UY26038A1 - Difenilureas w-carboxiarilicas sustituidas como inhibidoras de la raf-quinasa - Google Patents
Difenilureas w-carboxiarilicas sustituidas como inhibidoras de la raf-quinasaInfo
- Publication number
- UY26038A1 UY26038A1 UY26038A UY26038A UY26038A1 UY 26038 A1 UY26038 A1 UY 26038A1 UY 26038 A UY26038 A UY 26038A UY 26038 A UY26038 A UY 26038A UY 26038 A1 UY26038 A1 UY 26038A1
- Authority
- UY
- Uruguay
- Prior art keywords
- substituted
- group
- raf
- members
- aryl
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- -1 aryl ureas Chemical class 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 102000009929 raf Kinases Human genes 0.000 abstract 2
- 108010077182 raf Kinases Proteins 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 239000011593 sulfur Substances 0.000 abstract 2
- UDXPZWPTWCVPCT-UHFFFAOYSA-N 3-[4-(carbamoylamino)phenoxy]-N-methylbenzamide Chemical compound CNC(=O)C1=CC=CC(OC=2C=CC(NC(N)=O)=CC=2)=C1 UDXPZWPTWCVPCT-UHFFFAOYSA-N 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 235000013877 carbamide Nutrition 0.000 abstract 1
- 230000010261 cell growth Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
Classifications
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- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/192—Radicals derived from carboxylic acids from aromatic carboxylic acids
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- A61K31/17—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
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- A61K31/235—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids having an aromatic ring attached to a carboxyl group
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- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
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- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/13—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
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Abstract
Compuestos que son inhibidores de la enzima raf-quinasa, que se describen en general como ureas arílicas, incluyendo análogos tanto arílicos como heteroarílicos, que inhiben el pasaje de la raf-quinasa. Así pues, el invento se refiere a compuestos, composiciones y métodos para el tratamiento del crecimiento de las células cancerosas trasmitido por la raf-quinasa cuando se administra un compuesto de fórmula (I): A-D-B o una sal farmacéutica aceptable del mismo, en donde: D es NH-C(O)-NH, A es una porción sustituida de hasta 40 átomos de carbono de la fórmula: L-(M-L1)q, donde L es una estructura cíclica de 5 o 6 miembro unida directamente a D, L1 comprende una parte cíclica sustituida con al menos 5 miembros, M es un grupo de puente que tiene al menos un átomo, q es un entero de 1 a 3, y cada estructura cíclica de L y L1 contiene 0 a 4 miembros del grupo que consta de nitrógeno, oxígeno y azufre; B es una porción arílica o heteroarílica sustituida o no, que puede ser hasta tricíclica, de hasta 30 átomos de carbono con al menos una estructura cíclica de 6 miembros unida directamente a D que contiene 0 a 4 miembros del grupo que consta de notrógeno, oxígeno y azufre, donde L1 es sustituida por al menos un sustituyente seleccionado dentro del grupo que consta de SO2Rx, C(O)Rx y C(NRy)Rz. Por ejemplo: N-(3-ter-butilfenil)-N'-(4-(3-(N-metilcarbamoil)fenoxi)fenilurea.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
UY0001032230A UY32230A (es) | 1999-02-25 | 2009-11-09 | Difenilureas (omega)-carboxiarilicas sustituidas como inhibidoras de la raf-quinasa |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US25726699A | 1999-02-25 | 1999-02-25 | |
US42522899A | 1999-10-22 | 1999-10-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
UY26038A1 true UY26038A1 (es) | 2000-09-29 |
Family
ID=38812171
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UY26038A UY26038A1 (es) | 1999-02-25 | 2000-02-25 | Difenilureas w-carboxiarilicas sustituidas como inhibidoras de la raf-quinasa |
UY0001032230A UY32230A (es) | 1999-02-25 | 2009-11-09 | Difenilureas (omega)-carboxiarilicas sustituidas como inhibidoras de la raf-quinasa |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UY0001032230A UY32230A (es) | 1999-02-25 | 2009-11-09 | Difenilureas (omega)-carboxiarilicas sustituidas como inhibidoras de la raf-quinasa |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP1690853B1 (es) |
CA (1) | CA2549558C (es) |
DK (1) | DK1690853T3 (es) |
SI (2) | SI1690853T1 (es) |
UA (1) | UA73731C2 (es) |
UY (2) | UY26038A1 (es) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2002353147A1 (en) * | 2001-12-13 | 2003-06-30 | Abbott Laboratories | 3-(phenyl-alkoxy)-5-(phenyl)-pyridine derivatives and related compounds as kinase inhibitors for the treatment of cancer |
CA2824028A1 (en) * | 2011-01-06 | 2012-07-12 | Beta Pharma Canada Inc. | Novel ureas for the treatment and prevention of cancer |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH479557A (de) * | 1961-09-11 | 1969-10-15 | Wander Ag Dr A | Verfahren zur Herstellung neuer mehrbasischer Verbindungen |
CH575208A5 (es) | 1973-07-30 | 1976-05-14 | Ciba Geigy Ag | |
JPS57185219A (en) * | 1981-05-12 | 1982-11-15 | Chugai Pharmaceut Co Ltd | Remedy for cancer |
JPH0222650A (ja) * | 1988-07-11 | 1990-01-25 | Konica Corp | ハロゲン化銀カラー写真感光材料 |
JPH0223337A (ja) * | 1988-07-12 | 1990-01-25 | Konica Corp | 新規なカプラーを含有するハロゲン化銀写真感光材料 |
US4973675A (en) * | 1989-04-13 | 1990-11-27 | University Of Tennessee Research Center | Hybrid nitrosoureidoanthracyclines having antitumor activity |
FR2683818B1 (fr) | 1991-11-14 | 1993-12-31 | Adir Cie | Nouveaux derives de 3-sulfonylamino-2-(1h)-quinoleinone, leur procede de preparation et les compositions pharmaceutiques qui les contiennent. |
US5447957A (en) * | 1994-06-02 | 1995-09-05 | Smithkline Beecham Corp. | Anti-inflammatory compounds |
WO1995033458A1 (en) * | 1994-06-02 | 1995-12-14 | Smithkline Beecham Corporation | Anti-inflammatory compounds |
AU7340096A (en) * | 1995-11-07 | 1997-05-29 | Kirin Beer Kabushiki Kaisha | Quinoline derivatives and quinazoline derivatives inhibiting autophosphorylation of growth factor receptor originating in platelet and pharmaceutical compositions containing the same |
CZ59398A3 (cs) | 1996-06-29 | 1998-07-15 | Samjin Pharmaceutical Co., Ltd. | Piperazinové deriváty a způsob jejich přípravy |
WO1998052559A1 (en) * | 1997-05-23 | 1998-11-26 | Bayer Corporation | Raf kinase inhibitors |
JP4344960B2 (ja) * | 1997-05-23 | 2009-10-14 | バイエル、コーポレイション | アリール尿素によるp38キナーゼ活性の阻害 |
AU9802198A (en) * | 1997-10-21 | 1999-05-10 | Pharmacia & Upjohn Company | Antiinflammatory thiadiazolyl ureas which act as lfa-1 and mac-1 inhibitors |
SK286564B6 (sk) * | 1997-12-22 | 2009-01-07 | Bayer Corporation | Substituované arylmočoviny ako inhibítory rafkinázy a farmaceutický prípravok s ich obsahom |
JP4403482B2 (ja) * | 1997-12-22 | 2010-01-27 | バイエル コーポレイション | 置換複素環尿素合成のための中間体およびその製造方法 |
AU762077B2 (en) * | 1997-12-22 | 2003-06-19 | Bayer Healthcare Llc | Inhibition of p38 kinase activity using aryl and heteroaryl substituted heterocyclic ureas |
DK1042305T3 (da) * | 1997-12-22 | 2005-09-19 | Bayer Pharmaceuticals Corp | Inhibering af p38-kinase ved anvendelse af symmetriske og asymmetriske diphenylurinstoffer |
ES2377847T3 (es) * | 1999-01-13 | 2012-04-02 | Bayer Healthcare Llc | Difenil ureas sustituidas con omega-carboxi arilo como agentes inhibidores de la cinasa p38 |
-
2000
- 2000-01-12 EP EP05028442A patent/EP1690853B1/en not_active Expired - Lifetime
- 2000-01-12 DK DK05028442.1T patent/DK1690853T3/da active
- 2000-01-12 SI SI200031058T patent/SI1690853T1/sl unknown
- 2000-01-12 CA CA2549558A patent/CA2549558C/en not_active Expired - Lifetime
- 2000-01-12 SI SI200030837T patent/SI1140840T1/sl unknown
- 2000-02-25 UY UY26038A patent/UY26038A1/es not_active IP Right Cessation
- 2000-12-01 UA UA2001075426A patent/UA73731C2/uk unknown
-
2009
- 2009-11-09 UY UY0001032230A patent/UY32230A/es unknown
Also Published As
Publication number | Publication date |
---|---|
UA73731C2 (en) | 2005-09-15 |
CA2549558C (en) | 2010-08-31 |
SI1140840T1 (sl) | 2006-06-30 |
UY32230A (es) | 2010-06-30 |
SI1690853T1 (sl) | 2010-07-30 |
CA2549558A1 (en) | 2000-07-20 |
EP1690853A1 (en) | 2006-08-16 |
EP1690853B1 (en) | 2010-03-10 |
DK1690853T3 (da) | 2010-06-07 |
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