AR004413A1 - Compuestos de tiol que poseen actividad inhibitoria de metalopeptidasa; proceso para preparar dichos derivados; composiciones farmaceuticas que loscontienen - Google Patents

Compuestos de tiol que poseen actividad inhibitoria de metalopeptidasa; proceso para preparar dichos derivados; composiciones farmaceuticas que loscontienen

Info

Publication number
AR004413A1
AR004413A1 ARP960105957A ARP960105957A AR004413A1 AR 004413 A1 AR004413 A1 AR 004413A1 AR P960105957 A ARP960105957 A AR P960105957A AR P960105957 A ARP960105957 A AR P960105957A AR 004413 A1 AR004413 A1 AR 004413A1
Authority
AR
Argentina
Prior art keywords
group
groups
alkyl
phenyl
branched
Prior art date
Application number
ARP960105957A
Other languages
English (en)
Original Assignee
Zambon Spa
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 Zambon Spa filed Critical Zambon Spa
Publication of AR004413A1 publication Critical patent/AR004413A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/26Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three 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
    • 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
    • A61K31/41Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/54Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/55Acids; Esters
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D241/00Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/10Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D241/12Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic 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
    • C07D277/22Heterocyclic 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
    • C07D277/30Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic 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
    • C07D307/38Heterocyclic 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
    • C07D307/54Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic 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
    • C07D333/06Heterocyclic 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
    • C07D333/24Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Treatment Of Fiber Materials (AREA)
  • Preliminary Treatment Of Fibers (AREA)
  • Medicines Containing Plant Substances (AREA)

Abstract

El invento se refiere a fórmula (I), donde R es un grupo mercapto o un grupo R4COS convertible en el organismo a un grupo mercapto; R1 es un grupoalquilo C2-C4 recto o ramificado o un grupo arilo o arilalquilo que tiene entre 1 y 6 átomosde carbono en la fracción alquilo donde el arilo es unfenilo o un heterociclo aromático de 5 ó 6 miembros con uno o dos heteroátomos seleccionados del grupo consistente en nitrógeno, oxígeno y azufre, sustituidooptativamente con uno o mássustituyen tes, los mismos o diferentes, seleccionados del grupo formado por átomos de halógeno, grupos hidroxi, alcoxi,alquilo, alquiltio, alquilsulfonilo o alcoxicarbonilo que tienen entre 1 y 6 átomos de carbono en la fracciónalquilo, grupos alquilo C1-C3 que contienenuno o más átomos de fluor, grupos carboxi, grupos nitro, grupos amino o aminocarbonilo, grupos acilamino, grupos aminosulfonilo, grupos mono- ódi-alquilamino o mono- ó dialquilaminocarbonilo quetienen entre 1 y 6 á tomos en la fracción alquilo; R2 es un átomo de hidrógeno, un alquilo C1-C4 recto oramificado o un grupo bencilo; R3 es un grupo fenilo sustituido con un heterociclo aromático de 5 ó 6 miembros con uno o dosheteroátomosseleccionados del g rupo consistente en nitrógeno, oxígeno y azufre, estando los grupos fenilo y heterocíclico sustituidos optativamente con uno o mássustituyentes, los mismos o diferentes, según se indica para R1; R4 es un grupoalquilo C1-C4 recto o ramificado o un grupo fenilo; procedimiento para supreparación y composiciones farmacéuticas que los contiene como ingredientes activos. Los compuestos de fórmula (I) están dotados de una actividad mixtainhibitoria de ACE yNEP y son útiles en el tratamiento de enfermedades cardiovasculares.
ARP960105957A 1995-12-28 1996-12-27 Compuestos de tiol que poseen actividad inhibitoria de metalopeptidasa; proceso para preparar dichos derivados; composiciones farmaceuticas que loscontienen AR004413A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT95MI002773A IT1277737B1 (it) 1995-12-28 1995-12-28 Derivati tiolici ad attivita' inibitrice delle metallopeptidasi

Publications (1)

Publication Number Publication Date
AR004413A1 true AR004413A1 (es) 1998-11-04

Family

ID=11372827

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP960105957A AR004413A1 (es) 1995-12-28 1996-12-27 Compuestos de tiol que poseen actividad inhibitoria de metalopeptidasa; proceso para preparar dichos derivados; composiciones farmaceuticas que loscontienen

Country Status (31)

Country Link
EP (1) EP0877740B1 (es)
JP (1) JP2000502687A (es)
KR (1) KR19990076809A (es)
CN (1) CN1071325C (es)
AP (1) AP1186A (es)
AR (1) AR004413A1 (es)
AT (1) ATE292123T1 (es)
AU (1) AU713156B2 (es)
BG (1) BG63942B1 (es)
BR (1) BR9612373A (es)
CA (1) CA2241414A1 (es)
CZ (1) CZ204698A3 (es)
DE (1) DE69634543D1 (es)
EA (1) EA000991B1 (es)
EE (1) EE03766B1 (es)
GE (1) GEP19991871B (es)
HK (1) HK1018008A1 (es)
IL (1) IL124915A (es)
IS (1) IS1885B (es)
IT (1) IT1277737B1 (es)
NO (1) NO310914B1 (es)
NZ (1) NZ325785A (es)
OA (1) OA10704A (es)
PL (1) PL188151B1 (es)
RO (1) RO119882B1 (es)
SK (1) SK282977B6 (es)
TR (1) TR199801229T2 (es)
UA (1) UA62923C2 (es)
UY (1) UY24425A1 (es)
WO (1) WO1997024342A1 (es)
ZA (1) ZA9610891B (es)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1289522B1 (it) * 1996-12-24 1998-10-15 Zambon Spa Processo per la preparazione di eteroaril-fenilalanine
MY153569A (en) 1998-01-20 2015-02-27 Mitsubishi Tanabe Pharma Corp Inhibitors of ?4 mediated cell adhesion
US8168616B1 (en) 2000-11-17 2012-05-01 Novartis Ag Combination comprising a renin inhibitor and an angiotensin receptor inhibitor for hypertension
GB0203665D0 (en) * 2002-02-15 2002-04-03 Glaxo Group Ltd Process
MY140707A (en) 2002-02-28 2010-01-15 Mitsubishi Tanabe Pharma Corp Process for preparing a phenylalanine derivative and intermediates thereof
EP1481967B1 (en) 2002-03-05 2011-05-04 Sumitomo Chemical Company, Limited Process for the preparation of biaryl compounds
TW200407310A (en) * 2002-06-07 2004-05-16 Glaxo Group Ltd Compounds
GB0213122D0 (en) * 2002-06-07 2002-07-17 Glaxo Group Ltd Compounds
US7045653B2 (en) 2002-12-23 2006-05-16 Pfizer, Inc. Pharmaceuticals
GB0327839D0 (en) 2003-12-01 2003-12-31 Novartis Ag Organic compounds
US20080161321A1 (en) 2004-03-17 2008-07-03 David Louis Feldman Use of Renin Inhibitors in Therapy
EP2414625B1 (en) 2009-04-03 2014-05-07 Statoil Petroleum AS Equipment and method for reinforcing a borehole of a well while drilling
CN102811989A (zh) 2010-02-03 2012-12-05 Meh联合公司 作为具有选择性和生物活性的等排物的多取代氟甲烷
TW201136582A (en) 2010-03-16 2011-11-01 Novartis Ag Improved pharmaceutical compositions of aliskiren and methods of delivery

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4401677A (en) * 1981-10-09 1983-08-30 E. R. Squibb & Sons, Inc. Enkephalinase inhibitors
FR2652087B1 (fr) * 1989-09-15 1993-10-15 Bioprojet Ste Civile Derives d'amino-acides, leur procede de preparation et leurs applications therapeutiques.
FR2682952B1 (fr) * 1991-10-25 1993-12-03 Institut Nal Sante Recherc Medic Nouveaux n-(mercaptoacyl) amino-acides, leur preparation et les compositions pharmaceutiques qui les contiennent.
IT1273455B (it) * 1995-01-27 1997-07-08 Zambon Spa Derivati tiolici ad attivita' inibitrice delle metallopeptidasi

Also Published As

Publication number Publication date
AP9801264A0 (en) 1998-06-30
PL327580A1 (en) 1998-12-21
NZ325785A (en) 1999-09-29
AP1186A (en) 2003-07-07
KR19990076809A (ko) 1999-10-15
SK88998A3 (en) 1998-12-02
EE03766B1 (et) 2002-06-17
JP2000502687A (ja) 2000-03-07
CA2241414A1 (en) 1997-07-10
DE69634543D1 (de) 2005-05-04
IL124915A (en) 2001-10-31
RO119882B1 (ro) 2005-05-30
EP0877740A1 (en) 1998-11-18
HK1018008A1 (en) 1999-12-10
GEP19991871B (en) 1999-12-06
BR9612373A (pt) 1999-07-13
AU713156B2 (en) 1999-11-25
PL188151B1 (pl) 2004-12-31
EP0877740B1 (en) 2005-03-30
ATE292123T1 (de) 2005-04-15
IS4780A (is) 1998-06-22
CN1071325C (zh) 2001-09-19
EA199800544A1 (ru) 1999-02-25
ZA9610891B (en) 1997-06-27
SK282977B6 (sk) 2003-01-09
CZ204698A3 (cs) 1998-11-11
OA10704A (en) 2002-11-28
ITMI952773A1 (it) 1997-06-28
NO982977D0 (no) 1998-06-26
WO1997024342A1 (en) 1997-07-10
AU1301897A (en) 1997-07-28
IS1885B (is) 2003-08-15
ITMI952773A0 (es) 1995-12-28
NO310914B1 (no) 2001-09-17
IL124915A0 (en) 1999-01-26
EA000991B1 (ru) 2000-08-28
CN1206411A (zh) 1999-01-27
IT1277737B1 (it) 1997-11-12
BG102553A (en) 1999-04-30
NO982977L (no) 1998-08-27
BG63942B1 (bg) 2003-07-31
EE9800192A (et) 1998-12-15
TR199801229T2 (xx) 1998-09-21
UA62923C2 (en) 2004-01-15
UY24425A1 (es) 1997-01-09

Similar Documents

Publication Publication Date Title
AR004413A1 (es) Compuestos de tiol que poseen actividad inhibitoria de metalopeptidasa; proceso para preparar dichos derivados; composiciones farmaceuticas que loscontienen
ES2196396T3 (es) Compuestos heteroaromaticos de 5 miembros conteniendo oxigeno o azufre como inhibidores del factor xa.
DE60014393D1 (de) Aminobenzophenone als inhibitoren von il-1beta und tnf-alpha
IS2833B (is) 1,5 Bensóþíósepín og notkun þeirra gegn fitublæði
DK0494819T3 (da) Hidtil ukendte phenylimidazolidiner, deres fremstilling, anvendelse som lægemidler samt farmaceutiske præparater med indhold heraf
ATE30021T1 (de) Indolinon-(2)-derivate, verfahren zu ihrer herstellung, diese verbindungen enthaltende arzneimittel und zwischenprodukte.
ATE12042T1 (de) Aminosaeurederivate und ihre therapeutische verwendung.
TW430660B (en) Novel benzindole derivatives for neuron cell protection, processes for production, and the pharmaceutical compounds containing them
GR862248B (en) Substituted heterocyclic indoles intermediates method for their preparation and their use as medicaments
FI913478A0 (fi) Diazinderivat.
TR199901765T2 (xx) S�lfomid-metalloproteaz inhibit�rleri
AR024837A1 (es) Derivados de n-(iminometil)aminas, compuestos intermediarios para su preparacion, medicamento y composicion farmaceutica que los contienen y uso de dichos derivados para la produccion de medicamentos.
DE60034961D1 (de) Aminobenzophenone als inhibitoren von il-1beta und tnf-alpha
NO180196C (no) Analogifremgangsmåte for fremstilling av terapeutisk aktive amino- og nitroholdige, tricykliske forbindelser
ES2164164T3 (es) Derivados de aminotetrazol utiles como inhibidores de oxido nitrico sintasa.
HUP0001294A2 (hu) Proteáz inhibitor hatású (heterociklil-karbonil)-hidrazid-származékok, eljárás előállításukra és alkalmazásuk
UY25211A1 (es) Inhibidores de isoquinolinilguanidina uroquinasa
SE9701304D0 (sv) Compounds
AR002761A1 (es) Un compuesto derivado del triazol, su uso, una composicion farmaceutica que lo contiene, un metodo de tratamiento o prevencion de una infeccion fungica enun paciente humano mediante dicho compuesto o composicion, y procedimiento y compuestos intermedios para prepararlo.
YU86601A (sh) Derivati purina, postupak za njihovo dobijanje i farmaceutski preparati koji ih sadrže
BR9501612A (pt) Composto bicíclicos aromáticos utilização de um composto composição farmacêutica composição cosmética e utilização de uma composição cosmética
PT1202959E (pt) Aminobenzofenonas como inibidores de il-1-beta e tnf-alfa
MXPA04005940A (es) Acidos 3-(imidazolil)-2-aminopropanoicos.
HUP0004142A2 (hu) 5-HT1F agonista hatású karboxamidszármazékok és a vegyületeket tartalmazó gyógyászati készítmények
BG104717A (en) Water soluble azoles as broad-spectrum antifungals

Legal Events

Date Code Title Description
FC Refusal