BR9916314A - Tricyclic farnesyl transferase protein inhibitors - Google Patents
Tricyclic farnesyl transferase protein inhibitorsInfo
- Publication number
- BR9916314A BR9916314A BR9916314-4A BR9916314A BR9916314A BR 9916314 A BR9916314 A BR 9916314A BR 9916314 A BR9916314 A BR 9916314A BR 9916314 A BR9916314 A BR 9916314A
- Authority
- BR
- Brazil
- Prior art keywords
- group
- farnesyl transferase
- compounds
- protein inhibitors
- transferase protein
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/12—Heterocyclic 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 linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/14—Heterocyclic 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
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)
- Hematology (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Electroluminescent Light Sources (AREA)
Abstract
Patente de Invenção: <B>"INIBIDORES TRICìCLICOS DA PROTEìNA FARNESIL TRANSFERASE"<D>. Estão descritos compostos de fórmula (1.0) onde R^ 13^ representa um anel imidazol; R^ 14^ representa um grupo carbamato, uréia, amida ou sulfonamida; R^ 8^ representa H quando a cadeia alquila entre o grupo amida e o grupo imidazol R^ 13^ é substituída, ou R^ 8^ representa um substituinte tal como arilalquila, heteroarilalquila ou cicloalquila; e os outros substituintes são como definidos neste relatório. Também estão descritos compostos onde R^ 8^ é H, e a cadeia alquila entre o grupo amida e o grupo imidazol R^ 13^ é não-substituída. Também está descrito um método de tratamento de câncer e um método de inibição da proteína farnesil transferase usando os compostos descritos.Invention Patent: <B> "TRICYCLIC INHIBITORS OF PROTEIN FARNESIL TRANSFERASE" <D>. Compounds of formula (1.0) are described where R3 13 represents an imidazole ring; R ^ 14 ^ represents a carbamate, urea, amide or sulfonamide group; R ^ 8 ^ represents H when the alkyl chain between the amide group and the imidazole group R ^ 13 ^ is substituted, or R ^ 8 ^ represents a substituent such as arylalkyl, heteroarylalkyl or cycloalkyl; and the other substituents are as defined in this report. Also described are compounds where R ^8 8 is H, and the alkyl chain between the amide group and the imidazole group R ^13 ^ is unsubstituted. Also described is a method of treating cancer and a method of inhibiting the farnesyl transferase protein using the described compounds.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US21639898A | 1998-12-18 | 1998-12-18 | |
PCT/US1999/027939 WO2000037459A1 (en) | 1998-12-18 | 1999-12-16 | Tricyclic farnesyl protein transferase inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
BR9916314A true BR9916314A (en) | 2001-10-02 |
Family
ID=22806914
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR9916314-4A BR9916314A (en) | 1998-12-18 | 1999-12-16 | Tricyclic farnesyl transferase protein inhibitors |
Country Status (20)
Country | Link |
---|---|
EP (1) | EP1140902A1 (en) |
JP (1) | JP2002533336A (en) |
KR (1) | KR20010081116A (en) |
CN (1) | CN1326850C (en) |
AR (1) | AR021718A1 (en) |
AU (1) | AU776558B2 (en) |
BR (1) | BR9916314A (en) |
CA (1) | CA2354779A1 (en) |
CO (1) | CO5160350A1 (en) |
CZ (1) | CZ20011950A3 (en) |
HU (1) | HUP0202152A2 (en) |
IL (1) | IL143408A0 (en) |
NO (1) | NO20012961L (en) |
NZ (1) | NZ511878A (en) |
PE (1) | PE20001342A1 (en) |
PL (1) | PL348293A1 (en) |
SK (1) | SK7592001A3 (en) |
TR (1) | TR200101755T2 (en) |
WO (1) | WO2000037459A1 (en) |
ZA (1) | ZA200104233B (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU776558B2 (en) | 1998-12-18 | 2004-09-16 | Schering Corporation | Tricyclic farnesyl protein transferase inhibitors |
US7342016B2 (en) | 2000-08-30 | 2008-03-11 | Schering Corporation | Farnesyl protein transferase inhibitors as antitumor agents |
US6645966B2 (en) | 2001-01-22 | 2003-11-11 | Schering Corporation | Treatment of malaria with farnesyl protein transferase inhibitors |
WO2002080895A2 (en) * | 2001-04-06 | 2002-10-17 | Schering Corporation | Treatment of malaria with farsenyl protein transferase inhibitors |
CA2590979A1 (en) * | 2004-12-13 | 2006-06-22 | Schering Corporation | Novel farnesyl protein transferase inhibitors and their use to treat cancer |
CN101128202A (en) | 2004-12-14 | 2008-02-20 | 先灵公司 | Farnesyl protein transferase inhibitors and methods for treating proliferative diseases |
WO2007084498A1 (en) * | 2006-01-19 | 2007-07-26 | Schering Corporation | Piperazine derivatives as farnesyl protein transferase inhibitors |
US9988365B2 (en) | 2014-03-19 | 2018-06-05 | Vps-3, Inc. | 2-(2,4-difluorophenyl)-1,1-difluoro-1-(5-substituted-pyridin-2-yl)-3-(1H-tetrazol-1-yl)propan-2-ols and processes for their preparation |
KR102441242B1 (en) * | 2014-03-19 | 2022-09-07 | 브이피에스-3, 엘엘씨 | 2-(2,4-difluorophenyl)-1,1-difluoro-1-(5-substituted-pyridin-2-yl)-3-(1h-tetrazol-1-yl)propan-2-ols and processes for their preparation |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL111235A (en) * | 1993-10-15 | 2001-03-19 | Schering Plough Corp | Pharmaceutical compositions for inhibition of g-protein function and for treatment of proliferative diseases containing tricyclic compounds some such compounds and process for preparing part of them |
IL117798A (en) * | 1995-04-07 | 2001-11-25 | Schering Plough Corp | Tricyclic compounds useful for inhibition of g-protein function and for treatment of proliferative diseases and pharmaceutical compositions comprising them |
US5801175A (en) * | 1995-04-07 | 1998-09-01 | Schering Corporation | Tricyclic compounds useful for inhibition of G-protein function and for treatment of proliferative diseases |
US5712280A (en) * | 1995-04-07 | 1998-01-27 | Schering Corporation | Tricyclic compounds useful for inhibition of G-protein function and for treatment of proliferative diseases |
PE92098A1 (en) * | 1996-07-31 | 1998-12-31 | Schering Corp | TRICYCLIC N-CYANOIMINES USEFUL AS PROTEIN TRANSFERASE INHIBITORS FARNESILO |
EP0989983B1 (en) * | 1997-06-17 | 2004-08-11 | Schering Corporation | Benzpyrido cycloheptane compounds useful for inhibition of farnesyl protein transferase |
AU776558B2 (en) | 1998-12-18 | 2004-09-16 | Schering Corporation | Tricyclic farnesyl protein transferase inhibitors |
-
1999
- 1999-12-16 AU AU20307/00A patent/AU776558B2/en not_active Ceased
- 1999-12-16 TR TR2001/01755T patent/TR200101755T2/en unknown
- 1999-12-16 SK SK759-2001A patent/SK7592001A3/en unknown
- 1999-12-16 BR BR9916314-4A patent/BR9916314A/en not_active IP Right Cessation
- 1999-12-16 CA CA002354779A patent/CA2354779A1/en not_active Abandoned
- 1999-12-16 CN CNB99816206XA patent/CN1326850C/en not_active Expired - Fee Related
- 1999-12-16 CO CO99078843A patent/CO5160350A1/en unknown
- 1999-12-16 EP EP99963980A patent/EP1140902A1/en not_active Withdrawn
- 1999-12-16 KR KR1020017007632A patent/KR20010081116A/en active IP Right Grant
- 1999-12-16 NZ NZ511878A patent/NZ511878A/en unknown
- 1999-12-16 PL PL99348293A patent/PL348293A1/en not_active Application Discontinuation
- 1999-12-16 HU HU0202152A patent/HUP0202152A2/en unknown
- 1999-12-16 IL IL14340899A patent/IL143408A0/en unknown
- 1999-12-16 JP JP2000589531A patent/JP2002533336A/en active Pending
- 1999-12-16 WO PCT/US1999/027939 patent/WO2000037459A1/en active Application Filing
- 1999-12-16 CZ CZ20011950A patent/CZ20011950A3/en unknown
- 1999-12-16 AR ARP990106461A patent/AR021718A1/en unknown
- 1999-12-17 PE PE1999001295A patent/PE20001342A1/en not_active Application Discontinuation
-
2001
- 2001-05-23 ZA ZA200104233A patent/ZA200104233B/en unknown
- 2001-06-15 NO NO20012961A patent/NO20012961L/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
CO5160350A1 (en) | 2002-05-30 |
NO20012961L (en) | 2001-08-16 |
CZ20011950A3 (en) | 2001-12-12 |
CN1334811A (en) | 2002-02-06 |
TR200101755T2 (en) | 2001-09-21 |
IL143408A0 (en) | 2002-04-21 |
CA2354779A1 (en) | 2000-06-29 |
HUP0202152A2 (en) | 2002-10-28 |
NZ511878A (en) | 2003-10-31 |
NO20012961D0 (en) | 2001-06-15 |
ZA200104233B (en) | 2002-08-22 |
SK7592001A3 (en) | 2002-03-05 |
WO2000037459A1 (en) | 2000-06-29 |
AU776558B2 (en) | 2004-09-16 |
AR021718A1 (en) | 2002-07-31 |
PE20001342A1 (en) | 2000-12-09 |
CN1326850C (en) | 2007-07-18 |
EP1140902A1 (en) | 2001-10-10 |
JP2002533336A (en) | 2002-10-08 |
PL348293A1 (en) | 2002-05-20 |
AU2030700A (en) | 2000-07-12 |
KR20010081116A (en) | 2001-08-27 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE A 5O, 6O E 7O ANUIDADES. |
|
B08K | Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette] |
Free format text: REFERENTE AO DESPACHO 8.6 PUBLICADO NA RPI 1913 DE 04/09/2007. |