CL2011000273A1 - Uso de un inhibidor de la enzima fosfohidrolasa de acido fosfatidico (pap) o combinacion de inhibidores, en que el inhibidor es d(+) propranolol, y la combinacion es mezcla racemica de propranolol o d(+) propranolol junto con desipramina, para preparar un medicamento util en el tratamiento del cancer. - Google Patents
Uso de un inhibidor de la enzima fosfohidrolasa de acido fosfatidico (pap) o combinacion de inhibidores, en que el inhibidor es d(+) propranolol, y la combinacion es mezcla racemica de propranolol o d(+) propranolol junto con desipramina, para preparar un medicamento util en el tratamiento del cancer.Info
- Publication number
- CL2011000273A1 CL2011000273A1 CL2011000273A CL2011000273A CL2011000273A1 CL 2011000273 A1 CL2011000273 A1 CL 2011000273A1 CL 2011000273 A CL2011000273 A CL 2011000273A CL 2011000273 A CL2011000273 A CL 2011000273A CL 2011000273 A1 CL2011000273 A1 CL 2011000273A1
- Authority
- CL
- Chile
- Prior art keywords
- propranolol
- inhibitor
- combination
- pap
- cancer
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 4
- 206010028980 Neoplasm Diseases 0.000 title abstract 2
- 102000001107 Phosphatidate Phosphatase Human genes 0.000 title abstract 2
- 108010069394 Phosphatidate Phosphatase Proteins 0.000 title abstract 2
- 201000011510 cancer Diseases 0.000 title abstract 2
- AQHHHDLHHXJYJD-CQSZACIVSA-N (R)-(+)-propranolol Chemical group C1=CC=C2C(OC[C@H](O)CNC(C)C)=CC=CC2=C1 AQHHHDLHHXJYJD-CQSZACIVSA-N 0.000 title 2
- AQHHHDLHHXJYJD-UHFFFAOYSA-N propranolol Chemical compound C1=CC=C2C(OCC(O)CNC(C)C)=CC=CC2=C1 AQHHHDLHHXJYJD-UHFFFAOYSA-N 0.000 title 2
- HCYAFALTSJYZDH-UHFFFAOYSA-N Desimpramine Chemical compound C1CC2=CC=CC=C2N(CCCNC)C2=CC=CC=C21 HCYAFALTSJYZDH-UHFFFAOYSA-N 0.000 title 1
- 229960003914 desipramine Drugs 0.000 title 1
- 239000003814 drug Substances 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- 229960003712 propranolol Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/133—Amines having hydroxy groups, e.g. sphingosine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
- A61K31/138—Aryloxyalkylamines, e.g. propranolol, tamoxifen, phenoxybenzamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
- A61K31/366—Lactones having six-membered rings, e.g. delta-lactones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/5415—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with carbocyclic ring systems, e.g. phenothiazine, chlorpromazine, piroxicam
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Uso de compuestos inhibidores de la enzima fosfohidrolasa de acido fosfatídico (PAP); su uso en el tratamiento del cáncer.
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CL2011000273A CL2011000273A1 (es) | 2011-02-08 | 2011-02-08 | Uso de un inhibidor de la enzima fosfohidrolasa de acido fosfatidico (pap) o combinacion de inhibidores, en que el inhibidor es d(+) propranolol, y la combinacion es mezcla racemica de propranolol o d(+) propranolol junto con desipramina, para preparar un medicamento util en el tratamiento del cancer. |
| AU2012239822A AU2012239822A1 (en) | 2011-02-08 | 2012-02-06 | Inhibitors of phosphatidic acid phosphohydrolase (PAP), including D-propranolol and analogs thereof, alone or in combination with desipramine, for the treatment of cancers that depend on the epidermal growth factor receptor (EGFR), oncogenic variants thereof and other members of the ErbB/HER family |
| CA2826785A CA2826785A1 (en) | 2011-02-08 | 2012-02-06 | Inhibitors of phosphatidic acid phosphohydrolase (pap), including d-propranolol and analogs thereof, alone or in combination with desipramine, for the treatment of cancers that depend on the epidermal growth factor receptor (egfr), oncogenic variants thereof and other members of the erbb/her family |
| MX2013009091A MX2013009091A (es) | 2011-02-08 | 2012-02-06 | Inhibidores de la enzima fosfohidrolasa de acido fosfatidico (pap), que incluyen d-propanolol y analogos del mismo, solos o en combinacion con desipramine, para el tratamiento de canceres que dependen del factor de crecimiento epidermal (egfr) sus variantes oncogenicas y otros miembros de su familia erbb/her. |
| BR112013020125A BR112013020125A2 (pt) | 2011-02-08 | 2012-02-06 | inibidores de ácido fosfatídico fosfohidrolase (pap), incluindo de d-propanonol e seus análogos sozinhos ou em combinação com desipramina para o tratamento de cânceres que dependem do receptor do fator de crescimento epidérmico (egfr), suas variáveis oncogênicas e outros membros da família erbb/her |
| US13/984,012 US9345710B2 (en) | 2011-02-08 | 2012-02-06 | Inhibitors of phosphatidic acid phosphohydrolase (PAP) enzymes for the treatment of cancers that depend on members of the ErbB/HER tyrosine kinase receptor family |
| CN201280017339.1A CN103635186A (zh) | 2011-02-08 | 2012-02-06 | 包括d-普萘洛尔和其类似物的磷脂酸磷酸水解酶(pap)的抑制剂,单独或与地昔帕明组合用于治疗依赖于表皮生长因子受体(egfr)、其致癌变体和erbb/her家族其他成员的癌症 |
| JP2013552810A JP2014505078A (ja) | 2011-02-08 | 2012-02-06 | 上皮細胞増殖因子受容体(EGFR)、その発癌性変異体およびErbB/HERファミリーの他のメンバーに依存する癌の処置用の、単独またはデシプラミンと組み合わせたD−プロプラノロールおよびその類似体を含むホスファチジン酸ホスホヒドロラーゼ(PAP)の阻害剤 |
| EP12717035.5A EP2674156A1 (en) | 2011-02-08 | 2012-02-06 | Inhibitors of phosphatidic acid phosphohydrolase (pap), including d-propranolol and analogs thereof, alone or in combination with desipramine, for the treatment of cancers that depend on the epidermal growth factor receptor (egfr), oncogenic variants thereof and other members of the erbb/her family |
| PCT/CL2012/000005 WO2012135970A1 (es) | 2011-02-08 | 2012-02-06 | Inhibidores de sfohidrolasa de ácido fosfatídico (pap), incluyendo d-propranolol y análogos, solos o en combinación con desipramina, para bloquear cánceres dependientes del egfr, sus variantes oncogénicas y otros miembros de su familia erbb/her |
| RU2013137960/15A RU2013137960A (ru) | 2011-02-08 | 2012-02-06 | ИНГИБИТОРЫ ФОСФОГИДРОЛАЗ ФОСФАТИДНОЙ КИСЛОТЫ (РАР), ВКЛЮЧАЯ D-ПРОПРАНАЛОЛ И АНАЛОГИ, ОТДЕЛЬНО ИЛИ В КОМБИНАЦИИ С ДЕЗИПРАМИНОМ ДЛЯ ЛЕЧЕНИЯ ВИДОВ РАКА, КОТОРЫЕ ЗАВИСЯТ ОТ РЕЦЕПТОРА ЭПИДЕРМАЛЬНОГО ФАКТОРА РОСТА (FGFR), ЕГО ОНКОГЕННЫХ ВАРИАНТОВ И ДРУГИХ ЧЛЕНОВ СЕМЕЙСТВА ТИРОЗИНКИНАЗНЫХ РЕЦЕПТОРОВ ErbB/HER |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CL2011000273A CL2011000273A1 (es) | 2011-02-08 | 2011-02-08 | Uso de un inhibidor de la enzima fosfohidrolasa de acido fosfatidico (pap) o combinacion de inhibidores, en que el inhibidor es d(+) propranolol, y la combinacion es mezcla racemica de propranolol o d(+) propranolol junto con desipramina, para preparar un medicamento util en el tratamiento del cancer. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2011000273A1 true CL2011000273A1 (es) | 2011-06-17 |
Family
ID=46000592
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2011000273A CL2011000273A1 (es) | 2011-02-08 | 2011-02-08 | Uso de un inhibidor de la enzima fosfohidrolasa de acido fosfatidico (pap) o combinacion de inhibidores, en que el inhibidor es d(+) propranolol, y la combinacion es mezcla racemica de propranolol o d(+) propranolol junto con desipramina, para preparar un medicamento util en el tratamiento del cancer. |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US9345710B2 (es) |
| EP (1) | EP2674156A1 (es) |
| JP (1) | JP2014505078A (es) |
| CN (1) | CN103635186A (es) |
| AU (1) | AU2012239822A1 (es) |
| BR (1) | BR112013020125A2 (es) |
| CA (1) | CA2826785A1 (es) |
| CL (1) | CL2011000273A1 (es) |
| MX (1) | MX2013009091A (es) |
| RU (1) | RU2013137960A (es) |
| WO (1) | WO2012135970A1 (es) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB201720401D0 (en) * | 2017-12-07 | 2018-01-24 | Vib Vzw | Means and methods to treat torsin related neurologicl diseases |
| CN116785308B (zh) * | 2023-06-30 | 2025-08-19 | 华南农业大学 | Plpp3调控细胞氧化应激在人卵巢颗粒细胞中的应用 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU1831395A (en) | 1994-01-14 | 1995-08-01 | Cell Therapeutics, Inc. | Method for treating diseases mediated by cellular proliferation in response to pdgf, egf, fgf and vegf |
| WO2003097855A2 (en) | 2002-05-14 | 2003-11-27 | Baylor College Of Medicine | Small molecule inhibitors of her2 expression |
| EP1509230B1 (en) | 2002-06-05 | 2007-01-03 | Cedars-Sinai Medical Center | Gefitinib (iressa) for the treatment of cancer |
| AU2005249205A1 (en) | 2004-06-03 | 2005-12-15 | F. Hoffmann-La Roche Ag | Treatment with gemcitabine and an EGFR-inhibitor |
| US20060009506A1 (en) | 2004-07-09 | 2006-01-12 | Odyssey Thera, Inc. | Drugs for the treatment of neoplastic disorders |
| WO2008112297A2 (en) | 2007-03-13 | 2008-09-18 | Yale University | Methods of treating cancer by interfering with igf-i receptor signaling |
| WO2009070609A2 (en) | 2007-11-27 | 2009-06-04 | The Board Of Regents Of The University Of Texas System | Therapeutic targeting of il-6 using sirna in neutral liposomes |
| CN102006875A (zh) | 2008-02-08 | 2011-04-06 | 帕纳德制药公司 | 吡铂和贝伐单抗治疗结直肠癌的用途 |
| AU2009221765B2 (en) | 2008-03-05 | 2015-05-07 | Vicus Therapeutics, Llc | Compositions and methods for mucositis and oncology therapies |
| WO2012030234A1 (en) * | 2010-09-01 | 2012-03-08 | Swee Thong Tan | Methods and compositions for treating cancer |
-
2011
- 2011-02-08 CL CL2011000273A patent/CL2011000273A1/es unknown
-
2012
- 2012-02-06 WO PCT/CL2012/000005 patent/WO2012135970A1/es not_active Ceased
- 2012-02-06 US US13/984,012 patent/US9345710B2/en not_active Expired - Fee Related
- 2012-02-06 CN CN201280017339.1A patent/CN103635186A/zh active Pending
- 2012-02-06 RU RU2013137960/15A patent/RU2013137960A/ru not_active Application Discontinuation
- 2012-02-06 JP JP2013552810A patent/JP2014505078A/ja active Pending
- 2012-02-06 MX MX2013009091A patent/MX2013009091A/es not_active Application Discontinuation
- 2012-02-06 AU AU2012239822A patent/AU2012239822A1/en not_active Abandoned
- 2012-02-06 EP EP12717035.5A patent/EP2674156A1/en not_active Withdrawn
- 2012-02-06 BR BR112013020125A patent/BR112013020125A2/pt not_active IP Right Cessation
- 2012-02-06 CA CA2826785A patent/CA2826785A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| RU2013137960A (ru) | 2015-03-20 |
| US20140142087A1 (en) | 2014-05-22 |
| EP2674156A1 (en) | 2013-12-18 |
| BR112013020125A2 (pt) | 2016-11-01 |
| WO2012135970A8 (es) | 2013-09-19 |
| MX2013009091A (es) | 2014-05-27 |
| CA2826785A1 (en) | 2012-10-11 |
| AU2012239822A1 (en) | 2013-10-10 |
| CN103635186A (zh) | 2014-03-12 |
| WO2012135970A1 (es) | 2012-10-11 |
| JP2014505078A (ja) | 2014-02-27 |
| US9345710B2 (en) | 2016-05-24 |
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