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EA200000409A1 - Compounds, pharmaceutical compositions, methods for inhibiting cell death in a cell or tissue, methods of treating or REDUCE cell death, treatment or prophylaxis of polycystic kidney or anemia / erythropoiesis in an animal way to protect an organ or tissue of mammals from extinction CELLS, METHOD FOR REDUCTION OR PREVENTION CELL DEFENSE IN ORGAN OR TREATMENT OF DONOR AFTER THEIR TRANSPLANTATION, THE WAY TO REDUCE OR PREVENT THE DESTRUCTION OF SPERM OR EGGS - Google Patents

Compounds, pharmaceutical compositions, methods for inhibiting cell death in a cell or tissue, methods of treating or REDUCE cell death, treatment or prophylaxis of polycystic kidney or anemia / erythropoiesis in an animal way to protect an organ or tissue of mammals from extinction CELLS, METHOD FOR REDUCTION OR PREVENTION CELL DEFENSE IN ORGAN OR TREATMENT OF DONOR AFTER THEIR TRANSPLANTATION, THE WAY TO REDUCE OR PREVENT THE DESTRUCTION OF SPERM OR EGGS

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Publication number
EA200000409A1
EA200000409A1 EA200000409A EA200000409A EA200000409A1 EA 200000409 A1 EA200000409 A1 EA 200000409A1 EA 200000409 A EA200000409 A EA 200000409A EA 200000409 A EA200000409 A EA 200000409A EA 200000409 A1 EA200000409 A1 EA 200000409A1
Authority
EA
Eurasian Patent Office
Prior art keywords
organ
tissue
cell
treatment
methods
Prior art date
Application number
EA200000409A
Other languages
Russian (ru)
Inventor
Джон Гюастелла
Джон Э. Дроуэ
Ю Янг
Суй Хионг Кай
Джон Ф. У. Киана
Original Assignee
Сайтовиэ, Инк.
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 Сайтовиэ, Инк. filed Critical Сайтовиэ, Инк.
Publication of EA200000409A1 publication Critical patent/EA200000409A1/en

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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic 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
    • C07D233/64Heterocyclic 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 substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/64Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
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    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
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    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
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    • A61P37/00Drugs for immunological or allergic disorders
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    • AHUMAN NECESSITIES
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    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/02Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C237/22Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06Esters of carbamic acids
    • C07C271/08Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/22Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
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    • C07C323/00Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
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    • C07C323/51Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C323/60Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton with the carbon atom of at least one of the carboxyl groups bound to nitrogen atoms
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    • C07D277/08Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D277/12Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
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    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
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    • C07K5/06Dipeptides
    • C07K5/06191Dipeptides containing heteroatoms different from O, S, or N
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    • C12N2810/00Vectors comprising a targeting moiety
    • C12N2810/40Vectors comprising a peptide as targeting moiety, e.g. a synthetic peptide, from undefined source

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Abstract

Настоящее изобретение относится к новым дипептидам, представленным общей формулой (I), где R-Rи AA определены в описании изобретения. Настоящее изобретение относится к открытию соединений, имеющих формулу (I), которые являются сильными ингибиторами апоптотической гибели клеток. Следовательно, ингибиторы по настоящему изобретению могут замедлять или блокировать гибель клеток, которая наблюдается при ряде клинических состояний, сопровождающихся потерей клеток, тканей или целых органов.Международная заявка была опубликована вместе с отчетом о международном поиске.The present invention relates to new dipeptides represented by the general formula (I), where R-R and AA are defined in the specification. The present invention relates to the discovery of compounds having the formula (I), which are strong inhibitors of apoptotic cell death. Therefore, the inhibitors of the present invention can slow down or block cell death, which is observed in a number of clinical conditions involving loss of cells, tissues, or entire organs. The international application was published along with an international search report.

EA200000409A 1997-10-10 1998-10-09 Compounds, pharmaceutical compositions, methods for inhibiting cell death in a cell or tissue, methods of treating or REDUCE cell death, treatment or prophylaxis of polycystic kidney or anemia / erythropoiesis in an animal way to protect an organ or tissue of mammals from extinction CELLS, METHOD FOR REDUCTION OR PREVENTION CELL DEFENSE IN ORGAN OR TREATMENT OF DONOR AFTER THEIR TRANSPLANTATION, THE WAY TO REDUCE OR PREVENT THE DESTRUCTION OF SPERM OR EGGS EA200000409A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US6167697P 1997-10-10 1997-10-10
PCT/US1998/021232 WO1999018781A1 (en) 1997-10-10 1998-10-09 Dipeptide apoptosis inhibitors and the use thereof

Publications (1)

Publication Number Publication Date
EA200000409A1 true EA200000409A1 (en) 2000-10-30

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Family Applications (1)

Application Number Title Priority Date Filing Date
EA200000409A EA200000409A1 (en) 1997-10-10 1998-10-09 Compounds, pharmaceutical compositions, methods for inhibiting cell death in a cell or tissue, methods of treating or REDUCE cell death, treatment or prophylaxis of polycystic kidney or anemia / erythropoiesis in an animal way to protect an organ or tissue of mammals from extinction CELLS, METHOD FOR REDUCTION OR PREVENTION CELL DEFENSE IN ORGAN OR TREATMENT OF DONOR AFTER THEIR TRANSPLANTATION, THE WAY TO REDUCE OR PREVENT THE DESTRUCTION OF SPERM OR EGGS

Country Status (10)

Country Link
EP (1) EP1033910A4 (en)
JP (1) JP4439111B2 (en)
KR (1) KR100580333B1 (en)
CN (1) CN1138472C (en)
AU (1) AU741203B2 (en)
BR (1) BR9814817A (en)
CA (1) CA2306692C (en)
EA (1) EA200000409A1 (en)
NO (1) NO20001323L (en)
WO (1) WO1999018781A1 (en)

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NZ580884A (en) 2007-05-02 2012-02-24 Vertex Pharma Thiazoles and pyrazoles useful as kinase inhibitors
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EP1033910A4 (en) 2004-11-24
CA2306692A1 (en) 1999-04-22
CN1138472C (en) 2004-02-18
NO20001323D0 (en) 2000-03-14
AU741203B2 (en) 2001-11-22
AU9793098A (en) 1999-05-03
WO1999018781A1 (en) 1999-04-22
CN1301131A (en) 2001-06-27
JP4439111B2 (en) 2010-03-24
JP2001519358A (en) 2001-10-23
CA2306692C (en) 2010-09-21
BR9814817A (en) 2002-01-08
NO20001323L (en) 2000-06-13
KR100580333B1 (en) 2006-05-16
KR20010031053A (en) 2001-04-16
EP1033910A1 (en) 2000-09-13

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