AR012989A1 - Novedosos inhibidores de sulfonamida de la farnesil-protein trasnferasa. - Google Patents

Novedosos inhibidores de sulfonamida de la farnesil-protein trasnferasa.

Info

Publication number
AR012989A1
AR012989A1 ARP980102859A ARP980102859A AR012989A1 AR 012989 A1 AR012989 A1 AR 012989A1 AR P980102859 A ARP980102859 A AR P980102859A AR P980102859 A ARP980102859 A AR P980102859A AR 012989 A1 AR012989 A1 AR 012989A1
Authority
AR
Argentina
Prior art keywords
novel sulfonamide
farnesil
protein transferase
sulfonamide inhibitors
inhibitors
Prior art date
Application number
ARP980102859A
Other languages
English (en)
Spanish (es)
Original Assignee
Schering 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 Schering Corp filed Critical Schering Corp
Publication of AR012989A1 publication Critical patent/AR012989A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D221/00Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
    • C07D221/02Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
    • C07D221/04Ortho- or peri-condensed ring systems
    • C07D221/06Ring systems of three rings
    • C07D221/16Ring systems of three rings containing carbocyclic rings other than six-membered
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
ARP980102859A 1997-06-17 1998-06-16 Novedosos inhibidores de sulfonamida de la farnesil-protein trasnferasa. AR012989A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US87705097A 1997-06-17 1997-06-17

Publications (1)

Publication Number Publication Date
AR012989A1 true AR012989A1 (es) 2000-11-22

Family

ID=25369146

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP980102859A AR012989A1 (es) 1997-06-17 1998-06-16 Novedosos inhibidores de sulfonamida de la farnesil-protein trasnferasa.

Country Status (14)

Country Link
EP (1) EP0989980A1 (fr)
JP (1) JP2002507192A (fr)
KR (1) KR20010013826A (fr)
CN (1) CN1267290A (fr)
AR (1) AR012989A1 (fr)
AU (1) AU8253698A (fr)
CA (1) CA2293358C (fr)
CO (1) CO4940475A1 (fr)
HU (1) HUP0004627A2 (fr)
IL (1) IL133393A0 (fr)
NZ (1) NZ501619A (fr)
PE (1) PE86199A1 (fr)
WO (1) WO1998057949A1 (fr)
ZA (1) ZA985218B (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6689789B2 (en) 1997-06-17 2004-02-10 Schering Corporation Compounds useful for inhibition of farnesyl protein transferase
US7517884B2 (en) 1998-03-30 2009-04-14 Kalypsys Inc. Sulfonyl-substituted bicyclic compounds as modulators of PPAR
US7342016B2 (en) 2000-08-30 2008-03-11 Schering Corporation Farnesyl protein transferase inhibitors as antitumor agents
EP1337522B1 (fr) * 2000-11-29 2007-08-29 Schering Corporation Inhibiteurs de farnesyl proteine transferase
CA2585172C (fr) 2004-10-29 2014-08-12 Kalypsys, Inc. Composes bicycliques a substitution sulfonyle, modulateurs des ppars
HUE040020T2 (hu) 2005-10-25 2019-02-28 Kalypsys Inc PPAR modulátorok sói és eljárások metabolikus betegségek kezelésére
WO2008091863A1 (fr) 2007-01-23 2008-07-31 Kalypsys, Inc. Composés bicycliques substitués par sulfonyle utilisés comme modulateurs de ppar dans le traitement de la stéatohépatite non alcoolique
US9796717B2 (en) * 2013-02-19 2017-10-24 Icahn School Of Medicine At Mount Sinai Tricyclic heterocycles as anticancer agents

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL111257A0 (en) * 1993-10-15 1994-12-29 Schering Corp Tricyclic sulfonamide compounds useful for inhibition of g-protein function and for treatment of proliferative diseases
IL117797A0 (en) * 1995-04-07 1996-08-04 Pharmacopeia Inc Tricyclic compounds useful for inhibition of G-protein function and for treatment of proliferative diseases
IL117798A (en) * 1995-04-07 2001-11-25 Schering Plough Corp Tricyclic compounds useful for inhibiting the function of protein - G and for the treatment of malignant diseases, and pharmaceutical preparations containing them

Also Published As

Publication number Publication date
ZA985218B (en) 1998-12-15
IL133393A0 (en) 2001-04-30
HUP0004627A2 (hu) 2001-10-28
PE86199A1 (es) 1999-09-24
CA2293358C (fr) 2008-08-05
NZ501619A (en) 2002-02-01
EP0989980A1 (fr) 2000-04-05
CA2293358A1 (fr) 1998-12-23
JP2002507192A (ja) 2002-03-05
CO4940475A1 (es) 2000-07-24
WO1998057949A1 (fr) 1998-12-23
KR20010013826A (ko) 2001-02-26
CN1267290A (zh) 2000-09-20
AU8253698A (en) 1999-01-04

Similar Documents

Publication Publication Date Title
Chesney et al. Effect of platelet-activating factor (PAF) on human platelets
Hanover et al. Synthesis of N-and O-linked glycopeptides in oviduct membrane preparations.
Naghshineh et al. Activation of adipocyte adenylate cyclase by protein kinase C.
MX9207449A (es) Inhibidores de la enzima proteolitica derivada de sacarina.
MX9206008A (es) Inhibidores de enzima proteolitica, derivados de sacarina 2-substituida.
TR199800825T2 (xx) Farnesil protein transferini inhibe eden (imidazol-5-il) metil-2-kinolinon t�revleri.
BR9814340A (pt) Derivados de indol como inibidores de fator xa
UA32556C2 (uk) (1r,4ar,8ar)-1,2,3,4,5,6,7,8-пергідроізохінолін-1- карбоніл-(l)-пролініл- (l)-аргінін альдегід для використання як антитромбового препарату і фармацевтична композиція на його основі
DE69432035D1 (de) Saccharinderivate als proteolytische Enzyminhibitoren
BR9713178A (pt) Inbidores espirocìclicos da metaloprotease.
Fenton et al. Biogenesis of the mitochondrial enzyme methylmalonyl-CoA mutase. Synthesis and processing of a precursor in a cell-free system and in cultured cells.
Malemud et al. Identification of neutral proteases in human neutrophil granules that degrade articular cartilage proteoglycan
BR0112337A (pt) Derivados de fosfolipìdeos de ácido valpróico e suas misturas
BR0317284A (pt) Inibidores aminocianopiridina de proteìna quinase-2 ativada com proteìna quinase ativada com mitógeno
AR012989A1 (es) Novedosos inhibidores de sulfonamida de la farnesil-protein trasnferasa.
EA200000240A1 (ru) Соединения, препятствующие эффекту раннего превращения лекарственных средств
Hope et al. Secretory phospholipase A2 inhibitors and calmodulin antagonists as inhibitors of cytosolic phospholipase A2
CO5011061A1 (es) Inhibicion de las metaloprotesas de matriz por acidos biariloxobutiricos sustituidos y composiciones farmaceuticas que los contienen
BR9913190A (pt) Modulação de proteìnas quinase de linhagemmúltipla
AR009809A1 (es) Derivados de 10,13,15-trioxatriciclo[9.2.1(9.6)]-pentadecanona, procedimientos para su preparacion y medicamentos que contienen estos compuestos
EA199800544A1 (ru) Тиольные производные, обладающие ингибирующей активностью в отношении металлопептидаз
ES2150461T3 (es) Derivados de amidinofenilalanina, proceso para su preparacion, su empleo y agentes que los contienen como anticoagulantes.
Keraly et al. Inhibition by ticlopidine of PAF-acether-induced in vitro aggregation of rabbit and human platelets
ATE299140T1 (de) Farnesyl-protein transferase inhibitoren
BR0308601A (pt) inibidores de carboxipeptidase b de plasma

Legal Events

Date Code Title Description
FB Suspension of granting procedure