PE20110843A1 - Derivados de 5-(1h-imidazol-5-il)-2-fenilpirimidina, como inhibidores de prostaglandina d sintasa hematopoyetica - Google Patents
Derivados de 5-(1h-imidazol-5-il)-2-fenilpirimidina, como inhibidores de prostaglandina d sintasa hematopoyeticaInfo
- Publication number
- PE20110843A1 PE20110843A1 PE2011000665A PE2011000665A PE20110843A1 PE 20110843 A1 PE20110843 A1 PE 20110843A1 PE 2011000665 A PE2011000665 A PE 2011000665A PE 2011000665 A PE2011000665 A PE 2011000665A PE 20110843 A1 PE20110843 A1 PE 20110843A1
- Authority
- PE
- Peru
- Prior art keywords
- prostaglandin
- hematopoyetic
- phenylpyrimidine
- imidazol
- inhibitors
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 150000003180 prostaglandins Chemical class 0.000 title abstract 2
- -1 2-PYRIDYL Chemical class 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 2
- 102100029100 Hematopoietic prostaglandin D synthase Human genes 0.000 abstract 1
- 101710082112 Hematopoietic prostaglandin D synthase Proteins 0.000 abstract 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 abstract 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 abstract 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- WSFSSNUMVMOOMR-BJUDXGSMSA-N methanone Chemical compound O=[11CH2] WSFSSNUMVMOOMR-BJUDXGSMSA-N 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- BHMBVRSPMRCCGG-OUTUXVNYSA-N prostaglandin D2 Chemical compound CCCCC[C@H](O)\C=C\[C@@H]1[C@@H](C\C=C/CCCC(O)=O)[C@@H](O)CC1=O BHMBVRSPMRCCGG-OUTUXVNYSA-N 0.000 abstract 1
- BHMBVRSPMRCCGG-UHFFFAOYSA-N prostaglandine D2 Natural products CCCCCC(O)C=CC1C(CC=CCCCC(O)=O)C(O)CC1=O BHMBVRSPMRCCGG-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
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- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
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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
- A61K31/435—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
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- 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- 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
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- C07D401/14—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 three or more hetero rings
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- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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- Orthopedic Medicine & Surgery (AREA)
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
REFERIDA A UN COMPUESTO DE FORMULA I, DONDE R1 ES ALQUILO C1-C6, CICLOALQUILO C3-C6, FENILO, 2-PIRIDILO, 3-PIRIDILO, ENTRE OTROS; R2 ES FENILO, 3-FLUOROFENIL, 2-PIRIDIL, PIRIDIN, ENTRE OTROS; W ES ENLACE COVALENTE, O, S, SO, SO2, CO, NH, ENTRE OTROS; Y1, Y2 E Y3 FORMAN JUNTO AL N UN ANILLO DE PREFERENCIA PIRIMIDIN; U1, U2, U3, U4 FORMAN UN ANILLO DE PREFERENCIA 4-IL-OMIDAZOL, 3-PIRAZOL, OXAZOL. SON COMPUESTOS PREFERIDOS: ACIDO-2-(2-FENILPIRIMIDINA-5-IL)TIAZOL-4-CARBOXILICO; FENIL-(5-(2-(PIRIDIN-3-IL)-1H-IMIDAZOL-5-IL)PIRIMIDINA-2-IL)METANONA; ENTRE OTROS. DICHOS COMPUESTOS SON INHIBIDORES DE PROSTAGLANDINA D HEMATOPOYETICA (H-PGDS) UTILES EN EL TRATAMIENTO Y PREVENCION DE ENFERMEDADES Y AFECCIONES MEDIADAS POR PROSTAGLANDINA D2
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9894208P | 2008-09-22 | 2008-09-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20110843A1 true PE20110843A1 (es) | 2011-12-08 |
Family
ID=42038293
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2011000665A PE20110843A1 (es) | 2008-09-22 | 2009-09-22 | Derivados de 5-(1h-imidazol-5-il)-2-fenilpirimidina, como inhibidores de prostaglandina d sintasa hematopoyetica |
Country Status (21)
| Country | Link |
|---|---|
| US (3) | US8536185B2 (es) |
| EP (1) | EP2350059B1 (es) |
| JP (1) | JP2014001228A (es) |
| KR (2) | KR101406433B1 (es) |
| AP (1) | AP3272A (es) |
| AU (1) | AU2009292931B2 (es) |
| BR (1) | BRPI0919004A2 (es) |
| CA (1) | CA2736955C (es) |
| CL (2) | CL2011000604A1 (es) |
| CO (1) | CO6362005A2 (es) |
| CR (1) | CR20110196A (es) |
| EC (1) | ECSP11010995A (es) |
| IL (3) | IL211629A0 (es) |
| MX (1) | MX2011003011A (es) |
| MY (1) | MY154000A (es) |
| NI (1) | NI201100056A (es) |
| NZ (1) | NZ592297A (es) |
| PE (1) | PE20110843A1 (es) |
| PH (1) | PH12013502370A1 (es) |
| SG (1) | SG2014014013A (es) |
| WO (1) | WO2010033977A2 (es) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8536185B2 (en) | 2008-09-22 | 2013-09-17 | Cayman Chemical Company, Incorporated | Multiheteroaryl compounds as inhibitors of H-PGDS and their use for treating prostaglandin D2 mediated diseases |
| CA2758731A1 (en) * | 2009-04-23 | 2010-10-28 | Merck Sharp & Dohme Corp. | 2-alkyl piperidine mglur5 receptor modulators |
| EP2611796B1 (en) * | 2010-09-01 | 2016-04-20 | Ambit Biosciences Corporation | An optically active pyrazolylaminoquinazoline, and pharmaceutical compositions and methods of use thereof |
| US9199975B2 (en) | 2011-09-30 | 2015-12-01 | Asana Biosciences, Llc | Biaryl imidazole derivatives for regulating CYP17 |
| US8809372B2 (en) | 2011-09-30 | 2014-08-19 | Asana Biosciences, Llc | Pyridine derivatives |
| EP2912458B1 (en) | 2012-10-24 | 2018-07-18 | NYU Winthrop Hospital | Non-invasive biomarker to identify subjects at risk of preterm delivery |
| ES2903153T3 (es) * | 2013-07-10 | 2022-03-31 | Cnbm Bengbu Design & Res Institute For Glass Industry Co Ltd | Módulo solar con soporte de módulo aislado eléctricamente, procedimiento para su fabricación y uso de una capa adhesiva para sujetar el soporte de módulo |
| RU2690679C2 (ru) * | 2014-02-11 | 2019-06-05 | Мерк Патент Гмбх | Новые пиримидинимидазоламины в качестве модуляторов активности киназы |
| WO2017103851A1 (en) | 2015-12-17 | 2017-06-22 | Astex Therapeutics Limited | Quinoline-3-carboxamides as h-pgds inhibitors |
| JOP20190072A1 (ar) | 2016-10-13 | 2019-04-07 | Glaxosmithkline Ip Dev Ltd | مشتقات 1، 3 سيكلوبوتان ثنائي الاستبدال أو آزيتيدين كمثبطات للإنزيم المخلق للبروستاجلاندين d المكون للدم |
| US11149035B2 (en) | 2017-06-13 | 2021-10-19 | Glaxosmithkline Intellectual Property Dfvelopment Limited | Chemical compounds as H—PGDS inhibitors |
| US20200264188A1 (en) | 2017-09-13 | 2020-08-20 | Progenity, Inc. | Preeclampsia biomarkers and related systems and methods |
| CN111479814A (zh) | 2017-12-13 | 2020-07-31 | 葛兰素史密斯克莱知识产权发展有限公司 | 作为h-pgds抑制剂的稠合的吡啶 |
| WO2020095215A1 (en) | 2018-11-08 | 2020-05-14 | Glaxosmithkline Intellectual Property Development Limited | Chemical compounds |
| EP4070113A4 (en) | 2019-12-04 | 2023-12-20 | Biora Therapeutics, Inc. | ASSESSMENT OF PREECAMPSIA USING FREE AND DISSOCIATE PLACENTAL GROWTH FACTOR ASSAYS |
| EP3916015A1 (en) | 2020-05-28 | 2021-12-01 | Geneuro SA | Anti-herv-w envelope protein antibody for use in the treatment of psychotic diseases |
| EP4169575A4 (en) | 2020-06-19 | 2023-10-25 | Sato Pharmaceutical Co., Ltd. | Condensed ring compounds that inhibit h-pgds |
| KR20240121786A (ko) | 2021-12-17 | 2024-08-09 | 사토 세이야쿠 가부시키가이샤 | H-pgds를 저해하는 아자인돌 유도체 |
| CN115403526A (zh) * | 2022-09-21 | 2022-11-29 | 韶远科技(上海)有限公司 | 一种5-乙酰基嘧啶的制备方法 |
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