CN101945874A - 作为抗癌剂的3-取代的-4-氧代-3,4-二氢-咪唑并[5,1-d][1,2,3,5]-四嗪-8-甲酰胺类 - Google Patents
作为抗癌剂的3-取代的-4-氧代-3,4-二氢-咪唑并[5,1-d][1,2,3,5]-四嗪-8-甲酰胺类 Download PDFInfo
- Publication number
- CN101945874A CN101945874A CN2008801269450A CN200880126945A CN101945874A CN 101945874 A CN101945874 A CN 101945874A CN 2008801269450 A CN2008801269450 A CN 2008801269450A CN 200880126945 A CN200880126945 A CN 200880126945A CN 101945874 A CN101945874 A CN 101945874A
- Authority
- CN
- China
- Prior art keywords
- independently
- compound according
- saturated aliphatic
- compound
- alkylene
- 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.)
- Pending
Links
- RBORGIJOCTWMNM-UHFFFAOYSA-N NC(c(nc[n]12)c1N=NN(CO)C2=O)=O Chemical compound NC(c(nc[n]12)c1N=NN(CO)C2=O)=O RBORGIJOCTWMNM-UHFFFAOYSA-N 0.000 description 4
- 0 *N1N=Nc2c(C(N)=O)nc[n]2C1=O Chemical compound *N1N=Nc2c(C(N)=O)nc[n]2C1=O 0.000 description 3
- IRJLFDHRTDDHFP-UHFFFAOYSA-N NC(c(nc[nH]1)c1N=N)=O Chemical compound NC(c(nc[nH]1)c1N=N)=O IRJLFDHRTDDHFP-UHFFFAOYSA-N 0.000 description 2
- JHGYHIRPZKSABQ-UHFFFAOYSA-N C#CCN1N=Nc2c(C(N)=O)nc[n]2C1=O Chemical compound C#CCN1N=Nc2c(C(N)=O)nc[n]2C1=O JHGYHIRPZKSABQ-UHFFFAOYSA-N 0.000 description 1
- YOXXWQMYZAJVMT-UHFFFAOYSA-N CCC(CN1N=Nc2c(C(N)=O)nc[n]2C1=O)=O Chemical compound CCC(CN1N=Nc2c(C(N)=O)nc[n]2C1=O)=O YOXXWQMYZAJVMT-UHFFFAOYSA-N 0.000 description 1
- LULCUBZLVBTNMV-UHFFFAOYSA-N CN(C)C(CN1N=Nc2c(C(N)=O)nc[n]2C1=O)=O Chemical compound CN(C)C(CN1N=Nc2c(C(N)=O)nc[n]2C1=O)=O LULCUBZLVBTNMV-UHFFFAOYSA-N 0.000 description 1
- VTVKZBUVVRXUSD-UHFFFAOYSA-N CN1N=Nc2c(C=O)nc[n]2C1=O Chemical compound CN1N=Nc2c(C=O)nc[n]2C1=O VTVKZBUVVRXUSD-UHFFFAOYSA-N 0.000 description 1
- OSPCVVQIISNXLL-RUETXSTFSA-N C[C@H](c1ccc(C2C(C)C2)cc1)N1N=Nc2c(C(N)=O)nc[n]2C1=O Chemical compound C[C@H](c1ccc(C2C(C)C2)cc1)N1N=Nc2c(C(N)=O)nc[n]2C1=O OSPCVVQIISNXLL-RUETXSTFSA-N 0.000 description 1
- ZMVUVOGQYFTORE-UHFFFAOYSA-N C[Si+](C)(C)CCOCN1N=Nc2c(C(N)=O)nc[n]2C1=O Chemical compound C[Si+](C)(C)CCOCN1N=Nc2c(C(N)=O)nc[n]2C1=O ZMVUVOGQYFTORE-UHFFFAOYSA-N 0.000 description 1
- SVTGUCIIMFSDOZ-UHFFFAOYSA-N C[Si+](C)(C)CCOCN=C=O Chemical compound C[Si+](C)(C)CCOCN=C=O SVTGUCIIMFSDOZ-UHFFFAOYSA-N 0.000 description 1
- RICWJULAEOPTAC-UHFFFAOYSA-N C[Si](C)(C)#CCN1N=Nc2c(C(N)=O)nc[n]2C1=O Chemical compound C[Si](C)(C)#CCN1N=Nc2c(C(N)=O)nc[n]2C1=O RICWJULAEOPTAC-UHFFFAOYSA-N 0.000 description 1
- BPXKZEMBEZGUAH-UHFFFAOYSA-N C[Si](C)(C)CCOCCl Chemical compound C[Si](C)(C)CCOCCl BPXKZEMBEZGUAH-UHFFFAOYSA-N 0.000 description 1
- XTAAYHOHCWQHCR-UHFFFAOYSA-N C[Si](C)(C)CCOCN1N=Nc2c(C(N)=O)nc[n]2C1=O Chemical compound C[Si](C)(C)CCOCN1N=Nc2c(C(N)=O)nc[n]2C1=O XTAAYHOHCWQHCR-UHFFFAOYSA-N 0.000 description 1
- HAGVFGQYIUJBNM-UHFFFAOYSA-N C[Si](C)(C)CCOCN=C=O Chemical compound C[Si](C)(C)CCOCN=C=O HAGVFGQYIUJBNM-UHFFFAOYSA-N 0.000 description 1
- SSEWJYFCBNVBAI-UHFFFAOYSA-N NC(c(nc[n]12)c1N=NN(CC(O)=O)C2=O)=O Chemical compound NC(c(nc[n]12)c1N=NN(CC(O)=O)C2=O)=O SSEWJYFCBNVBAI-UHFFFAOYSA-N 0.000 description 1
- JGUFREYWKHEKTR-UHFFFAOYSA-N NC(c(nc[n]12)c1N=NN(CNC(OCC1c3ccccc3-c3ccccc13)=O)C2=O)=O Chemical compound NC(c(nc[n]12)c1N=NN(CNC(OCC1c3ccccc3-c3ccccc13)=O)C2=O)=O JGUFREYWKHEKTR-UHFFFAOYSA-N 0.000 description 1
- HHCAFEAKBZJVMO-UHFFFAOYSA-N O=C(NCN=C=O)OCC1c2ccccc2-c2ccccc12 Chemical compound O=C(NCN=C=O)OCC1c2ccccc2-c2ccccc12 HHCAFEAKBZJVMO-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/10—Compounds having one or more C—Si linkages containing nitrogen having a Si-N linkage
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (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 |
|---|---|---|---|
| US1452007P | 2007-12-18 | 2007-12-18 | |
| US61/014,520 | 2007-12-18 | ||
| PCT/GB2008/004140 WO2009077741A2 (en) | 2007-12-18 | 2008-12-16 | 3-substituted-4-oxo-3,4-dihydro-imidazo-[5,1-d][1,2,3,5-tetrazine-8-carboxylic acid amides and their use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN101945874A true CN101945874A (zh) | 2011-01-12 |
Family
ID=40427129
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2008801269450A Pending CN101945874A (zh) | 2007-12-18 | 2008-12-16 | 作为抗癌剂的3-取代的-4-氧代-3,4-二氢-咪唑并[5,1-d][1,2,3,5]-四嗪-8-甲酰胺类 |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US8450479B2 (enExample) |
| EP (2) | EP2698370A3 (enExample) |
| JP (1) | JP2011506588A (enExample) |
| CN (1) | CN101945874A (enExample) |
| AR (1) | AR071548A1 (enExample) |
| AU (1) | AU2008337261A1 (enExample) |
| CA (1) | CA2709749A1 (enExample) |
| IL (1) | IL206453A0 (enExample) |
| PE (1) | PE20091101A1 (enExample) |
| TW (1) | TW200934782A (enExample) |
| WO (1) | WO2009077741A2 (enExample) |
| ZA (1) | ZA201004554B (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108276415A (zh) * | 2018-02-08 | 2018-07-13 | 台州职业技术学院 | 一种烷氧化三唑并四嗪类化合物及其制备方法和应用 |
| CN113271939A (zh) * | 2018-08-09 | 2021-08-17 | 伊利诺伊大学董事会 | 咪唑四嗪化合物 |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20091101A1 (es) | 2007-12-18 | 2009-07-26 | Pharminox Ltd | AMIDAS DE ACIDO 3-SUBSTITUIDO-4-OXO-3,4-DIHIDRO-IMIDAZO[5,1-d] [1,2,3,5-TETRACINA-8-CARBOXILICO Y SU EMPLEO |
| US9024018B2 (en) * | 2009-06-23 | 2015-05-05 | Pharminox Limited | 3-substituted-8-substituted-3H-imidazo[5,1-d][1,2,3,5]tetrazin-4-one compounds and their use |
| WO2011107726A1 (en) | 2010-03-01 | 2011-09-09 | Pharminox Ltd | Methods and intermediates for the synthesis of 4-oxo-3,4-dihydro-imidazo[5,1-d][1,2,3,5]tetrazines |
| WO2012085501A1 (en) | 2010-12-20 | 2012-06-28 | Pharminox Limited | 8 - sulfo - imidazotetrazin- 4 - one compounds and their use as anticancer drug |
| RU2545458C2 (ru) * | 2013-08-01 | 2015-03-27 | Автономная Некоммерческая Организация "Научно-Исследовательский Центр Биотехнологии Антибиотиков И Других Биологически Активных Веществ "Биоан" | ПРОТИВОТУБЕРКУЛЕЗНОЕ ЛЕКАРСТВЕННОЕ СРЕДСТВО: КОМПОЗИЦИЯ ИМИДАЗО[1,2-b]ТЕТРАЗИНА С ПИРАЗИНАМИДОМ |
| WO2020106558A1 (en) | 2018-11-20 | 2020-05-28 | Merck Sharp & Dohme Corp. | Substituted amino triazolopyrimidine and amino triazolopyrazine adenosine receptor antagonists, pharmaceutical compositions and their use |
| WO2020106560A1 (en) | 2018-11-20 | 2020-05-28 | Merck Sharp & Dohme Corp. | Substituted amino triazolopyrimidine and amino triazolopyrazine adenosine receptor antagonists, pharmaceutical compositions and their use |
| PE20211768A1 (es) | 2018-11-30 | 2021-09-07 | Merck Sharp & Dohme | Derivados de amino triazolo quinazolina 9-sustituidos como antagonistas del receptor de adenosina, composiciones farmaceuticas y su uso |
| JP2022511778A (ja) | 2018-11-30 | 2022-02-01 | メルク・シャープ・アンド・ドーム・コーポレーション | アデノシン受容体拮抗薬としての7-、8-及び10-置換されたアミノトリアゾロキナゾリン誘導体、医薬組成物及びそれらの使用 |
| GB201907813D0 (en) | 2019-05-31 | 2019-07-17 | Univ Nottingham | Therapeutic compounds |
| KR102571751B1 (ko) | 2020-03-24 | 2023-08-25 | 삼성에스디아이 주식회사 | 리튬 이차 전지의 전해질용 첨가제, 리튬 이차 전지용 전해질 및 이를 포함하는 리튬 이차 전지 |
| WO2022266468A1 (en) * | 2021-06-18 | 2022-12-22 | Yale University | Anti-cancer compounds and methods of use |
| US20240400572A1 (en) * | 2021-09-23 | 2024-12-05 | Yale University | Compounds and methods for treating cancers that are mgmt deficient regardless of mmr status |
| US20250129083A1 (en) * | 2022-02-01 | 2025-04-24 | The Board Of Trustees Of The University Of Illinois | Imidazotetrazine compounds and treatment of tmz-resistant cancers |
| TW202515538A (zh) * | 2023-08-04 | 2025-04-16 | 美商莫迪菲生物科學有限公司 | 氟烷氧基伸烷基-二氫咪唑并〔5,1-d〕四嗪酮化合物及相關化合物以及其在治療醫學疾患中之用途 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5260291A (en) * | 1981-08-24 | 1993-11-09 | Cancer Research Campaign Technology Limited | Tetrazine derivatives |
| CN1742723A (zh) * | 2004-09-02 | 2006-03-08 | 天津倍方科技发展有限公司 | 含有替莫唑胺-8-羧酸酯的药物组合物以及该类化合物用于制备抗肿瘤药物的用途 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| OA07174A (fr) | 1981-08-24 | 1984-04-30 | May & Baker Ltd | Nouvelles imidazotétrazionones, leur préparation et les médicaments qui les contiennent. |
| GB2125402B (en) | 1982-08-17 | 1985-11-13 | May & Baker Ltd | New tetrazine derivatives |
| US4504475A (en) | 1983-05-24 | 1985-03-12 | Warner Lambert Company | 3-(Haloethyl)-4-oxopyrazolo[5,1-D]-1,2,3,5-tetrazine-8-carboxamide compounds |
| GB9504361D0 (en) | 1995-03-04 | 1995-04-26 | Glaxo Spa | Heterocyclic compounds |
| AR035419A1 (es) | 2001-01-18 | 2004-05-26 | Schering Corp | Un proceso para preparar compuestos imidazo-tetrazin-4-ona, compuestos intermediarios, sales de adicion de acidos, un proceso para preparar la temozolomida, un proceso para preparar intermediarios |
| PE20091101A1 (es) | 2007-12-18 | 2009-07-26 | Pharminox Ltd | AMIDAS DE ACIDO 3-SUBSTITUIDO-4-OXO-3,4-DIHIDRO-IMIDAZO[5,1-d] [1,2,3,5-TETRACINA-8-CARBOXILICO Y SU EMPLEO |
| GB0807103D0 (en) | 2008-04-18 | 2008-05-21 | Univ Bradford The | Compounds |
| US9024018B2 (en) | 2009-06-23 | 2015-05-05 | Pharminox Limited | 3-substituted-8-substituted-3H-imidazo[5,1-d][1,2,3,5]tetrazin-4-one compounds and their use |
-
2008
- 2008-12-12 PE PE2008002071A patent/PE20091101A1/es not_active Application Discontinuation
- 2008-12-16 EP EP20130175051 patent/EP2698370A3/en not_active Withdrawn
- 2008-12-16 WO PCT/GB2008/004140 patent/WO2009077741A2/en not_active Ceased
- 2008-12-16 JP JP2010538886A patent/JP2011506588A/ja active Pending
- 2008-12-16 EP EP08861839A patent/EP2229393A2/en not_active Withdrawn
- 2008-12-16 CA CA2709749A patent/CA2709749A1/en not_active Abandoned
- 2008-12-16 AU AU2008337261A patent/AU2008337261A1/en not_active Abandoned
- 2008-12-16 CN CN2008801269450A patent/CN101945874A/zh active Pending
- 2008-12-16 US US12/808,604 patent/US8450479B2/en not_active Expired - Fee Related
- 2008-12-18 TW TW097149411A patent/TW200934782A/zh unknown
- 2008-12-18 AR ARP080105534A patent/AR071548A1/es unknown
-
2010
- 2010-06-17 IL IL206453A patent/IL206453A0/en unknown
- 2010-06-28 ZA ZA2010/04554A patent/ZA201004554B/en unknown
-
2013
- 2013-05-24 US US13/901,680 patent/US20130338104A1/en not_active Abandoned
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5260291A (en) * | 1981-08-24 | 1993-11-09 | Cancer Research Campaign Technology Limited | Tetrazine derivatives |
| CN1742723A (zh) * | 2004-09-02 | 2006-03-08 | 天津倍方科技发展有限公司 | 含有替莫唑胺-8-羧酸酯的药物组合物以及该类化合物用于制备抗肿瘤药物的用途 |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108276415A (zh) * | 2018-02-08 | 2018-07-13 | 台州职业技术学院 | 一种烷氧化三唑并四嗪类化合物及其制备方法和应用 |
| CN108276415B (zh) * | 2018-02-08 | 2019-07-05 | 台州职业技术学院 | 一种烷氧化三唑并四嗪类化合物及其制备方法和应用 |
| CN113271939A (zh) * | 2018-08-09 | 2021-08-17 | 伊利诺伊大学董事会 | 咪唑四嗪化合物 |
| US12234240B2 (en) | 2018-08-09 | 2025-02-25 | The Board Of Trustees Of The University Of Illinois | Substituted imidazo[5,1-d][1,2,3,5]tetrazines for the treatment of cancer |
| CN113271939B (zh) * | 2018-08-09 | 2025-03-07 | 伊利诺伊大学董事会 | 咪唑四嗪化合物 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2011506588A (ja) | 2011-03-03 |
| PE20091101A1 (es) | 2009-07-26 |
| WO2009077741A3 (en) | 2009-12-03 |
| EP2698370A2 (en) | 2014-02-19 |
| EP2698370A3 (en) | 2014-07-16 |
| AR071548A1 (es) | 2010-06-30 |
| EP2229393A2 (en) | 2010-09-22 |
| US8450479B2 (en) | 2013-05-28 |
| US20100286088A1 (en) | 2010-11-11 |
| IL206453A0 (en) | 2010-12-30 |
| CA2709749A1 (en) | 2009-06-25 |
| AU2008337261A1 (en) | 2009-06-25 |
| ZA201004554B (en) | 2011-09-28 |
| WO2009077741A2 (en) | 2009-06-25 |
| TW200934782A (en) | 2009-08-16 |
| US20130338104A1 (en) | 2013-12-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101945874A (zh) | 作为抗癌剂的3-取代的-4-氧代-3,4-二氢-咪唑并[5,1-d][1,2,3,5]-四嗪-8-甲酰胺类 | |
| TWI841759B (zh) | 可用於治療流感病毒感染之化合物 | |
| EP2614061B1 (en) | Quinoline and quinoxaline derivatives as kinase inhibitors | |
| EP3002285B1 (en) | Tetrahydrocarboline derivative | |
| EP2585467B1 (en) | Pyrazolo[1,5-a]pyrimidines and -triazines as antiviral agents | |
| EP2794611B1 (en) | Pyrazolo[1,5-a]pyrimidines as antiviral agents | |
| CN102906090B (zh) | 1-(5-叔丁基-2-苯基-2h-吡唑-3-基)-3-[2-氟-4-(1-甲基-2-氧代-2,3-二氢-1h-咪唑并[4,5-b]吡啶-7-基氧基)-苯基]-脲和相关化合物及它们在治疗中的应用 | |
| CN108366994B (zh) | 新型Jak1选择性抑制剂及其用途 | |
| KR101561756B1 (ko) | 이미다조 피라진 | |
| EP4137484A1 (en) | Tricyclic compounds as egfr inhibitors | |
| EP2445915B1 (en) | 3-substituted-8-substituted-3h imidazo[5,1-d][1,2,3,5-tetrazin-4-one compounds and their use | |
| EP2740730B1 (en) | Dibenzooxepin derivative | |
| CN109311893B (zh) | 含有取代环戊基的吡咯并嘧啶化合物 | |
| CN1269801A (zh) | 作为抗病毒剂的嘌呤非环核苷 | |
| KR20240131416A (ko) | 거대고리 화합물 및 키나제 억제제로서의 용도 | |
| WO2019080724A1 (zh) | 核苷磷酸类化合物及其制备方法和用途 | |
| HK1152526A (en) | 3-substituted-4-0x0-3, 4-dihydro-imidazo- [5, 1-d] [1,2,3,5] -tetrazine-8-carboxylic acid amides as anticancer agents | |
| CN114341128A (zh) | 双功能蛋白降解靶向嵌合体类化合物及其制备方法和医药用途 | |
| US20210198282A1 (en) | Salts of compounds and crystals thereof | |
| WO2012085501A1 (en) | 8 - sulfo - imidazotetrazin- 4 - one compounds and their use as anticancer drug | |
| HK40035878A (en) | Cyclic di-nucleotide compounds and methods of use | |
| EP4212511A1 (en) | Aromatic ethylene compound and preparation method therefor, and intermediate, pharmaceutical composition, and application thereof | |
| AU740264C (en) | Antiviral agents | |
| HK1172321B (en) | 3-substituted-8-substituted-3h imidazo[5,1-d][1,2,3,5-tetrazin-4-one compounds and their use | |
| HK1181754B (en) | Quinoline and quinoxaline derivatives as kinase inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| REG | Reference to a national code |
Ref country code: HK Ref legal event code: DE Ref document number: 1152526 Country of ref document: HK |
|
| C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20110112 |
|
| REG | Reference to a national code |
Ref country code: HK Ref legal event code: WD Ref document number: 1152526 Country of ref document: HK |