KR880011328A - 신규 화합물들 - Google Patents

신규 화합물들 Download PDF

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KR880011328A
KR880011328A KR1019880003345A KR880003345A KR880011328A KR 880011328 A KR880011328 A KR 880011328A KR 1019880003345 A KR1019880003345 A KR 1019880003345A KR 880003345 A KR880003345 A KR 880003345A KR 880011328 A KR880011328 A KR 880011328A
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immunoglobulin
amidinophenyl
human
pyridyldithio
propionyl
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앤소니 가드윈 스미스 리차아드
배러트 캘린드지언 사키스
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데이빗 로버츠
비이참 그루우프 피이엘시이
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Publication of KR880011328A publication Critical patent/KR880011328A/ko

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    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/62—Oxygen or sulfur atoms
    • C07D213/70—Sulfur atoms
    • C07D213/71—Sulfur atoms to which a second hetero atom is attached
    • 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
    • A61K47/50—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68—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 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 an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6801—Drug-antibody or immunoglobulin conjugates defined by the pharmacologically or therapeutically active agent
    • A61K47/6803—Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates
    • A61K47/6811—Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates the drug being a protein or peptide, e.g. transferrin or bleomycin
    • A61K47/6815—Enzymes
    • 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
    • A61K47/50—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68—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 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 an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6889—Conjugates wherein the antibody being the modifying agent and wherein the linker, binder or spacer confers particular properties to the conjugates, e.g. peptidic enzyme-labile linkers or acid-labile linkers, providing for an acid-labile immuno conjugate wherein the drug may be released from its antibody conjugated part in an acidic, e.g. tumoural or environment
    • 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

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Abstract

내용없음

Description

신규 화합물들
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
제1도는 유로키나제와같은 아미도분해 활성이 실시예 1의 화합물에 노출된 적혈구로부터 검출할 수 있었으나 예비 가수분해된 화합물 혹은 조절되지 않은 유로키나제에 노출된 세포로부터는 검출할 수 없었음을 나타낸다.
제2도는 방출된 활성이 섬유소 용해성이며, 비특이 IgG와의 배합체나 처리되지 않은 적혈구 자체는 그런 활성을 방출하지 못함을 보여준다.

Claims (15)

  1. 피브린 용해 활성의 원인이 되는 효소 상의 촉매자리가, 가역 결합기에 의해 거기에 결합되어 있고 혈전증 물질의 성분과 관련된 항원에 대항하는 특이적 면역글로불린 또는 그의 단편에 의해서 블로킹된 피브린 용해 효소 유도체.
  2. 제1항에 있어서, 효소상의 촉매 자리가 하기 일반 구조식(Ⅰ)의 기에 의해 블로킹된 유도체.
    (Im)-B-A-X
    여기서 (Im)은 단백질 부착기를 포함하도록 아미노산 곁사슬 특이시약으로 처리함으로써 임의로 개질된 앞서 정의한 특이적 면역 글로불린이며, X는 하기 일반 구조식의 아실기이며.
    (여기서 R은 방향족 또는 지방족 잔기임). A는 산소, 황 및 C1-6알킬기에 의해 임의 치환된 질소로부터 선택된 적어도 하나의 이종 원자를 포함하는 브리징기이며, B는 (Im)상의 단백질 부착기에 결합된 선형의 친수성 결합기이다.
  3. 제3항에 있어서 -B-A-X가 하기 구조식을 갖는 유도체
    -S-(CH2)2-CONH-(CH2)n-NH여기서 n은 2 내지 8의 정수이다.
  4. 제1항 내지 제3항중 어느 한 항에 있어서, 결합기가 하기로부터 유도되는 유도체.
    4'-아미디노페닐 4-N-[4-N-(3-[2-피리딜디티오]프로피오닐)아미노부틸]아미노벤조에이트 ; 4'-아미디노페닐 4-N-[4-N-(3-[2-피리딜디티오]프로피오닐)아미노헥실]아미노벤조에이트 : 4'-아미디노페닐 4-N-[3-N-(3-[2-피리딜디티오]프로피오닐)아미노프로틸]아미노벤조에이트 : 4'-아미디노페닐 4-N-[5-N-(3-[2-피리딜디티오]프로피오닐)아미노펜틸]아미노팬탈에이트 : 4'-아미디노페닐 4-N-[8-N-(3-[2-피리딜디티오]프로피오닐)아미노-3,6-디옥사옥틸]아미노벤조에이트 또는 4'-아미디노페닐 4-N-[2-N-(3-[2-피리딜디티오]프로피오닐)아미노에틸]아미노벤조에이트.
  5. 제1항 내지 제4항중 어느 한 항에 있어서, 피브린 용해 효소가 플라스미노겐 활성제인 유도체.
  6. 제5항에 있어서, 피브린 용해 효소가 조직 플라스미노겐 활성제 또는 고분자량의 유로키나제인 유도체.
  7. 제1항 내지 제6항중 어느 한 항에 있어서, 특이적 면역글로불린이 토끼 항-[인간 적형구막 당단백질] 면역글로불린 G 또는 쥐 모노클로날 항-(인간 피브린) 면역글로불린 G인 유도체.
  8. 4-N-[2-N'-(3-4'-부티리미노-(N"-ε-lys 토기 항-[인간 적혈구만 당단백질]면역 글로분린 G)] 디티오프로피오닐)아미노에틸]아미노벤조일-O-(ser-356) 인간 고분자량 유로키나제, 4-N-[2-N'-(3-4'-부티리미노-(N"-ε-lys 토기 항-[인간 적혈구만 당단백질]면역 글로분린 G)] 디티오프로피오닐)아미노에틸]아미노벤조일-O-(ser-478) 인간 조직 플라스미노겐 활성제, 4-N-[8-N'-(3-4'-부티리미노-(N"-ε-lys 토기 항-[인간 적혈구만 당단백질]면역글루불린 G)] 디티오프로피오닐)아미노-3,6-디옥사옥틸]아미노벤조일-O-(ser-478) 인간 조직 플라스미노겐 활성제, 4-N-[2-N'-(3-4'-부티리미노-(N"-ε-lys 토기 항-[인간 적혈구만 당단백질]면역 글로분린 G)] 디티오프로피오닐)아미노펜틸]아미노벤조일-O-(ser-478) 인간 조직 플라스미노겐 활성제, 4-N-[2-N'-(3-4'-부티리미노-(N"-ε-lys 토기 항-[인간 적혈구만 당단백질]면역 글로분린 G)] 디티오프로피오닐)아미노부틸]아미노벤조일-O-(ser-478) 인간 조직 플라스미노겐 활성제, 4-N-[2-N'-(3-4'-부티리미노-(N"-ε-lys 토기 항-[인간 적혈구만 당단백질]면역 글로분린 G)] 디티오프로피오닐)아미노에틸]아미노벤조일-O-(ser-478) 인간 조직 플라스미노겐 활성제, 또는 4-N-[2 N' (3-[4'-부티리미노 (N"-ε-lys토끼 항-[인간 적혈구막 당단백질]면역글루불린 G)[디티오프로피오닐)아미노프로필]아미노벤조일 O (ser-478)인간 조직 플라스미노겐 활성제.
  9. 단백질 부착기를 포함하도록 임이 개조된 특이적 면역글로불린, 피브린 용해효소 및 앞서 정의한 가역 결합기를 형성시키기 위해 단백질 아미노기 또는 단백질 부착기와 반응할 수 있는 부분 및 효소의 촉매자리와 반응할 수 있는 부분을 가진 결합제를 함께 반응시키는 것을 포함하는, 제1항에 따르는 유도체의 제조방법.
  10. 제약한적으로 허용가능한 담체와 조합된 제1항에 따르는 유도체를 포함하는 제약학적 조성물.
  11. 제1항에 있어서 활성 치료 물질로 사용하기 위한 유도체.
  12. 제1항에 있어서, 혈정증의 치료 및/또는 예방을 위한 유도체.
  13. 현정증을 치료 및/또는 예방하는 약제를 제조하기 위한 제1항의 유도체의 사용.
  14. 하기 일반구조식(Ⅲ)의 화합물.
    여기서 n은 3 내지 8의 정수이며, Z는 카운터 이온이며 R1내지 R4의 각각은 수소 또는 아미디노페닐 에스테르의 반응성을 증가시키는 전자 끄는 부분을 나타낸다.
  15. 4'-아미디노페닐 4-N-[4-N-(3-[2-피리딜디티오]프로피오닐)아미노부틸]아미노벤조에이트, 4'-아미디노페닐 4-N-[6-N-(3-[2-피리딜디티오]프로피오닐)아미노헥실]아미노벤조에이트, 4'-아미디노페닐 4-N-[3-N-(3-[2-피리딜디티오]프로피오닐)아미노프로필]아미노벤조에이트 또는, 4'-아미디노페닐 4'-N-[5-N-(3-[2-피리딜디티오]프로피오닐)아미노부틸]아미노벤조에이트, 또는 이들의 염.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019880003345A 1987-03-27 1988-03-26 신규 화합물들 KR880011328A (ko)

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GB878707369A GB8707369D0 (en) 1987-03-27 1987-03-27 Enzyme derivatives
GB8707369 1987-03-27

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EP (1) EP0284413A3 (ko)
JP (1) JPS63269980A (ko)
KR (1) KR880011328A (ko)
AU (1) AU609105B2 (ko)
DK (1) DK165088A (ko)
GB (1) GB8707369D0 (ko)
NZ (1) NZ224025A (ko)
PT (1) PT87096B (ko)
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* Cited by examiner, † Cited by third party
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WO1992018139A1 (en) * 1991-04-09 1992-10-29 Brigham And Women's Hospital Chimeric molecule with plasminogen activator activity and affinity for atherosclerotic plaques
US5331109A (en) * 1992-04-06 1994-07-19 Biosite Diagnostics Incorporated Phencyclidine derivatives and protein and polypeptide phencyclidine derivative conjugates and labels
US5470997A (en) * 1992-04-06 1995-11-28 Biosite Diagnostics Incorporated Amphetamine derivatives and protein and polypeptide amphetamine derivative conjugates and labels

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* Cited by examiner, † Cited by third party
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NZ191320A (en) * 1978-09-07 1982-09-14 Beecham Group Ltd In vivo fibrinolytic enzyme having active site blocked by hydrolytically removable group pharmaceutical compositions
EP0109653A3 (en) * 1982-11-17 1986-01-29 Otsuka Pharmaceutical Co., Ltd. Process for preparing urokinase complex
GB8334498D0 (en) * 1983-12-24 1984-02-01 Beecham Group Plc Compounds
GB8334499D0 (en) * 1983-12-24 1984-02-01 Beecham Group Plc Derivatives
GB8400653D0 (en) * 1984-01-11 1984-02-15 Beecham Group Plc Conjugates
EP0266032A1 (en) * 1986-08-29 1988-05-04 Beecham Group Plc Modified fibrinolytic enzyme

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GB8707369D0 (en) 1987-04-29
AU609105B2 (en) 1991-04-26
JPS63269980A (ja) 1988-11-08
PT87096A (pt) 1988-04-01
PT87096B (pt) 1992-07-31
AU1376588A (en) 1988-09-29
DK165088D0 (da) 1988-03-25
DK165088A (da) 1988-09-28
EP0284413A3 (en) 1990-06-13
ZA882145B (en) 1989-01-25
NZ224025A (en) 1991-02-26
EP0284413A2 (en) 1988-09-28

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