CN104583214B - 人类免疫缺陷病毒复制的抑制剂 - Google Patents
人类免疫缺陷病毒复制的抑制剂 Download PDFInfo
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- CN104583214B CN104583214B CN201380043596.7A CN201380043596A CN104583214B CN 104583214 B CN104583214 B CN 104583214B CN 201380043596 A CN201380043596 A CN 201380043596A CN 104583214 B CN104583214 B CN 104583214B
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- tert
- butoxy
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- 0 CCCC1c(cc(*2OC(C)(C)C(C)(C)O2)cc2)c2OCC1 Chemical compound CCCC1c(cc(*2OC(C)(C)C(C)(C)O2)cc2)c2OCC1 0.000 description 6
- FCEPMBPRKFZEKD-DXSDROHOSA-N CC(CCCOC(C)(CC1)CCN1c1c([C@@H](C(O)=O)OC(C)(C)C)c(C)nc2cc-3n[n]12)C(C)Oc1ccc(C)cc1-c1cccc-3c1 Chemical compound CC(CCCOC(C)(CC1)CCN1c1c([C@@H](C(O)=O)OC(C)(C)C)c(C)nc2cc-3n[n]12)C(C)Oc1ccc(C)cc1-c1cccc-3c1 FCEPMBPRKFZEKD-DXSDROHOSA-N 0.000 description 2
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- SHTARJXBKXRLHD-YWGMWZHNSA-N CC(C)(C)O[C@H](C(O)=O)c(c(C)nc1cc-2n[n]11)c1N(CC1)CCC1(C)/[O]=C/C=C/COc1ccccc1-c1cccc-2c1 Chemical compound CC(C)(C)O[C@H](C(O)=O)c(c(C)nc1cc-2n[n]11)c1N(CC1)CCC1(C)/[O]=C/C=C/COc1ccccc1-c1cccc-2c1 SHTARJXBKXRLHD-YWGMWZHNSA-N 0.000 description 1
- RWJFMBQQPUZFBB-YTTGMZPUSA-N CC(C)(C)O[C@H](C(O)=O)c(c(C)nc1cc-2n[n]11)c1N(CC1)CCC1(C)OCCCCOc1ccc(C)cc1-c1cccc-2c1 Chemical compound CC(C)(C)O[C@H](C(O)=O)c(c(C)nc1cc-2n[n]11)c1N(CC1)CCC1(C)OCCCCOc1ccc(C)cc1-c1cccc-2c1 RWJFMBQQPUZFBB-YTTGMZPUSA-N 0.000 description 1
- QNHCUEYHMKHFHZ-RSUXDYMJSA-N CC(C)(C)O[C@H](C(OC)=O)c(c(C)nc1c2)c(-c(cc3)cc4c3OCC[C@@H]4CCCCOc3c-4cccc3)[n]1nc2-c1cc-4ccc1 Chemical compound CC(C)(C)O[C@H](C(OC)=O)c(c(C)nc1c2)c(-c(cc3)cc4c3OCC[C@@H]4CCCCOc3c-4cccc3)[n]1nc2-c1cc-4ccc1 QNHCUEYHMKHFHZ-RSUXDYMJSA-N 0.000 description 1
- WYJHJSXIVTYJCF-WXCKSCCKSA-N CC(C)(C)O[C@H](C(OC)=O)c(c(C)nc1cc(-c2cc(-c3ccccc3CCC=C)ccc2)n[n]11)c1N(CC1)CCC1(C)/C=C/C=C Chemical compound CC(C)(C)O[C@H](C(OC)=O)c(c(C)nc1cc(-c2cc(-c3ccccc3CCC=C)ccc2)n[n]11)c1N(CC1)CCC1(C)/C=C/C=C WYJHJSXIVTYJCF-WXCKSCCKSA-N 0.000 description 1
- VSSVWSWBAXPTAW-BHVANESWSA-N CC(C)(C)O[C@H](C(OC)=O)c(c(C)nc1cc(-c2cc(-c3ccccc3CCC=C)ccc2)n[n]11)c1N1CCC(C)(COCC=C)CC1 Chemical compound CC(C)(C)O[C@H](C(OC)=O)c(c(C)nc1cc(-c2cc(-c3ccccc3CCC=C)ccc2)n[n]11)c1N1CCC(C)(COCC=C)CC1 VSSVWSWBAXPTAW-BHVANESWSA-N 0.000 description 1
- QYRFWBZEHOWGKT-GXHSSAHRSA-N CC(C)(C)O[C@H](C(OC)=O)c(c(C)nc1cc-2n[n]11)c1N(CC1)CCC1(C)/C=C/C=C/CCc1ccccc1-c1cccc-2c1 Chemical compound CC(C)(C)O[C@H](C(OC)=O)c(c(C)nc1cc-2n[n]11)c1N(CC1)CCC1(C)/C=C/C=C/CCc1ccccc1-c1cccc-2c1 QYRFWBZEHOWGKT-GXHSSAHRSA-N 0.000 description 1
- MNZYQPOQYYFAGP-UHFFFAOYSA-N CC(C)(C)[O-]c(c(-c1c(CC(OC)=O)c(C)nc2cc(-c3cc(-c(cccc4)c4O)ccc3)n[n]12)c1Cl)cc2c1N(CC=C)CCO2 Chemical compound CC(C)(C)[O-]c(c(-c1c(CC(OC)=O)c(C)nc2cc(-c3cc(-c(cccc4)c4O)ccc3)n[n]12)c1Cl)cc2c1N(CC=C)CCO2 MNZYQPOQYYFAGP-UHFFFAOYSA-N 0.000 description 1
- UUEURGUMLLFHCB-UHFFFAOYSA-N CCCCN(CCCOCC=C)c1c(C(C(OC)=O)OC(C)(C)C)c(C)nc2cc(-c3cc(-c(c(O)c4)ccc4F)ccc3)n[n]12 Chemical compound CCCCN(CCCOCC=C)c1c(C(C(OC)=O)OC(C)(C)C)c(C)nc2cc(-c3cc(-c(c(O)c4)ccc4F)ccc3)n[n]12 UUEURGUMLLFHCB-UHFFFAOYSA-N 0.000 description 1
- JFTCISYZLOUDEY-HOYUZMNJSA-N C[C@@H](CC=C)NC1=C(c2cccc(-c3n[n]4c(N(CC5)CCC5(C)OCC=C)c([C@@H](C(OC)=O)OC(C)(C)C)c(C)nc4c3)c2)C(F)=CCC1 Chemical compound C[C@@H](CC=C)NC1=C(c2cccc(-c3n[n]4c(N(CC5)CCC5(C)OCC=C)c([C@@H](C(OC)=O)OC(C)(C)C)c(C)nc4c3)c2)C(F)=CCC1 JFTCISYZLOUDEY-HOYUZMNJSA-N 0.000 description 1
- OHGLFRRMTJLYEZ-ASMAMLKCSA-N C[C@@H](CC=C)Oc(c(-c1cccc(-c2n[n]3c(N(CC4)CCC4(C)[U]CC=C)c(/C(/C(OC)=O)=[O-]/C(C)(C)C)c(C)nc3c2)c1)c1C)ccc1Cl Chemical compound C[C@@H](CC=C)Oc(c(-c1cccc(-c2n[n]3c(N(CC4)CCC4(C)[U]CC=C)c(/C(/C(OC)=O)=[O-]/C(C)(C)C)c(C)nc3c2)c1)c1C)ccc1Cl OHGLFRRMTJLYEZ-ASMAMLKCSA-N 0.000 description 1
- IWAMSFNYGNTSRC-ROPHLPQBSA-N C[C@@H](CC=C)Oc(c(-c1cccc(-c2n[n]3c(N(CC4)CCC4(C)[U]CC=C)c(CC(OC)=O)c(C)nc3c2)c1)c1)cc(C)c1[I]1CCC1 Chemical compound C[C@@H](CC=C)Oc(c(-c1cccc(-c2n[n]3c(N(CC4)CCC4(C)[U]CC=C)c(CC(OC)=O)c(C)nc3c2)c1)c1)cc(C)c1[I]1CCC1 IWAMSFNYGNTSRC-ROPHLPQBSA-N 0.000 description 1
- PWKDVHTWIQOLIJ-WYOOIXGGSA-N C[C@@H](CCCCOC(C)(CC1)CCN1c1c([C@@H](C(O)=O)OC(C)(C)C)c(C)nc2cc-3n[n]12)Oc1ccc(C(F)(F)F)cc1-c1cccc-3c1 Chemical compound C[C@@H](CCCCOC(C)(CC1)CCN1c1c([C@@H](C(O)=O)OC(C)(C)C)c(C)nc2cc-3n[n]12)Oc1ccc(C(F)(F)F)cc1-c1cccc-3c1 PWKDVHTWIQOLIJ-WYOOIXGGSA-N 0.000 description 1
- LLYNGOSRZKSYAX-UDNBHOFDSA-N C[C@@H](CCCOC(C)(CC1)CCN1c1c([C@@H](C(O)=O)OC(C)(C)C)c(C)nc2cc-3n[n]12)Oc1ccccc1-c1cccc-3c1 Chemical compound C[C@@H](CCCOC(C)(CC1)CCN1c1c([C@@H](C(O)=O)OC(C)(C)C)c(C)nc2cc-3n[n]12)Oc1ccccc1-c1cccc-3c1 LLYNGOSRZKSYAX-UDNBHOFDSA-N 0.000 description 1
Classifications
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5383—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- C07D471/22—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 systems contains four or more hetero rings
-
- 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
- C07D487/12—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 three hetero rings
- C07D487/16—Peri-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/22—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/16—Peri-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Virology (AREA)
- AIDS & HIV (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261683772P | 2012-08-16 | 2012-08-16 | |
| US61/683,772 | 2012-08-16 | ||
| US201361818572P | 2013-05-02 | 2013-05-02 | |
| US61/818,572 | 2013-05-02 | ||
| US13/959,268 | 2013-08-05 | ||
| US13/959,268 US8906929B2 (en) | 2012-08-16 | 2013-08-05 | Inhibitors of human immunodeficiency virus replication |
| PCT/US2013/054532 WO2014028384A1 (en) | 2012-08-16 | 2013-08-12 | Inhibitors of human immunodeficiency virus replication |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN104583214A CN104583214A (zh) | 2015-04-29 |
| CN104583214B true CN104583214B (zh) | 2017-06-09 |
Family
ID=50100460
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201380043596.7A Expired - Fee Related CN104583214B (zh) | 2012-08-16 | 2013-08-12 | 人类免疫缺陷病毒复制的抑制剂 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US8906929B2 (enExample) |
| EP (1) | EP2888266B1 (enExample) |
| JP (1) | JP6214657B2 (enExample) |
| KR (1) | KR20150042830A (enExample) |
| CN (1) | CN104583214B (enExample) |
| AU (1) | AU2013302873B2 (enExample) |
| BR (1) | BR112015003175A2 (enExample) |
| CA (1) | CA2882077A1 (enExample) |
| EA (1) | EA201590358A1 (enExample) |
| ES (1) | ES2619960T3 (enExample) |
| IL (1) | IL237154A (enExample) |
| MX (1) | MX2015001899A (enExample) |
| SG (1) | SG11201500887QA (enExample) |
| TW (1) | TW201412750A (enExample) |
| WO (1) | WO2014028384A1 (enExample) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG186820A1 (en) | 2010-07-02 | 2013-02-28 | Gilead Sciences Inc | Napht- 2 -ylacetic acid derivatives to treat aids |
| BR112012033689A2 (pt) | 2010-07-02 | 2019-09-24 | Gilead Sciences Inc | derivados de ácido 2-quinolinil-acético como compostos de hiv antivirais |
| ES2615734T3 (es) | 2011-04-21 | 2017-06-08 | Gilead Sciences, Inc. | Compuestos de benzotiazol y su uso farmacéutico |
| US9376392B2 (en) | 2012-01-04 | 2016-06-28 | Gilead Sciences, Inc. | 2-(tert-butoxy)-2-(7-methylquinolin-6-yl) acetic acid derivatives for treating AIDS |
| US9284323B2 (en) | 2012-01-04 | 2016-03-15 | Gilead Sciences, Inc. | Naphthalene acetic acid derivatives against HIV infection |
| MX2014005002A (es) | 2012-04-20 | 2014-07-09 | Gilead Sciences Inc | Derivados de acido benzotiazol-6-il acetico y su uso para tratar una infeccion por vih. |
| US8906929B2 (en) | 2012-08-16 | 2014-12-09 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
| CN105189510B (zh) * | 2013-03-13 | 2017-05-17 | 百时美施贵宝公司 | 人免疫缺陷病毒复制的抑制剂 |
| WO2014159076A1 (en) * | 2013-03-14 | 2014-10-02 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
| WO2015123182A1 (en) * | 2014-02-12 | 2015-08-20 | Bristol-Myers Squibb Company | Pyrazolopyrimidine macrocycles as inhibitors of human immunodeficiency virus replication |
| ES2654242T3 (es) | 2014-02-12 | 2018-02-12 | Viiv Healthcare (No.5) Limited | Macrociclos de benzotiazol como inhibidores de la réplica del virus de la inmunodeficiencia humana |
| EP3152215A1 (en) * | 2014-02-18 | 2017-04-12 | ViiV Healthcare UK (No.5) Limited | Pyrazolopyrimidine macrocycles as inhibitors of human immunodeficiency virus replication |
| US9409922B2 (en) | 2014-02-18 | 2016-08-09 | Bristol-Myers Squibb Company | Imidazopyridine macrocycles as inhibitors of human immunodeficiency virus replication |
| WO2015126758A1 (en) * | 2014-02-18 | 2015-08-27 | Bristol-Myers Squibb Company | Imidazopyrimidine macrocycles as inhibitors of human immunodeficiency virus replication |
| WO2015126376A1 (en) * | 2014-02-19 | 2015-08-27 | Bristol-Myers Squibb Company | Pyrazolopyrimidine macrocycles as inhibitors of human immunodeficiency virus replication |
| US9273067B2 (en) | 2014-02-19 | 2016-03-01 | Bristol-Myers Squibb Company | Pyrazolopyrimidine macrocycles as inhibitors of human immunodeficiency virus replication |
| PT3107913T (pt) | 2014-02-19 | 2018-09-28 | Viiv Healthcare Uk No 5 Ltd | Inibidores da replicação do vírus da imunodeficiência humana |
| ES2670010T3 (es) | 2014-02-20 | 2018-05-29 | VIIV Healthcare UK (No.5) Limited | Macrociclos de ácido piridin-3-il acético como inhibidores de replicación del virus de inmunodeficiencia humana |
| WO2015174511A1 (ja) * | 2014-05-16 | 2015-11-19 | 塩野義製薬株式会社 | Ｈｉｖ複製阻害作用を有する３環性複素環誘導体 |
| MA43120A (fr) | 2015-05-29 | 2018-09-05 | Shionogi & Co | Dérivé tricyclique contenant de l'azote présentant une activité inhibitrice de la réplication du vih |
| JP2018522924A (ja) * | 2015-08-10 | 2018-08-16 | ヴィーブ ヘルスケア ユーケー（ナンバー５）リミテッド | ヒト免疫不全ウイルス複製の阻害剤としてのイミダゾピリジン大環状化合物 |
| CA3057261A1 (en) | 2017-04-06 | 2018-10-11 | Inventiva | New compounds inhibitors of the yap/taz-tead interaction and their use in the treatment of malignant mesothelioma |
| EP3632908A1 (en) | 2018-10-02 | 2020-04-08 | Inventiva | Inhibitors of the yap/taz-tead interaction and their use in the treatment of cancer |
| SI3938047T1 (sl) | 2019-03-22 | 2022-10-28 | Gilead Sciences, Inc. | Premoščene triciklične karbamoilpiridonske spojine in njihova farmacevtska uporaba |
| WO2021173522A1 (en) | 2020-02-24 | 2021-09-02 | Gilead Sciences, Inc. | Tetracyclic compounds for treating hiv infection |
| KR20230079137A (ko) | 2020-09-30 | 2023-06-05 | 길리애드 사이언시즈, 인코포레이티드 | 가교된 트리사이클릭 카르바모일피리돈 화합물 및 이의 용도 |
| PT4196479T (pt) | 2021-01-19 | 2024-01-03 | Gilead Sciences Inc | Compostos de piridotriazinas substituídos e suas utilizações |
| TWI856796B (zh) | 2022-04-06 | 2024-09-21 | 美商基利科學股份有限公司 | 橋聯三環胺甲醯基吡啶酮化合物及其用途 |
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| WO2009111653A2 (en) * | 2008-03-05 | 2009-09-11 | Biocryst Pharmaceuticals, Inc. | Antiviral therapeutic agents |
| CN102036996A (zh) * | 2008-03-19 | 2011-04-27 | 百时美施贵宝公司 | 作为hiv整合酶抑制剂的桥接杂环 |
| WO2012033735A1 (en) * | 2010-09-08 | 2012-03-15 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
| CN102459183A (zh) * | 2009-05-15 | 2012-05-16 | 吉联亚科学股份有限公司 | 人类免疫缺陷病毒复制的抑制剂 |
| WO2012065963A2 (en) * | 2010-11-15 | 2012-05-24 | Katholieke Universiteit Leuven | Novel antiviral compounds |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB427857A (en) | 1934-08-02 | 1935-05-01 | Newsum Sons & Company Ltd H | A new or improved system of construction for skeleton structures, particularly vehicle body frames and door frames |
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- 2013-08-12 CN CN201380043596.7A patent/CN104583214B/zh not_active Expired - Fee Related
- 2013-08-12 KR KR20157006290A patent/KR20150042830A/ko not_active Withdrawn
- 2013-08-12 CA CA2882077A patent/CA2882077A1/en active Pending
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Also Published As
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|---|---|
| BR112015003175A2 (pt) | 2017-08-08 |
| US8906929B2 (en) | 2014-12-09 |
| KR20150042830A (ko) | 2015-04-21 |
| US20140051692A1 (en) | 2014-02-20 |
| MX2015001899A (es) | 2015-05-07 |
| JP2015524841A (ja) | 2015-08-27 |
| EA201590358A1 (ru) | 2015-05-29 |
| ES2619960T3 (es) | 2017-06-27 |
| AU2013302873A1 (en) | 2015-04-02 |
| AU2013302873B2 (en) | 2017-02-02 |
| TW201412750A (zh) | 2014-04-01 |
| CN104583214A (zh) | 2015-04-29 |
| JP6214657B2 (ja) | 2017-10-18 |
| EP2888266A1 (en) | 2015-07-01 |
| CA2882077A1 (en) | 2014-02-20 |
| IL237154A (en) | 2017-03-30 |
| EP2888266B1 (en) | 2017-01-11 |
| WO2014028384A1 (en) | 2014-02-20 |
| IL237154A0 (en) | 2015-04-30 |
| SG11201500887QA (en) | 2015-03-30 |
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