AR073949A1 - Agonistas del receptor aril-gpr120 y usos de los mismos - Google Patents
Agonistas del receptor aril-gpr120 y usos de los mismosInfo
- Publication number
- AR073949A1 AR073949A1 ARP090104033A ARP090104033A AR073949A1 AR 073949 A1 AR073949 A1 AR 073949A1 AR P090104033 A ARP090104033 A AR P090104033A AR P090104033 A ARP090104033 A AR P090104033A AR 073949 A1 AR073949 A1 AR 073949A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- substituted
- 6alkyl
- 6alkynyl
- independently selected
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- A61K31/415—1,2-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/04—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
- C07D249/06—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles with aryl radicals directly attached to ring atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/32—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/24—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/06—1,2,3-Thiadiazoles; Hydrogenated 1,2,3-thiadiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/40—Radicals substituted by oxygen atoms
- C07D307/42—Singly bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/14—Radicals substituted by singly bound hetero atoms other than halogen
- C07D333/16—Radicals substituted by singly bound hetero atoms other than halogen by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Diabetes (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Furan Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Se proveen agonistas aril-GPR120. Estos compuestos son de utilidad para el tratamiento de enfermedades metabolicas, incluyendo diabetes Tipo II y las enfermedades asociadas con un control pobre de la glucemia. Reivindicacion 1: Un compuesto caracterizado porque responde a la Formula (1) o una sal farmacéuticamente aceptable del mismo, donde Q representa un grupo arilo monocíclico o bicíclico de entre 5 y 10 miembros, un grupo heteroarilo monocíclico o bicíclico de ente 5 y 10 miembros, un grupo cicloalquilo monocíclico o bicíclico de entre 5 y 10 miembros, un grupo heterocicloalquilo monocíclico o bicíclico de entre 5 y 10 miembros, o un grupo bicíclico de entre 8 y 10 miembros donde un arilo o un anillo heteroarilo de 5 o 6 miembros está fusionado a un anillo cicloalquilo o heterocicloalquilo de 5 o 6 miembros; E1, E2 y E3 se seleccionan en forma independiente entre el grupo que consiste en C, N y S; E4 se selecciona entre el grupo que consiste en C y N; X se selecciona entre el grupo que consiste en -CH2-, -C(O)- y -C(O)CH2-; Y se selecciona entre el grupo que consiste en -CH2-, -NH- y -O-; Z se selecciona entre el grupo que consiste en -(CR4R5)n-, -S-, -C(O)- y -CR4=CR5-; V se selecciona entre el grupo que consiste en un enlace, -(CR4R5)n-, -CR4=CR5-, y -O-CR4R5-; W se selecciona entre el grupo que consiste en H, C1-6alquilo y C1-6alquilo sustituido; R1 se selecciona en forma independiente entre el grupo que consiste en halo, C1-6alquilo, C1-6alquilo sustituido, C3-7cicloalquilo, C3-7cicloalquilo sustituido, C2-6alquenilo, C2-6alquenilo sustituido, C2-6alquinilo, C2-6alquinilo sustituido, CN, -ORa, -NRaRb, -C(O)Ra, -C(O)ORa, -NRaC(O)Rb, -SRa, -S(O)Ra y -S(O)2Ra; R2 se selecciona en forma independiente entre el grupo que consiste en halo, C1-6alquilo, C1-6alquilo9 sustituido, C3-7cicloalquilo, C3-7cicloalquilo sustituido, C2-6alquenilo, C2-6alquenilo sustituido, C2-6alquinilo, C2-6alquinilo sustituido, ariloxi, ariloxi sustituido, CN, -ORa, -NRaRb, -C(O)Ra, -C(O)ORa, -C(O)NRaRb, -NRaC(O)Rb, -SRa, -S(O)Ra y -S(O)2Ra; cada uno de Ra y Rb se selecciona en forma independiente entre el grupo que consiste en H, C1-6alquilo, C1-6alquilo sustituido, C3-7cicloalquilo, C2-6alquenilo y C2-6alquinilo; R4 se selecciona en forma independiente entre el grupo que consiste en H, halo, C1-6alquilo, C1-6alquilo sustituido, C1-6alcoxi y C1-6alcoxi sustituido; R5 se selecciona en forma independiente entre el grupo que consiste en H, halo, C1-6alquilo, C1-6alquilo sustituido y C1-6alcoxi; R6 se selecciona entre el grupo que consiste en halo, C1-6alquilo, C1-6alquilo sustituido, C1-6alcoxi, C1-6alcoxi sustituido, arilo, arilo sustituido, heteroarilo y heteroarilo sustituido; opcionalmente R4 y R5 se ciclizan para formar un anillo C3-7 saturado o un grupo espiro C3-7cicloalquilo; el subíndice b es 0, 1, 2, 3 o 4; el subíndice g es 0, 1 o 2; y el subíndice n es en forma independiente 1, 2 o 3.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10731408P | 2008-10-21 | 2008-10-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR073949A1 true AR073949A1 (es) | 2010-12-15 |
Family
ID=41480108
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP090104033A AR073949A1 (es) | 2008-10-21 | 2009-10-20 | Agonistas del receptor aril-gpr120 y usos de los mismos |
Country Status (22)
Country | Link |
---|---|
US (1) | US20100216827A1 (es) |
EP (2) | EP2350016A2 (es) |
JP (2) | JP2012506386A (es) |
KR (1) | KR20110082145A (es) |
CN (1) | CN102186825A (es) |
AR (1) | AR073949A1 (es) |
AU (1) | AU2009307656B2 (es) |
BR (1) | BRPI0920237A2 (es) |
CA (1) | CA2740366A1 (es) |
CL (1) | CL2011000899A1 (es) |
CO (1) | CO6382155A2 (es) |
CR (1) | CR20110201A (es) |
EA (1) | EA022417B1 (es) |
EC (1) | ECSP11010989A (es) |
IL (1) | IL212144A0 (es) |
MX (1) | MX2011004125A (es) |
NI (1) | NI201100075A (es) |
NZ (1) | NZ592603A (es) |
TW (1) | TW201020241A (es) |
UA (1) | UA107917C2 (es) |
WO (1) | WO2010048207A2 (es) |
ZA (1) | ZA201102815B (es) |
Families Citing this family (99)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AR074760A1 (es) | 2008-12-18 | 2011-02-09 | Metabolex Inc | Agonistas del receptor gpr120 y usos de los mismos en medicamentos para el tratamiento de diabetes y el sindrome metabolico. |
US8299117B2 (en) | 2010-06-16 | 2012-10-30 | Metabolex Inc. | GPR120 receptor agonists and uses thereof |
RU2576316C2 (ru) | 2010-11-03 | 2016-02-27 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Пестицидная композиция, способ контроля вредителей, способ контроля эндопаразитов, эктопаразитов или обоих и способ усиления жизнестойкости растений |
CN102816067A (zh) * | 2011-06-09 | 2012-12-12 | 中国医学科学院医药生物技术研究所 | 一种4-羟基苯酰丙烯酸衍生物、其制备方法及其应用 |
EP2545964A1 (en) | 2011-07-13 | 2013-01-16 | Phenex Pharmaceuticals AG | Novel FXR (NR1H4) binding and activity modulating compounds |
MX361458B (es) | 2011-08-23 | 2018-12-06 | Asana Biosciences Llc | Compuestos de pirimido-piridazinona y uso de los mismos. |
KR102006039B1 (ko) | 2011-10-26 | 2019-07-31 | 다우 아그로사이언시즈 엘엘씨 | 살충 조성물 및 그와 관련된 방법 |
EP2602248A1 (en) | 2011-12-05 | 2013-06-12 | University Of Leicester | Novel pyrrole compounds |
WO2013104257A1 (zh) | 2012-01-12 | 2013-07-18 | 江苏恒瑞医药股份有限公司 | 多环类衍生物、其制备方法及其在医药上的应用 |
EP2805718B1 (en) | 2012-01-17 | 2018-04-04 | EA Pharma Co., Ltd. | Heterocyclic amide derivative and pharmaceutical product containing same |
IN2014MN01839A (es) * | 2012-02-28 | 2015-07-03 | Piramal Entpr Ltd | |
WO2013134562A1 (en) | 2012-03-09 | 2013-09-12 | Inception 2, Inc. | Triazolone compounds and uses thereof |
CN104302640A (zh) | 2012-03-16 | 2015-01-21 | 埃克希金医药品有限公司 | 3,5-二氨基吡唑激酶抑制剂 |
US9708288B2 (en) | 2012-04-27 | 2017-07-18 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
RU2623233C2 (ru) | 2012-04-27 | 2017-06-23 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Пестицидные композиции и относящиеся к ним способы |
US9282739B2 (en) | 2012-04-27 | 2016-03-15 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
CN104780915A (zh) | 2012-07-11 | 2015-07-15 | 埃尔舍利克斯治疗公司 | 包含他汀、双胍和用于减小心脏代谢风险的其它药剂的组合物 |
RU2015116540A (ru) | 2012-10-11 | 2016-12-10 | Мерк Шарп И Доум Корп. | Замещенные соединения спиропиперидинила, применяемые в качестве агонистов gpr120 |
KR101942752B1 (ko) | 2012-11-05 | 2019-01-28 | 주식회사 엘지화학 | Gpr120 효능제로서의 티오아릴 유도체 |
WO2014089364A1 (en) | 2012-12-06 | 2014-06-12 | Quanticel Pharmaceuticals, Inc | Histone demethylase inhibitors |
CA2894281C (en) | 2012-12-20 | 2021-04-20 | Inception 2, Inc. | Triazolone compounds and uses thereof |
KR102422559B1 (ko) | 2013-03-14 | 2022-07-18 | 얀센 파마슈티카 엔.브이. | Gpr120의 작용제로서 유용한 벤조 융합된 헤테로사이클릭 유도체 |
JP6333355B2 (ja) | 2013-03-14 | 2018-05-30 | ヤンセン ファーマシューティカ エヌ.ベー. | Gpr120のアゴニストとして有用な二環式ピロール誘導体 |
WO2014159054A1 (en) | 2013-03-14 | 2014-10-02 | Janssen Pharmaceutica Nv | Gpr120 agonists for the treatment of type ii diabetes |
CA2912747C (en) | 2013-06-27 | 2021-05-04 | Lg Life Sciences Ltd. | Biaryl derivatives as gpr120 agonists |
PE20160880A1 (es) | 2013-09-06 | 2016-09-22 | Inception 2 Inc | Compuestos de triazolona y usos de los mismos |
NZ631142A (en) | 2013-09-18 | 2016-03-31 | Axikin Pharmaceuticals Inc | Pharmaceutically acceptable salts of 3,5-diaminopyrazole kinase inhibitors |
CN105636441B (zh) | 2013-10-17 | 2018-06-15 | 美国陶氏益农公司 | 制备杀虫化合物的方法 |
CA2925914A1 (en) | 2013-10-17 | 2015-04-23 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
JP2016536295A (ja) | 2013-10-17 | 2016-11-24 | ダウ アグロサイエンシィズ エルエルシー | 有害生物防除性化合物の製造方法 |
MX2016004946A (es) | 2013-10-17 | 2016-06-28 | Dow Agrosciences Llc | Procesos para la preparacion de compuestos plaguicidas. |
KR20160072155A (ko) | 2013-10-17 | 2016-06-22 | 다우 아그로사이언시즈 엘엘씨 | 살충성 화합물의 제조 방법 |
MX2016004948A (es) | 2013-10-17 | 2016-06-28 | Dow Agrosciences Llc | Procesos para la preparacion de un compuesto pesticida. |
CN105636445B (zh) | 2013-10-17 | 2018-12-07 | 美国陶氏益农公司 | 制备杀虫化合物的方法 |
RU2656391C2 (ru) | 2013-10-22 | 2018-06-05 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Пестицидные композиции и связанные с ними способы |
US9788546B2 (en) | 2013-10-22 | 2017-10-17 | Dow Agrosciences Llc | Synergistic pesticidal compositions and related methods |
KR20160074621A (ko) | 2013-10-22 | 2016-06-28 | 다우 아그로사이언시즈 엘엘씨 | 상승작용적 살충 조성물 및 관련 방법 |
RU2656888C2 (ru) | 2013-10-22 | 2018-06-07 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Пестицидные композиции и связанные с ними способы |
AR098091A1 (es) | 2013-10-22 | 2016-05-04 | Dow Agrosciences Llc | Composiciones pesticidas sinérgicas y métodos relacionados |
AR098105A1 (es) | 2013-10-22 | 2016-05-04 | Dow Agrosciences Llc | Composiciones plaguicidas y métodos relacionados |
MX2016005308A (es) | 2013-10-22 | 2016-08-08 | Dow Agrosciences Llc | Composiciones pesticidas sinergicas y metodos relacionados. |
US9155304B2 (en) | 2013-10-22 | 2015-10-13 | Dow Agrosciences Llc | Synergistic pesticidal compositions and related methods |
AR098092A1 (es) | 2013-10-22 | 2016-05-04 | Dow Agrosciences Llc | Composiciones plaguicidas sinérgicas y los métodos relacionados |
CA2927206A1 (en) | 2013-10-22 | 2015-04-30 | Dow Agrosciences Llc | Synergistic pesticidal compositions and related methods |
CN105828611A (zh) | 2013-10-22 | 2016-08-03 | 美国陶氏益农公司 | 协同杀虫组合物和相关方法 |
MX2016005319A (es) | 2013-10-22 | 2016-08-12 | Dow Agrosciences Llc | Composiciones pesticidas y metodos relacionados. |
NZ720113A (en) | 2013-10-22 | 2017-06-30 | Dow Agrosciences Llc | Synergistic pesticidal compositions and related methods |
AU2014340407B2 (en) | 2013-10-22 | 2017-05-04 | Dow Agrosciences Llc | Synergistic pesticidal compositions and related methods |
JP2016535022A (ja) | 2013-10-22 | 2016-11-10 | ダウ アグロサイエンシィズ エルエルシー | 農薬組成物および関連する方法 |
JP2016538265A (ja) | 2013-10-22 | 2016-12-08 | ダウ アグロサイエンシィズ エルエルシー | 相乗的有害生物防除組成物および関連する方法 |
TWI651049B (zh) | 2013-10-22 | 2019-02-21 | 陶氏農業科學公司 | 殺蟲組成物及相關方法 |
DK3107901T3 (da) | 2014-02-19 | 2020-06-22 | Piramal Entpr Ltd | Forbindelser til brug som gpr120 agonister |
CA2941445A1 (en) * | 2014-03-07 | 2015-09-11 | Janssen Pharmaceutica Nv | Isothiazole derivatives as gpr120 agonists for the treatment of type ii diabetes |
CA2941442C (en) * | 2014-03-07 | 2022-01-11 | Janssen Pharmaceutica Nv | Bicyclic pyrrole derivatives useful as agonists of gpr120 |
US9067898B1 (en) | 2014-03-07 | 2015-06-30 | Janssen Pharmaceutica Nv | Isothiazole derivatives as GPR120 agonists for the treatment of type II diabetes |
US8912227B1 (en) | 2014-03-07 | 2014-12-16 | Janssen Pharmaceutica Nv | Bicyclic pyrrole derivatives useful as agonists of GPR120 |
US10273230B2 (en) | 2014-07-25 | 2019-04-30 | Piramal Enterprises Limited | Substituted phenyl alkanoic acid compounds as GPR120 agonists and uses thereof |
US9249122B1 (en) | 2014-07-31 | 2016-02-02 | Dow Agrosciences Llc | Process for the preparation of 3-(3-chloro-1H-pyrazol-1-yl)pyridine |
EP3186229A4 (en) | 2014-07-31 | 2018-01-10 | Dow AgroSciences LLC | Process for the preparation of 3-(3-chloro-1h-pyrazol-1-yl)pyridine |
CA2954345A1 (en) | 2014-07-31 | 2016-02-04 | Dow Agrosciences Llc | Process for the preparation of 3-(3-chloro-1h-pyrazol-1-yl)pyridine |
HRP20220522T1 (hr) | 2014-08-04 | 2022-06-10 | Nuevolution A/S | Proizvoljno kondenzirani heterociklil-supstituirani derivati pirimidina koji su korisni za liječenje upalnih, metaboličkih, onkoloških i autoimunih bolesti |
WO2016028328A1 (en) | 2014-08-19 | 2016-02-25 | Dow Agrosciences Llc | Process for the preparation of 3-(3-chloro-1h-pyrazol-1-yl)pyridine |
AU2015308350B2 (en) | 2014-08-29 | 2020-03-05 | Tes Pharma S.R.L. | Inhibitors of alpha-amino-beta-carboxymuconic acid semialdehyde decarboxylase |
WO2016038540A1 (en) * | 2014-09-11 | 2016-03-17 | Piramal Enterprises Limited | Fused heterocyclic compounds as gpr120 agonists |
AR098113A1 (es) | 2014-09-12 | 2016-05-04 | Dow Agrosciences Llc | Proceso para la preparación de 3-(3-cloro-1h-pirazol-1-il)piridina |
AR103264A1 (es) | 2014-12-23 | 2017-04-26 | Axikin Pharmaceuticals Inc | Derivados de 3,5-aminopirazol como inhibidores de quinasa rc |
AU2015367977B9 (en) * | 2014-12-24 | 2020-02-06 | Lg Chem, Ltd | Biaryl derivative as GPR120 agonist |
WO2016125182A1 (en) | 2015-02-05 | 2016-08-11 | Piramal Enterprises Limited | Compounds containing carbon-carbon linker as gpr120 agonists |
TWI698430B (zh) | 2015-02-13 | 2020-07-11 | 南北兄弟藥業投資有限公司 | 三環化合物及其在藥物中的應用 |
CN104610156A (zh) * | 2015-02-13 | 2015-05-13 | 佛山市赛维斯医药科技有限公司 | 一种环丙基酰肼和腈基苯类gpr119激动剂、制备方法及其用途 |
CN104557717A (zh) * | 2015-02-13 | 2015-04-29 | 佛山市赛维斯医药科技有限公司 | 酰肼类gpr119激动剂、制备方法及其用途 |
CN105272889B (zh) * | 2015-07-30 | 2017-11-24 | 四川大学 | 一种人造革用环保低碳发泡剂及其制备方法 |
US9908873B2 (en) | 2015-08-12 | 2018-03-06 | Janssen Pharmaceutica Nv | GPR40 agonists for the treatment of type II diabetes |
US9856245B2 (en) | 2015-08-12 | 2018-01-02 | Janssen Pharmaceutica Nv | GPR40 agonists for the treatment of type II diabetes |
US9920040B2 (en) | 2015-08-12 | 2018-03-20 | Janssen Pharmaceutica Nv | GPR40 agonists for the treatment of type II diabetes |
CN106478616B (zh) * | 2015-08-27 | 2020-05-12 | 江苏恒瑞医药股份有限公司 | 一种gpr40激动剂的结晶形式及其制备方法 |
WO2017201683A1 (en) * | 2016-05-25 | 2017-11-30 | Merck Sharp & Dohme Corp. | Substituted tetrahydroisoquinoline compounds useful as gpr120 agonists |
CA3026512A1 (en) | 2016-06-13 | 2017-12-21 | Gilead Sciences, Inc. | Fxr (nr1h4) modulating compounds |
CA2968836A1 (en) | 2016-06-13 | 2017-12-13 | Gilead Sciences, Inc. | Fxr (nr1h4) modulating compounds |
CN110121343B (zh) * | 2016-09-12 | 2023-11-03 | 整体健康 | 用作gpr120调节剂的双环化合物 |
US10800773B2 (en) | 2016-09-12 | 2020-10-13 | Integral Health, Inc. | Monocyclic compounds useful as GPR120 modulators |
US10233155B2 (en) | 2016-12-29 | 2019-03-19 | Dow Agrosciences Llc | Processes for the preparation of pesticide compounds |
WO2018125815A1 (en) | 2016-12-29 | 2018-07-05 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
WO2018170067A1 (en) * | 2017-03-14 | 2018-09-20 | Dana-Farber Cancer Institute, Inc. | Small molecule sensitization of bax activation for induction of cell death |
EP4122464B1 (en) | 2017-03-28 | 2024-05-15 | Gilead Sciences, Inc. | Therapeutic combinations for treating liver diseases |
CN109420175A (zh) * | 2017-09-01 | 2019-03-05 | 任洁 | 基于cox的血糖调节机制 |
CN111108105B (zh) | 2017-09-22 | 2023-03-31 | 朱比兰特埃皮帕德有限公司 | 作为pad抑制剂的杂环化合物 |
PL3697785T3 (pl) | 2017-10-18 | 2023-08-07 | Jubilant Epipad LLC | Związki imidazopirydynowe jako inhibitory pad |
JP7279057B6 (ja) | 2017-11-06 | 2024-02-15 | ジュビラント プローデル エルエルシー | Pd1/pd-l1活性化の阻害剤としてのピリミジン誘導体 |
LT3704120T (lt) | 2017-11-24 | 2024-06-25 | Jubilant Episcribe Llc | Heterocikliniai junginiai kaip prmt5 inhibitoriai |
CN112105610B (zh) * | 2018-03-13 | 2024-01-26 | 朱比连特普罗德尔有限责任公司 | 作为pd1/pd-l1相互作用/活化的抑制剂的双环化合物 |
CN111868035A (zh) * | 2018-03-15 | 2020-10-30 | 阿克萨姆股份公司 | 取代的吡唑ffa4/gpr120受体激动剂 |
EP4360632A3 (en) | 2019-01-15 | 2024-06-19 | Gilead Sciences, Inc. | Fxr (nr1h4) modulating compounds |
EP3927683A1 (en) | 2019-02-19 | 2021-12-29 | Gilead Sciences, Inc. | Solid forms of fxr agonists |
MX2022007265A (es) | 2019-12-20 | 2022-09-09 | Nuevolution As | Compuestos activos frente a receptores nucleares. |
MX2022012260A (es) | 2020-03-31 | 2022-11-30 | Nuevolution As | Compuestos activos frente a receptores nucleares. |
US11613532B2 (en) | 2020-03-31 | 2023-03-28 | Nuevolution A/S | Compounds active towards nuclear receptors |
CN112876352A (zh) * | 2021-01-15 | 2021-06-01 | 南京艾美斐生物医药科技有限公司 | 一种gpr120蛋白受体抑制剂及其制备和应用 |
CN115572223A (zh) * | 2022-10-17 | 2023-01-06 | 聊城大学 | 一种苯丙酸衍生物及其用途 |
Family Cites Families (58)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US639527A (en) | 1894-11-30 | 1899-12-19 | Frank B Cook | Drop-restoring device for telephone-switchboards. |
US3536809A (en) * | 1969-02-17 | 1970-10-27 | Alza Corp | Medication method |
US3598123A (en) | 1969-04-01 | 1971-08-10 | Alza Corp | Bandage for administering drugs |
US3845770A (en) * | 1972-06-05 | 1974-11-05 | Alza Corp | Osmatic dispensing device for releasing beneficial agent |
US3916899A (en) | 1973-04-25 | 1975-11-04 | Alza Corp | Osmotic dispensing device with maximum and minimum sizes for the passageway |
US4008719A (en) | 1976-02-02 | 1977-02-22 | Alza Corporation | Osmotic system having laminar arrangement for programming delivery of active agent |
DE3300795A1 (de) * | 1983-01-12 | 1984-07-12 | Bayer Ag, 5090 Leverkusen | Substituierte 4-imidazolyl-pyrazole, verfahren zu ihrer herstellung sowie diese enthaltende arzneimittel |
US5032577A (en) | 1986-12-31 | 1991-07-16 | Abbott Laboratories | Peptidylaminodiols |
US5013556A (en) * | 1989-10-20 | 1991-05-07 | Liposome Technology, Inc. | Liposomes with enhanced circulation time |
CZ293211B6 (cs) * | 1995-02-13 | 2004-03-17 | G. D. Searle & Co. Corporate Patent Dept. | Substituované izoxazoly pro léčení zánětů |
DE19648793A1 (de) * | 1996-11-26 | 1998-05-28 | Basf Ag | Neue Benzamide und deren Anwendung |
JPH11263775A (ja) * | 1997-09-08 | 1999-09-28 | Sankyo Co Ltd | ヒドロキシアニリン誘導体 |
JP3694774B2 (ja) * | 1997-10-31 | 2005-09-14 | 大鵬薬品工業株式会社 | フェニルカルボン酸誘導体 |
ATE451346T1 (de) * | 1998-03-10 | 2009-12-15 | Ono Pharmaceutical Co | Carbonsäurederivate und medikamente die diese als aktiven wirkstoff enthalten |
HUP0104038A3 (en) * | 1998-11-09 | 2002-07-29 | Black James Foundation | Gastrin and cholecystokinin receptor ligand imidazole derivatives pharmaceutical compositions containing them and process for their preparation |
AU7073400A (en) * | 1999-08-27 | 2001-03-26 | Eli Lilly And Company | Biaryl-oxa(thia)zole derivatives and their use as ppars modulators |
TWI262185B (en) * | 1999-10-01 | 2006-09-21 | Eisai Co Ltd | Carboxylic acid derivatives having anti-hyperglycemia and anti-hyperlipemia action, and pharmaceutical composition containing the derivatives |
US6921767B2 (en) | 2000-06-15 | 2005-07-26 | Pharmacia Corporation | Cycloalkyl alkanoic acids as integrin receptor antagonists derivatives |
AR036237A1 (es) * | 2001-07-27 | 2004-08-25 | Bayer Corp | Derivados del acido indan acetico, intermediarios, y metodo para su preparacion, composicion farmaceutica y el uso de dichos derivados para la manufactura de un medicamento |
ATE381542T1 (de) * | 2001-08-13 | 2008-01-15 | Phenex Pharmaceuticals Ag | Nr1h4-kern-rezeptor-bindende verbindungen |
ATE415160T1 (de) * | 2002-02-25 | 2008-12-15 | Lilly Co Eli | Modulatoren von peroxisome proliferator- aktivierten rezeptoren |
WO2003099793A1 (en) * | 2002-05-24 | 2003-12-04 | Takeda Pharmaceutical Company Limited | 1,2-azole derivatives with hypoglycemic and hypolipidemic activity |
WO2004011446A1 (en) * | 2002-07-26 | 2004-02-05 | Bayer Pharmaceuticals Corporation | Indane, dihydrobenzofuran, and tetrahydronaphthalene carboxylic acid derivatives and their use as antidiabetics |
WO2004011445A1 (ja) | 2002-07-31 | 2004-02-05 | Nippon Soda Co.,Ltd. | アミノサリチル酸アミド誘導体、製造法及び農園芸用殺菌剤 |
AR041481A1 (es) * | 2002-10-07 | 2005-05-18 | Hoffmann La Roche | Derivados de acido arilpropionico-oxazol y su uso como agonistas de ppar |
MXPA05004743A (es) * | 2002-11-08 | 2005-08-03 | Hoffmann La Roche | Derivados 4-alcoxioxazol sustituidos como agonistas ppar. |
EP1562915A1 (en) * | 2002-11-22 | 2005-08-17 | SmithKline Beecham Corporation | Farnesoid x receptor agonists |
GB0228417D0 (en) * | 2002-12-05 | 2003-01-08 | Cancer Rec Tech Ltd | Pyrazole compounds |
US7504433B2 (en) * | 2003-01-06 | 2009-03-17 | Eli Lilly And Company | Thiophene derivative PPAR modulators |
PA8594401A1 (es) * | 2003-02-21 | 2004-09-16 | Pfizer | Acidos carboxilicos de heteroarilo condensado como agonista del ppar |
SE0301232D0 (sv) * | 2003-04-25 | 2003-04-25 | Astrazeneca Ab | Novel use |
EP1630152A4 (en) * | 2003-05-30 | 2009-09-23 | Takeda Pharmaceutical | CONNECTION WITH CONDENSED RING |
JP4235505B2 (ja) * | 2003-08-08 | 2009-03-11 | 高周波熱錬株式会社 | 等速自在継手の外輪の内表面の焼入れ方法 |
US7470807B2 (en) * | 2003-08-14 | 2008-12-30 | Asahi Kasei Pharma Corporation | Substituted arylalkanoic acid derivatives and use thereof |
CN100404088C (zh) * | 2003-09-17 | 2008-07-23 | 张荣士 | 复合式棒球棒 |
WO2005049589A2 (en) * | 2003-10-14 | 2005-06-02 | Cadila Healthcare Limited | Heterocyclic compounds for the treatment of hyperlipidemia, diabetes, obesity and similar diseases |
WO2005051890A1 (en) * | 2003-11-19 | 2005-06-09 | Smithkline Beecham Corporation | Aminophenylcyclopropyl carboxylic acids and derivatives as agonists to gpr40 |
WO2005054213A1 (ja) * | 2003-12-02 | 2005-06-16 | Shionogi & Co., Ltd. | ペルオキシソーム増殖活性化受容体アゴニスト活性を有するイソキサゾール誘導体 |
AU2004311909A1 (en) * | 2003-12-22 | 2005-07-21 | Eli Lilly And Company | Triazole, oxadiazole and thiadiazole derivative as PPAR modulators for the treatment of diabetes |
EP1737809B1 (en) * | 2004-02-27 | 2013-09-18 | Amgen, Inc | Compounds, pharmaceutical compositions and methods for use in treating metabolic disorders |
WO2005087710A1 (ja) * | 2004-03-15 | 2005-09-22 | Takeda Pharmaceutical Company Limited | アミノフェニルプロパン酸誘導体 |
ATE427941T1 (de) * | 2004-07-27 | 2009-04-15 | Astellas Pharma Inc | Thiazolderivate mit vap-1-hemmender wirkung |
US20080051418A1 (en) * | 2004-11-26 | 2008-02-28 | Tsuyoshi Maekawa | Arylalkanoic Acid Derivative |
US8153694B2 (en) * | 2005-07-29 | 2012-04-10 | Takeda Pharmaceutical Company Limited | Cyclopropanecarboxylic acid compound |
EP1940767A2 (en) * | 2005-09-07 | 2008-07-09 | Plexxikon, Inc. | Pparactive compounds |
JP2007230909A (ja) * | 2006-03-01 | 2007-09-13 | Univ Of Tokyo | 置換イソキサゾール誘導体 |
EP2001844A2 (en) * | 2006-03-14 | 2008-12-17 | Amgen, Inc | Bicyclic carboxylic acid derivatives useful for treating metabolic disorders |
WO2007140183A1 (en) * | 2006-05-24 | 2007-12-06 | Eli Lilly And Company | Fxr agonists |
US8183275B2 (en) * | 2006-10-20 | 2012-05-22 | Merck Sharp & Dohme Corp. | Substituted imidazoles as bombesin receptor subtype-3 modulators |
JP5399262B2 (ja) * | 2006-12-08 | 2014-01-29 | エグゼリクシス パテント カンパニー エルエルシー | Lxrおよびfxrのモジュレーター |
US8394841B2 (en) * | 2007-02-22 | 2013-03-12 | Irm Llc | Compounds and methods for modulating G protein-coupled receptors |
MX2009008998A (es) * | 2007-02-23 | 2009-09-02 | Lilly Co Eli | Moduladores del receptor activado por proliferador de peroxisoma. |
WO2008108602A1 (en) * | 2007-03-07 | 2008-09-12 | Dong-A Pharm. Co., Ltd. | Novel phenylpropionic acid derivatives as peroxisome proliferator-activated gamma receptor modulators, method of the same, and pharmaceutical composition comprising the same |
GB0722077D0 (en) * | 2007-11-09 | 2007-12-19 | Smithkline Beecham Corp | Compounds |
AU2008333320B2 (en) * | 2007-12-04 | 2012-12-20 | F. Hoffmann-La Roche Ag | Isoxazolo-pyrazine derivatives |
US7943619B2 (en) * | 2007-12-04 | 2011-05-17 | Hoffmann-La Roche Inc. | Isoxazolo-pyridazine derivatives |
DK2227467T3 (en) * | 2007-12-04 | 2015-01-19 | Hoffmann La Roche | Isoxazolo-pyridine derivatives |
AR074760A1 (es) * | 2008-12-18 | 2011-02-09 | Metabolex Inc | Agonistas del receptor gpr120 y usos de los mismos en medicamentos para el tratamiento de diabetes y el sindrome metabolico. |
-
2009
- 2009-10-20 MX MX2011004125A patent/MX2011004125A/es not_active Application Discontinuation
- 2009-10-20 EA EA201170504A patent/EA022417B1/ru not_active IP Right Cessation
- 2009-10-20 US US12/582,610 patent/US20100216827A1/en not_active Abandoned
- 2009-10-20 UA UAA201106189A patent/UA107917C2/ru unknown
- 2009-10-20 EP EP09744008A patent/EP2350016A2/en not_active Withdrawn
- 2009-10-20 CA CA2740366A patent/CA2740366A1/en not_active Abandoned
- 2009-10-20 WO PCT/US2009/061356 patent/WO2010048207A2/en active Application Filing
- 2009-10-20 NZ NZ592603A patent/NZ592603A/xx not_active IP Right Cessation
- 2009-10-20 JP JP2011532337A patent/JP2012506386A/ja not_active Ceased
- 2009-10-20 EP EP13190133.2A patent/EP2690095A1/en not_active Withdrawn
- 2009-10-20 BR BRPI0920237A patent/BRPI0920237A2/pt not_active IP Right Cessation
- 2009-10-20 AR ARP090104033A patent/AR073949A1/es unknown
- 2009-10-20 AU AU2009307656A patent/AU2009307656B2/en not_active Ceased
- 2009-10-20 KR KR1020117009622A patent/KR20110082145A/ko active Search and Examination
- 2009-10-20 CN CN2009801413846A patent/CN102186825A/zh active Pending
- 2009-10-21 TW TW098135635A patent/TW201020241A/zh unknown
-
2011
- 2011-04-05 IL IL212144A patent/IL212144A0/en unknown
- 2011-04-14 ZA ZA2011/02815A patent/ZA201102815B/en unknown
- 2011-04-15 NI NI201100075A patent/NI201100075A/es unknown
- 2011-04-15 CR CR20110201A patent/CR20110201A/es unknown
- 2011-04-18 EC EC2011010989A patent/ECSP11010989A/es unknown
- 2011-04-20 CL CL2011000899A patent/CL2011000899A1/es unknown
- 2011-05-12 CO CO11058452A patent/CO6382155A2/es active IP Right Grant
-
2014
- 2014-04-14 JP JP2014082658A patent/JP2014132037A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
CO6382155A2 (es) | 2012-02-15 |
EP2690095A1 (en) | 2014-01-29 |
EP2350016A2 (en) | 2011-08-03 |
ECSP11010989A (es) | 2011-08-31 |
NZ592603A (en) | 2013-02-22 |
AU2009307656A1 (en) | 2010-04-29 |
JP2014132037A (ja) | 2014-07-17 |
WO2010048207A2 (en) | 2010-04-29 |
CN102186825A (zh) | 2011-09-14 |
TW201020241A (en) | 2010-06-01 |
ZA201102815B (en) | 2012-06-27 |
CA2740366A1 (en) | 2010-04-29 |
KR20110082145A (ko) | 2011-07-18 |
CR20110201A (es) | 2011-08-29 |
MX2011004125A (es) | 2011-05-19 |
AU2009307656B2 (en) | 2015-07-02 |
BRPI0920237A2 (pt) | 2015-12-29 |
EA201170504A1 (ru) | 2011-12-30 |
EA022417B1 (ru) | 2015-12-30 |
WO2010048207A3 (en) | 2010-06-17 |
NI201100075A (es) | 2012-03-15 |
JP2012506386A (ja) | 2012-03-15 |
US20100216827A1 (en) | 2010-08-26 |
CL2011000899A1 (es) | 2011-09-30 |
IL212144A0 (en) | 2011-06-30 |
UA107917C2 (ru) | 2015-03-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR073949A1 (es) | Agonistas del receptor aril-gpr120 y usos de los mismos | |
PE20181269A1 (es) | Agonistas del receptor de apelina y metodos de uso | |
CL2020003260A1 (es) | Compuestos de naftiridinona sustituidos útiles como activadores de células t | |
CO2017005992A2 (es) | Compuestos de triazolopirimidina y usos de los mismos | |
PE20160208A1 (es) | Compuestos de pirimidinodiona contra estados cardiacos | |
CU24385B1 (es) | Compuestos éteres de arilo útiles para tratar cancer de célula renal | |
CL2022000485A1 (es) | Compuestos de piridopirimidinonilo sustituidos útiles como activadores de células t | |
PE20141191A1 (es) | Compuestos como inhibidores de bace | |
PE20161243A1 (es) | Compuesto heterociclico fusionado | |
PE20191245A1 (es) | Compuestos de tiazolcarboxamidas y piridinacarboxamida utiles como inhibidores de quinasa pim | |
UY35641A (es) | PROCEDIMIENTO DE SÍNTESIS PARA PREPARAR ANÁLOGOS MACROCÍCLICOS C1-CETO DE HALICONDRINA B, E INTERMEDIARIOS ÚTILES INCLUYENDO INTERMEDIARIOS CONTENIENDO GRUPOS ?SO2-(p-TOLILO) | |
PE20120645A1 (es) | Inhibidores de epoxicetona proteasa de tripeptidos cristalinos | |
CL2012000953A1 (es) | Procedimientos de preparacion de derivados espiro[furo[2,3-f][1,3]benzodioxol-7,3`-indol]-2`(1`h)-onas. | |
UY37774A (es) | Compuestos 5-cianoindol sustituidos y usos de los mismos | |
ECSP014067A (es) | Activadores de fenil glucoquinasa para-aril o heterociclico sustituida | |
PE20190806A1 (es) | Agonistas heterociclicos del receptor de apelina (apj) y usos de los mismos | |
CL2009001044A1 (es) | Compuestos cristalinos derivados de heterociclos puenteados por un alqueno; utiles en el tratamiento de enfermedades metabolicas, enfermedades circulatorias, enfermedades del snc, entre otras enfermedades. | |
PE20161476A1 (es) | Derivados de indolin-2-ona o pirrolo-piridin-2-ona | |
AR094527A1 (es) | Derivados de poliglicol bis-[3-(7-ter-butil-2-oxo-3-fenil-3h-benzofuran-5-il)-propanoilo] como estabilizantes de material orgánico | |
PE20190339A1 (es) | 1h-pirazolo[4,3-b] piridinas como inhibidores de pde1 | |
AR110119A1 (es) | Proceso para la purificación de pirazolpiridazinas | |
AR059190A1 (es) | Composiciones pesticidas a base de derivados de 3 - piridilo, semillas y metodos de control de plagas y de proteccion de plantas en crecimiento que las utilizan, derivados de 3-piridilo, procedimientos para su preparacion y mezclas pesticidas sinergicas que los utilizan como principio activo. | |
PE20191488A1 (es) | Activador de nrf2 | |
PE20170949A1 (es) | Espiroindolinas para el tratamiento y profilaxis de infeccion por virus respiratorio sincitial (rsv) | |
CL2019001406A1 (es) | Moduladores de ror gamma (rory). |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FB | Suspension of granting procedure |