MX2016013529A - Derivados de amidas y sales farmaceuticamente aceptables de los mismos, método de preparación de los mismos y aplicación médica de los mismos. - Google Patents

Derivados de amidas y sales farmaceuticamente aceptables de los mismos, método de preparación de los mismos y aplicación médica de los mismos.

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Publication number
MX2016013529A
MX2016013529A MX2016013529A MX2016013529A MX2016013529A MX 2016013529 A MX2016013529 A MX 2016013529A MX 2016013529 A MX2016013529 A MX 2016013529A MX 2016013529 A MX2016013529 A MX 2016013529A MX 2016013529 A MX2016013529 A MX 2016013529A
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MX
Mexico
Prior art keywords
preparation
method therefor
amide derivatives
pharmaceutically acceptable
acceptable salts
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MX2016013529A
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English (en)
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MX368504B (es
Inventor
Hu Qiyue
Wang Bin
He Wei
Sun Piaoyang
Dong Qing
Jin Fangfang
Li Xin
Liu Xianbo
Original Assignee
Shanghai hengrui pharmaceutical co ltd
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Application filed by Shanghai hengrui pharmaceutical co ltd filed Critical Shanghai hengrui pharmaceutical co ltd
Publication of MX2016013529A publication Critical patent/MX2016013529A/es
Publication of MX368504B publication Critical patent/MX368504B/es

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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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 system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non 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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    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C209/00Preparation of compounds containing amino groups bound to a carbon skeleton
    • C07C209/44Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of carboxylic acids or esters thereof in presence of ammonia or amines, or by reduction of nitriles, carboxylic acid amides, imines or imino-ethers
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    • C07C233/46Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
    • C07C233/47Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
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Abstract

La presente invención se refiere a derivados de amida y sales farmacéuticamente aceptables de los mismos, al método de preparación de los mismos y a la aplicación medicinal de los mismos. Específicamente, la presente invención se refiere a derivados de amida representados por la fórmula general (I), al método de preparación de los mismos, a composiciones farmacéuticas que contienen los derivados, y a su uso como agente terapéutico, especialmente como inhibidor de la prostaglandina E sintasa-1 microsomal (mPGES-1), y a su uso en la preparación de medicamentos para el tratamiento y/o la prevención de enfermedades o trastornos tales como inflamación y/o dolor, etc. La definición de cada grupo sustituyente en la fórmula general (I) es la misma que la definición en la descripción. (ver Fórmula).
MX2016013529A 2014-04-14 2015-03-31 Derivados de amidas y sales farmaceuticamente aceptables de los mismos, método de preparación de los mismos y aplicación médica de los mismos. MX368504B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201410148152 2014-04-14
PCT/CN2015/075531 WO2015158204A1 (zh) 2014-04-14 2015-03-31 酰胺类衍生物及其可药用盐、其制备方法及其在医药上的应用

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Publication Number Publication Date
MX2016013529A true MX2016013529A (es) 2017-05-09
MX368504B MX368504B (es) 2019-10-04

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US (1) US10081629B2 (es)
EP (1) EP3133068B1 (es)
JP (1) JP6688445B2 (es)
KR (1) KR20160134865A (es)
CN (1) CN105636951B (es)
AU (1) AU2015246577B2 (es)
BR (1) BR112016023679A2 (es)
CA (1) CA2944357A1 (es)
DK (1) DK3133068T3 (es)
ES (1) ES2838625T3 (es)
HU (1) HUE052925T2 (es)
MX (1) MX368504B (es)
PT (1) PT3133068T (es)
RU (1) RU2681537C2 (es)
TW (1) TWI714527B (es)
WO (1) WO2015158204A1 (es)

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WO2021040393A1 (ko) * 2019-08-26 2021-03-04 국제약품 주식회사 인돌 카복사미드 유도체 및 그를 포함하는 약제학적 조성물
EP4045083B1 (en) 2019-10-18 2024-01-10 Forty Seven, Inc. Combination therapies for treating myelodysplastic syndromes and acute myeloid leukemia
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JP2023509881A (ja) 2019-12-24 2023-03-10 カルナバイオサイエンス株式会社 ジアシルグリセロールキナーゼ調節化合物
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