EA202092250A1 - Комбинированные продукты для лечения rsv - Google Patents
Комбинированные продукты для лечения rsvInfo
- Publication number
- EA202092250A1 EA202092250A1 EA202092250A EA202092250A EA202092250A1 EA 202092250 A1 EA202092250 A1 EA 202092250A1 EA 202092250 A EA202092250 A EA 202092250A EA 202092250 A EA202092250 A EA 202092250A EA 202092250 A1 EA202092250 A1 EA 202092250A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- compounds
- methyl
- compound
- imidazo
- pyridin
- Prior art date
Links
- 229940126062 Compound A Drugs 0.000 abstract 6
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 6
- 206010061603 Respiratory syncytial virus infection Diseases 0.000 abstract 3
- -1 YM-543403 Chemical compound 0.000 abstract 3
- 230000002401 inhibitory effect Effects 0.000 abstract 2
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 2
- 229940127557 pharmaceutical product Drugs 0.000 abstract 2
- QZSZPSDRJPPZDZ-OAQYLSRUSA-N (9bs)-9b-(4-chlorophenyl)-1-(pyridine-3-carbonyl)-2,3-dihydroimidazo[5,6]pyrrolo[1,2-a]pyridin-5-one Chemical compound C1=CC(Cl)=CC=C1[C@]1(C2=CN=CC=C2C2=O)N2CCN1C(=O)C1=CC=CN=C1 QZSZPSDRJPPZDZ-OAQYLSRUSA-N 0.000 abstract 1
- MTPVBMVUENFFLL-HXUWFJFHSA-N 1-(2-fluorophenyl)-3-[(3s)-2-oxo-5-phenyl-1,3-dihydro-1,4-benzodiazepin-3-yl]urea Chemical compound FC1=CC=CC=C1NC(=O)N[C@@H]1C(=O)NC2=CC=CC=C2C(C=2C=CC=CC=2)=N1 MTPVBMVUENFFLL-HXUWFJFHSA-N 0.000 abstract 1
- KSHJXDWYTZJUEI-UHFFFAOYSA-N 1-cyclopropyl-3-[[1-(4-hydroxybutyl)benzimidazol-2-yl]methyl]imidazo[4,5-c]pyridin-2-one Chemical compound N=1C2=CC=CC=C2N(CCCCO)C=1CN(C1=O)C2=CN=CC=C2N1C1CC1 KSHJXDWYTZJUEI-UHFFFAOYSA-N 0.000 abstract 1
- BLUJRJMLDHEMRX-UHFFFAOYSA-N 2-[[2-hydroxy-5-[(5-methyltetrazol-1-yl)iminomethyl]phenyl]-(4-hydroxyphenyl)methyl]-4-[(5-methyltetrazol-1-yl)iminomethyl]phenol Chemical compound Cc1nnnn1N=Cc1ccc(O)c(c1)C(c1ccc(O)cc1)c1cc(C=Nn2nnnc2C)ccc1O BLUJRJMLDHEMRX-UHFFFAOYSA-N 0.000 abstract 1
- DKORMNNYNRPTBJ-UHFFFAOYSA-N 2-[[6-[[2-(3-hydroxypropyl)-5-methylanilino]methyl]-2-(3-morpholin-4-ylpropylamino)benzimidazol-1-yl]methyl]-6-methylpyridin-3-ol Chemical compound CC1=CC=C(CCCO)C(NCC=2C=C3N(CC=4C(=CC=C(C)N=4)O)C(NCCCN4CCOCC4)=NC3=CC=2)=C1 DKORMNNYNRPTBJ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 abstract 1
- CKCODSNUWCBRIS-UHFFFAOYSA-N 5-[[4,6-bis[3-[bis(3-amino-3-oxo-propyl)sulfamoyl]anilino]-1,3,5-triazin-2-yl]amino]-2-[4-[[4,6-bis[3-[bis(3-amino-3-oxo-propyl)sulfamoyl]anilino]-1,3,5-triazin-2-yl]amino]-2-sulfo-phenyl]benzenesulfonic acid Chemical compound NC(=O)CCN(CCC(N)=O)S(=O)(=O)C1=CC=CC(NC=2N=C(NC=3C=C(C(C=4C(=CC(NC=5N=C(NC=6C=C(C=CC=6)S(=O)(=O)N(CCC(N)=O)CCC(N)=O)N=C(NC=6C=C(C=CC=6)S(=O)(=O)N(CCC(N)=O)CCC(N)=O)N=5)=CC=4)S(O)(=O)=O)=CC=3)S(O)(=O)=O)N=C(NC=3C=C(C=CC=3)S(=O)(=O)N(CCC(N)=O)CCC(N)=O)N=2)=C1 CKCODSNUWCBRIS-UHFFFAOYSA-N 0.000 abstract 1
- GTQTUABHRCWVLL-UHFFFAOYSA-N C(CCN1C(=CC2=CC(=CC=C12)Cl)CN1C2=C(N(C1=O)CC(F)(F)F)C=CN=C2)S(=O)(=O)C Chemical compound C(CCN1C(=CC2=CC(=CC=C12)Cl)CN1C2=C(N(C1=O)CC(F)(F)F)C=CN=C2)S(=O)(=O)C GTQTUABHRCWVLL-UHFFFAOYSA-N 0.000 abstract 1
- SWWRPROUTDGFFV-UHFFFAOYSA-N CCS(=O)(=O)CCc1c(CN2C(=O)N(C3CC3)c4ccncc24)nc5cc(Cl)ccn15 Chemical compound CCS(=O)(=O)CCc1c(CN2C(=O)N(C3CC3)c4ccncc24)nc5cc(Cl)ccn15 SWWRPROUTDGFFV-UHFFFAOYSA-N 0.000 abstract 1
- VTCJNYICQADBJD-UHFFFAOYSA-N N-(2-fluoro-6-methylphenyl)-6-[4-[[5-methyl-2-(7-oxa-2-azaspiro[3.5]nonan-2-yl)pyridine-3-carbonyl]amino]benzoyl]-4,5-dihydrothieno[3,2-d][1]benzazepine-2-carboxamide Chemical compound FC1=C(C(=CC=C1)C)NC(=O)C1=CC2=C(C3=C(N(CC2)C(C2=CC=C(C=C2)NC(C2=C(N=CC(=C2)C)N2CC4(C2)CCOCC4)=O)=O)C=CC=C3)S1 VTCJNYICQADBJD-UHFFFAOYSA-N 0.000 abstract 1
- ALMZSKFFZDETDT-UHFFFAOYSA-N O=S(=O)(C)CCCN1C2=C(C=C(Cl)C=C2)N=C1CN1C2=C(N(C1=O)C1CC1)C=CN=C2 Chemical compound O=S(=O)(C)CCCN1C2=C(C=C(Cl)C=C2)N=C1CN1C2=C(N(C1=O)C1CC1)C=CN=C2 ALMZSKFFZDETDT-UHFFFAOYSA-N 0.000 abstract 1
- IWUCXVSUMQZMFG-AFCXAGJDSA-N Ribavirin Chemical compound N1=C(C(=O)N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 IWUCXVSUMQZMFG-AFCXAGJDSA-N 0.000 abstract 1
- 239000013066 combination product Substances 0.000 abstract 1
- 229940127555 combination product Drugs 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- GOFXWTVKPWJNGD-UWJYYQICSA-N n-[2-[(2s)-2-[5-[(3s)-3-aminopyrrolidin-1-yl]-6-methylpyrazolo[1,5-a]pyrimidin-2-yl]piperidine-1-carbonyl]-4-chlorophenyl]methanesulfonamide Chemical compound CC1=CN2N=C([C@H]3N(CCCC3)C(=O)C=3C(=CC=C(Cl)C=3)NS(C)(=O)=O)C=C2N=C1N1CC[C@H](N)C1 GOFXWTVKPWJNGD-UWJYYQICSA-N 0.000 abstract 1
- 229960000402 palivizumab Drugs 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical compound OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 abstract 1
- ZETYKEPFFRMVBX-UHFFFAOYSA-N rfi 641 Chemical compound NC(=O)CN(CC(N)=O)S(=O)(=O)C1=CC=CC(NC=2N=C(NC=3C=C(C(C=4C(=CC(NC=5N=C(NC=6C=C(C=CC=6)S(=O)(=O)N(CC(N)=O)CC(N)=O)N=C(NC=6C=C(C=CC=6)S(=O)(=O)N(CC(N)=O)CC(N)=O)N=5)=CC=4)S(O)(=O)=O)=CC=3)S(O)(=O)=O)N=C(NC=3C=C(C=CC=3)S(=O)(=O)N(CC(N)=O)CC(N)=O)N=2)=C1 ZETYKEPFFRMVBX-UHFFFAOYSA-N 0.000 abstract 1
- 229960000329 ribavirin Drugs 0.000 abstract 1
- HZCAHMRRMINHDJ-DBRKOABJSA-N ribavirin Natural products O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1N=CN=C1 HZCAHMRRMINHDJ-DBRKOABJSA-N 0.000 abstract 1
Classifications
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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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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- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
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- C—CHEMISTRY; METALLURGY
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- C07K16/08—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from viruses
- C07K16/10—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from viruses from RNA viruses
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
Изобретение направлено на комбинацию ингибирующего RSV соединения A, т.е. 3-({5-хлор-1-[3-(метилсульфонил)пропил]-1H-индол-2-ил}метил)-1-(2,2,2-трифторэтил)-1,3-дигидро-2H-имидазо[4,5-c]пиридин-2-она, и одного или нескольких ингибирующих RSV соединений B, выбранных из рибавирина, GS-5806, MDT-637, BTA-9881, BMS-433771, YM-543403, A-60444, TMC-353121, RFI-641, CL-387626, MBX-300, AZ-27, MEDI8897, CR9501, паливизумаба, 3-({5-хлор-1-[3-(метилсульфонил)пропил]-1H-бензимидазол-2-ил}метил)-1-циклопропил-1,3-дигидро-2H-имидазо[4,5-c]пиридин-2-она, 3-[[7-хлор-3-(2-этилсульфонилэтил)имидазо[1,2-a]пиридин-2-ил]метил]-1-циклопропилимидазо[4,5-c]пиридин-2-она, N-(2-фтор-6-метилфенил)-6-(4-(5-метил-2-(7-окса-2-азаспиро[3.5]нонан-2-ил)никотинамидо)бензоил)-5,6-дигидро-4H-бензо[b]тиено[2,3-d]азепин-2-карбоксамида и 4-амино-8-[3-[[2-(3,4-диметоксифенил)этил]амино]пропил]-6,6-диметил-2-(4-метил-3-нитрофенил)-3H-имидазо[4,5-h]изохинолин-7,9-(6H,8H)-диона, предназначенную для лечения или уменьшения интенсивности RSV-инфекции. Настоящее изобретение дополнительно относится к комбинированному продукту на основе соединения A и одного или нескольких соединений B, к фармацевтическому продукту, содержащему соединение A и одно или несколько соединений B, к применению комбинации соединения A и одного или нескольких соединений B или фармацевтического продукта, содержащего соединение A и одно или несколько соединений B, для лечения RSV-инфекции и к способу лечения или уменьшения интенсивности RSV-инфекции у субъекта, нуждающегося в этом, предусматривающему введение комбинации соединения A и одного или нескольких соединений B в эффективном количестве указанному субъекту.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
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| EP16154035 | 2016-02-03 |
Publications (1)
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| EA202092250A1 true EA202092250A1 (ru) | 2020-12-11 |
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| Application Number | Title | Priority Date | Filing Date |
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| EA202092251A EA202092251A1 (ru) | 2016-02-03 | 2017-02-02 | Комбинированные продукты для лечения rsv |
| EA201891655A EA037206B1 (ru) | 2016-02-03 | 2017-02-02 | Комбинация для лечения и ослабления rsv инфекции и фармацевтическая композиция на её основе |
| EA202092250A EA202092250A1 (ru) | 2016-02-03 | 2017-02-02 | Комбинированные продукты для лечения rsv |
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| Application Number | Title | Priority Date | Filing Date |
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| EA202092251A EA202092251A1 (ru) | 2016-02-03 | 2017-02-02 | Комбинированные продукты для лечения rsv |
| EA201891655A EA037206B1 (ru) | 2016-02-03 | 2017-02-02 | Комбинация для лечения и ослабления rsv инфекции и фармацевтическая композиция на её основе |
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| US (1) | US10363253B2 (ru) |
| EP (2) | EP3411028B1 (ru) |
| JP (1) | JP7065030B2 (ru) |
| KR (1) | KR20180108598A (ru) |
| CN (2) | CN112245429A (ru) |
| AU (2) | AU2017214246B2 (ru) |
| BR (1) | BR112018014958A2 (ru) |
| CA (1) | CA3006488A1 (ru) |
| CL (3) | CL2018001808A1 (ru) |
| EA (3) | EA202092251A1 (ru) |
| ES (1) | ES2877808T3 (ru) |
| IL (2) | IL259669B (ru) |
| MX (2) | MX2018009422A (ru) |
| MY (1) | MY197217A (ru) |
| PH (2) | PH12018501649B1 (ru) |
| SG (1) | SG11201806581TA (ru) |
| UA (1) | UA124099C2 (ru) |
| WO (1) | WO2017134133A1 (ru) |
| ZA (1) | ZA201805205B (ru) |
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| WO2016055791A1 (en) | 2014-10-10 | 2016-04-14 | Pulmocide Limited | Novel 5,6-dihydro-4H-benzo[b]thieno-[2,3-d]azepine derivative |
| US10160772B2 (en) | 2014-12-18 | 2018-12-25 | Pulmocide Limited | 5,6-dihydro-4H-benzo[b]thieno-[2,3-d]azepine derivatives |
| US10626126B2 (en) | 2016-04-08 | 2020-04-21 | Pulmocide Limited | Compounds |
| TW201936193A (zh) * | 2017-12-05 | 2019-09-16 | 愛爾蘭商健生科學愛爾蘭無限公司 | 使用組合產品治療ｒｓｖ |
| US20240109894A1 (en) * | 2019-10-30 | 2024-04-04 | Janssen Sciences Ireland Unlimited Company | Synthesis of 3-({5-chloro-1-[3-(methylsulfonyl)propyl]-1h-indol-2-yl} methyl)-1-(2,2,2-trifluoroethyl)-1,3-dihydro-2h-imidazo[4,5-c]pyridin-2-one |
| CN114014856B (zh) * | 2021-11-26 | 2023-12-22 | 嘉兴安谛康生物科技有限公司 | 作为呼吸道合胞病毒抗病毒剂的咪唑并吡啶类衍生物 |
| CN116077494A (zh) * | 2023-01-11 | 2023-05-09 | 黑龙江中医药大学 | 一种治疗呼吸道合胞病毒的药物组合物及其制备方法 |
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| TWI515187B (zh) * | 2010-12-16 | 2016-01-01 | 健生科學愛爾蘭無限公司 | 作為呼吸道融合病毒抗病毒劑之吲哚類 |
| JP6469081B2 (ja) * | 2013-04-25 | 2019-02-13 | ヤンセン ファッシンズ アンド プリベンション ベーフェーＪａｎｓｓｅｎ Ｖａｃｃｉｎｅｓ ＆ Ｐｒｅｖｅｎｔｉｏｎ Ｂ．Ｖ． | 安定化された可溶性融合前ｒｓｖｆポリペプチド |
| BR112016003348B1 (pt) * | 2013-08-21 | 2023-03-07 | Alios Biopharma, Inc | Compostos antivirais ou sais farmaceuticamente aceitáveis dos mesmos, composição farmacêutica e seus usos |
| WO2016055791A1 (en) * | 2014-10-10 | 2016-04-14 | Pulmocide Limited | Novel 5,6-dihydro-4H-benzo[b]thieno-[2,3-d]azepine derivative |
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