ES2190199T3 - Agentes anti-tumorales. - Google Patents
Agentes anti-tumorales.Info
- Publication number
- ES2190199T3 ES2190199T3 ES99909099T ES99909099T ES2190199T3 ES 2190199 T3 ES2190199 T3 ES 2190199T3 ES 99909099 T ES99909099 T ES 99909099T ES 99909099 T ES99909099 T ES 99909099T ES 2190199 T3 ES2190199 T3 ES 2190199T3
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- hydrogen
- tumor agents
- akanesulphonyloxy
- alkanesulphonyloxy
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—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
- 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
- C07D295/135—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 separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C219/00—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C219/34—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having amino groups and esterified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (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)
- Steroid Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Saccharide Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
Un agente anti - tumoral de la fórmula I **(Fórmula)** en la cual R1 es hidrógeno, (1 - 4C)alquilo, (3 - 4C) - alquenilo, (3 - 4C)alquinilo, hidroxi - (1 - 4C)alquilo, (1 - 4C)alcoxi - (1 - 4C)alquilo, amino - (1 - 4C)alquilo, (1 - 4C) - alquilamino - (1 - 4C)alquilo, di [(1 - 4C)alquil]amino - (1 - 4C) - alquilo, pirrolidin - 1 - il - (1 - 4C)alquilo, piperidino - (1 - 4C)alquilo, morfolino - (1 - 4C)alquilo, piperazin - 1 - il - (1 - 4C)alquilo, 4 - (1 - 4C)alquilpiperazin - 1 - il - (1 4C)alquilo, carboxi - (1 - 4C)alquilo, (1 - 4C)alcoxicarbonil - (1 - 4C) - alquilo, carbamoil - (1 - 4C) alquilo, N - (1 - 4C)alquil - carbamoil - (1 - 4C)alquilo, N, N - di - [(1 - 4C)alquil]carbamoil - (1 - 4C)alquilo, amino, (1 - 4C)alquilamino, (3 - 4C)alquenil - amino, (3 - 4C) alquinilamino, di - [(1 - 4C)alquil]amino, di - [(3 4C)alquenil]amino, di - [(3 - 4C)alquinil]amino, pirrol - idin - 1 - ilo, piperidino, morfolino, piperazin - 1 ilo, 4 - (1 - 4C) alquilpiperazin - 1 - ilo, hidroxi - (2 - 4C)alquilamino, (1 - 4C)alcoxi - (2 - 4C)alquilamino, amino - (2 - 4C)alquilamino, (1 - 4C)alquilamino - (2 - 4C)alquilamino, di - [(1 - 4C)alquil]amino - (2 4C)alquilamino, pirrolidin - 1 - il - (2 - 4C)alquilamino, piperidino - (2 - 4C)alquilamino, morfolino (2 - 4C)alquilamino, piperazin - 1 - il - (2 - 4)alquilamino, 4 - (1 - 4)alquil - piperazin - 1 - il - (2 4C)alquilamino, (2 - 4C)alcanoilamino, (2 - 4C)alcanoilamino - (2 - 4C)alquilamino, carboxi - (1 - 4C) alquilamino, (1 - 4C)alcoxicarbonil - (1 - 4C) - alquilamino, carbamoil - (1 - 4C)alquilamino, N - (1 4C)alquilcarbamoil - (1 - 4C)alquilamino, N, N - di - [(1 - 4C)alquil]carbamoil - (1 - 4C) - alquilamino, hidroxi, (1 - 4C) - alcoxi, hidroxi - (2 - 4C) - alcoxi, (1 - 4C)alcoxi - (2 - 4C)alcoxi, amino - (2 - 4C)alcoxi, (1 - 4C)alquilamino - (2 - 4C)alcoxi, di - [(1 - 4C)alquil]amino - (2 - 4C)alcoxi, pirrolidin - 1 - il - (2 4C)alcoxi, piperidino - (2 - 4C)alcoxi, morfolino - (2 - 4C)alcoxi, piperazin - 1 - il - (2 - 4C)alcoxi o 4 -(1 - 4C)alquilpiperazin - 1 - il - (2 - 4C)alcoxi; R2 es hidrógeno, (1 - 4C)alquilo, (3 - 4C)alquenilo, (3 - 4C) - alquinilo, hidroxi - (1 - 4C)alquilo, (1 4C)alcoxi - (1 - 4C) - alquilo, amino - (1 - 4C)alquilo, (1 - 4C)alquilamino - (1 - 4C) - alquilo, di [(1 - 4C)alquil]amino - (1 - 4C)alquilo, pirrolidin - 1 - il - (1 - 4C)alquilo, piperidino - (1 - 4C)alquilo, morfolino - (1 - 4C)alquilo, piperazin - 1 - il - (1 - 4C)alquilo, 4 - (1 - 4C)alquilpiperazin - 1 - il - (1 4C)alquilo, carboxi - (1 - 4C) - alquilo, (1 - 4C)alcoxicarbonil - (1 - 4C)alquilo, carbamoil - (1 - 4C)alquilo, N - (1 - 4C)alquilcarbamoil - (1 - 4C)alquilo, N, N - di - [(1 - 4C)alquil]carbamoil - (1 - 4C)alquilo, amino, (1 - 4C)alquilamino, (3 - 4C)alquenilamino, (3 - 4C)alquinilamino, di - [(1 - 4C)alquil]amino, di - [(3 4C)alquenil]amino, di - [(3 - 4C)alquinil]amino, pirrolidin - 1 - ilo, piperidino, morfolino, piperazin - 1 - ilo, 4 - (1 - 4C)alquilpiperazin - 1 - ilo, hidroxi - (2 - 4C)alquilamino, (1 - 4C)alcoxi- (2 - 4C) - alquilamino, amino - (2 - 4C)alquilamino, (1 - 4C)alquilamino - (2 - 4C)alquilamino, di - [(1 - 4C)alquil]amino (2 - 4C)alquil - amino, pirrolidin - 1 - il - (2 - 4C)alquilamino, piperidino - (2 - 4C)alquilamino, morfolino - (2 - 4C)alquilamino, piperazin - 1 - il - (2 - 4C)alquilamino, 4 - (1 - 4C)alquilpiperazin 1 - il - (2 - 4C)alquilamino, (2 - 4C)alcanoilamino, (2 - 4C)alcanoilamino - (2 - 4C)alquilamino, carboxi (1 - 4C)alquilamino, (1 - 4C) - alcoxicarbonil - (1 - 4C)alquilamino, carbamoil - (1 - 4C)alquil - amino, N - (1 - 4C)alquilcarbamoil - (1 - 4C)alquilamino, , N - di - [(1 - 4C)alquil]carbamoil - (1 - 4C)alquilamino, hidroxi, (1 - 4C)alcoxi, hidroxi - (2 - 4C)alcoxi, (1 - 4C)alcoxi - (2 - 4C) - alcoxi, amino - (2 - 4C)alcoxi, (1 - 4C)alquilamino - (2 - 4C) - alcoxi, di - [(1 - 4C)alquil]amino - (2 - 4C)alcoxi, pirrolidin - 1 - il - (2 4C)alcoxi, piperidino - (2 - 4C)alcoxi, morfolino - (2 - 4C)alcoxi, piperazin - 1 - il - (2 - 4C)alcoxi o 4 - (1 - 4C) - alquilpiperazin - 1 - il - (2 - 4C)alcoxi; R3 es hidrógeno, (1 - 4C)alquilo, (3 - 4C)alquenilo, (3 - 4C) - alquinilo, hidroxi - (1 - 4C)alquilo, (1 4C)alcoxi - (1 - 4C) - alquilo, amino - (1 - 4C)alquilo, (1 - 4C)alquilamino - (1 - 4C) - alquilo, di [(1 - 4C)alquil]amino - (1 - 4C)alquilo, pirrolidin - 1 - il - (1 - 4C)alquilo, piperidino - (1 - 4C)alquilo, morfolino - (1 - 4C)alquilo, piperazin - 1 - il - (1 - 4C)alquilo, 4 - (1 - 4C)alquilpiperazin - 1 - il - (1 4C)alquilo, carboxi - (1 - 4C) - alquilo, (1 - 4C)alcoxicarbonil - (1 - 4C)alquilo, carbamoil - (1 - 4C)alquilo, N - (1 - 4C)alquilcarbamoil - (1 - 4C)alquilo, N, N - di - [(1 - 4C)alquil]carbamoil - (1 - 4C)alquilo, amino, (1 - 4C) - alquilamino, (3 - 4C)alquenilamino, (3 - 4C)alquinilamino, di - [(1 - 4C)alquil]amino, di - [(3 4C)alquenil]amino, di - [(3 - 4C)alquinil]amino, pirrolidin - 1 - ilo, piperidino, morfolino, piperazin - 1 - ilo, 4 - (1 - 4C)alquilpiperazin - 1 - ilo, hidroxi - (2 - 4C)alquilamino, (1 - 4C)alcoxi - (2 - 4C)alquilamino, amino - (2 - 4C)alquilamino, (1 - 4C)alquilamino - (2 - 4C)alquilamino, di - [(1 - 4C)alquil]amino (2 - 4C)alquilamino, pirrolidin - 1 - il - (2 - 4C)alquilamino, piperidino - (2 - 4C)alquilamino, morfolino - (2 - 4C)alquilamino, piperazin - 1 - il - (2 - 4C)alquilamino, 4 - (1 - 4C)alquilpiperazin - 1 - il (2 - 4C)alquilamino, (2 - 4C)alcanoilamino, (2 - 4C)alcanoilamino - (2 - 4C)alquilamino, carboxi - (1 4C)alquilamino, (1 - 4C)alcoxicarbonil - (1 - 4C)alquilamino, carbamoil - (1 - 4C)alquilamino, N - (1 4C) - alquilcarbamoil - (1 - 4C)alquilamino, N, N - di - [(1 - 4C) - alquil]carbamoil - (1 - 4C)alquilamino, hidroxi, (1 - 4C)alcoxi, hidroxi - (2 - 4C)alcoxi, (1 - 4C)alcoxi - (2 - 4C)alcoxi, amino - (2 - 4C)alcoxi, (1 - 4C)alquilamino - (2 - 4C)alcoxi, di - [(1 - 4C)alquil]amino - (2 - 4C)alcoxi, pirrolidin - 1 - il - (2 4C)alcoxi, piperidino - (2 - 4C)alcoxi, morfolino - (2 - 4C)alcoxi, piperazin - 1 - il - (2 - 4C)alcoxi o 4 - (1 - 4C)alquilpiperazin - 1 - il - (2 - 4C)alcoxi; R4 es (1 - 4C)alquilo; R5 es (1 - 4C)alquilo; R6 es hidrógeno o (1 - 4C)alquilo; R7 es hidrógeno o (1 - 4C)alquilo; X es oxígeno; m es 1 ó 2 y cada R8 es independientemente hidrógeno, halógeno, hidroxi, (1 - 4C)alcoxi, (2 4C)alqueniloxi, (2 - 4C) - alquiniloxi, (1 - 4C)alquilo, (3 - 4C)alquenilo, (3 - 4C) - alquinilo, amino, (1 - 4C)alquilamino, di - [(1 - 4C)alquil] - amino, ciano, (2 - 4C alcanoilamino, carboxi, (1 - 4C)alcoxi carbonilo, carbamoílo, N - (1 - 4C)alquilcarbamoílo o N, N - di - [(1 - 4C)alquil]carbamoílo; Y1 es halógeno, (1 - 4C)alcanosulfoniloxi, bencenosulfonil - oxi o fenil - (1 - 4C)alcanosulfoniloxi; e Y2 es halógeno, (1 - 4C)alcanosulfoniloxi, bencenosulfonil - oxi o fenil - (1 - 4C)alcanosulfoniloxi; y en la cual cualquier grupo heterocíclico en R1, R2 o R3 está sustituido opcionalmente con 1, 2 ó 3 sustituyentes (1 - 4C)alquilo, y en la cual cualquier grupo fenilo en Y1 o Y2 cuando Y1 e Y2 es bencenosulfoniloxi o fenil - (1 - 4C)alcanosulfoniloxi está sustituido opcionalmente con 1, 2 ó 3 sustituyentes seleccionados de halógeno, nitro, ciano, trifluorometilo, hidroxi, amino, (1 - 4C)alquilo, (1 - 4C)alcoxi, (1 - 4C)alquilamino y di - [(1 - 4C)alquil]amino; o una de sus sales farmacéuticamente aceptables; con la condición de que al menos uno de R1, R2, y R3 es distinto de hidrógeno.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB9805866.2A GB9805866D0 (en) | 1998-03-20 | 1998-03-20 | Anti-tumour agents |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2190199T3 true ES2190199T3 (es) | 2003-07-16 |
Family
ID=10828858
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES99909099T Expired - Lifetime ES2190199T3 (es) | 1998-03-20 | 1999-03-16 | Agentes anti-tumorales. |
Country Status (18)
Country | Link |
---|---|
US (1) | US6346633B1 (es) |
EP (1) | EP1064253B1 (es) |
JP (1) | JP2002507590A (es) |
KR (1) | KR20010042055A (es) |
CN (1) | CN1293654A (es) |
AT (1) | ATE231835T1 (es) |
AU (1) | AU756651B2 (es) |
BR (1) | BR9908932A (es) |
CA (1) | CA2324361A1 (es) |
DE (1) | DE69905142T2 (es) |
DK (1) | DK1064253T3 (es) |
ES (1) | ES2190199T3 (es) |
GB (1) | GB9805866D0 (es) |
IL (1) | IL138589A (es) |
NO (1) | NO20004662L (es) |
NZ (1) | NZ505856A (es) |
WO (1) | WO1999048857A1 (es) |
ZA (1) | ZA200004387B (es) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9805868D0 (en) | 1998-03-20 | 1998-05-13 | Zeneca Ltd | Anti-tumour agents |
US20060099712A1 (en) * | 2004-11-08 | 2006-05-11 | Eastman Kodak Company | Correlation of anti-cancer activity of dyes with redox potentials |
BR112018076639A2 (pt) * | 2016-06-27 | 2019-04-02 | Systems Oncology, Llc | quimioterapias de combinação |
US20220185785A1 (en) * | 2019-04-12 | 2022-06-16 | TONIX Pharmaceuticals Holding Corp | Inhibitors of cd40-cd154 binding |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2862107D1 (en) | 1977-12-02 | 1982-11-18 | Takeda Chemical Industries Ltd | Glucosamine-peptide derivatives and their pharmaceutical compositions |
JPS58177934A (ja) * | 1982-04-13 | 1983-10-18 | Takeda Chem Ind Ltd | ベンゾキノン誘導体 |
NZ240785A (en) * | 1991-11-28 | 1995-08-28 | Cancer Res Campaign Tech | Substituted nitro aniline derivatives and medicaments |
GB9805868D0 (en) | 1998-03-20 | 1998-05-13 | Zeneca Ltd | Anti-tumour agents |
-
1998
- 1998-03-20 GB GBGB9805866.2A patent/GB9805866D0/en not_active Ceased
-
1999
- 1999-03-16 IL IL13858999A patent/IL138589A/en not_active IP Right Cessation
- 1999-03-16 CA CA002324361A patent/CA2324361A1/en not_active Abandoned
- 1999-03-16 KR KR1020007010399A patent/KR20010042055A/ko not_active Application Discontinuation
- 1999-03-16 BR BR9908932-7A patent/BR9908932A/pt not_active IP Right Cessation
- 1999-03-16 US US09/646,459 patent/US6346633B1/en not_active Expired - Fee Related
- 1999-03-16 DE DE69905142T patent/DE69905142T2/de not_active Expired - Fee Related
- 1999-03-16 NZ NZ505856A patent/NZ505856A/xx unknown
- 1999-03-16 DK DK99909099T patent/DK1064253T3/da active
- 1999-03-16 EP EP99909099A patent/EP1064253B1/en not_active Expired - Lifetime
- 1999-03-16 AU AU28468/99A patent/AU756651B2/en not_active Ceased
- 1999-03-16 AT AT99909099T patent/ATE231835T1/de not_active IP Right Cessation
- 1999-03-16 JP JP2000537842A patent/JP2002507590A/ja active Pending
- 1999-03-16 CN CN99804243A patent/CN1293654A/zh active Pending
- 1999-03-16 WO PCT/GB1999/000787 patent/WO1999048857A1/en not_active Application Discontinuation
- 1999-03-16 ES ES99909099T patent/ES2190199T3/es not_active Expired - Lifetime
-
2000
- 2000-08-24 ZA ZA200004387A patent/ZA200004387B/xx unknown
- 2000-09-19 NO NO20004662A patent/NO20004662L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
EP1064253A1 (en) | 2001-01-03 |
ATE231835T1 (de) | 2003-02-15 |
DK1064253T3 (da) | 2003-06-23 |
ZA200004387B (en) | 2001-10-31 |
GB9805866D0 (en) | 1998-05-13 |
DE69905142T2 (de) | 2003-10-16 |
EP1064253B1 (en) | 2003-01-29 |
US6346633B1 (en) | 2002-02-12 |
BR9908932A (pt) | 2005-10-25 |
JP2002507590A (ja) | 2002-03-12 |
NZ505856A (en) | 2002-09-27 |
CA2324361A1 (en) | 1999-09-30 |
KR20010042055A (ko) | 2001-05-25 |
NO20004662D0 (no) | 2000-09-19 |
NO20004662L (no) | 2000-11-17 |
AU756651B2 (en) | 2003-01-16 |
DE69905142D1 (de) | 2003-03-06 |
IL138589A (en) | 2004-08-31 |
CN1293654A (zh) | 2001-05-02 |
IL138589A0 (en) | 2001-10-31 |
WO1999048857A1 (en) | 1999-09-30 |
AU2846899A (en) | 1999-10-18 |
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