WO2005012230A1 - DIAMIDAS DE AMINOACIDOS EN POSICION NO α UTILES COMO ADYUVANTES PARA LA ADMINISTRACION DE AGENTES BIOLOGICOS ACTIVOS - Google Patents

DIAMIDAS DE AMINOACIDOS EN POSICION NO α UTILES COMO ADYUVANTES PARA LA ADMINISTRACION DE AGENTES BIOLOGICOS ACTIVOS Download PDF

Info

Publication number
WO2005012230A1
WO2005012230A1 PCT/ES2004/000346 ES2004000346W WO2005012230A1 WO 2005012230 A1 WO2005012230 A1 WO 2005012230A1 ES 2004000346 W ES2004000346 W ES 2004000346W WO 2005012230 A1 WO2005012230 A1 WO 2005012230A1
Authority
WO
WIPO (PCT)
Prior art keywords
aromatic
mmol
compound
reaction
added
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.)
Ceased
Application number
PCT/ES2004/000346
Other languages
English (en)
Spanish (es)
French (fr)
Inventor
Jean Sarkis Mardiguian
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Laboratorios Farmaceuticos Rovi SA
Original Assignee
Laboratorios Farmaceuticos Rovi SA
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Laboratorios Farmaceuticos Rovi SA filed Critical Laboratorios Farmaceuticos Rovi SA
Priority to DK04742074T priority Critical patent/DK1652836T3/da
Priority to AU2004261417A priority patent/AU2004261417C1/en
Priority to US10/563,994 priority patent/US7462735B2/en
Priority to DE602004007665T priority patent/DE602004007665T2/de
Priority to BRPI0413032-4A priority patent/BRPI0413032A/pt
Priority to PL04742074T priority patent/PL1652836T3/pl
Priority to EP04742074A priority patent/EP1652836B1/en
Priority to CA002533639A priority patent/CA2533639A1/en
Priority to JP2006521597A priority patent/JP4343227B2/ja
Publication of WO2005012230A1 publication Critical patent/WO2005012230A1/es
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/16—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
    • A61K47/18—Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/28—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton
    • C07C237/42—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
    • 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
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/164—Amides, e.g. hydroxamic acids of a carboxylic acid with an aminoalcohol, e.g. ceramides
    • 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
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/17—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C233/81—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • C07C233/82—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
    • C07C233/83—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom of an acyclic saturated carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/42—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/44—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/56—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/42—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/44—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/58—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring with carbon atoms of carboxamide groups and singly-bound oxygen atoms, bound in ortho-position to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/64—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring with carbon atoms of carboxamide groups and singly-bound oxygen atoms, bound in ortho-position to carbon atoms of the same non-condensed six-membered aromatic ring having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring

Definitions

  • the present invention relates to new amino acid diamides in non- ⁇ position useful as adjuvants for the administration of biological active ingredients.
  • the compounds according to the invention facilitate oral, intraduodenal, intracolonic and pulmonary administration of heparin, low molecular weight heparins, very low molecular weight heparins and other glycosaminoglycans and derivatives.
  • Heparin is currently used in parenteral administration for prevention and treatment of deep vein thrombosis. Heparin and related derivatives are ineffective or are destroyed in the gastro-intestinal tract by acidic or enzymatic hydrolysis. Additionally, the size and ionic charge of the molecules could impede absorption.
  • heparin Several adjuvants (eg, non-ionic surfactants) have been employed to improve oral absorption of heparin. Recently, modified amino acids have been used to facilitate the administration of various biological agents, in particular heparin (WO 98/34632, WO 01/51454, WO 97/36480).
  • adjuvants eg, non-ionic surfactants
  • modified amino acids have been used to facilitate the administration of various biological agents, in particular heparin (WO 98/34632, WO 01/51454, WO 97/36480).
  • R ⁇ ⁇ is selected from the group consisting of the alkyl, halogen, N0 2 , OH, OCH 3 functional groups alone or associated and R 2 is selected from the group consisting of the functional groups H, alkyl, halogen, NO 2 , OH , OCH 3 .
  • Structure D synthesized by the applicant have no effect on the colonic absorption of bemiparin (see table).
  • Table 1 shows the Anti Xa / ml Activity in plasma after intracolonic administration in Bemiparin rat and the association of Bemiparin together with the compounds of examples 1, 2 and 3, as shown therein:
  • Another feature of the invention relates to the importance of the nature and position of the Ri substituent as well as the length of the chain (value of n).
  • the applicant has also discovered that derivatives that have the substituents Cl or N0 2 in position 3 are at least as active as derivatives that have an OH in position 1.
  • the products of the invention are usable in the form of an acid or in the form of a soluble, biologically acceptable salt, or of a pharmaceutical composition containing a heparin or a heparin derivative (ester, amide, oligosaccharides, etc.) as well as an adjuvant known for its favorable action (polyethylene glycol, alginate, chitosan and derivatives, propylene glycol, carbopol, etc).
  • One of the preferred compositions consists in associating one of the products described above with a low molecular weight heparin as bemiparin for oral use in the prevention and treatment of venous and arterial thrombosis.
  • Another application of the products of the invention is to associate them with any non-anticoagulant derivative of heparin for oral use in areas such as inflammation, allergy and cancer.
  • the products of the invention favor oral absorption, especially by the colonic route, of glycosaminoglycans and oligosaccharides of glycosaminoglycans.
  • Figure 1 shows the intracolonic absorption in rat of bemiparin and the compounds of examples 4, 5 and 9, which are shown below.
  • Figure 2 shows the intracolonic rat absorption of the compounds of examples 10, 11 and 17, which are shown below.
  • Figure 3 shows the intracolonic absorption in association rat of the pharmaceutical composition RO-14 together with the product of example 4.
  • Plasma concentration is determined by assessing the inhibitory capacity of factor Xa.
  • the rat is used because it is one of the species commonly used in this type of test. 2. Description of the test method
  • the animals will be distributed randomly in the different experimental groups, leaving one animal in reserve per group: On the day of the trial the treatments will be administered intracolonicly, prior anesthesia with ketamine. Administration will be carried out by a catheter of approximately 8 cm, attached to a 1 ml syringe. The catheter will be fully inserted into the colon through the anus and the test product will be slowly administered within the color.
  • Plasma freezing (- 20 + 5 ° C) until determination of anti factor Xa activity.
  • a control group will be included that will not receive any treatment. Only one blood sample per animal will be taken under the same conditions as the treated group, this being considered the baseline value of anti Xa activity.
  • the anti Xa activity will be assessed by chromogenic method (Kit evaluation anti anti FXa activity).
  • the mean, the standard deviation (D.E.M.) and the standard error of the mean (E.E.M.) of each experimental group will be calculated. If deemed appropriate, the values obtained in the different experimental groups will be compared using a statistical analysis.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Pain & Pain Management (AREA)
  • Hematology (AREA)
  • Rheumatology (AREA)
  • Immunology (AREA)
  • Pulmonology (AREA)
  • Diabetes (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Cosmetics (AREA)
PCT/ES2004/000346 2003-07-28 2004-07-23 DIAMIDAS DE AMINOACIDOS EN POSICION NO α UTILES COMO ADYUVANTES PARA LA ADMINISTRACION DE AGENTES BIOLOGICOS ACTIVOS Ceased WO2005012230A1 (es)

Priority Applications (9)

Application Number Priority Date Filing Date Title
DK04742074T DK1652836T3 (da) 2003-07-28 2004-07-23 Aminosyrediamider i non-alfa-stilling, som egner sig som adjuvanser til administration af aktrive biologiske midler
AU2004261417A AU2004261417C1 (en) 2003-07-28 2004-07-23 Amino acid diamides in non alpha position useful as adjuvants for the administration of active biological agents
US10/563,994 US7462735B2 (en) 2003-07-28 2004-07-23 Amino acid diamides in non α position which are useful as adjuvants for administration of biological active agents
DE602004007665T DE602004007665T2 (de) 2003-07-28 2004-07-23 Aminosäurediamide in nicht-alpha-stellung, die sich als adjuvantien für die verabreichung biologisch aktiver mittel eignen
BRPI0413032-4A BRPI0413032A (pt) 2003-07-28 2004-07-23 diamidas de aminoacidos em uma posição não-(alfa), úteis como adjuvantes na administração de agentes biológicos ativos
PL04742074T PL1652836T3 (pl) 2003-07-28 2004-07-23 Diamidy nie-α-aminokwasów użyteczne jako środki wspomagające do podawania środków biologicznie czynnych
EP04742074A EP1652836B1 (en) 2003-07-28 2004-07-23 Amino acid diamides in non alpha position useful as adjuvants for the administration of active biological agents
CA002533639A CA2533639A1 (en) 2003-07-28 2004-07-23 Amino acid diamides in non alpha position useful as adjuvants for the administration of active biological agents
JP2006521597A JP4343227B2 (ja) 2003-07-28 2004-07-23 生物活性剤の投与のためのアジュバントとして有効である非α位のアミノ酸ジアミド

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ES200301781A ES2222822B1 (es) 2003-07-28 2003-07-28 Diamidas de aminoacidos en posicion no alfa utiles como adyuvantes para la administracion de agentes biologicos activos.
ESP200301781 2003-07-28

Publications (1)

Publication Number Publication Date
WO2005012230A1 true WO2005012230A1 (es) 2005-02-10

Family

ID=34112519

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/ES2004/000346 Ceased WO2005012230A1 (es) 2003-07-28 2004-07-23 DIAMIDAS DE AMINOACIDOS EN POSICION NO α UTILES COMO ADYUVANTES PARA LA ADMINISTRACION DE AGENTES BIOLOGICOS ACTIVOS

Country Status (17)

Country Link
US (1) US7462735B2 (enExample)
EP (1) EP1652836B1 (enExample)
JP (1) JP4343227B2 (enExample)
KR (1) KR100970216B1 (enExample)
CN (1) CN100475776C (enExample)
AT (1) ATE367373T1 (enExample)
AU (1) AU2004261417C1 (enExample)
BR (1) BRPI0413032A (enExample)
CA (1) CA2533639A1 (enExample)
DE (1) DE602004007665T2 (enExample)
DK (1) DK1652836T3 (enExample)
ES (2) ES2222822B1 (enExample)
PL (1) PL1652836T3 (enExample)
PT (1) PT1652836E (enExample)
RU (1) RU2368599C2 (enExample)
WO (1) WO2005012230A1 (enExample)
ZA (1) ZA200600165B (enExample)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2296529A1 (es) * 2006-08-07 2008-04-16 Laboratorios Farmaceuticos Rovi, S.A. Composicion farmaceutica con promotores de absorcion.
CN104230745A (zh) * 2014-07-10 2014-12-24 南京医科大学 一类n-苄基取代的氨基水杨酸与4-氨基丁酸的酰胺衍生物及其药物用途

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2060253A1 (en) 2007-11-14 2009-05-20 Laboratorios Farmaceuticos Rovi, S.A. Pharmaceutical forms for the release of active compounds
US8802156B2 (en) 2007-11-14 2014-08-12 Laboratorios Farmacéuticos Rovi, S.A. Pharmaceutical forms for the release of active compounds
EP2213282A1 (en) 2009-01-30 2010-08-04 Laboratorios Farmaceuticos Rovi, S.A. Pharmaceutical forms for the release of active compounds

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000007979A2 (en) * 1998-08-07 2000-02-17 Emisphere Technologies, Inc. Compounds and compositions for delivering active agents
US20020006614A1 (en) * 1998-11-23 2002-01-17 Timothy J. Mitchison Detecting structural or synthetic information about chemical compounds
US20030008900A1 (en) * 1997-02-07 2003-01-09 Emisphere Technologies, Inc. Compounds and compositions for delivering active agents
WO2003015774A1 (en) * 2001-08-17 2003-02-27 Astrazeneca Ab Compounds effecting glucokinase
US20030045579A1 (en) * 1995-03-31 2003-03-06 Emisphere Technologies, Inc. Compounds and compositions for delivering active agents

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5965121A (en) * 1995-03-31 1999-10-12 Emisphere Technologies, Inc. Compounds and compositions for delivering active agents
US5650386A (en) * 1995-03-31 1997-07-22 Emisphere Technologies, Inc. Compositions for oral delivery of active agents

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030045579A1 (en) * 1995-03-31 2003-03-06 Emisphere Technologies, Inc. Compounds and compositions for delivering active agents
US20030008900A1 (en) * 1997-02-07 2003-01-09 Emisphere Technologies, Inc. Compounds and compositions for delivering active agents
WO2000007979A2 (en) * 1998-08-07 2000-02-17 Emisphere Technologies, Inc. Compounds and compositions for delivering active agents
US20020006614A1 (en) * 1998-11-23 2002-01-17 Timothy J. Mitchison Detecting structural or synthetic information about chemical compounds
WO2003015774A1 (en) * 2001-08-17 2003-02-27 Astrazeneca Ab Compounds effecting glucokinase

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2296529A1 (es) * 2006-08-07 2008-04-16 Laboratorios Farmaceuticos Rovi, S.A. Composicion farmaceutica con promotores de absorcion.
ES2296529B1 (es) * 2006-08-07 2009-04-01 Laboratorios Farmaceuticos Rovi, S.A. Composicion farmaceutica con promotores de absorcion.
CN104230745A (zh) * 2014-07-10 2014-12-24 南京医科大学 一类n-苄基取代的氨基水杨酸与4-氨基丁酸的酰胺衍生物及其药物用途

Also Published As

Publication number Publication date
KR100970216B1 (ko) 2010-07-16
AU2004261417B2 (en) 2010-07-01
ATE367373T1 (de) 2007-08-15
ES2222822A1 (es) 2005-02-01
CN100475776C (zh) 2009-04-08
DE602004007665D1 (de) 2007-08-30
EP1652836B1 (en) 2007-07-18
RU2368599C2 (ru) 2009-09-27
US7462735B2 (en) 2008-12-09
AU2004261417A1 (en) 2005-02-10
PT1652836E (pt) 2007-10-23
ZA200600165B (en) 2007-03-28
DE602004007665T2 (de) 2008-05-15
AU2004261417C1 (en) 2011-02-24
KR20060079184A (ko) 2006-07-05
ES2289534T3 (es) 2008-02-01
RU2006101630A (ru) 2007-09-10
ES2222822B1 (es) 2005-12-16
US20070191302A1 (en) 2007-08-16
PL1652836T3 (pl) 2007-12-31
DK1652836T3 (da) 2007-11-05
JP2007533600A (ja) 2007-11-22
CN1829682A (zh) 2006-09-06
EP1652836A1 (en) 2006-05-03
BRPI0413032A (pt) 2006-10-03
CA2533639A1 (en) 2005-02-10
JP4343227B2 (ja) 2009-10-14

Similar Documents

Publication Publication Date Title
KR100655808B1 (ko) 혈관 손상제로서 콜치놀 유도체, 그것의 용도 및 제조 방법
AU2004281536B2 (en) Novel alanyl-amino peptidase inhibitors for functionally influencing different cells and treating immunological, inflammatory, neuronal, and other diseases
JP2001507676A (ja) 抗血栓性有機硝酸塩
CN105120866A (zh) 与毒性醛相关的疾病和治疗
RS53679B1 (sr) Furazanobenzimidazoli kao prolekovi za lečenje neoplastičnih ili autoimunskih bolesti
WO2005012230A1 (es) DIAMIDAS DE AMINOACIDOS EN POSICION NO α UTILES COMO ADYUVANTES PARA LA ADMINISTRACION DE AGENTES BIOLOGICOS ACTIVOS
WO2023208170A1 (zh) 蛋白酶抑制剂及其制备方法和应用
RU2417217C2 (ru) Устойчивые и стабильные при хранении солевые кластеры соли аммония и минеральной соли с анионами двухосновных кислот и способ их получения
ES2660467T3 (es) Procedimiento para la preparación de ésteres de ácido (indol-1-il)-acético sustituidos en posición 3
WO2021125345A1 (ja) 血管拡張剤およびその用途
MXPA06001025A (en) Amino acid diamides in non alpha position useful as adjuvants for the administration of active biological agents
CN112500314B (zh) 一种化合物及其制法和在制备治疗糖代谢紊乱疾病的药物中的应用
CN102223883A (zh) 用于治疗抑郁症、焦虑症、精神分裂症、睡眠障碍和癫痫症的琥珀酸的胆碱盐
ES2987705T3 (es) Métodos y composiciones de los profármacos isoindolin-1,3-diona e isoindol útiles para el tratamiento del cáncer, colitis ulcerosa y enfermedades inflamatorias relacionadas
Naser et al. Synthesis and preliminary pharmacological evaluation of new analogues of diclofenac as potential anti-inflammatory agents
CN105153163A (zh) 2,9-二取代嘌呤-6-氨基异羟肟酸类组蛋白去乙酰化酶抑制剂及制备方法和应用
CN110204493A (zh) 三环类xor抑制剂及其制备方法和应用
CN108218777A (zh) 一种硫取代苯基吡唑类xor抑制剂及制备与应用
PT98851A (pt) Processo para a preparacao de derivados de diazepina uteis como agentes terapeuticos
EP3753559A1 (en) Colitis improving agent
CN108186645A (zh) 嘌呤衍生物的应用
CN119504644A (zh) 一种苯并噻唑偶联异羟肟酸类化合物及其制备方法和应用
CN120058611A (zh) 1-芳基-5-吡唑啉酮类化合物及其药物组合物和应用
CN104892640A (zh) 2-苯基-6-苯甲酰基-噻唑并[3,2-b][1,2,4]-三氮唑类衍生物及应用
CN114957148A (zh) 富马酸衍生物及其制备方法和医药用途

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200480022040.0

Country of ref document: CN

AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): BW GH GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 2006/00165

Country of ref document: ZA

Ref document number: 200600165

Country of ref document: ZA

WWE Wipo information: entry into national phase

Ref document number: 12006500090

Country of ref document: PH

WWE Wipo information: entry into national phase

Ref document number: 2004742074

Country of ref document: EP

ENP Entry into the national phase

Ref document number: 2533639

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: 544948

Country of ref document: NZ

Ref document number: 06006399

Country of ref document: CO

WWE Wipo information: entry into national phase

Ref document number: PA/a/2006/001025

Country of ref document: MX

Ref document number: 2004261417

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: 1020067001803

Country of ref document: KR

WWE Wipo information: entry into national phase

Ref document number: 2006521597

Country of ref document: JP

Ref document number: 344/CHENP/2006

Country of ref document: IN

ENP Entry into the national phase

Ref document number: 2004261417

Country of ref document: AU

Date of ref document: 20040723

Kind code of ref document: A

WWP Wipo information: published in national office

Ref document number: 2004261417

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: DZP2006000099

Country of ref document: DZ

WWE Wipo information: entry into national phase

Ref document number: 2006101630

Country of ref document: RU

Ref document number: A20060056

Country of ref document: BY

WWP Wipo information: published in national office

Ref document number: 2004742074

Country of ref document: EP

DPEN Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed from 20040101)
WWP Wipo information: published in national office

Ref document number: 1020067001803

Country of ref document: KR

WWE Wipo information: entry into national phase

Ref document number: 10563994

Country of ref document: US

Ref document number: 2007191302

Country of ref document: US

ENP Entry into the national phase

Ref document number: PI0413032

Country of ref document: BR

WWG Wipo information: grant in national office

Ref document number: 2004742074

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 10563994

Country of ref document: US