-11-01 | 美商美國禮來大藥廠 | Sstr4促效劑鹽 |
| AU2024236692A1 (en) | 2023-03-10 | 2025-10-16 | Eli Lilly And Company | Methods for the preparation and dose regimens for use of sstr4 agonists and salts thereof |
| JP2026509366A (ja) | 2023-03-10 | 2026-03-18 | イーライ リリー アンド カンパニー | Sstr4アゴニスト及びその塩の調製のための方法 |
| WO2024245077A1 (zh) * | 2023-05-29 | 2024-12-05 | 武汉熙瑞医药科技有限公司 | 3-氮杂-双环[3.1.0]己烷衍生物、其制备方法及其应用 |
| WO2025027049A1 (en) * | 2023-08-02 | 2025-02-06 | Boehringer Ingelheim International Gmbh | (2s,5r)-5-(hydroxymethyl)morpholine-2-carboxamides as agonists of sstr4 |
| WO2025096300A1 (en) | 2023-10-30 | 2025-05-08 | Eli Lilly And Company | Novel methods for the preparation of 3-azabicylco[3.1,0]hexane-6-carboxamide derivatives |
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| WO2026030052A1 (en) | 2024-07-31 | 2026-02-05 | Fmc Corporation | Fungicidal substituted azoles |
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| US6159941A (en) | 1996-05-14 | 2000-12-12 | Novo Nordisk A/S | Use of somatostatin agonists and antagonists for treating diseases related to the eye |
| US6355613B1 (en) | 1996-07-31 | 2002-03-12 | Peptor Limited | Conformationally constrained backbone cyclized somatostatin analogs |
| US6057338A (en) | 1997-04-04 | 2000-05-02 | Merck & Co., Inc. | Somatostatin agonists |
| US6063796A (en) | 1997-04-04 | 2000-05-16 | Merck & Co., Inc. | Somatostatin agonists |
| US20100004339A1 (en) | 2003-10-06 | 2010-01-07 | Oy Juvantia Pharma Ltd. | Somatostatin Receptor 1 and/or 4 Selective Agonists and Antagonists |
| FI20031454A0 (fi) | 2003-10-06 | 2003-10-06 | Juvantia Pharma Ltd Oy | Selektiivisiä somatostatiinireseptori 1 ja/tai 4 -agonisteja ja -antagonisteja |
| RS20060190A (sr) | 2003-10-14 | 2008-08-07 | Pfizer Products Inc., | Biciklični /3.1.0/ derivati kao inhibitori transportera glicina |
| CA2672373C (en) | 2006-12-19 | 2011-08-30 | Pfizer Products Inc. | Nicotinamide derivatives as inhibitors of h-pgds and their use for treating prostaglandin d2 mediated diseases |
| WO2010059922A1 (en) | 2008-11-21 | 2010-05-27 | Ligand Pharmaceuticals Incorporated | Pyrrolidine carboxamide compounds |
| US8835472B2 (en) | 2010-09-02 | 2014-09-16 | Boehringer Ingelheim International Gmbh | Compounds, pharmaceutical compositions and uses thereof |
| EP2685828A4 (en) | 2011-03-17 | 2014-08-13 | Merck Sharp & Dohme | SUBSTITUTED 3-AZABICYCLO [3,1,0-] HEXAN DERIVATIVES AS CCR2 ANTAGONISTS |
| CN102675290B (zh) * | 2011-03-18 | 2014-11-12 | 山东亨利医药科技有限责任公司 | 含有并环的二氢吡唑类化合物 |
| KR101556318B1 (ko) * | 2013-05-15 | 2015-10-01 | 한국과학기술연구원 | 칼슘이온 채널 조절제로서 유효한 6-피라졸일아미도-3-치환된 아자바이사이클로[3.1.0]헥산 유도체 |
| US9371282B2 (en) * | 2013-05-17 | 2016-06-21 | Centrexion Therapeutics Corporation | Somatostatin receptor subtype 4 (SSTR4) agonists |
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