AR004501A1 - Una sal de orotato de un compuesto triazol - Google Patents
Una sal de orotato de un compuesto triazolInfo
- Publication number
- AR004501A1 AR004501A1 ARP960103666A AR10366696A AR004501A1 AR 004501 A1 AR004501 A1 AR 004501A1 AR P960103666 A ARP960103666 A AR P960103666A AR 10366696 A AR10366696 A AR 10366696A AR 004501 A1 AR004501 A1 AR 004501A1
- Authority
- AR
- Argentina
- Prior art keywords
- amino
- cyano
- individual
- lower alkyl
- cancer
- Prior art date
Links
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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/20—Interleukins [IL]
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4192—1,2,3-Triazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/191—Tumor necrosis factors [TNF], e.g. lymphotoxin [LT], i.e. TNF-beta
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/21—Interferons [IFN]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
- A61K38/2292—Thymosin; Related peptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- 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
- 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
- C07D233/66—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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/88—Nitrogen atoms, e.g. allantoin
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Zoology (AREA)
- Gastroenterology & Hepatology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Endocrinology (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Un método para prevenir o inhibir el crecimiento de un cáncer en un individuo, que consiste en administrar a un individuo que lo necesite, unacantidad terapéuticamente efectiva de una composición que comprende una sal de 5-aminoimidazol-4 -carboxamida y/o 5-amino ó 1,2,3-triazoles 5-amino oaminosubstituidos de la fórmula (I), 5-amino-1H-imidazol + sales -4- carboxamida, y (II), en la cual un ácido orgánico o un ácido inorgánico estáunido al R2 y en donde R1 es (III), en donde p es 0 a 2; m es 0 a 4; y n es 0 a 5; X es O, S, SO, SO2, CO, CHCN, CH2 ó C=NR6, en donde R6 es hidrógeno, alquiloinferior, hidroxi, alcoxi inferior, amino, alquilamino inferior, dialquilamino inferior o ciano; y R4 y R5 son independientementeha lógeno, ciano,trifluorometil, alcanoil inferior, nitro, alquil inferior, alcoxi inferior, carboxi, carbalcoxi inferior, trifluorometoxi, acetamido, alquiltio inferior,alquilsulfinil inferior, alquilsulfonil inferior, triclorovinilo,trifluorometiltio, trifluorometil sulfinilo ó trifluorometil sulfonilo; R2 esamino, mono o dialquil amino inferior, acetamido, acetimido, ureido,formamido, formimido o guanidino; y R3 es carbamoilo, ciano, carbazoilo, amidino o N-hidroxicarbamoilo;en donde los grupos alquil inferior, que contienen alquil inferior, alcoxi inferior, y alcanoil inferior, contienenn de 1 a 3 átomos decarbono, en la preparación de una composición administrable a un individuo como un agente para prevenir o inhib irel crecimiento de un cáncer. Se describenmétodos y composiciones para la prevención y/o inhibición de neoplasmas metastásicos primario y secundario. Individuos con un alto riesgo de desarrollode neoplasias y pacientes con cáncer que se som eten aterapias convencionales pueden ser tratados con una dosis efectiva de una sal de aminoimidazol
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/505,439 US5728707A (en) | 1995-07-21 | 1995-07-21 | Treatment and prevention of primary and metastatic neoplasms with salts of aminoimidazole carboxamide |
US08/684,297 US5861406A (en) | 1995-07-21 | 1996-07-18 | Treatment and prevention of neoplasms with salts of aminoimidazole carboxamide and 5-amino or substituted amino 1,2,3-triazoles |
Publications (1)
Publication Number | Publication Date |
---|---|
AR004501A1 true AR004501A1 (es) | 1998-12-16 |
Family
ID=24010320
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP960103666A AR004501A1 (es) | 1995-07-21 | 1996-07-19 | Una sal de orotato de un compuesto triazol |
Country Status (4)
Country | Link |
---|---|
US (2) | US5728707A (es) |
KR (1) | KR100477910B1 (es) |
CN (1) | CN101273988B (es) |
AR (1) | AR004501A1 (es) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2686899B1 (fr) * | 1992-01-31 | 1995-09-01 | Rhone Poulenc Rorer Sa | Nouveaux polypeptides biologiquement actifs, leur preparation et compositions pharmaceutiques les contenant. |
EP0840608B1 (en) * | 1995-07-21 | 2004-10-06 | Savvipharm Inc. | Orotate salts of 5-amino or substituted amino 1,2,3-triazoles for treatment of neoplasms |
US6184227B1 (en) * | 1995-07-21 | 2001-02-06 | Savvipharm Inc. | Salts of aminoimidazole carboxamide useful in the prevention and treatment of liver diseases |
US6413533B1 (en) * | 1998-05-07 | 2002-07-02 | The University Of Tennessee Research Corporation | Method for chemoprevention of prostate cancer |
US20040176470A1 (en) * | 1998-05-07 | 2004-09-09 | Steiner Mitchell S. | Method for treatment and chemoprevention of prostate cancer |
US20040092602A1 (en) * | 1998-05-07 | 2004-05-13 | Steiner Mitchell S. | Method for treatment and chemoprevention of prostate cancer |
EP1100507B1 (en) * | 1998-07-31 | 2007-01-24 | Sacks, Meir S. | Use of a combination comprising a precursor of uric acid and antioxidant for the treatment of neurodegenerative deseases |
EA010263B1 (ru) * | 1999-11-08 | 2008-06-30 | Те Юниверсити Оф Теннесси Рисерч Корпорейшн | Способ химиопрофилактики рака предстательной железы |
EP1278544A4 (en) * | 2000-04-12 | 2004-08-18 | Human Genome Sciences Inc | ALBUMIN FUSION PROTEINS |
US20050100991A1 (en) * | 2001-04-12 | 2005-05-12 | Human Genome Sciences, Inc. | Albumin fusion proteins |
US6462017B1 (en) * | 2000-05-01 | 2002-10-08 | Sciclone Pharmaceuticals, Inc. | Method of reducing side effects of chemotherapy in cancer patients |
CU22999A1 (es) * | 2001-12-04 | 2004-10-12 | Centro Inmunologia Molecular | Método de tratamiento de enfermedades malignas e infecciosas crónicas |
EP1401477A4 (en) * | 2001-05-25 | 2005-02-02 | Human Genome Sciences | CHIMIOKINE BETA-1 HYBRID PROTEINS |
EP2277910A1 (en) | 2001-12-21 | 2011-01-26 | Human Genome Sciences, Inc. | Albumin fusion proteins |
EP1463752A4 (en) * | 2001-12-21 | 2005-07-13 | Human Genome Sciences Inc | ALBUMIN FUSION PROTEINS |
US7531560B2 (en) * | 2004-11-10 | 2009-05-12 | Boehringer Ingelheim Pharmaceuticals, Inc. | Anti-cytokine heterocyclic compounds |
US7601834B2 (en) * | 2005-02-22 | 2009-10-13 | Savvipharm Inc | Compositions and methods of reducing side effects and toxicity of methotrexate when given as orotate derivatives |
US8034823B2 (en) * | 2005-02-22 | 2011-10-11 | Savvipharm Inc | Method of increasing drug oral bioavailability and compositions of less toxic orotate salts |
US20060270641A1 (en) * | 2005-05-31 | 2006-11-30 | Steiner Mitchell S | Method for chemoprevention of prostate cancer |
US8017129B2 (en) * | 2006-06-15 | 2011-09-13 | SciClone Pharmaceuticals International Ltd | Use of thymosin alpha 1 for preparing a medicament for the treatment of stage IV malignant melanoma |
US7750018B2 (en) * | 2006-12-06 | 2010-07-06 | Tactical Therapeutics, Inc | Use of carboxiamidotriazole (CAI) orotate in macular degeneration |
US20080300166A1 (en) * | 2007-06-01 | 2008-12-04 | Sciclone Pharmaceuticals, Inc. | Treatment of Melanoma with Alpha Thymosin Peptides |
US8461192B2 (en) * | 2007-09-13 | 2013-06-11 | The University Of South Florida | Method of selectively inhibiting PKCiota |
CN104817507A (zh) * | 2009-09-04 | 2015-08-05 | 巧妙疗法股份有限公司 | 用于制备5-氨基或取代的氨基1,2,3-三唑和三唑乳清酸盐制剂的新组合物和方法 |
US9089570B2 (en) | 2010-09-03 | 2015-07-28 | Tactical Therapeutics Inc | Compositions for treating cancers having acquired resitance to prior chemotherapeutic and targeted drugs using carboxyamidotriazole orotate |
KR102443370B1 (ko) | 2015-11-20 | 2022-09-15 | 동우 화인켐 주식회사 | 실리콘 질화막 식각액 조성물 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1210865B (de) * | 1962-03-05 | 1966-02-17 | Fujisawa Pharmaceutical Co | Verfahren zur Herstellung des 2, 6-dioxo-tetrahydropyrimidin-4-carbonsauren Salzes des 4-Amino-5-imidazolcarbonsaeureamids |
US3997518A (en) * | 1970-12-09 | 1976-12-14 | Beecham Group Limited | 2-Alkyl-4-carboxyalkyl-5-(3,3'-dimethyltriazeno)-imidazoles |
HU190597B (en) * | 1983-07-11 | 1986-09-29 | Chinoin Gyogyszer Es Vegyeszeti Termekek Gyara Rt,Hu | Process for preparing synrtgetic pharmaceutical compositions |
US4590201A (en) * | 1984-02-02 | 1986-05-20 | Merck & Co., Inc. | 5-amino or substituted amino 1,2,3-triazoles |
US4847257A (en) * | 1987-08-20 | 1989-07-11 | Merck & Co., Inc. | 5-Amino or substituted amino 1,2,3,-triazoles useful as antiproliferative agents |
US5498620A (en) * | 1989-05-19 | 1996-03-12 | The United States Of America As Represented By The Department Of Health And Human Services | Signal transduction inhibitor 1,2,3-triazolo compounds |
US5132315A (en) * | 1989-05-19 | 1992-07-21 | The United States Of America As Represented By The Department Of Health And Human Services | Therapeutic application of an anti-invasive compound |
US5359078A (en) * | 1989-05-19 | 1994-10-25 | The United States Of America As Represented By The Department Of Health And Human Services | Signal transduction inhibitor compounds |
-
1995
- 1995-07-21 US US08/505,439 patent/US5728707A/en not_active Expired - Lifetime
-
1996
- 1996-07-18 US US08/684,297 patent/US5861406A/en not_active Expired - Lifetime
- 1996-07-18 CN CN2007100960133A patent/CN101273988B/zh not_active Expired - Lifetime
- 1996-07-18 KR KR10-1998-0700429A patent/KR100477910B1/ko not_active IP Right Cessation
- 1996-07-19 AR ARP960103666A patent/AR004501A1/es active IP Right Grant
Also Published As
Publication number | Publication date |
---|---|
CN101273988A (zh) | 2008-10-01 |
KR19990035773A (ko) | 1999-05-25 |
KR100477910B1 (ko) | 2005-06-16 |
US5861406A (en) | 1999-01-19 |
US5728707A (en) | 1998-03-17 |
CN101273988B (zh) | 2011-12-14 |
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Legal Events
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