EA200501768A1 - Вич-пролекарства, способные расщепляться под действием cd26 - Google Patents

Вич-пролекарства, способные расщепляться под действием cd26

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Publication number
EA200501768A1
EA200501768A1 EA200501768A EA200501768A EA200501768A1 EA 200501768 A1 EA200501768 A1 EA 200501768A1 EA 200501768 A EA200501768 A EA 200501768A EA 200501768 A EA200501768 A EA 200501768A EA 200501768 A1 EA200501768 A1 EA 200501768A1
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Eurasian Patent Office
Prior art keywords
group
alkyl group
prodrugs
acid
alkyl
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EA200501768A
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English (en)
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EA009727B1 (ru
Inventor
Херман Аугустинус Де Кок
Пит Том Берт Поль Вигеринк
Ян Бальзарини
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Тиботек Фармасьютикалз Лтд.
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Publication of EA200501768A1 publication Critical patent/EA200501768A1/ru
Publication of EA009727B1 publication Critical patent/EA009727B1/ru

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    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/04Ortho-condensed systems
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
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    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/62Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
    • A61K47/64Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent
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    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
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    • A61P31/12Antivirals
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    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/15Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/16Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
    • C07C311/17Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
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    • C07C311/22Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
    • C07C311/29Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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    • C07H15/20Carbocyclic rings
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    • C07K5/06Dipeptides
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    • C07K9/003Peptides being substituted by heterocyclic radicals, e.g. bleomycin, phleomycin
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Abstract

В настоящем изобретении предлагаются новые пролекарства, которые представляют собой конъюгаты терапевтического соединения и пептида, при этом конъюгат способен расщепляться под действием дипептидилпептидазы, более предпочтительно под действием CD26, известной также как DPPIV (дипептидиламинопептидаза IV). Пролекарства по настоящему изобретению имеют формулу (I) или представляют собой его стереоизомерные формы и его соли, где n составляет от 1 до 5; Y обозначает пролин, аланин, гидроксипролин, дигидроксипролин, тиазолидинкарбоновую кислоту (тиопролин), дегидропролин, пипеколиновую кислоту (L-гомопролин), азетидинкарбоновую кислоту, азиридинкарбоновую кислоту, глицин, серин, валин, лейцин, изолейцин и треонин; X выбирают из любой аминокислоты с D- или L-конфигурацией; X и Y в каждом повторе фрагмента [Y-X] выбирают независимо один от другого и независимо от других повторов; Z обозначает прямую связь или бивалентную насыщенную углеводородную группу с прямой или разветвленной цепью, содержащую от 1 до 4 атомов углерода; Rобозначает арильную, гетероарильную группу, арилоксигруппу, гетероарилоксигруппу, арилокси Cалкильную группу, гетероциклоалкилоксигруппу, гетероциклоакил Cалкоксигруппу, гетероарилокси Cалкильную группу, гетероарил Cалкилоксигруппу; Rобозначает арил Cалкильную группу; Rобозначает Cалкильную, Cалкенильную или Cциклоакил Cалкильную группу; Rобозначает водород или Cалкильную группу. В настоящем изобретении предлагается также применение указанных пролекарств в качестве лекарственных средств, а также способ получения указанных пролекарств.
EA200501768A 2003-05-08 2004-05-10 Вич-пролекарства, способные расщепляться под действием cd26 EA009727B1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0310593.9A GB0310593D0 (en) 2003-05-08 2003-05-08 Peptidic prodrugs
PCT/EP2004/050753 WO2004099135A2 (en) 2003-05-08 2004-05-10 Hiv prodrugs cleavable by cd26

Publications (2)

Publication Number Publication Date
EA200501768A1 true EA200501768A1 (ru) 2006-04-28
EA009727B1 EA009727B1 (ru) 2008-02-28

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EA200501768A EA009727B1 (ru) 2003-05-08 2004-05-10 Вич-пролекарства, способные расщепляться под действием cd26

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US (2) US20080214648A1 (ru)
EP (2) EP1620130A1 (ru)
JP (2) JP2007526872A (ru)
KR (1) KR20060008300A (ru)
CN (1) CN1784244A (ru)
AP (1) AP2005003465A0 (ru)
AT (1) ATE375172T1 (ru)
AU (2) AU2004235988A1 (ru)
BR (1) BRPI0410158A (ru)
CA (2) CA2525191A1 (ru)
DE (1) DE602004009435T2 (ru)
DK (1) DK1624897T3 (ru)
EA (1) EA009727B1 (ru)
ES (1) ES2295879T3 (ru)
GB (1) GB0310593D0 (ru)
MX (1) MXPA05012019A (ru)
NO (1) NO20055826L (ru)
NZ (1) NZ543946A (ru)
PT (1) PT1624897E (ru)
UA (1) UA82221C2 (ru)
WO (2) WO2004098644A1 (ru)
ZA (1) ZA200509940B (ru)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2005319578A1 (en) 2004-11-24 2006-06-29 Neopro Labs, Llc Methods and compositions for treating conditions
DK1831361T3 (da) 2004-12-23 2012-05-14 Campina Nederland Holding Bv Proteinhydrolysat beriget med peptider, som inhiberer DPP-IV, og deres anvendelse
JP2009517464A (ja) 2005-11-30 2009-04-30 カンピーナ ネーダーランド ホールディング ビー.ブイ. グルカゴン様ペプチド1の活性を増強するタンパク質加水分解物の使用
CA2647835A1 (en) 2006-03-28 2007-10-04 Neopro Labs, Llc Methods and compositions for treating conditions
JP2010527377A (ja) 2007-05-17 2010-08-12 ネオプロ ラブス,エルエルシー ペプチドの結晶形および非結晶形
WO2009058662A2 (en) * 2007-10-30 2009-05-07 Indiana University Research And Technology Corporation Glucagon antagonists
CN101983066B (zh) 2008-01-30 2016-06-29 印第安那大学科技研究公司 基于酯的胰岛素前药
WO2009129305A2 (en) 2008-04-15 2009-10-22 Tsrl, Inc. Prodrugs of neuraminidase inhibitors
CA2737253C (en) * 2008-09-12 2017-08-15 Cadila Pharmaceuticals Ltd. Novel dipeptidyl peptidase iv (dp-iv) compounds
WO2010053550A2 (en) 2008-11-04 2010-05-14 Anchor Therapeutics, Inc. Cxcr4 receptor compounds
CA2747195A1 (en) * 2008-12-19 2010-07-15 Indiana University Research And Technology Corporation Dipeptide linked medicinal agents
KR20110110174A (ko) 2008-12-19 2011-10-06 인디애나 유니버시티 리서치 앤드 테크놀로지 코퍼레이션 아미드 기반 글루카곤 슈퍼패밀리 펩티드 프로드럭
WO2011061590A1 (en) 2009-11-17 2011-05-26 Hetero Research Foundation Novel carboxamide derivatives as hiv inhibitors
EP2566494B1 (en) * 2010-02-26 2017-11-29 Acer Therapeutics, Inc. Cxcr4 receptor compounds
CA2803164C (en) 2010-06-24 2018-08-21 Indiana University Research And Technology Corporation Amide-based insulin prodrugs
US10426740B1 (en) 2010-08-18 2019-10-01 Avm Biotechnology, Llc Compositions and methods to inhibit stem cell and progenitor cell binding to lymphoid tissue and for regenerating germinal centers in lymphatic tissues
CN105683180B (zh) 2013-11-05 2020-01-21 阿斯利康(瑞典)有限公司 Nmda拮抗剂前药
EP3192794A4 (en) * 2014-09-11 2018-06-27 Shionogi & Co., Ltd. Sustained hiv protease inhibitor
EP3197912B1 (en) * 2014-09-24 2023-01-04 Indiana University Research & Technology Corporation Lipidated amide-based insulin prodrugs
KR102633963B1 (ko) * 2015-05-29 2024-02-05 애로우헤드 파마슈티컬스 인코포레이티드 생물학적으로 절단가능한 테트라펩티드 연결제
KR102509006B1 (ko) 2017-04-01 2023-03-13 에이브이엠 바이오테크놀로지, 엘엘씨 세포 면역치료요법 전 세포독성 사전컨디셔닝의 대체
CA3067674A1 (en) * 2017-06-29 2019-01-03 Ureka Sarl Pro-drug peptide with improved pharmaceutical properties
EP3488851A1 (en) 2018-10-03 2019-05-29 AVM Biotechnology, LLC Immunoablative therapies
CN111233955B (zh) * 2020-02-28 2022-06-10 南京缘聚医药科技有限公司 一类噻唑酮甲酰胞嘧啶衍生物及其药物用途

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL55431A (en) * 1978-08-24 1982-07-30 Yeda Res & Dev Anthracycline type antibiotics,their preparation and pharmaceutical compositions comprising them
WO1987007276A1 (en) * 1986-05-30 1987-12-03 Fuji Kagaku Kogyo Kabushiki Kaisha Novel 5-fluorouridine compounds and process for their preparation
US5627035A (en) * 1990-08-22 1997-05-06 Syntello Vaccine Development Ab Peptides that block human immunodeficiency virus and methods of use thereof
US5968942A (en) * 1992-08-25 1999-10-19 G. D. Searle & Co. α- and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors
US5843946A (en) * 1992-08-25 1998-12-01 G.D. Searle & Co. α-and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors
US6046190A (en) * 1992-08-25 2000-04-04 G.D. Searle & Co. Hydroxyethylamino sulphonamides useful as retroviral protease inhibitors
US5830897A (en) * 1992-08-27 1998-11-03 G. D. Searle & Co. α- and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors
SI0769967T1 (sl) * 1994-08-19 2008-06-30 Wallone Region Konjugati vsebujoäśi protitumorna sredstva in njihova uporaba
WO1997000268A1 (en) * 1995-06-15 1997-01-03 Pfizer Inc. Process for preparing derivatives of azabicyclo naphthyridine carboxylic acid comprising a dipeptide
CZ389398A3 (cs) * 1996-05-29 1999-07-14 Prototek, Inc. Proléčiva thalidomidu a jejich použití pro modulaci funkce T-buněk
US6177404B1 (en) * 1996-10-15 2001-01-23 Merck & Co., Inc. Conjugates useful in the treatment of benign prostatic hyperplasia
US5783689A (en) * 1996-11-12 1998-07-21 University Of Notre Dame Antibacterial and antifungal nucleosides
AU4828199A (en) * 1998-06-23 2000-01-10 Board Of Trustees Of The University Of Illinois, The Multi-drug resistant retroviral protease inhibitors and associated methods
DE19828113A1 (de) * 1998-06-24 2000-01-05 Probiodrug Ges Fuer Arzneim Prodrugs von Inhibitoren der Dipeptidyl Peptidase IV
US7425541B2 (en) * 1998-12-11 2008-09-16 Medarex, Inc. Enzyme-cleavable prodrug compounds
US6613879B1 (en) * 1999-05-14 2003-09-02 Boehringer Ingelheim Pharma Kg FAP-activated anti-tumour compounds
CA2401340A1 (en) * 2000-02-28 2001-09-07 The University Of British Columbia Compositions and methods for the treatment of inflammatory disease using topoisomerase inhibitors
CA2411545A1 (en) * 2000-06-14 2002-01-03 Medarex, Inc. Tripeptide prodrug compounds
US6849622B2 (en) * 2000-10-06 2005-02-01 Tanabe Seiyaku Co., Ltd. Aliphatic nitrogenous five-membered ring compounds
UA74912C2 (en) * 2001-07-06 2006-02-15 Merck & Co Inc Beta-aminotetrahydroimidazo-(1,2-a)-pyrazines and tetratriazolo-(4,3-a)-pyrazines as inhibitors of dipeptylpeptidase for the treatment or prevention of diabetes
AU2002360487A1 (en) * 2001-12-04 2003-06-17 Ashim K. Mitra Acyclovir-peptide analogs
AU2003296601A1 (en) * 2002-12-10 2004-06-30 F. Hoffmann-La Roche Ag Antiviral nucleoside derivatives
AU2004212786A1 (en) * 2003-02-21 2004-09-02 Tripep Ab Glycinamide derivative for inhibiting HIV replication

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PT1624897E (pt) 2008-01-17
DK1624897T3 (da) 2008-02-11
DE602004009435T2 (de) 2008-07-24
NZ543946A (en) 2008-09-26
JP2007526872A (ja) 2007-09-20
AU2004236371B2 (en) 2009-12-17
US20070275900A1 (en) 2007-11-29
JP2006525235A (ja) 2006-11-09
CA2517338A1 (en) 2004-11-18
US8236756B2 (en) 2012-08-07
ES2295879T3 (es) 2008-04-16
UA82221C2 (ru) 2008-03-25
CN1784244A (zh) 2006-06-07
EA009727B1 (ru) 2008-02-28
ZA200509940B (en) 2007-04-25
AP2005003465A0 (en) 2005-12-31
NO20055826D0 (no) 2005-12-08
WO2004099135A3 (en) 2005-02-17
NO20055826L (no) 2006-02-08
EP1624897B1 (en) 2007-10-10
EP1620130A1 (en) 2006-02-01
US20080214648A1 (en) 2008-09-04
ATE375172T1 (de) 2007-10-15
BRPI0410158A (pt) 2006-05-16
EP1624897A2 (en) 2006-02-15
KR20060008300A (ko) 2006-01-26
AU2004235988A1 (en) 2004-11-18
WO2004099135A2 (en) 2004-11-18
GB0310593D0 (en) 2003-06-11
CA2525191A1 (en) 2004-11-18
DE602004009435D1 (de) 2007-11-22
MXPA05012019A (es) 2006-02-03
WO2004098644A1 (en) 2004-11-18

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