MX2012006485A - Piridinon hidroxiclicopentil carboxamidas: inhibidores de la integrasa del vih con aplicaciones terapeuticas. - Google Patents
Piridinon hidroxiclicopentil carboxamidas: inhibidores de la integrasa del vih con aplicaciones terapeuticas.Info
- Publication number
- MX2012006485A MX2012006485A MX2012006485A MX2012006485A MX2012006485A MX 2012006485 A MX2012006485 A MX 2012006485A MX 2012006485 A MX2012006485 A MX 2012006485A MX 2012006485 A MX2012006485 A MX 2012006485A MX 2012006485 A MX2012006485 A MX 2012006485A
- Authority
- MX
- Mexico
- Prior art keywords
- hiv
- compounds
- pyridinone
- methods
- carboxamides
- Prior art date
Links
- 229940099797 HIV integrase inhibitor Drugs 0.000 title 1
- CZHZKOWQWCXDDE-UHFFFAOYSA-N O=C1C=CC=CN1.ONC(=O)C1CCCC1 Chemical class O=C1C=CC=CN1.ONC(=O)C1CCCC1 CZHZKOWQWCXDDE-UHFFFAOYSA-N 0.000 title 1
- 239000003084 hiv integrase inhibitor Substances 0.000 title 1
- 230000001225 therapeutic effect Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- 238000000034 method Methods 0.000 abstract 3
- 208000030507 AIDS Diseases 0.000 abstract 2
- 230000036436 anti-hiv Effects 0.000 abstract 2
- 208000015181 infectious disease Diseases 0.000 abstract 2
- AUKREADUEIPTFY-UHFFFAOYSA-N 3-cyclopentyl-1h-pyridin-2-one Chemical class O=C1NC=CC=C1C1CCCC1 AUKREADUEIPTFY-UHFFFAOYSA-N 0.000 abstract 1
- 108010002459 HIV Integrase Proteins 0.000 abstract 1
- 102100034343 Integrase Human genes 0.000 abstract 1
- 108010061833 Integrases Proteins 0.000 abstract 1
- 239000003242 anti bacterial agent Substances 0.000 abstract 1
- 229940088710 antibiotic agent Drugs 0.000 abstract 1
- 239000003443 antiviral agent Substances 0.000 abstract 1
- 229940121357 antivirals Drugs 0.000 abstract 1
- 150000003857 carboxamides Chemical class 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 239000003937 drug carrier Substances 0.000 abstract 1
- 239000002955 immunomodulating agent Substances 0.000 abstract 1
- 229940121354 immunomodulator Drugs 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 230000010076 replication Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229940124597 therapeutic agent Drugs 0.000 abstract 1
- 229960005486 vaccine Drugs 0.000 abstract 1
- -1 vaccines Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4412—Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (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)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Oncology (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicinal Preparation (AREA)
Abstract
Se describen nuevas ciclopentil piridinon dicetocarboxamidas sustituidas con oxi, quirales y aquirales, y sus derivados y métodos para sus preparaciones. Los compuestos incluyen tautómeros, regioisómeros e isómeros geométricos. Estas carboxamidas complejas se diseñan como inhibidores de la replicación del VIH a través de la inhibición de la integrasa del VIH. Los compuestos son útiles en la prevención o tratamiento de la infección por el VIH y en el tratamiento del SIDA y el Complejo Relacionado con el SIDA (ARC, por sus siglas en inglés), ya sea como los compuestos, o como sales farmacéuticamente aceptables, con portadores farmacéuticamente aceptables, utilizados solos o en combinación con antivirales, inmunomoduladores, antibióticos, vacunas y otros agentes terapéuticos, especialmente otros compuestos anti-VIH (incluyendo otros agentes anti-integrasa del VIH), que pueden utilizarse para crear preparaciones combinadas anti-VIH. También se describen métodos para tratar el SIDA y el ARC y métodos para tratar o prevenir la infección por VIH.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US28367509P | 2009-12-07 | 2009-12-07 | |
| US32042910P | 2010-04-02 | 2010-04-02 | |
| PCT/US2010/059183 WO2011071849A2 (en) | 2009-12-07 | 2010-12-07 | Pyridinone hydroxycyclopentyl carboxamides: hiv integrase inhibitors with therapeutic applications |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2012006485A true MX2012006485A (es) | 2012-08-23 |
Family
ID=44146132
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2012006485A MX2012006485A (es) | 2009-12-07 | 2010-12-07 | Piridinon hidroxiclicopentil carboxamidas: inhibidores de la integrasa del vih con aplicaciones terapeuticas. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US8703801B2 (es) |
| EP (1) | EP2509949B1 (es) |
| JP (1) | JP2013512957A (es) |
| KR (1) | KR20120094098A (es) |
| CN (1) | CN102753526B (es) |
| AU (1) | AU2010328325B2 (es) |
| CA (1) | CA2783540C (es) |
| EA (1) | EA201270651A1 (es) |
| IL (1) | IL220113A0 (es) |
| MX (1) | MX2012006485A (es) |
| MY (1) | MY172005A (es) |
| NZ (1) | NZ600873A (es) |
| PH (1) | PH12012501095A1 (es) |
| SG (1) | SG181524A1 (es) |
| WO (1) | WO2011071849A2 (es) |
| ZA (1) | ZA201204147B (es) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2012006485A (es) | 2009-12-07 | 2012-08-23 | Univ Georgia | Piridinon hidroxiclicopentil carboxamidas: inhibidores de la integrasa del vih con aplicaciones terapeuticas. |
| KR101406201B1 (ko) * | 2011-10-19 | 2014-06-12 | 한국생명공학연구원 | 인제난 타입의 디테르펜 화합물 및 이를 포함하는 바이러스 감염 질환의 치료 또는 예방용 약학적 조성물 |
| EP3578563B1 (en) | 2011-12-22 | 2021-04-14 | Geron Corporation | Guanine analogs as telomerase substrates and telomere length affectors |
| WO2013148174A1 (en) | 2012-03-31 | 2013-10-03 | University Of Georgia Research Foundation, Inc. | New anti-mycobacterial drugs against tuberculosis |
| CN103524396B (zh) * | 2012-09-29 | 2018-05-25 | 中国医学科学院医药生物技术研究所 | 含吲哚环的二脒类衍生物及其制备方法和应用 |
| JP6767011B2 (ja) * | 2015-09-18 | 2020-10-14 | ヤマサ醤油株式会社 | 抗dnaウィルス活性などの生理活性を有するヌクレオシド誘導体 |
| JP2019502363A (ja) | 2015-10-30 | 2019-01-31 | エヌビーイー セラピューティクス アクチェン ゲゼルシャフト | 抗ror1抗体 |
| UA125718C2 (uk) | 2016-01-20 | 2022-05-25 | Зе Скріппс Ресеарч Інстітьют | Композиції антитіл до ror1 і пов'язані з ними способи |
| WO2019030240A1 (en) | 2017-08-07 | 2019-02-14 | Nbe-Therapeutics Ag | ANTIBODIES BINDING TO A LINEAR HUMAN CS1 EPITOPE |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN2234616Y (zh) * | 1995-01-05 | 1996-09-04 | 上海市临床检验中心 | 一种试剂盒 |
| AU757409B2 (en) | 1998-06-03 | 2003-02-20 | Merck & Co., Inc. | Hiv integrase inhibitors |
| EP1082121A4 (en) | 1998-06-03 | 2003-02-05 | Merck & Co Inc | HIV integrase |
| JP2002516858A (ja) | 1998-06-03 | 2002-06-11 | メルク エンド カムパニー インコーポレーテッド | Hivインテグラーゼ阻害薬 |
| CA2353961A1 (en) | 1998-12-25 | 2000-07-06 | Shionogi & Co., Ltd. | Heteroaromatic derivatives having an inhibitory activity against hiv integrase |
| EP1196384A4 (en) | 1999-06-25 | 2002-10-23 | Merck & Co Inc | 1- (AROMATIC OR HETEROAROMATICALLY SUBSTITUTED) -3- (HETEROAROMATICALLY SUBSTITUTED) -1,3-PROPANDIONS AND THEIR APPLICATIONS |
| US20030171406A1 (en) | 2000-06-13 | 2003-09-11 | Akihiko Sato | Medicinal compositions containing propenone derivatives |
| WO2002030426A1 (en) | 2000-10-12 | 2002-04-18 | Merck & Co., Inc. | Aza- and polyaza-naphthalenyl-carboxamides useful as hiv integrase inhibitors |
| JP2003014923A (ja) | 2001-07-04 | 2003-01-15 | Hamamatsu Photonics Kk | 薄膜作成方法及び薄膜作成装置 |
| EP3406596A1 (en) | 2002-11-20 | 2018-11-28 | Japan Tobacco Inc. | 4-oxoquinoline compound and use thereof as hiv integrase inhibitor |
| US7115601B2 (en) | 2004-05-18 | 2006-10-03 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
| WO2005113509A1 (en) | 2004-05-20 | 2005-12-01 | Japan Tobacco Inc. | Novel 4-oxoquinoline compound and use thereof as hiv integrase inhibitor |
| US7176196B2 (en) | 2004-05-28 | 2007-02-13 | Bristol-Myers Squibb Company | Bicyclic heterocycles as HIV integrase inhibitors |
| US7157447B2 (en) | 2004-05-28 | 2007-01-02 | Bristol-Myers Squibb Company | Bicyclic heterocycles as HIV integrase inhibitors |
| US20070232644A1 (en) | 2004-09-07 | 2007-10-04 | Pfizer Inc. | Inhibitors of the Hiv Integrase Enzyme |
| CN101014572B (zh) | 2004-09-15 | 2011-07-06 | 盐野义制药株式会社 | 具有hiv整合酶抑制活性的氨基甲酰基吡啶酮衍生物 |
| US7745459B2 (en) | 2004-09-21 | 2010-06-29 | Japan Tobacco Inc. | Quinolizinone compound and use thereof as HIV integrase inhibitor |
| UA87884C2 (uk) * | 2004-12-03 | 2009-08-25 | Мерк Энд Ко., Инк. | Безводна кристалічна калієва сіль інгібітора віл-інтегрази |
| US7250421B2 (en) * | 2005-01-31 | 2007-07-31 | University Of Georgia Research Foundation, Inc. | Diketo acids with nucleobase scaffolds: anti-HIV replication inhibitors targeted at HIV integrase |
| WO2007106450A2 (en) | 2006-03-10 | 2007-09-20 | University Of Georgia Research Foundation, Inc. | Diketo acids with nucleobase scaffolds: anti-hiv replication inhibitors targeted at hiv integrase in combination therapy |
| US20100092427A1 (en) * | 2006-07-19 | 2010-04-15 | The University Of Georgia Research Foundation | Pyridinone Diketo Acids: Inhibitors of HIV Replication in Combination Therapy |
| CN101516369A (zh) * | 2006-07-19 | 2009-08-26 | 佐治亚大学研究基金会 | 吡啶酮二酮酸:用于组合治疗的hiv复制抑制剂 |
| MX2009004081A (es) * | 2006-10-20 | 2009-06-18 | Cpd Llc | Metodo para restaurar el efecto de incretina. |
| MX2012006485A (es) | 2009-12-07 | 2012-08-23 | Univ Georgia | Piridinon hidroxiclicopentil carboxamidas: inhibidores de la integrasa del vih con aplicaciones terapeuticas. |
-
2010
- 2010-12-07 MX MX2012006485A patent/MX2012006485A/es active IP Right Grant
- 2010-12-07 PH PH1/2012/501095A patent/PH12012501095A1/en unknown
- 2010-12-07 WO PCT/US2010/059183 patent/WO2011071849A2/en not_active Ceased
- 2010-12-07 MY MYPI2012002470A patent/MY172005A/en unknown
- 2010-12-07 EP EP10836497.7A patent/EP2509949B1/en active Active
- 2010-12-07 SG SG2012041331A patent/SG181524A1/en unknown
- 2010-12-07 CA CA2783540A patent/CA2783540C/en active Active
- 2010-12-07 NZ NZ600873A patent/NZ600873A/en not_active IP Right Cessation
- 2010-12-07 KR KR1020127017575A patent/KR20120094098A/ko not_active Withdrawn
- 2010-12-07 JP JP2012543189A patent/JP2013512957A/ja not_active Ceased
- 2010-12-07 EA EA201270651A patent/EA201270651A1/ru unknown
- 2010-12-07 AU AU2010328325A patent/AU2010328325B2/en not_active Ceased
- 2010-12-07 US US13/513,448 patent/US8703801B2/en active Active
- 2010-12-07 CN CN201080063257.1A patent/CN102753526B/zh not_active Expired - Fee Related
-
2012
- 2012-06-03 IL IL220113A patent/IL220113A0/en unknown
- 2012-06-06 ZA ZA2012/04147A patent/ZA201204147B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2783540A1 (en) | 2011-06-16 |
| CN102753526B (zh) | 2014-11-26 |
| SG181524A1 (en) | 2012-07-30 |
| US8703801B2 (en) | 2014-04-22 |
| EP2509949A4 (en) | 2013-04-17 |
| PH12012501095A1 (en) | 2015-04-22 |
| ZA201204147B (en) | 2013-02-27 |
| NZ600873A (en) | 2014-08-29 |
| JP2013512957A (ja) | 2013-04-18 |
| EA201270651A1 (ru) | 2013-01-30 |
| MY172005A (en) | 2019-11-11 |
| CN102753526A (zh) | 2012-10-24 |
| AU2010328325B2 (en) | 2015-02-05 |
| KR20120094098A (ko) | 2012-08-23 |
| EP2509949A2 (en) | 2012-10-17 |
| WO2011071849A3 (en) | 2011-10-06 |
| AU2010328325A1 (en) | 2012-06-21 |
| WO2011071849A2 (en) | 2011-06-16 |
| US20120282218A1 (en) | 2012-11-08 |
| EP2509949B1 (en) | 2014-04-23 |
| CA2783540C (en) | 2018-04-24 |
| IL220113A0 (en) | 2012-07-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant or registration |