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PE20010319A1 - ANTAGONISTS OF IL-8 RECEPTORS - Google Patents

ANTAGONISTS OF IL-8 RECEPTORS

Info

Publication number
PE20010319A1
PE20010319A1 PE2000000589A PE0005892000A PE20010319A1 PE 20010319 A1 PE20010319 A1 PE 20010319A1 PE 2000000589 A PE2000000589 A PE 2000000589A PE 0005892000 A PE0005892000 A PE 0005892000A PE 20010319 A1 PE20010319 A1 PE 20010319A1
Authority
PE
Peru
Prior art keywords
alkyl
aryl
group
ring
halosustituted
Prior art date
Application number
PE2000000589A
Other languages
Spanish (es)
Inventor
Katherine L Widdowson
John G Gleason
Gregory M Benson
Original Assignee
Smithkline Beecham Corp
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 Smithkline Beecham Corp filed Critical Smithkline Beecham Corp
Publication of PE20010319A1 publication Critical patent/PE20010319A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/46Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D317/48Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
    • C07D317/62Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to atoms of the carbocyclic ring
    • C07D317/66Nitrogen atoms not forming part of a nitro radical
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/13Amines
    • A61K31/155Amidines (), e.g. guanidine (H2N—C(=NH)—NH2), isourea (N=C(OH)—NH2), isothiourea (—N=C(SH)—NH2)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/275Nitriles; Isonitriles
    • A61K31/277Nitriles; Isonitriles having a ring, e.g. verapamil
    • 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
    • A61K31/357Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having two or more oxygen atoms in the same ring, e.g. crown ethers, guanadrel
    • A61K31/36Compounds containing methylenedioxyphenyl groups, e.g. sesamin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/02Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/20Antivirals for DNA viruses
    • A61P31/22Antivirals for DNA viruses for herpes viruses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00Antiparasitic agents
    • A61P33/02Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
    • A61P33/06Antimalarials
    • 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
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C279/00Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
    • C07C279/28Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of guanidine groups bound to cyano groups, e.g. cyanoguanidines, dicyandiamides
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Virology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Rheumatology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Urology & Nephrology (AREA)
  • Molecular Biology (AREA)
  • Biotechnology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

SE REFIERE AL USO COMPUESTOS QUE CONTIENEN GUANIDINA DE FORMULA I, DONDE: Z ES CN, OR11, C(O)NR15R16, R18, C(O)R11, S(O)2R17; R ES UN GRUPO CON UN H IONIZABLE Y UN pKa MENOR A 10; R1 ES H, HALOGENO, NITRO, CIANO, ALQUILO C1-C10 HALOSUSTITUIDO, (CR8R8)qS(O)tR4, OH, (CR8R8)qNR4R5, ENTRE OTROS; q ES 0-10, t ES 0-2; v ES 0-4; R4 Y R5 SON H, ALQUILO C1-C4, ARILO, (ARIL)-ALQUILO C1-C4, HETEROARILO, HETEROCICLICO,ENTRE OTROS; O JUNTO CON N FORMAN UN ANILLO DE 5 A 7 MIEMBROS; Y ES H, HALOGENO, NITRO, CIANO, ALQUILO C1-C10 HALOSUSTITUIDO, ALQUENILO C2-C10, ALCOXI C1-C10, ENTRE OTROS; R6 Y R7 SON H, ALQUILO C1-C4; R6 Y R7 JUNTO A N FORMAN UN ANILLO DE 5 A 7 MIEMBROS; R8 ES H, ALQUILO C1-C4; R11 ES H, ALQUILO C1-C4, ENTRE OTROS; R15 Y R16 SON H, ALQUILO C1-C4, ARILO, ENTRE OTROS; R17 ES ALQUILO C1-C4, NR15R16, OR11, ARILO, ENTRE OTROS; R18 ES ALQUILO C1-C4, ARILO, ARIL-ALQUILO C1-C4, ENTRE OTROS; W ES UN GRUPO a, ENTRE OTROS; E` ES UN GRUPO b, ENTRE OTROS; W1 ES UN GRUPO c, ENTRE OTROS; E ES UN GRUPO d; * ES EL PUNTO DE UNION DEL ANILLO. LOS COMPUESTOS DE GUANIDINA INHIBE LA UNION DE QUIMIOQUINAS GROO, GROß, GROÛ, NAP-2 AL RECEPTOR O, ß DE INTERLEUQUINA IL-8 Y PUEDEN SER UTILES PARA EL TRATAMIENTO DE MALARIA, RESTENOSIS, ANGIOGENESIS, ATEROSCLEROSIS, OSTEOPOROSIS, GINGIVITIS, ENFERMEDADES CAUSADAS POR VIRUS DE LA HEPATITIS ßREFERS TO THE USE OF COMPOUNDS CONTAINING GUANIDINE OF FORMULA I, WHERE: Z IS CN, OR11, C (O) NR15R16, R18, C (O) R11, S (O) 2R17; R IS A GROUP WITH A H IONIZABLE AND A pKa LESS THAN 10; R1 IS H, HALOGEN, NITRO, CYANE, C1-C10 HALOSUSTITUTED ALKYL, (CR8R8) qS (O) tR4, OH, (CR8R8) qNR4R5, AMONG OTHERS; q IS 0-10, t IS 0-2; v ES 0-4; R4 AND R5 ARE H, C1-C4 ALKYL, ARYL, (ARYL) -C1-C4 ALKYL, HETEROARYL, HETEROCYCLIC, AMONG OTHERS; OR TOGETHER WITH N, THEY FORM A RING OF 5 TO 7 MEMBERS; AND IT IS H, HALOGEN, NITRO, CYANE, C1-C10 HALOSUSTITUTED ALKYL, C2-C10 ALKYL, C1-C10 ALCOXY, AMONG OTHERS; R6 AND R7 ARE H, C1-C4 ALKYL; R6 AND R7 TOGETHER WITH N FORM A RING OF 5 TO 7 MEMBERS; R8 IS H, C1-C4 ALKYL; R11 IS H, C1-C4 ALKYL, AMONG OTHERS; R15 AND R16 ARE H, C1-C4 ALKYL, ARYL, AMONG OTHERS; R17 IS C1-C4 ALKYL, NR15R16, OR11, ARYL, AMONG OTHERS; R18 IS C1-C4 ALKYL, ARYL, ARYL-C1-C4 ALKYL, AMONG OTHERS; W IS A GROUP a, AMONG OTHERS; E` IS A GROUP b, AMONG OTHERS; W1 IS A GROUP c, AMONG OTHERS; E IS A GROUP d; * IS THE JOINT POINT OF THE RING. GUANIDINE COMPOUNDS INHIBIT THE BINDING OF CHEMOKINES GROO, GROß, GROÛ, NAP-2 TO THE IL-8 INTERLEUQUIN O, ß RECEPTOR AND MAY BE USEFUL FOR THE TREATMENT OF MALARIA, RESTENOSIS, ANGIOGENESIS, ATHEROSCLEROMEDOSIS, CABINETS FOR HEPATITIS VIRUS ß

PE2000000589A 1999-06-16 2000-06-14 ANTAGONISTS OF IL-8 RECEPTORS PE20010319A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US13967499P 1999-06-16 1999-06-16

Publications (1)

Publication Number Publication Date
PE20010319A1 true PE20010319A1 (en) 2001-05-24

Family

ID=22487784

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2000000589A PE20010319A1 (en) 1999-06-16 2000-06-14 ANTAGONISTS OF IL-8 RECEPTORS

Country Status (22)

Country Link
EP (1) EP1191934A4 (en)
JP (1) JP2003501471A (en)
KR (1) KR20020009635A (en)
CN (1) CN1494424A (en)
AR (1) AR029368A1 (en)
AU (1) AU766086B2 (en)
BR (1) BR0010985A (en)
CA (1) CA2377397A1 (en)
CZ (1) CZ20014490A3 (en)
EC (2) ECSP003525A (en)
HK (1) HK1044716A1 (en)
HU (1) HUP0202019A3 (en)
IL (1) IL146214A0 (en)
MX (1) MXPA01013287A (en)
NO (1) NO20016065D0 (en)
NZ (1) NZ515232A (en)
PE (1) PE20010319A1 (en)
PL (1) PL352218A1 (en)
TR (1) TR200103690T2 (en)
UY (1) UY26209A1 (en)
WO (1) WO2000076516A1 (en)
ZA (1) ZA200110203B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6642215B2 (en) * 2001-05-24 2003-11-04 Leo Pharma A/S Method of modulating NF-kB activity

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0344425B1 (en) * 1988-03-30 1993-12-08 Warner-Lambert Company N-[[(2,6-disubstituted)phenyl]-N'- arylalkyl] ureas as antihypercholesterolemic and antiatherosclerotic agents
US5780483A (en) * 1995-02-17 1998-07-14 Smithkline Beecham Corporation IL-8 receptor antagonists
AR008290A1 (en) * 1996-08-15 1999-12-29 Smithkline Beecham Corp NEW COMPOUNDS CONTAINING GUANIDINE USEFUL AS ANTAGONISTS OF IL-8 RECEPTORS, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM PROCEDURE FOR THE PREPARATION OF SUCH COMPOUNDS AND PROCEDURE FOR THE PREPARATION OF INTERMEDIARIES.

Also Published As

Publication number Publication date
NO20016065L (en) 2001-12-12
MXPA01013287A (en) 2002-06-04
CA2377397A1 (en) 2000-12-21
JP2003501471A (en) 2003-01-14
EP1191934A1 (en) 2002-04-03
AU5748200A (en) 2001-01-02
ECSP003525A (en) 2002-01-25
IL146214A0 (en) 2002-07-25
HUP0202019A2 (en) 2002-10-28
AR029368A1 (en) 2003-06-25
TR200103690T2 (en) 2002-05-21
EP1191934A4 (en) 2004-02-04
AU766086B2 (en) 2003-10-09
KR20020009635A (en) 2002-02-01
HUP0202019A3 (en) 2003-03-28
ECSP003528A (en) 2002-01-25
ZA200110203B (en) 2002-09-11
BR0010985A (en) 2002-03-26
PL352218A1 (en) 2003-08-11
NO20016065D0 (en) 2001-12-12
WO2000076516A1 (en) 2000-12-21
NZ515232A (en) 2004-02-27
UY26209A1 (en) 2000-12-29
CN1494424A (en) 2004-05-05
HK1044716A1 (en) 2002-11-01
CZ20014490A3 (en) 2002-07-17

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