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MX2013014241A - Derivados de indanona, sales farmaceuticamente aceptables o isomeros opticos de los mismos, metodo de preparacion de los mismos, y composiciones farmaceuticas que contienen los mismos como ingrediente activo para prevención o tratamiento de enfermedades virales. - Google Patents

Derivados de indanona, sales farmaceuticamente aceptables o isomeros opticos de los mismos, metodo de preparacion de los mismos, y composiciones farmaceuticas que contienen los mismos como ingrediente activo para prevención o tratamiento de enfermedades virales.

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Publication number
MX2013014241A
MX2013014241A MX2013014241A MX2013014241A MX2013014241A MX 2013014241 A MX2013014241 A MX 2013014241A MX 2013014241 A MX2013014241 A MX 2013014241A MX 2013014241 A MX2013014241 A MX 2013014241A MX 2013014241 A MX2013014241 A MX 2013014241A
Authority
MX
Mexico
Prior art keywords
same
preventing
viral
pharmaceutically acceptable
active ingredient
Prior art date
Application number
MX2013014241A
Other languages
English (en)
Other versions
MX363405B (es
Inventor
Johan Neyts
Young Sik Jung
Chong Kgo Lee
Hae Soon Kim
Hee Chun Jeong
Pil Ho Kim
Soo Bong Han
Jin Soo Shin
Hendrik Jan Thibaut
Original Assignee
Univ Leuven Kath
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Univ Leuven Kath filed Critical Univ Leuven Kath
Publication of MX2013014241A publication Critical patent/MX2013014241A/es
Publication of MX363405B publication Critical patent/MX363405B/es

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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/93Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems condensed with a ring other than six-membered
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    • C07ORGANIC CHEMISTRY
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    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/78Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/79Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
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    • C07C233/30Carboxylic 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 doubly-bound oxygen atoms
    • C07C233/32Carboxylic 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 doubly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
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    • C07D209/56Ring systems containing three or more rings
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Abstract

Se describen derivados de indanona, sales farmacéuticamente aceptables de los mismos o enantiómeros, un método de preparación de los mismos, y una composición farmacéutica para la prevención o tratamiento de enfermedades virales, que comprenden los mismos como un ingrediente activo. Los derivados de indanona tienen excelente actividad inhibitoria contra picornavirus incluyendo virus coxsackie, enterovirus, ecovirus, poliovirus y rinovirus, así como exhiben baja citotoxicidad, de modo que pueden ser útiles como un ingrediente activo de una composición farmacéutica para la prevención y tratamiento de enfermedades virales incluyendo poliomielitis, parálisis, conjuntivitis hemorrágica aguda, meningitis viral, enfermedad de manos-pies y boca, enfermedad vesicular, hepatitis A, miositis, miocarditis, pancreatitis, diabetes, mialgia epidémica, encefalitis, gripe, herpangina, enfermedad de pies y boca, asma, enfermedad pulmonar obstructiva crónica, neumonía, sinusitis u otitis media.
MX2013014241A 2011-06-16 2012-06-18 Derivados de indanona, sales farmaceuticamente aceptables o isomeros opticos de los mismos, metodo de preparacion de los mismos, y composiciones farmaceuticas que contienen los mismos como ingrediente activo para prevención o tratamiento de enfermedades virales. MX363405B (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
KR20110058705 2011-06-16
PCT/KR2012/004806 WO2012173448A2 (ko) 2011-06-16 2012-06-18 인다논 유도체, 이의 약학적으로 허용되는 염 또는 이의 광학 이성질체, 이의 제조방법 및 이를 유효성분으로 함유하는 바이러스성 질환의 예방 또는 치료용 약학적 조성물
KR1020120065022A KR101391746B1 (ko) 2011-06-16 2012-06-18 인다논 유도체, 이의 약학적으로 허용되는 염 또는 이의 광학 이성질체, 이의 제조방법 및 이를 유효성분으로 함유하는 바이러스성 질환의 예방 또는 치료용 약학적 조성물

Publications (2)

Publication Number Publication Date
MX2013014241A true MX2013014241A (es) 2014-05-14
MX363405B MX363405B (es) 2019-03-22

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MX2013014241A MX363405B (es) 2011-06-16 2012-06-18 Derivados de indanona, sales farmaceuticamente aceptables o isomeros opticos de los mismos, metodo de preparacion de los mismos, y composiciones farmaceuticas que contienen los mismos como ingrediente activo para prevención o tratamiento de enfermedades virales.

Country Status (12)

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US (2) US9464067B2 (es)
EP (2) EP2722042B1 (es)
JP (2) JP5906309B2 (es)
KR (1) KR101391746B1 (es)
CN (1) CN103764140B (es)
AU (1) AU2012270311B2 (es)
BR (1) BR112013032306B1 (es)
CA (3) CA2838703C (es)
EA (1) EA026149B1 (es)
ES (1) ES2743199T3 (es)
MX (1) MX363405B (es)
WO (1) WO2012173448A2 (es)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2743199T3 (es) * 2011-06-16 2020-02-18 Korea Res Inst Chemical Tech Derivados de indanona, sales farmacéuticamente aceptables o isómeros ópticos de los mismos, método de preparación para los mismos y composiciones farmacéuticas que los contienen como ingrediente activo para prevenir o tratar enfermedades virales
WO2014092514A1 (ko) * 2012-12-14 2014-06-19 한국화학연구원 신규한 화합물, 이의 약학적으로 허용가능한 염 또는 이의 광학 이성질체, 이의 제조방법 및 이를 유효성분으로 함유하는 바이러스성 질환의 예방 또는 치료용 약학적 조성물
CN104211666B (zh) * 2013-05-31 2017-11-14 中国人民解放军军事医学科学院毒物药物研究所 2,3‑环氧丁二酰胺类化合物、其制备方法和用途
CN104744283A (zh) * 2015-02-09 2015-07-01 西北师范大学 茚酮羧酸酯的三氟甲基化方法
WO2020055858A1 (en) * 2018-09-10 2020-03-19 Cocrystal Pharma, Inc. Pyridopyrazine and pyridotriazine inhibitors of influenza virus replication
JP7592748B2 (ja) * 2020-04-20 2024-12-02 ノバルティス アーゲー 抗ウイルス1,3-ジ-オキソ-インデン化合物
CN120590351A (zh) * 2020-04-20 2025-09-05 诺华股份有限公司 抗病毒素1,3-二氧代茚化合物
CN113512027B (zh) * 2021-07-20 2022-06-14 华南理工大学 一种茚酮并喹喔啉衍生物及其制备方法与应用
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