AR100137A1 - Compuestos 4-amino-imidazoquinolina - Google Patents
Compuestos 4-amino-imidazoquinolinaInfo
- Publication number
- AR100137A1 AR100137A1 ARP150101179A ARP150101179A AR100137A1 AR 100137 A1 AR100137 A1 AR 100137A1 AR P150101179 A ARP150101179 A AR P150101179A AR P150101179 A ARP150101179 A AR P150101179A AR 100137 A1 AR100137 A1 AR 100137A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkylsulfonyl
- alkoxycarbonyl
- alkoxy
- halogen
- Prior art date
Links
- RSYUXZQXNGSKGO-UHFFFAOYSA-N 1h-imidazo[4,5-h]quinolin-4-amine Chemical class NC1=CC2=CC=CN=C2C2=C1N=CN2 RSYUXZQXNGSKGO-UHFFFAOYSA-N 0.000 title abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 11
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical group 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- -1 cyano, carboxyl Chemical group 0.000 abstract 3
- 150000002431 hydrogen Chemical group 0.000 abstract 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 2
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000005223 heteroarylcarbonyl group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 208000035473 Communicable disease Diseases 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 239000000556 agonist Substances 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- A61K31/4188—1,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
-
- 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
- A61P31/20—Antivirals for DNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Virology (AREA)
- Biotechnology (AREA)
- Molecular Biology (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
La presente solicitud se refiere a compuestos 4-amino-imidazoquinolina y sales farmacéuticamente aceptables de los mismos. Estos compuestos son agonistas de RTT y, por lo tanto, pueden resultar útiles como medicamentos para el tratamiento de enfermedades tales como el cáncer o enfermedades infecciosas. Reivindicación 1: Compuesto de fórmula (1) en la que: R¹ es alquilo C₁₋₇ o alcoxi C₁₋₇-alquilo C₁₋₇; R² se selecciona de entre el grupo que consiste de hidrógeno, halógeno, hidroxialquilo C₁₋₇, alcoxi-alquilo C₁₋₇, carboxilo, carboxil-alquilo C₁₋₇, carboxil-alquenilo C₂₋₇, aminocarbonil-alquilo C₁₋₇, aminocarbonil-alquenilo C₂₋₇, alquilamino C₁₋₇-carbonil-alquilo C₁₋₇, alquilamino C₁₋₇-carbonil-alquenilo C₂₋₇, alcoxicarbonil C₁₋₇-alquilo C₁₋₇, alcoxicarbonil C₁₋₇-alquenilo C₂₋₇, alquil C₁₋₇-sulfonil-alquilo C₁₋₇, sulfamoil-alquilo C₁₋₇, alquil C₁₋₇-sulfamoil-alquilo C₁₋₇, fenilo, encontrándose dicho fenilo no sustituido o sustituido con uno, dos o tres grupos seleccionados de entre el grupo que consiste de alquilo C₁₋₇, cicloalquilo C₁₋₇, halógeno, halógeno-alquilo C₁₋₇, halógeno-alcoxi C₁₋₇, hidroxi, hidroxi-alquilo C₁₋₇, alcoxi C₁₋₇, ciano, carboxilo, alcoxicarbonilo C₁₋₇, alcoxicarbonil C₁₋₇-alquilo C₁₋₇, alquilsulfonilo C₁₋₇, hidroxi-alquilsulfonilo C₁₋₇, alcoxi C₁₋₇-alquilsulfonilo C₁₋₇, carboxil-alquilsulfonilo C₁₋₇, alcoxicarbonil C₁₋₇-alquilsulfonilo C₁₋₇, amino, alquilamino C₁₋₇, di-alquilamino C₁₋₇ y nitro, y fenoxi, encontrándose dicho fenoxi no sustituido o sustituido con uno, dos o tres grupos seleccionados de entre el grupo que consiste de alquilo C₁₋₇, cicloalquilo C₁₋₇, halógeno, halógeno-alquilo C₁₋₇, halógeno-alcoxi C₁₋₇, hidroxi, hidroxi-alquilo C₁₋₇, alcoxi C₁₋₇, ciano, carboxilo, alcoxicarbonilo C₁₋₇, alcoxicarbonil C₁₋₇-alquilo C₁₋₇, alquilsulfonilo C₁₋₇, hidroxi-alquilsulfonilo C₁₋₇, alcoxi C₁₋₇-alquilsulfonilo C₁₋₇, carboxil-alquilsulfonilo C₁₋₇, alcoxicarbonil C₁₋₇-alquilsulfonilo C₁₋₇, amino, alquilamino C₁₋₇, di-alquilamino C₁₋₇ y nitro; R³ es hidrógeno o halógeno; R⁴ se selecciona de entre el grupo que consiste de: -O-(CH₂)ₘ-NHR⁵, y -O-(CO)-(CH₂)ₙ-NHR⁶, en la que: m se selecciona de entre 1, 2 ó 3, n se selecciona de entre 1 ó 2; R⁵ se selecciona de entre el grupo que consiste de hidrógeno, hidroxialquilo C₁₋₇, aminoalquilo C₁₋₇, alquilcarbonilo C₁₋₇, fenilcarbonilo, heteroarilcarbonilo, carboxilo carboxil-alquilo C₁₋₇ y alcoxicarbonilamino C₁₋₇-alquilcarbonilo C₁₋₇; y R⁶ se selecciona de entre el grupo que consiste de hidrógeno, hidroxialquilo C₁₋₇, aminoalquilo C₁₋₇, alquilcarbonilo C₁₋₇, fenilcarbonilo, heteroarilcarbonilo, carboxilo, carboxil-alquilo C₁₋₇ y alcoxicarbonilamino C₁₋₄-alquilcarbonilo C₁₋₇; o sales farmacéuticamente aceptables de los mismos.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14165349 | 2014-04-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR100137A1 true AR100137A1 (es) | 2016-09-14 |
Family
ID=50489008
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP150101179A AR100137A1 (es) | 2014-04-22 | 2015-04-20 | Compuestos 4-amino-imidazoquinolina |
Country Status (22)
| Country | Link |
|---|---|
| US (2) | US9334268B2 (es) |
| EP (1) | EP3134402B1 (es) |
| JP (1) | JP6367366B2 (es) |
| KR (1) | KR101905292B1 (es) |
| CN (1) | CN106232599B (es) |
| AR (1) | AR100137A1 (es) |
| BR (1) | BR112016017261B1 (es) |
| CA (1) | CA2938280C (es) |
| DK (1) | DK3134402T3 (es) |
| ES (1) | ES2804101T3 (es) |
| HR (1) | HRP20201043T1 (es) |
| HU (1) | HUE049656T2 (es) |
| LT (1) | LT3134402T (es) |
| MA (1) | MA39898B1 (es) |
| MX (1) | MX377916B (es) |
| PL (1) | PL3134402T3 (es) |
| PT (1) | PT3134402T (es) |
| RS (1) | RS60430B1 (es) |
| RU (1) | RU2698902C2 (es) |
| SI (1) | SI3134402T1 (es) |
| TW (1) | TWI607007B (es) |
| WO (1) | WO2015162075A1 (es) |
Families Citing this family (78)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108368140A (zh) * | 2015-12-14 | 2018-08-03 | 葛兰素史密丝克莱恩生物有限公司 | 作为tlr7和tlr8激动剂的peg化的咪唑并喹啉类 |
| UA124802C2 (uk) | 2015-12-17 | 2021-11-24 | Мерк Патент Гмбх | Поліциклічні антагоністи tlr7/8 і їх застосування в лікуванні імунних розладів |
| JP6918838B2 (ja) | 2016-05-23 | 2021-08-11 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | 第三級アミド基を有するベンズアゼピンジカルボキサミド化合物 |
| EP3464274B1 (en) | 2016-05-23 | 2020-05-27 | H. Hoffnabb-La Roche Ag | Benzazepine dicarboxamide compounds with secondary amide function |
| JP7012668B2 (ja) | 2016-06-12 | 2022-02-14 | エフ・ホフマン－ラ・ロシュ・アクチェンゲゼルシャフト | ジヒドロピリミジニルベンズアゼピンジカルボキサミド化合物 |
| CN115317603A (zh) | 2016-07-07 | 2022-11-11 | 小利兰·斯坦福大学托管委员会 | 抗体佐剂缀合物 |
| KR20240019867A (ko) | 2016-08-08 | 2024-02-14 | 메르크 파텐트 게엠베하 | Tlr7/8 안타고니스트 및 이의 용도 |
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| US10757485B2 (en) * | 2017-08-25 | 2020-08-25 | Honda Motor Co., Ltd. | System and method for synchronized vehicle sensor data acquisition processing using vehicular communication |
| WO2019084060A1 (en) | 2017-10-24 | 2019-05-02 | Silverback Therapeutics, Inc. | CONJUGATES AND METHODS OF USE FOR THE SELECTIVE DELIVERY OF IMMUNOMODULATORY AGENTS |
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| CN111511740B (zh) | 2017-12-20 | 2023-05-16 | 3M创新有限公司 | 用作免疫应答调节剂的带有支链连接基团的酰胺取代的咪唑并[4,5-c]喹啉化合物 |
| AU2018392213B2 (en) | 2017-12-20 | 2021-03-04 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 3'3' cyclic dinucleotides with phosphonate bond activating the STING adaptor protein |
| CN108299421B (zh) * | 2018-01-30 | 2020-09-29 | 中国医学科学院药用植物研究所 | 一种瑞喹莫德的酰化衍生物及制备方法与应用 |
| JP7050165B2 (ja) | 2018-02-26 | 2022-04-07 | ギリアード サイエンシーズ， インコーポレイテッド | Ｈｂｖ複製阻害剤としての置換ピロリジン化合物 |
| JP7251893B2 (ja) | 2018-02-28 | 2023-04-04 | スリーエム イノベイティブ プロパティズ カンパニー | Ｎ－１分枝基を有する置換イミダゾ［４，５－ｃ］キノリン化合物 |
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| US11142750B2 (en) | 2018-04-12 | 2021-10-12 | Precision Biosciences, Inc. | Optimized engineered meganucleases having specificity for a recognition sequence in the Hepatitis B virus genome |
| WO2019211799A1 (en) | 2018-05-03 | 2019-11-07 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 2'3'-cyclic dinucleotide analogue comprising a cyclopentanyl modified nucleotide |
| WO2019224765A1 (en) | 2018-05-24 | 2019-11-28 | 3M Innovative Properties Company | N-1 branched cycloalkyl substituted imidazo[4,5-c]quinoline compounds, compositions, and methods |
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| CN110526918B (zh) * | 2018-05-25 | 2021-09-03 | 江苏恒瑞医药股份有限公司 | 一种吡唑并杂芳基类衍生物的晶型及制备方法 |
| WO2020028097A1 (en) | 2018-08-01 | 2020-02-06 | Gilead Sciences, Inc. | Solid forms of (r)-11-(methoxymethyl)-12-(3-methoxypropoxy)-3,3-dimethyl-8-0x0-2,3,8,13b-tetrahydro-1h-pyrido[2,1-a]pyrrolo[1,2-c] phthalazine-7-c arboxylic acid |
| BR112021002642A2 (pt) | 2018-08-16 | 2021-05-04 | Innate Tumor Immunity, Inc. | compostos de 4-amino-1h-imidazo[4,5-c]quinolina substituídos e métodos aprimorados para a preparação dos mesmos |
| EP3846807B1 (en) * | 2018-09-07 | 2023-08-02 | Birdie Biopharmaceuticals, Inc. | Imidazoquinoline compounds and uses thereof |
| WO2020056192A1 (en) * | 2018-09-12 | 2020-03-19 | Silverback Therapeutics, Inc. | Antibody conjugates of toll-like receptor agonists |
| US20200113912A1 (en) | 2018-09-12 | 2020-04-16 | Silverback Therapeutics, Inc. | Methods and Compositions for the Treatment of Disease with Immune Stimulatory Conjugates |
| AU2019372046B2 (en) | 2018-10-31 | 2022-05-26 | Gilead Sciences, Inc. | Substituted 6-azabenzimidazole compounds as HPK1 inhibitors |
| EP3873608A1 (en) | 2018-10-31 | 2021-09-08 | Gilead Sciences, Inc. | Substituted 6-azabenzimidazole compounds having hpk1 inhibitory activity |
| JP7538803B6 (ja) * | 2019-02-01 | 2024-09-10 | ユー，ニンフイ | イミダゾキノリンアミン誘導体、医薬組成物、その使用 |
| EP3935065A1 (en) | 2019-03-07 | 2022-01-12 | Institute of Organic Chemistry and Biochemistry ASCR, V.V.I. | 3'3'-cyclic dinucleotide analogue comprising a cyclopentanyl modified nucleotide as sting modulator |
| JP7350872B2 (ja) | 2019-03-07 | 2023-09-26 | インスティチュート オブ オーガニック ケミストリー アンド バイオケミストリー エーエスシーアール，ヴイ．ヴイ．アイ． | ３’３’－環状ジヌクレオチドおよびそのプロドラッグ |
| US12318403B2 (en) | 2019-03-07 | 2025-06-03 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 2′3′-cyclic dinucleotides and prodrugs thereof |
| EP3937984A1 (en) | 2019-03-15 | 2022-01-19 | Bolt Biotherapeutics, Inc. | Immunoconjugates targeting her2 |
| TWI751516B (zh) | 2019-04-17 | 2022-01-01 | 美商基利科學股份有限公司 | 類鐸受體調節劑之固體形式 |
| TWI751517B (zh) | 2019-04-17 | 2022-01-01 | 美商基利科學股份有限公司 | 類鐸受體調節劑之固體形式 |
| WO2020237025A1 (en) | 2019-05-23 | 2020-11-26 | Gilead Sciences, Inc. | Substituted exo-methylene-oxindoles which are hpk1/map4k1 inhibitors |
| CA3141085A1 (en) | 2019-06-19 | 2020-12-24 | Brenda Stevens | Anti-mesothelin antibodies and immunoconjugates thereof |
| CN112174903B (zh) * | 2019-07-01 | 2022-07-12 | 清华大学 | Tlr8的小分子调节剂 |
| US11339159B2 (en) * | 2019-07-17 | 2022-05-24 | Pfizer Inc. | Toll-like receptor agonists |
| WO2021034804A1 (en) | 2019-08-19 | 2021-02-25 | Gilead Sciences, Inc. | Pharmaceutical formulations of tenofovir alafenamide |
| KR20220074917A (ko) | 2019-09-30 | 2022-06-03 | 길리애드 사이언시즈, 인코포레이티드 | Hbv 백신 및 hbv를 치료하는 방법 |
| AU2020358726A1 (en) | 2019-10-01 | 2022-04-07 | Silverback Therapeutics, Inc. | Combination therapy with immune stimulatory conjugates |
| CN114599360A (zh) * | 2019-10-29 | 2022-06-07 | 骏达贸易有限公司 | 4-氨基-咪唑并喹啉化合物及其用途 |
| CN116057068A (zh) | 2019-12-06 | 2023-05-02 | 精密生物科学公司 | 对乙型肝炎病毒基因组中的识别序列具有特异性的优化的工程化大范围核酸酶 |
| WO2021168274A1 (en) | 2020-02-21 | 2021-08-26 | Silverback Therapeutics, Inc. | Nectin-4 antibody conjugates and uses thereof |
| AU2021237718B2 (en) | 2020-03-20 | 2023-09-21 | Gilead Sciences, Inc. | Prodrugs of 4'-C-substituted-2-halo-2'-deoxyadenosine nucleosides and methods of making and using the same |
| AU2021258392A1 (en) | 2020-04-19 | 2022-12-15 | Ludwig ENGLMEIER | Prophylaxis and treatment of coronavirus infection |
| JP2023526304A (ja) * | 2020-05-14 | 2023-06-21 | メルク ヘルスケア コマンディトゲゼルシャフト アウフ アクティーン | コロナウイルス感染症治療のためのｔｌｒ７／８拮抗薬 |
| EP4153590A4 (en) * | 2020-05-21 | 2024-06-19 | Ohio State Innovation Foundation | FUNCTIONAL LIPID DERIVATIVES AND THEIR USES |
| AU2021300362A1 (en) | 2020-07-01 | 2023-02-23 | ARS Pharmaceuticals, Inc. | Anti-ASGR1 antibody conjugates and uses thereof |
| WO2022153157A1 (en) * | 2021-01-13 | 2022-07-21 | Pfizer Inc. | A crystalline form of 2-((4-amino-2-(ethoxymethyl)-6,7-dimethyl-1 h-imidazo[4,5-c]pyridin-1-yl)methyl)-2-methylpropane-1,3-diol free base |
| JP2024506300A (ja) * | 2021-02-03 | 2024-02-13 | シージェン インコーポレイテッド | 免疫刺激化合物及びコンジュゲート体 |
| US20240209080A1 (en) | 2021-04-10 | 2024-06-27 | Profoundbio Us Co. | Folr1 binding agents, conjugates thereof and methods of using the same |
| TW202308699A (zh) | 2021-04-23 | 2023-03-01 | 美商普方生物製藥美國公司 | Ｃｄ７０結合劑、其結合物及其使用方法 |
| JP2024518558A (ja) | 2021-05-13 | 2024-05-01 | ギリアード サイエンシーズ， インコーポレイテッド | ＴＬＲ８調節化合物と抗ＨＢＶ ｓｉＲＮＡ治療薬との組合せ |
| CN117377671A (zh) | 2021-06-23 | 2024-01-09 | 吉利德科学公司 | 二酰基甘油激酶调节化合物 |
| EP4359413A1 (en) | 2021-06-23 | 2024-05-01 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
| CN117355531A (zh) | 2021-06-23 | 2024-01-05 | 吉利德科学公司 | 二酰基甘油激酶调节化合物 |
| CA3220923A1 (en) | 2021-06-23 | 2022-12-29 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
| TW202320857A (zh) | 2021-07-06 | 2023-06-01 | 美商普方生物製藥美國公司 | 連接子、藥物連接子及其結合物及其使用方法 |
| US20250025447A1 (en) * | 2021-11-03 | 2025-01-23 | Regents Of The University Of Minnesota | Toll-like receptor agonists and antagonists and uses thereof |
| CA3262320A1 (en) * | 2022-08-03 | 2024-02-08 | Regents Of The University Of Minnesota | Anti-PD-L1 Conjugates - Immunostimulating Drugs |
| CN120457128A (zh) * | 2022-11-09 | 2025-08-08 | 默克专利股份公司 | 作为免疫刺激剂以引发先天抗肿瘤免疫的Toll样受体7激动剂 |
| WO2024112932A1 (en) * | 2022-11-23 | 2024-05-30 | Regents Of The University Of Minnesota | Immunomodulators and immunomodulator conjugates |
| US20250115680A1 (en) | 2023-09-26 | 2025-04-10 | Profoundbio Us Co. | Ptk7 binding agents, conjugates thereof and methods of using the same |
| US20250296992A1 (en) | 2024-01-10 | 2025-09-25 | Genmab A/S | Slitrk6 binding agents, conjugates thereof and methods of using the same |
| WO2025181219A1 (en) | 2024-02-29 | 2025-09-04 | Genmab A/S | Egfr and c-met bispecific binding agents, conjugates thereof and methods of using the same |
| US20250345390A1 (en) | 2024-05-13 | 2025-11-13 | Gilead Sciences, Inc. | Combination therapies |
| US20250345389A1 (en) | 2024-05-13 | 2025-11-13 | Gilead Sciences, Inc. | Combination therapies |
| WO2025240246A1 (en) | 2024-05-13 | 2025-11-20 | Gilead Sciences, Inc. | Combination therapies with ribavirin |
| WO2025240242A1 (en) | 2024-05-13 | 2025-11-20 | Gilead Sciences, Inc. | Combination therapies with ribavirin |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69229114T2 (de) * | 1991-03-01 | 1999-11-04 | Minnesota Mining And Mfg. Co., Saint Paul | 1,2-substituierte 1h-imidazo[4,5-c]chinolin-4-amine |
| US6451810B1 (en) * | 1999-06-10 | 2002-09-17 | 3M Innovative Properties Company | Amide substituted imidazoquinolines |
| US6664265B2 (en) | 2000-12-08 | 2003-12-16 | 3M Innovative Properties Company | Amido ether substituted imidazoquinolines |
| US6861440B2 (en) * | 2001-10-26 | 2005-03-01 | Hoffmann-La Roche Inc. | DPP IV inhibitors |
| ES2318615T3 (es) * | 2001-11-16 | 2009-05-01 | Coley Pharmaceutical Group, Inc. | N-(4-(4-amino-2-etil-1h-imidazo(4,5-c)quinolin-1-il)butil)metanosulfonamida, una composicion farmaceutica que la comprende y uso de la misma. |
| EA200600540A1 (ru) * | 2003-09-05 | 2006-08-25 | Анадис Фармасьютикалз, Инк. | Введение лигандов tlr7 и их пролекарств для лечения инфекции вируса гепатита с |
| AR048289A1 (es) * | 2003-12-04 | 2006-04-19 | 3M Innovative Properties Co | Eteres de anillos imidazo sulfona sustituidos. |
| TW201402124A (zh) | 2005-08-19 | 2014-01-16 | Array Biopharma Inc | 作為類鐸受體（ｔｏｌｌ-ｌｉｋｅ ｒｅｃｅｐｔｏｒ）調節劑之８-經取代苯并氮雜呯 |
| ES2546213T3 (es) | 2008-03-03 | 2015-09-21 | Novartis Ag | Compuestos y composiciones como moduladores de la actividad de TLR |
| ES2545275T3 (es) | 2008-11-06 | 2015-09-09 | Ventirx Pharmaceuticals, Inc. | Métodos de síntesis de derivados de benzazepinas |
| EA019768B1 (ru) | 2009-02-11 | 2014-06-30 | Дзе Регентс Оф Дзе Юниверсити Оф Калифорния | СОЕДИНЕНИЯ, МОДУЛИРУЮЩИЕ АКТИВНОСТЬ Toll-ПОДОБНЫХ РЕЦЕПТОРОВ |
| EP3199159B1 (en) | 2009-08-07 | 2019-04-10 | GlaxoSmithKline Biologicals S.A. | Lipidated oxoadenine derivatives |
| JP2013512859A (ja) | 2009-12-03 | 2013-04-18 | 大日本住友製薬株式会社 | トール様受容体（ｔｌｒ）を介して作用するイミダゾキノリン |
| CN103118682A (zh) | 2010-04-30 | 2013-05-22 | 加利福尼亚大学校务委员会 | 合成tlr7激动剂的磷脂缀合物的用途 |
| RU2016141322A (ru) | 2010-10-01 | 2018-12-14 | Вентиркс Фармасьютикалз, Инк. | Терапевтическое применение агониста tlr и комбинированная терапия |
| WO2012066336A1 (en) | 2010-11-19 | 2012-05-24 | Astrazeneca Ab | Benzylamine compounds as toll -like receptor 7 agonists |
| WO2012167081A1 (en) | 2011-06-03 | 2012-12-06 | 3M Innovative Properties Company | Hydrazino 1h-imidazoquinolin-4-amines and conjugates made therefrom |
| WO2012167801A1 (ru) | 2011-06-07 | 2012-12-13 | Uglovsky Sergey Evgenievich | Импульсная установка для преобразования низкопотенциальной тепловой энергии в электрическую |
| WO2013033345A1 (en) | 2011-08-30 | 2013-03-07 | Regents Of The University Of Minnesota | Immunomodulators and immunomodulator conjugates |
| IN2014CN04251A (es) | 2011-11-09 | 2015-07-17 | Ascend Biopharmaceuticals Ltd | |
| WO2013166110A1 (en) | 2012-05-02 | 2013-11-07 | Yale University | Tlr-agonist-conjugated antibody recruiting molecules (tlr_arms) |
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