JP2004503501A - イミダゾピリジンおよびイミダゾピリミジン抗ウイルス剤 - Google Patents
イミダゾピリジンおよびイミダゾピリミジン抗ウイルス剤 Download PDFInfo
- Publication number
- JP2004503501A JP2004503501A JP2002510088A JP2002510088A JP2004503501A JP 2004503501 A JP2004503501 A JP 2004503501A JP 2002510088 A JP2002510088 A JP 2002510088A JP 2002510088 A JP2002510088 A JP 2002510088A JP 2004503501 A JP2004503501 A JP 2004503501A
- Authority
- JP
- Japan
- Prior art keywords
- embedded image
- nmr
- compound
- mmol
- alkyl
- 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.)
- Withdrawn
Links
- 0 *c1ccc2[n]c(CC(Nc3c(*)cc(*)cc3)=C)nc2c1 Chemical compound *c1ccc2[n]c(CC(Nc3c(*)cc(*)cc3)=C)nc2c1 0.000 description 4
- YEIWIHIEXMVQTM-UHFFFAOYSA-N CC(C)(C)[Si+](C)(C)OC(C)(C)CCCBr Chemical compound CC(C)(C)[Si+](C)(C)OC(C)(C)CCCBr YEIWIHIEXMVQTM-UHFFFAOYSA-N 0.000 description 1
- RBFVGQWGOARJRU-UHFFFAOYSA-N CC(C)(CCBr)O Chemical compound CC(C)(CCBr)O RBFVGQWGOARJRU-UHFFFAOYSA-N 0.000 description 1
- BGQUPQDZDIVJHO-UHFFFAOYSA-N CC(C)(CCCBr)O Chemical compound CC(C)(CCCBr)O BGQUPQDZDIVJHO-UHFFFAOYSA-N 0.000 description 1
- YLFLTKJZYMMIEJ-UHFFFAOYSA-N CC(C)(OC1(CCBr)CC1)[Si](C)(C)C Chemical compound CC(C)(OC1(CCBr)CC1)[Si](C)(C)C YLFLTKJZYMMIEJ-UHFFFAOYSA-N 0.000 description 1
- OFMGGGIHSWGTID-UHFFFAOYSA-N CC(C)CC[n]1c(ccc(F)c2)c2nc1CCl Chemical compound CC(C)CC[n]1c(ccc(F)c2)c2nc1CCl OFMGGGIHSWGTID-UHFFFAOYSA-N 0.000 description 1
- RUPBOZODOMLGPD-UHFFFAOYSA-N CC(C)CC[n]1c(ccc(F)c2)c2nc1CN(c(cncc1)c1N1Cc(cc2)ccc2NC(C)=O)C1=O Chemical compound CC(C)CC[n]1c(ccc(F)c2)c2nc1CN(c(cncc1)c1N1Cc(cc2)ccc2NC(C)=O)C1=O RUPBOZODOMLGPD-UHFFFAOYSA-N 0.000 description 1
- UTKOIXMHZRYRPG-UHFFFAOYSA-N CC(C)CC[n]1c(cccc2)c2nc1CCl Chemical compound CC(C)CC[n]1c(cccc2)c2nc1CCl UTKOIXMHZRYRPG-UHFFFAOYSA-N 0.000 description 1
- ZXDFIGVWGLXLHX-UHFFFAOYSA-N CC(C)CC[n]1c(cccc2)c2nc1CN(c(c(Cl)ncc1)c1N1C)C1=O Chemical compound CC(C)CC[n]1c(cccc2)c2nc1CN(c(c(Cl)ncc1)c1N1C)C1=O ZXDFIGVWGLXLHX-UHFFFAOYSA-N 0.000 description 1
- OFAIGIUXLBBBDM-UHFFFAOYSA-N CC(N1CCC[n]2c(cccc3)c3nc2CN(c2cnccc2N2C3CC3)C2=O)=C(C)OC1=O Chemical compound CC(N1CCC[n]2c(cccc3)c3nc2CN(c2cnccc2N2C3CC3)C2=O)=C(C)OC1=O OFAIGIUXLBBBDM-UHFFFAOYSA-N 0.000 description 1
- TWYPOIQAPJFZDE-UHFFFAOYSA-N CC(OCCCC[n]1c(cccc2)c2nc1CN(c1ncccc1N1C2CC2)C1=O)=O Chemical compound CC(OCCCC[n]1c(cccc2)c2nc1CN(c1ncccc1N1C2CC2)C1=O)=O TWYPOIQAPJFZDE-UHFFFAOYSA-N 0.000 description 1
- MWPLAEQDVABGHB-UHFFFAOYSA-N CS(CCC[n]1c(cccc2)c2nc1CN(c(cncc1)c1N1CC(F)(F)F)C1=O)O Chemical compound CS(CCC[n]1c(cccc2)c2nc1CN(c(cncc1)c1N1CC(F)(F)F)C1=O)O MWPLAEQDVABGHB-UHFFFAOYSA-N 0.000 description 1
- OVCZWXIPHUPKML-UHFFFAOYSA-N CS(CCC[n]1c(cccc2)c2nc1CN(c1cnccc1N1)C1=O)(=O)=O Chemical compound CS(CCC[n]1c(cccc2)c2nc1CN(c1cnccc1N1)C1=O)(=O)=O OVCZWXIPHUPKML-UHFFFAOYSA-N 0.000 description 1
- GDWRVZPLJSKFEI-UHFFFAOYSA-N CS([n]1c(cccc2)c2nc1CI)(=O)=O Chemical compound CS([n]1c(cccc2)c2nc1CI)(=O)=O GDWRVZPLJSKFEI-UHFFFAOYSA-N 0.000 description 1
- VSOHGVMOLNNITA-UHFFFAOYSA-N CS(c1ccc(CN(c(cncc2)c2N2Cc3nc(cc(cc4)F)c4[n]3CCCC#N)C2=O)cc1)(=O)=O Chemical compound CS(c1ccc(CN(c(cncc2)c2N2Cc3nc(cc(cc4)F)c4[n]3CCCC#N)C2=O)cc1)(=O)=O VSOHGVMOLNNITA-UHFFFAOYSA-N 0.000 description 1
- JZMCXQUBAGHKFV-UHFFFAOYSA-N CS(c1ccc(C[n]2c(cccc3)c3nc2CO)cc1)(=O)=O Chemical compound CS(c1ccc(C[n]2c(cccc3)c3nc2CO)cc1)(=O)=O JZMCXQUBAGHKFV-UHFFFAOYSA-N 0.000 description 1
- YEGPOODVPLXLMC-UHFFFAOYSA-N CSCCC[n]1c(ccc(F)c2)c2nc1CO Chemical compound CSCCC[n]1c(ccc(F)c2)c2nc1CO YEGPOODVPLXLMC-UHFFFAOYSA-N 0.000 description 1
- VWEPARILXXFAMM-UHFFFAOYSA-N N#CCCC[n]1c(cccc2)c2nc1CN(c(cncc1)c1N1C2CCC2)C1=O Chemical compound N#CCCC[n]1c(cccc2)c2nc1CN(c(cncc1)c1N1C2CCC2)C1=O VWEPARILXXFAMM-UHFFFAOYSA-N 0.000 description 1
- RXRAJRFLQDSYQR-UHFFFAOYSA-N N#CCCC[n]1c(cccc2)c2nc1CN(c(cncc1)c1N1CC2CC2)C1=O Chemical compound N#CCCC[n]1c(cccc2)c2nc1CN(c(cncc1)c1N1CC2CC2)C1=O RXRAJRFLQDSYQR-UHFFFAOYSA-N 0.000 description 1
- CQRHRXAGXJFCQG-UHFFFAOYSA-N N#CCCC[n]1c(cccc2)c2nc1CN(c1c(N2CC(F)(F)F)ncnc1)C2=O Chemical compound N#CCCC[n]1c(cccc2)c2nc1CN(c1c(N2CC(F)(F)F)ncnc1)C2=O CQRHRXAGXJFCQG-UHFFFAOYSA-N 0.000 description 1
- PZYGTDBHRZWAPU-UHFFFAOYSA-N NCCC[n]1c(cccc2)c2nc1CN(c1cnccc1N1C2CC2)C1=O Chemical compound NCCC[n]1c(cccc2)c2nc1CN(c1cnccc1N1C2CC2)C1=O PZYGTDBHRZWAPU-UHFFFAOYSA-N 0.000 description 1
- XBVSBTOFDDZBOB-UHFFFAOYSA-N O=C(c1c2cccc1)N(CCC[n]1c(cccc3)c3nc1CN(c(cncc1)c1N1C3CC3)C1=O)C2=O Chemical compound O=C(c1c2cccc1)N(CCC[n]1c(cccc3)c3nc1CN(c(cncc1)c1N1C3CC3)C1=O)C2=O XBVSBTOFDDZBOB-UHFFFAOYSA-N 0.000 description 1
- GMKAWSPJDNWZHA-UHFFFAOYSA-N O=C1N(C2CC2)c(ccnc2)c2N1Cc1nc(cccc2)c2[n]1CC=C(F)F Chemical compound O=C1N(C2CC2)c(ccnc2)c2N1Cc1nc(cccc2)c2[n]1CC=C(F)F GMKAWSPJDNWZHA-UHFFFAOYSA-N 0.000 description 1
- NAYQAXAODXUMJR-UHFFFAOYSA-N O=C1N(C2CC2)c(ccnc2)c2N1Cc1nc(cccc2)c2[n]1CCCCCl Chemical compound O=C1N(C2CC2)c(ccnc2)c2N1Cc1nc(cccc2)c2[n]1CCCCCl NAYQAXAODXUMJR-UHFFFAOYSA-N 0.000 description 1
- PNYWFSBGLRGQAN-UHFFFAOYSA-N O=C1N(CCC[n]2c(cccc3)c3nc2CN(c(cncc2)c2N2C3CC3)C2=O)CCC1 Chemical compound O=C1N(CCC[n]2c(cccc3)c3nc2CN(c(cncc2)c2N2C3CC3)C2=O)CCC1 PNYWFSBGLRGQAN-UHFFFAOYSA-N 0.000 description 1
- YPDSIEMYVQERLJ-UHFFFAOYSA-N O=C1Nc(ncnc2)c2N1 Chemical compound O=C1Nc(ncnc2)c2N1 YPDSIEMYVQERLJ-UHFFFAOYSA-N 0.000 description 1
- OLTRKEVNZLERIO-UHFFFAOYSA-N O=C1OC(CC[n]2c(cccc3)c3nc2CN(c2cnccc2N2C3CC3)C2=O)CN1 Chemical compound O=C1OC(CC[n]2c(cccc3)c3nc2CN(c2cnccc2N2C3CC3)C2=O)CN1 OLTRKEVNZLERIO-UHFFFAOYSA-N 0.000 description 1
- VGQKBYSJQHMIQZ-UHFFFAOYSA-N O=C1OC(CC[n]2c(cccc3)c3nc2COCc2ccccc2)CN1 Chemical compound O=C1OC(CC[n]2c(cccc3)c3nc2COCc2ccccc2)CN1 VGQKBYSJQHMIQZ-UHFFFAOYSA-N 0.000 description 1
- VPXFEKYELFBRHB-UHFFFAOYSA-N OC1(CCCBr)CC1 Chemical compound OC1(CCCBr)CC1 VPXFEKYELFBRHB-UHFFFAOYSA-N 0.000 description 1
- COZTZELDBNIRSO-UHFFFAOYSA-N OCCCC[n]1c(cccc2)c2nc1CN(c(cncc1)c1N1Cc2ccccc2)C1=O Chemical compound OCCCC[n]1c(cccc2)c2nc1CN(c(cncc1)c1N1Cc2ccccc2)C1=O COZTZELDBNIRSO-UHFFFAOYSA-N 0.000 description 1
- KSHJXDWYTZJUEI-UHFFFAOYSA-N OCCCC[n]1c(cccc2)c2nc1CN(c1cnccc1N1C2CC2)C1=O Chemical compound OCCCC[n]1c(cccc2)c2nc1CN(c1cnccc1N1C2CC2)C1=O KSHJXDWYTZJUEI-UHFFFAOYSA-N 0.000 description 1
- JVDFNTLWAQQNCE-UHFFFAOYSA-N OCCCC[n]1c(cccc2)c2nc1CN(c1cnccc1N1CC(F)(F)F)C1=O Chemical compound OCCCC[n]1c(cccc2)c2nc1CN(c1cnccc1N1CC(F)(F)F)C1=O JVDFNTLWAQQNCE-UHFFFAOYSA-N 0.000 description 1
- ANQAHRBJLMNFAK-UHFFFAOYSA-N OCCC[n]1c(cccc2)c2nc1CN(c(cncc1)c1N1C2CC2)C1=O Chemical compound OCCC[n]1c(cccc2)c2nc1CN(c(cncc1)c1N1C2CC2)C1=O ANQAHRBJLMNFAK-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Virology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US21144700P | 2000-06-13 | 2000-06-13 | |
| US26336301P | 2001-01-22 | 2001-01-22 | |
| PCT/US2001/014775 WO2001095910A1 (en) | 2000-06-13 | 2001-05-08 | Imidazopyridine and imidazopyrimidine antiviral agents |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004503501A true JP2004503501A (ja) | 2004-02-05 |
| JP2004503501A5 JP2004503501A5 (OSRAM) | 2006-06-01 |
Family
ID=26906145
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002510088A Withdrawn JP2004503501A (ja) | 2000-06-13 | 2001-05-08 | イミダゾピリジンおよびイミダゾピリミジン抗ウイルス剤 |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US6489338B2 (OSRAM) |
| EP (1) | EP1311268A4 (OSRAM) |
| JP (1) | JP2004503501A (OSRAM) |
| KR (1) | KR20030008151A (OSRAM) |
| CN (1) | CN1436079A (OSRAM) |
| AR (1) | AR029128A1 (OSRAM) |
| AU (2) | AU2001272906B2 (OSRAM) |
| BR (1) | BR0111569A (OSRAM) |
| CA (1) | CA2412327A1 (OSRAM) |
| CZ (1) | CZ20024078A3 (OSRAM) |
| HU (1) | HUP0400766A2 (OSRAM) |
| IL (1) | IL152889A0 (OSRAM) |
| MX (1) | MXPA02012204A (OSRAM) |
| NO (1) | NO20025977L (OSRAM) |
| NZ (1) | NZ523566A (OSRAM) |
| PE (1) | PE20011348A1 (OSRAM) |
| PL (1) | PL360290A1 (OSRAM) |
| RU (1) | RU2003100828A (OSRAM) |
| UY (1) | UY26758A1 (OSRAM) |
| WO (1) | WO2001095910A1 (OSRAM) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008546738A (ja) * | 2005-06-20 | 2008-12-25 | テイボテク・フアーマシユーチカルズ・リミテツド | 呼吸器シンシチウムウイルスに活性をもつ、1−(2−アミノ−3−(置換アルキル)−3h−ベンズイミダゾイルメチル)−3−置換−1,3−ジヒドロ−ベンゾイミダゾル−2−オン |
| JP2013545785A (ja) * | 2010-12-16 | 2013-12-26 | ヤンセン・アールアンドデイ・アイルランド | ベンゾイミダゾール呼吸合胞体ウイルス阻害剤 |
| JP2015519386A (ja) * | 2012-06-15 | 2015-07-09 | ヤンセン・アールアンドデイ・アイルランド | Rsウイルス抗ウイルス薬としての、複素環によって置換された新規1,3−ジヒドロ−2h−ベンゾイミダゾル−2−オン誘導体 |
| JP2015519381A (ja) * | 2012-06-11 | 2015-07-09 | ユーシービー バイオファルマ エスピーアールエル | Tnf−アルファ調節ベンゾイミダゾール |
| JP2016145236A (ja) * | 2010-12-16 | 2016-08-12 | ヤンセン・サイエンシズ・アイルランド・ユーシー | 呼吸合胞体ウイルスの抗ウイルス剤としてのインドール |
| JP2023500213A (ja) * | 2019-10-30 | 2023-01-05 | ヤンセン・サイエンシズ・アイルランド・アンリミテッド・カンパニー | 3-ニトロ-n-(2,2,2-トリフルオロエチル)-4-ピリジンアミンの合成 |
| JP2023500214A (ja) * | 2019-10-30 | 2023-01-05 | ヤンセン・サイエンシズ・アイルランド・アンリミテッド・カンパニー | 3-({5-クロロ-1-[3-(メチルスルホニル)プロピル]-1H-インドール-2イル}メチル)-1-(2,2,2-トリフルオロエチル)-1,3-ジヒドロ-2H-イミダゾ[4,5-c]ピリジン-2-オンの合成 |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6774134B2 (en) * | 2000-12-20 | 2004-08-10 | Bristol-Myers Squibb Company | Heterocyclic substituted 2-methyl-benzimidazole antiviral agents |
| WO2003049688A2 (en) * | 2001-12-10 | 2003-06-19 | Bristol-Myers Squibb Company | Bis hydrochloride monohydrate salt of rsv fusion inhibitor |
| US6919331B2 (en) * | 2001-12-10 | 2005-07-19 | Bristol-Myers Squibb Company | Substituted 2-methyl-benzimidazole respiratory syncytial virus antiviral agents |
| WO2004043913A2 (en) * | 2002-11-08 | 2004-05-27 | Trimeris, Inc. | Hetero-substituted benzimidazole compounds and antiviral uses thereof |
| WO2005016275A2 (en) * | 2003-08-05 | 2005-02-24 | 3M Innovative Properties Company | Formulations containing an immune response modifier |
| EP1682547B1 (en) | 2003-10-30 | 2012-10-24 | Boehringer Ingelheim (Canada) Ltd. | Rsv polymerase inhibitors |
| NZ551468A (en) | 2003-12-24 | 2010-05-28 | Biota Scient Management | Polycyclic agents for the treatment of respiratory syncytial virus infections |
| GB0406282D0 (en) * | 2004-03-19 | 2004-04-21 | Arrow Therapeutics Ltd | Therapeutic compounds |
| GB0406279D0 (en) * | 2004-03-19 | 2004-04-21 | Arrow Therapeutics Ltd | Therapeutic compounds |
| CN101027303A (zh) | 2004-07-27 | 2007-08-29 | 吉里德科学公司 | 咪唑并[4,5-d]嘧啶类、其应用和制备方法 |
| CN101203507B (zh) | 2005-06-20 | 2012-05-23 | 泰博特克药品有限公司 | 2-取代的苯并咪唑 |
| JP5094716B2 (ja) | 2005-06-20 | 2012-12-12 | テイボテク・フアーマシユーチカルズ | ヘテロシクリルアミノアルキル置換ベンズイミダゾール |
| TWI423972B (zh) | 2006-09-28 | 2014-01-21 | Biota Scient Management | 治療呼吸系融合細胞病毒感染之多環劑 |
| WO2009084544A1 (ja) * | 2007-12-27 | 2009-07-09 | Idemitsu Kosan Co., Ltd. | 含窒素複素環誘導体及びそれを用いた有機エレクトロルミネッセンス素子 |
| US20100278835A1 (en) | 2009-03-10 | 2010-11-04 | Astrazeneca Uk Limited | Novel compounds 660 |
| RU2407738C1 (ru) * | 2009-07-03 | 2010-12-27 | Общество с ограниченной ответственностью "Интеллектуальный Диалог" | Противовирусный активный компонент, фармацевтическая композиция, лекарственное средство, способ лечения вирусных заболеваний |
| TWI508968B (zh) | 2010-02-08 | 2015-11-21 | Biota Scient Management | 用於治療呼吸道融合性病毒感染的化合物 |
| WO2011115150A1 (ja) * | 2010-03-18 | 2011-09-22 | 興和株式会社 | ベンゾチアジン化合物の製造方法 |
| US8796303B2 (en) | 2010-11-26 | 2014-08-05 | Biota Scientific Management Pty Ltd. | Imidazo[2,1-G][1,7]naphthyridines for treating respiratory syncytial virus infections |
| TWI527814B (zh) | 2010-12-16 | 2016-04-01 | 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氮雜苯并咪唑類 |
| TWI501967B (zh) | 2010-12-16 | 2015-10-01 | Janssen R&D Ireland | 作為呼吸道融合病毒抗病毒劑之氮雜吲哚類 |
| TWI541241B (zh) * | 2010-12-16 | 2016-07-11 | 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咪唑并吡啶類 |
| CN103860538B (zh) * | 2011-03-23 | 2016-03-02 | 上海市第一人民医院 | 靶向人La蛋白的先导化合物及其在制备抗乙型肝炎病毒的药物中的用途 |
| CA2873916A1 (en) * | 2012-06-15 | 2013-12-19 | Janssen R&D Ireland | 4-substituted 1,3-dihydro-2h-benzimidazol-2-one derivatives substituted with benzimidazoles as respiratory syncytial virus antivira agents |
| JP2015523350A (ja) * | 2012-06-15 | 2015-08-13 | ヤンセン・アールアンドデイ・アイルランド | Rsウイルス抗ウイルス薬としての、ベンゾイミダゾールによって置換された新規1,3−ジヒドロ−2h−ベンゾイミダゾル−2−オン誘導体 |
| WO2013186335A1 (en) * | 2012-06-15 | 2013-12-19 | Janssen R&D Ireland | 1,3 -dihydro-2h-benzimidazol-2-one derivatives substituted with heterocycles as respiratory syncytial virus antiviral agents |
| MY172021A (en) * | 2012-10-16 | 2019-11-12 | Janssen Sciences Ireland Uc | Rsv antiviral compounds |
| JP2016145155A (ja) * | 2013-04-30 | 2016-08-12 | 日本農薬株式会社 | フタルアミド誘導体及び該誘導体を含有する農園芸用殺虫剤並びにその使用方法 |
| BR112016009757A8 (pt) * | 2013-10-29 | 2018-01-30 | Medivir Ab | “inibidores do vírus sincicial respiratório com base em quinazolina” |
| WO2015065336A1 (en) * | 2013-10-29 | 2015-05-07 | Medivir Ab | Respiratory syncytial virus inhibitors |
| CA3008653A1 (en) * | 2015-10-14 | 2017-04-20 | Zibo Biopolar Changsheng Pharmaceutical Co. Ltd. | Bruton's tyrosine kinase inhibitors |
| WO2019046364A1 (en) * | 2017-08-29 | 2019-03-07 | Emory University | INHIBITORS OF SYNCYTIAL RESPIRATORY VIRUS (RSV) REPLICATION AND USES THEREOF |
| EP4165034A1 (en) | 2020-06-11 | 2023-04-19 | Janssen Sciences Ireland Unlimited Company | Hemi (l)-tartrate forms 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 and pharmaceutical compositions comprising the same |
| WO2022184606A1 (en) * | 2021-03-01 | 2022-09-09 | Janssen Sciences Ireland Unlimited Company | Synthesis of rilematovir |
| JP2025502943A (ja) * | 2022-01-28 | 2025-01-30 | インシリコ メディシン アイピー リミテッド | エクトヌクレオチドピロホスファターゼ-ホスホジエステラーゼ1(enpp1)阻害剤およびその使用 |
| WO2025026383A1 (en) * | 2023-08-02 | 2025-02-06 | Insilico Medicine Ip Limited | Crytsalline forms of ectonucleotide pyrophosphatase-phosphodiesterase 1 (enpp1) inhibitors and uses thereof |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4324794A (en) | 1980-08-26 | 1982-04-13 | Research Triangle Institute | Inhibition of respiratory syncytial virus-induced cell fusion by amidino compounds |
| DK154078C (da) | 1981-02-06 | 1989-05-22 | Ucb Sa | Analogifremgangsmaade til fremstilling af 2-(2-(4-(diphenyl-methyl)-1-piperazinyl)ethoxy)-acetamider eller syreadditionssalte heraf |
| US5256668A (en) | 1993-03-17 | 1993-10-26 | American Home Products Corporation | Aminopyrimidine derivatives as antiviral agents for respiratory syncytial virus |
| BR9700939A (pt) | 1996-02-13 | 1998-09-01 | American Cyanamid Co | Compostos aniônicos contendo traiazina úteis como agentes antivirais |
| BR9908522A (pt) | 1998-01-29 | 2001-10-02 | Viropharma Inc | Composto, pró-droga, intermediário para a preparação de um composto, composição farmacêutica, processos para tratar e prevenir infecção por pneumovìrus, para tratar células em cultura, para tratar materiais biológicos, e, para preparar um composto |
| CA2338147A1 (en) | 1998-07-20 | 2000-02-03 | Kuo-Long Yu | Substituted benzimidazole antiviral agents |
| HRP20010934A2 (en) | 1999-06-28 | 2003-06-30 | Janssen Pharmaceutica Nv | Respiratory syncytial virus replication inhibitors |
-
2001
- 2001-04-23 US US09/840,279 patent/US6489338B2/en not_active Expired - Fee Related
- 2001-05-08 JP JP2002510088A patent/JP2004503501A/ja not_active Withdrawn
- 2001-05-08 EP EP01952114A patent/EP1311268A4/en not_active Withdrawn
- 2001-05-08 CN CN01811136A patent/CN1436079A/zh active Pending
- 2001-05-08 CZ CZ20024078A patent/CZ20024078A3/cs unknown
- 2001-05-08 AU AU2001272906A patent/AU2001272906B2/en not_active Ceased
- 2001-05-08 NZ NZ523566A patent/NZ523566A/en unknown
- 2001-05-08 KR KR1020027016924A patent/KR20030008151A/ko not_active Ceased
- 2001-05-08 AU AU7290601A patent/AU7290601A/xx active Pending
- 2001-05-08 IL IL15288901A patent/IL152889A0/xx unknown
- 2001-05-08 CA CA002412327A patent/CA2412327A1/en not_active Abandoned
- 2001-05-08 HU HU0400766A patent/HUP0400766A2/hu unknown
- 2001-05-08 BR BR0111569-3A patent/BR0111569A/pt not_active IP Right Cessation
- 2001-05-08 MX MXPA02012204A patent/MXPA02012204A/es unknown
- 2001-05-08 RU RU2003100828/15A patent/RU2003100828A/ru not_active Application Discontinuation
- 2001-05-08 PL PL36029001A patent/PL360290A1/xx not_active Application Discontinuation
- 2001-05-08 WO PCT/US2001/014775 patent/WO2001095910A1/en not_active Ceased
- 2001-06-11 UY UY26758A patent/UY26758A1/es not_active Application Discontinuation
- 2001-06-12 AR ARP010102772A patent/AR029128A1/es unknown
- 2001-06-13 PE PE2001000559A patent/PE20011348A1/es not_active Application Discontinuation
-
2002
- 2002-12-12 NO NO20025977A patent/NO20025977L/no not_active Application Discontinuation
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008546738A (ja) * | 2005-06-20 | 2008-12-25 | テイボテク・フアーマシユーチカルズ・リミテツド | 呼吸器シンシチウムウイルスに活性をもつ、1−(2−アミノ−3−(置換アルキル)−3h−ベンズイミダゾイルメチル)−3−置換−1,3−ジヒドロ−ベンゾイミダゾル−2−オン |
| JP2013545785A (ja) * | 2010-12-16 | 2013-12-26 | ヤンセン・アールアンドデイ・アイルランド | ベンゾイミダゾール呼吸合胞体ウイルス阻害剤 |
| JP2016145236A (ja) * | 2010-12-16 | 2016-08-12 | ヤンセン・サイエンシズ・アイルランド・ユーシー | 呼吸合胞体ウイルスの抗ウイルス剤としてのインドール |
| JP2015519381A (ja) * | 2012-06-11 | 2015-07-09 | ユーシービー バイオファルマ エスピーアールエル | Tnf−アルファ調節ベンゾイミダゾール |
| JP2015519386A (ja) * | 2012-06-15 | 2015-07-09 | ヤンセン・アールアンドデイ・アイルランド | Rsウイルス抗ウイルス薬としての、複素環によって置換された新規1,3−ジヒドロ−2h−ベンゾイミダゾル−2−オン誘導体 |
| JP2023500213A (ja) * | 2019-10-30 | 2023-01-05 | ヤンセン・サイエンシズ・アイルランド・アンリミテッド・カンパニー | 3-ニトロ-n-(2,2,2-トリフルオロエチル)-4-ピリジンアミンの合成 |
| JP2023500214A (ja) * | 2019-10-30 | 2023-01-05 | ヤンセン・サイエンシズ・アイルランド・アンリミテッド・カンパニー | 3-({5-クロロ-1-[3-(メチルスルホニル)プロピル]-1H-インドール-2イル}メチル)-1-(2,2,2-トリフルオロエチル)-1,3-ジヒドロ-2H-イミダゾ[4,5-c]ピリジン-2-オンの合成 |
Also Published As
| Publication number | Publication date |
|---|---|
| AU7290601A (en) | 2001-12-24 |
| NO20025977D0 (no) | 2002-12-12 |
| RU2003100828A (ru) | 2004-06-27 |
| KR20030008151A (ko) | 2003-01-24 |
| AR029128A1 (es) | 2003-06-04 |
| UY26758A1 (es) | 2002-01-31 |
| CN1436079A (zh) | 2003-08-13 |
| WO2001095910A1 (en) | 2001-12-20 |
| EP1311268A4 (en) | 2004-06-30 |
| BR0111569A (pt) | 2003-04-29 |
| NO20025977L (no) | 2003-01-29 |
| PE20011348A1 (es) | 2002-02-07 |
| HUP0400766A2 (hu) | 2004-07-28 |
| IL152889A0 (en) | 2003-06-24 |
| US6489338B2 (en) | 2002-12-03 |
| NZ523566A (en) | 2004-08-27 |
| CA2412327A1 (en) | 2001-12-20 |
| US20020016309A1 (en) | 2002-02-07 |
| MXPA02012204A (es) | 2003-10-15 |
| AU2001272906B2 (en) | 2004-08-26 |
| PL360290A1 (en) | 2004-09-06 |
| EP1311268A1 (en) | 2003-05-21 |
| CZ20024078A3 (cs) | 2003-08-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US6489338B2 (en) | Imidazopyridine and imidazopyrimidine antiviral agents | |
| AU2001272906A1 (en) | Imidazopyridine and imidazopyrimidine antiviral agents | |
| CA2903215C (en) | Perfluorinated cyclopropyl fused 1,3-oxazin-2-amine compounds as beta-secretase inhibitors and methods of use | |
| CN101351466B (zh) | Janus激酶3的杂环抑制剂 | |
| JP5227304B2 (ja) | 新規なヒドロキサム酸誘導体 | |
| AU2003214503B2 (en) | Tropane derivatives as CCR5 modulators | |
| AU2019416589A1 (en) | Heterocyclic compound intermediate, preparation method therefor and application thereof | |
| EP2123651A1 (en) | Condensed pyridine compound | |
| AU2003300902A1 (en) | Piperidine derivatives as CCR5 antagonists | |
| CA3053484A1 (en) | Aminotriazolopyridines as kinase inhibitors | |
| CA2943874A1 (en) | Substituted spirocyclic inhibitors of autotaxin | |
| JP2009522232A (ja) | Pdfインヒビター | |
| EA027247B1 (ru) | Новые производные пиридина | |
| AU2011343258A1 (en) | Azabenzimidazoles as respiratory syncytial virus antiviral agents | |
| EP0925299B1 (en) | Pyrazolopyridine compound and pharmaceutical use thereof | |
| JP2025505230A (ja) | 二環式ヘテロアリール化合物およびその使用 | |
| CA3059954A1 (en) | Substituted n-arylethyl-2-aminoquinoline-4-carboxamides and use thereof | |
| CN115698011B (zh) | Pb2抑制剂及其制备方法和用途 | |
| HK1123303B (en) | Heterocyclic janus kinase 3 inhibitors | |
| JP2023550798A (ja) | 抗コリン剤 | |
| WO2010025436A2 (en) | Nitrogen and sulfur-containing heterocycle derivatives | |
| ZA200210104B (en) | Imidazopyridine and imidazopyrimidine antiviral agents. | |
| MX2008000621A (es) | Inhibidores heterociclicos de cinasa 3 de janus. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20060405 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20060405 |
|
| A761 | Written withdrawal of application |
Free format text: JAPANESE INTERMEDIATE CODE: A761 Effective date: 20061030 |