CO5580760A2 - Esteres y amidas como agonistas ppar-alfa - Google Patents

Esteres y amidas como agonistas ppar-alfa

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Publication number
CO5580760A2
CO5580760A2 CO04050434A CO04050434A CO5580760A2 CO 5580760 A2 CO5580760 A2 CO 5580760A2 CO 04050434 A CO04050434 A CO 04050434A CO 04050434 A CO04050434 A CO 04050434A CO 5580760 A2 CO5580760 A2 CO 5580760A2
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CO
Colombia
Prior art keywords
substituted
unsubstituted
linear
arylalkyl
represents hydrogen
Prior art date
Application number
CO04050434A
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English (en)
Inventor
Debnath Bhuniya
Kumar Das Saibal
Gurram Ranga Madhavan
Javed Iqbal
Ranjan Chakrabarti
Reeba Kannimel Vikramadithy
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Reddys Lab Ltd Dr
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Application filed by Reddys Lab Ltd Dr filed Critical Reddys Lab Ltd Dr
Publication of CO5580760A2 publication Critical patent/CO5580760A2/es

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    • 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
    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • A61K31/3533,4-Dihydrobenzopyrans, e.g. chroman, catechin
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    • 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
    • A61K31/435Heterocyclic 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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    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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    • 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4709Non-condensed quinolines and containing further heterocyclic rings
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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    • A61K31/535Heterocyclic 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
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/541Non-condensed thiazines containing further heterocyclic rings
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    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/63Esters of sulfonic acids
    • C07C309/64Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms
    • C07C309/65Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms of a saturated carbon skeleton
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    • C07C309/72Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/73Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
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    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/50Compounds containing any of the groups, X being a hetero atom, Y being any atom
    • C07C311/52Y being a hetero atom
    • C07C311/53X and Y not being nitrogen atoms, e.g. N-sulfonylcarbamic acid

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  • Pain & Pain Management (AREA)
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Abstract

1.- Un compuesto caracterizado porque es de la fórmula general (I) sus derivados, sus análogos, sus formas tautoméricas, sus estereoisómeros, sus polimorfos, sus sales farmacéuticamente aceptables, sus solvatos farmacéuticamente aceptables en donde R1 representa hidrógeno, hidroxi, halógeno, (C1-C12) alquilo lineal o ramificado, (C1-C12) alcoxi lineal o ramificado, un grupo arilalquilo substituido o no substituido forman un enlace junto con el grupo adyacente R2; R2 representa hidrógeno, halógeno, (C1-C12) alquilo lineal o ramificado, (C1-C12) alcoxi lineal o ramificado, (C1-C12) alcanoilo, aroilo, arilalcanoilo, arilalquilo substituido o no substituido o R2 forman un enlace junto con R1; R3 representan un átomo de hidrógeno o un grupo substituido o no substituido seleccionado de grupos (C1-C12) alquilo lineal o ramificado, cicloalquilo, cicloalquilalquilo, cicloalquenilo, arilo, (C1-C12, alcanoilo, aroilo, arilalquilo, arilalcanoilo, heterociclilo, heteroarilo, heteroarilalquilo, alcoxialquilo, alcoxicarbonilo, ariloxicarbonilo, alquilaminocarbonilo, o arilaminocarbonilo; R4 representa hidrógeno o grupos substituidos o no substituidos seleccionados de grupos (C1-C12) alquilo lineal o ramificado, cicloalquilo, arilo, arilalquilo, heterociclilo, heteroarilo o heteroarilalquilo; Y representa oxígeno, NR7 o N(R7)O, donde R7 representa hidrógeno o grupos substituidos o no substituidos seleccionados de grupos (C1-C12) alquilo, arilo, arilalquilo, hidroxialquilo, alcanoilo, aroilo, arilalcanoilo, heterociclilo, heteroarilo, heteroarilalquilo, alcoxicarbonilo o arilalcoxicarbonilo; o R4 y R7 juntos forman una estructura cíclica substituida o no substituida de 5 ó 6 miembros que contiene átomos de carbono y un átomo de nitrógeno, la cual opcionalmente contiene uno o más heteroátomos adicionales seleccionados de oxígeno, azufre o nitrógeno; R5 representa hidrógeno o grupos substituidos o no substituidos seleccionados de grupos alquilo, alquenilo, cicloalquilo, cicloalquilalquilo, arilo, o arilalquilo; Ar representa grupos substituidos o no substituidos seleccionados de fenileno divalente, naftileno, piridilo, quinolinilo, benzofurilo, dihidrobenzofurilo, benzopiranilo, dihidrobenzopiranilo, indolilo, indolinilo, azaindolilo, ...
CO04050434A 2001-12-03 2004-05-31 Esteres y amidas como agonistas ppar-alfa CO5580760A2 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IN971MA2001 2001-12-03

Publications (1)

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CO5580760A2 true CO5580760A2 (es) 2005-11-30

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CO04050434A CO5580760A2 (es) 2001-12-03 2004-05-31 Esteres y amidas como agonistas ppar-alfa

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Country Link
US (2) US7314889B2 (es)
EP (1) EP1453795A2 (es)
JP (1) JP2005511686A (es)
KR (1) KR20040066866A (es)
CN (1) CN1697828A (es)
AU (1) AU2002351069A1 (es)
BR (1) BR0214675A (es)
CA (1) CA2469227A1 (es)
CO (1) CO5580760A2 (es)
EA (1) EA008947B1 (es)
HR (1) HRP20040485A2 (es)
HU (1) HUP0402550A3 (es)
IL (1) IL162185A0 (es)
MX (1) MXPA04005257A (es)
NO (1) NO20042805L (es)
NZ (1) NZ533311A (es)
PL (1) PL370554A1 (es)
RS (1) RS48104A (es)
UA (1) UA82835C2 (es)
WO (1) WO2003048116A2 (es)
ZA (1) ZA200404261B (es)

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CN110590615A (zh) * 2019-10-03 2019-12-20 南京施倍泰生物科技有限公司 一类新型阿魏酸磺酸酯衍生物及其制备方法和应用
CN110627690A (zh) * 2019-10-03 2019-12-31 南京施倍泰生物科技有限公司 一类新型对香豆酸磺酸酯衍生物及其制备方法和应用
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CN114685323B (zh) * 2022-04-24 2023-01-06 南京大学 一类基于肉桂酰胺结构的磺酸酚酯衍生物及其制备方法和应用
CN114773238B (zh) * 2022-04-24 2023-03-24 南京大学 一类苯丙烯酰化的对氯苯磺酰阿魏酸酯衍生物及其制备方法和应用

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SE9801992D0 (sv) 1998-06-04 1998-06-04 Astra Ab New 3-aryl-2-hydroxypropionic acid derivative I
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YU72201A (sh) 1999-04-28 2005-07-19 Aventis Pharma Deutschland Gmbh. Derivati di-aril kiseline kao ppar receptorski ligandi
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