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AR053673A1 - Derivados de (1,2,4) - ditiazoli (di) , inductores de glutation - s- transferasa y nadph quinona oxido- reductasa , para profilaxis y tratamiento de condiciones adversas asociadas con citotoxicidad en general y apoptosis en particular - Google Patents

Derivados de (1,2,4) - ditiazoli (di) , inductores de glutation - s- transferasa y nadph quinona oxido- reductasa , para profilaxis y tratamiento de condiciones adversas asociadas con citotoxicidad en general y apoptosis en particular

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Publication number
AR053673A1
AR053673A1 ARP060100413A ARP060100413A AR053673A1 AR 053673 A1 AR053673 A1 AR 053673A1 AR P060100413 A ARP060100413 A AR P060100413A AR P060100413 A ARP060100413 A AR P060100413A AR 053673 A1 AR053673 A1 AR 053673A1
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AR
Argentina
Prior art keywords
atom
4alkyl
unbranched
dialkyl
cyano
Prior art date
Application number
ARP060100413A
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English (en)
Inventor
Roelof W Feenstra
Hiskias G Keizer
Maria L Pras-Raves
Vliet Bernard J Van
Scharrenburg Gustaaf J M Van
Original Assignee
Solvay Pharm Bv
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Application filed by Solvay Pharm Bv filed Critical Solvay Pharm Bv
Publication of AR053673A1 publication Critical patent/AR053673A1/es

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    • C07ORGANIC CHEMISTRY
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    • C07D285/00Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
    • C07D285/01Five-membered rings
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K31/33Heterocyclic compounds
    • A61K31/38Heterocyclic compounds having sulfur as a ring hetero atom
    • A61K31/385Heterocyclic compounds having sulfur as a ring hetero atom having two or more sulfur atoms in the same ring
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic 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
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    • A61K31/41Heterocyclic 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
    • A61K31/425Thiazoles
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    • C07D417/04Heterocyclic 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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    • C07D417/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
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Abstract

También se refiere al uso de un compuesto descripto en la presente para la fabricacion de un medicamento util para la profilaxis y tratamiento de condiciones adversas asociadas con citotoxicidad en general y apoptosis en particular. Reivindicacion 2: Compuestos de la formula general (1) en donde las líneas punteadas entre el átomo de C numero 5 y sus átomos de N vecinos representan enlaces simples o dobles, con la condicion de que uno de los dos enlaces es un enlace simple y uno es un enlace doble, y con la condicion de que cuando el enlace doble está entre el átomo de C numero 5 y el átomo de N numero 4, R4 no existe y cuando el enlace doble está entre el átomo de C numero 5 y el átomo de N exo, R2no existe; R1, R2, R3 y R4 independientemente representan un grupo alquilo C1-4 ramificado o no ramificado, que contiene opcionalmente átomos de S o grupos sulfoxido, amida, cetona, tiocetona o sulfona, y está opcionalmente sustituido con halogeno, ciano, mono- o dialquil C1- 4amino, trifluorometilo, alcoxi C1-4 o hidroxilo, o R1 y R2 junto con el átomo de N al cual están unidos, forman un sistema de anillos de 4 a 8 miembros en el cual pueden estar presentes otros heteroátomos (sustituidos) elegidos de N, O y S, y el cual sistema de anillos puede estar opcionalmente sustituido con alquilo C1-4 ramificado o no ramificado, halogeno, ciano, mono- o dialquil C1-4amino, trifluorometilo, alcoxi C1-4 o hidroxilo lo el cual sistema de anillos contiene funciones amida, cetona, tiocetona, sulfona o sulfoxido, R3 representa H, alquilo C1-4 ramificado o no ramificado, que contiene opcionalmente átomos de S o grupos sulfoxido, amida, cetona, tiocetona o sulfona, y está opcionalmente sustituido con halogeno, ciano, mono- o dialquil C1-4amino, trifluorometilo, alcoxi C1-4, S-alquilo C1-4, SH o hidroxilo, o R3 representa un grupo arilo, opcionalmente sustituido con grupos alquilo C1-4 ramificado o no ramificado, arilo, alquil C1-4arilo, SH, S- alquilo C1-4, halogeno, ciano, mono- o dialquil C1-4amino, CF3, OCF3, SCF3, nitro, hidroxi o alcoxi C1-4, y los tautomeros, estereoisomeros N-oxidos de los mismos, así como las sales farmacologicamente aceptables, los hidratos y solvatos de dichos compuestos de formula (1) y sus tautomeros, estereoisomeros y N-oxidos.
ARP060100413A 2005-02-11 2006-02-06 Derivados de (1,2,4) - ditiazoli (di) , inductores de glutation - s- transferasa y nadph quinona oxido- reductasa , para profilaxis y tratamiento de condiciones adversas asociadas con citotoxicidad en general y apoptosis en particular AR053673A1 (es)

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EP05101004 2005-02-11

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AR053673A1 true AR053673A1 (es) 2007-05-16

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ARP060100413A AR053673A1 (es) 2005-02-11 2006-02-06 Derivados de (1,2,4) - ditiazoli (di) , inductores de glutation - s- transferasa y nadph quinona oxido- reductasa , para profilaxis y tratamiento de condiciones adversas asociadas con citotoxicidad en general y apoptosis en particular

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EP (1) EP1851209B1 (es)
JP (1) JP2008530051A (es)
KR (1) KR20070107119A (es)
CN (1) CN101142199A (es)
AR (1) AR053673A1 (es)
AU (1) AU2006212209B2 (es)
BR (1) BRPI0607547A2 (es)
CA (1) CA2597523A1 (es)
MX (1) MX2007009695A (es)
RU (1) RU2397162C2 (es)
SA (1) SA06270010B1 (es)
TW (1) TW200640888A (es)
UA (1) UA94398C2 (es)
WO (1) WO2006084854A2 (es)

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WO2018057989A1 (en) 2016-09-24 2018-03-29 Washington University INHIBITORS OF SARM1 NADase ACTIVITY AND USES THEREOF
JP6944690B2 (ja) * 2017-02-21 2021-10-06 株式会社アミンファーマ研究所 グルタチオン−s−トランスフェラーゼ(gst)の発現増強剤
KR102254668B1 (ko) * 2019-04-16 2021-05-24 연세대학교 산학협력단 Gstt1 단백질 또는 이를 암호화하는 유전자를 유효성분으로 포함하는 조성물

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AU4144172A (en) * 1971-04-26 1973-10-25 Ortho Pharma Corp Inducing infertility in the male
JPS4930837B2 (es) * 1971-08-19 1974-08-16
JPS5581804A (en) * 1978-12-15 1980-06-20 Nippon Tokushu Noyaku Seizo Kk Acaricide and fungicide for agriculture and gardening
JP2685120B2 (ja) * 1994-07-20 1997-12-03 工業技術院長 ジチアゾリウム塩の製造方法

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EP1851209A2 (en) 2007-11-07
EP1851209B1 (en) 2012-05-30
AU2006212209A1 (en) 2006-08-17
KR20070107119A (ko) 2007-11-06
UA94398C2 (ru) 2011-05-10
CA2597523A1 (en) 2006-08-17
WO2006084854A3 (en) 2006-11-02
CN101142199A (zh) 2008-03-12
TW200640888A (en) 2006-12-01
RU2397162C2 (ru) 2010-08-20
RU2007133809A (ru) 2009-03-20
SA06270010B1 (ar) 2010-11-22
JP2008530051A (ja) 2008-08-07
BRPI0607547A2 (pt) 2010-04-06
WO2006084854A2 (en) 2006-08-17
MX2007009695A (es) 2007-11-12
AU2006212209B2 (en) 2011-02-10

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