NO180417C - Syrelabile linkermolekyler - Google Patents

Syrelabile linkermolekyler

Info

Publication number
NO180417C
NO180417C NO920040A NO920040A NO180417C NO 180417 C NO180417 C NO 180417C NO 920040 A NO920040 A NO 920040A NO 920040 A NO920040 A NO 920040A NO 180417 C NO180417 C NO 180417C
Authority
NO
Norway
Prior art keywords
aralkyl
aryl
lower alkyl
acid
alkylene
Prior art date
Application number
NO920040A
Other languages
English (en)
Norwegian (no)
Other versions
NO180417B (no
NO920040L (no
NO920040D0 (no
Inventor
Petrus Johannes Boon
Franciscus Michael Kaspersen
Ebo Sybren Bos
Original Assignee
Akzo Nv
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 Akzo Nv filed Critical Akzo Nv
Publication of NO920040D0 publication Critical patent/NO920040D0/no
Publication of NO920040L publication Critical patent/NO920040L/no
Publication of NO180417B publication Critical patent/NO180417B/no
Publication of NO180417C publication Critical patent/NO180417C/no

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three 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
    • C07D307/60—Two oxygen atoms, e.g. succinic anhydride
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • 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
    • A61K47/62—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 a protein, peptide or polyamino acid
    • A61K47/65—Peptidic linkers, binders or spacers, e.g. peptidic enzyme-labile linkers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/10—Spiro-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/20—Carbocyclic rings
    • C07H15/24—Condensed ring systems having three or more rings
    • C07H15/252—Naphthacene radicals, e.g. daunomycins, adriamycins

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Saccharide Compounds (AREA)
  • Ultra Sonic Daignosis Equipment (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Medicinal Preparation (AREA)
  • Mushroom Cultivation (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyrrole Compounds (AREA)
NO920040A 1990-12-31 1992-01-02 Syrelabile linkermolekyler NO180417C (no)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP90203526 1990-12-31

Publications (4)

Publication Number Publication Date
NO920040D0 NO920040D0 (no) 1992-01-02
NO920040L NO920040L (no) 1992-07-01
NO180417B NO180417B (no) 1997-01-06
NO180417C true NO180417C (no) 1997-04-16

Family

ID=8205218

Family Applications (1)

Application Number Title Priority Date Filing Date
NO920040A NO180417C (no) 1990-12-31 1992-01-02 Syrelabile linkermolekyler

Country Status (17)

Country Link
US (1) US5306809A (fr)
EP (1) EP0495265B1 (fr)
JP (1) JPH04334377A (fr)
KR (1) KR920012063A (fr)
AT (1) ATE109476T1 (fr)
AU (1) AU646121B2 (fr)
CA (1) CA2058595A1 (fr)
DE (1) DE69103255T2 (fr)
DK (1) DK0495265T3 (fr)
ES (1) ES2061166T3 (fr)
FI (1) FI101678B1 (fr)
HU (1) HUT60484A (fr)
IE (1) IE65406B1 (fr)
NO (1) NO180417C (fr)
NZ (1) NZ241217A (fr)
PT (1) PT99954B (fr)
ZA (1) ZA9110203B (fr)

Families Citing this family (54)

* Cited by examiner, † Cited by third party
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US5505931A (en) * 1993-03-04 1996-04-09 The Dow Chemical Company Acid cleavable compounds, their preparation and use as bifunctional acid-labile crosslinking agents
EP0638583A1 (fr) * 1993-08-13 1995-02-15 Hoechst Aktiengesellschaft Aminosucre substances actives, un procédé pour leur préparation, et leur utilisation comme médicaments
DE4433890C2 (de) * 1994-09-22 1999-02-18 Deutsches Krebsforsch Konjugat aus einem Wirkstoff und einem nicht als körperfremd angesehenen, nativen Protein
WO1997023243A1 (fr) * 1995-12-22 1997-07-03 Bristol-Myers Squibb Company Segments de liaison hydrazone ramifies
DE19636889A1 (de) * 1996-09-11 1998-03-12 Felix Dr Kratz Antineoplastisch wirkende Transferrin- und Albuminkonjugate zytostatischer Verbindungen aus der Gruppe der Anthrazykline, Alkylantien, Antimetabolite und Cisplatin-Analoga und diese enthaltende Arzneimittel
US6030997A (en) * 1998-01-21 2000-02-29 Eilat; Eran Acid labile prodrugs
US6800616B2 (en) 1998-02-26 2004-10-05 Supergen, Inc. Treatment of HIV infections
CA2248592A1 (fr) 1998-08-31 2000-02-29 Christopher D. Batich Microspheres pour le traitement du cancer
US6140015A (en) * 1998-12-10 2000-10-31 International Business Machines Corporation Photoresist compositions with pendant polar-functionalized aromatic groups and acid-labile branching
TWI242000B (en) * 1998-12-10 2005-10-21 Univ Southern California Reversible aqueous pH sensitive lipidizing reagents, compositions and methods of use
CN1149219C (zh) * 1999-03-11 2004-05-12 阿登尼亚投资有限公司 治疗癌症的新化合物
US6706892B1 (en) * 1999-09-07 2004-03-16 Conjuchem, Inc. Pulmonary delivery for bioconjugation
BRPI0003386B8 (pt) * 2000-08-08 2021-05-25 Cristalia Produtos Quim Farmaceuticos Ltda pró-droga homo ou heterodiméricas úteis no tratamento de doenças ou disfunções mediadas por fosfodiesterases; composições farmacêuticas contendo a pró-droga ou seus sais farmacêuticos aceitáveis; processo de obtenção destas pró-drogas
MXPA03003401A (es) * 2000-10-16 2004-06-30 Neopharm Inc Formulacion liposomica de mitoxantrona.
US20100056762A1 (en) 2001-05-11 2010-03-04 Old Lloyd J Specific binding proteins and uses thereof
DK2163256T3 (en) 2001-05-11 2015-12-07 Ludwig Inst For Cancer Res Ltd Specific binding proteins and use thereof
GB0116143D0 (en) * 2001-07-02 2001-08-22 Amersham Pharm Biotech Uk Ltd Chemical capture reagent
KR100507968B1 (ko) * 2001-08-18 2005-08-17 한국과학기술연구원 자기집합체를 형성하는 항암제-키토산 복합체 및 그의제조방법
WO2003051113A1 (fr) * 2001-12-14 2003-06-26 The University Of Wyoming Methodes et compositions de liberation controlee de medicaments
US8361464B2 (en) 2002-03-01 2013-01-29 Immunomedics, Inc. Anthracycline-Antibody Conjugates for Cancer Therapy
CA2478522A1 (fr) * 2002-03-08 2003-09-18 Emory University Nouvelles constructions de facteurs viia de curcuminoides utilisees en tant que suppresseurs de la croissance tumorale et de l'angiogenese
US20050069551A1 (en) * 2002-03-08 2005-03-31 Emory University Cytotoxic compound-protein conjugates as suppressors of tumor growth and angiogenesis
EP1506218B1 (fr) * 2002-05-24 2017-04-12 Arrowhead Pharmaceuticals, Inc. Modification reversible de l'interaction membranaire
CN1733314A (zh) * 2004-08-11 2006-02-15 张阳德 半乳糖化白蛋白磁性阿霉素纳米粒的制备方法
US20060135459A1 (en) * 2004-11-09 2006-06-22 Epstein Alan L Targeted innate immunity
NZ556788A (en) 2005-01-05 2011-03-31 Biogen Idec Inc Humanized CRIPTO binding molecules with CDRs from murine B3F6
EP2083866A4 (fr) 2006-10-27 2011-12-28 Wei-Chiang Shen Interféron lipidisé et ses utilisations
JP5276017B2 (ja) * 2007-01-25 2013-08-28 デイナ ファーバー キャンサー インスティチュート，インコーポレイテッド Ｅｇｆｒ変異体仲介性疾患の治療における抗ｅｇｆｒ抗体の使用
CN101688229B (zh) * 2007-03-15 2013-06-12 路德维格癌症研究所 包含egfr抗体和src抑制剂的组合物及其在制备用于治疗哺乳动物癌症的药物中的用途
MX2010001757A (es) 2007-08-14 2010-09-14 Ludwig Inst Cancer Res Anticuerpo monoclonal 175 que activa el receptor egf y derivados y usos del mismo.
US8618096B2 (en) * 2008-07-21 2013-12-31 The Regents Of The University Of California Prodrug compositions and methods for using the same in treating cancer and malaria
JP5472288B2 (ja) * 2009-03-17 2014-04-16 国立大学法人 東京大学 タンパク質の電荷調節剤、及びタンパク質内包高分子ミセル複合体
US8535948B2 (en) * 2009-03-26 2013-09-17 Institute For Systems Biology Method to determine protein interaction sites
EP2448966B1 (fr) 2009-07-03 2018-11-14 Avipep Pty Ltd Immunoconjugués et leurs procédés de production
US20110076232A1 (en) * 2009-09-29 2011-03-31 Ludwig Institute For Cancer Research Specific binding proteins and uses thereof
SG181814A1 (en) 2009-12-23 2012-07-30 Avipep Pty Ltd Immuno-conjugates and methods for producing them 2
RU2013103763A (ru) 2010-07-02 2014-08-10 Ангиохем Инк. Короткие и содержащие d-аминокислоты полипептиды для терапевтических конъюгатов и их применения
WO2013012733A1 (fr) 2011-07-15 2013-01-24 Biogen Idec Ma Inc. Régions fc hétérodimères, molécules de liaison les comprenant, et méthodes associées
CA2845391C (fr) 2011-08-18 2021-01-19 Affinity Biosciences Pty Ltd Polypeptides solubles
JP6247226B2 (ja) 2012-01-10 2017-12-13 バイオジェン・エムエイ・インコーポレイテッドＢｉｏｇｅｎ ＭＡ Ｉｎｃ． 血液脳関門を越える治療分子の輸送の向上
GB201202268D0 (en) 2012-02-09 2012-03-28 Medical Res Council Intracellular immunity
WO2014057436A2 (fr) 2012-10-10 2014-04-17 Adamed Sp. Z O.O. Conjugué anticancéreux
WO2014124227A1 (fr) 2013-02-07 2014-08-14 Immunomedics, Inc. Forme de pro-médicament (p2pdox) de la 2-pyrrolinodoxorubicine fortement puissante conjuguée à des anticorps pour la thérapie ciblée du cancer
WO2014141094A1 (fr) 2013-03-14 2014-09-18 Adamed Sp. Z O.O. Conjugué anticancéreux
WO2015123595A1 (fr) 2014-02-14 2015-08-20 The Regents Of The University Of California Peroxydes cycliques utilisés en tant que promédicaments pour l'administration sélective d'agents
SG11201702627UA (en) 2014-10-03 2017-04-27 Engeneic Molecular Delivery Pty Ltd Enhanced loading of intact, bacterially derived vesicles with small molecule compounds
RU2740672C2 (ru) 2015-08-07 2021-01-19 ЭйЭлЭкс Онколоджи Инк. Конструкции, имеющие sirp-альфа домен или его вариант
EA034582B1 (ru) 2015-08-07 2020-02-21 АЭлЭкс ОНКОЛОДЖИ ИНК. Конструкции варианта sirp-альфа и их применение
WO2017088058A1 (fr) 2015-11-24 2017-06-01 Transfert Plus, S.E.C. Composés peptidiques et conjugués peptidiques destinés au traitement du cancer par chimiothérapie à médiation par un récepteur
WO2018118015A1 (fr) 2016-12-19 2018-06-28 Morehouse School Of Medicine Compositions et procédés pour traiter des maladies par inhibition de libération d'exosomes
US10800817B2 (en) 2016-12-19 2020-10-13 Morehouse School Of Medicine Compositions and methods for treating diseases by inhibiting exosome release
WO2020243338A1 (fr) 2019-05-31 2020-12-03 ALX Oncology Inc. Méthodes de traitement du cancer avec une protéine de fusion sirpalpha-fc en association avec un inhibiteur de point de contrôle immunitaire
US11180534B1 (en) 2021-06-04 2021-11-23 Morehouse School Of Medicine Compositions and methods for treating SARS-CoV-2 infections
WO2023137443A1 (fr) * 2022-01-14 2023-07-20 Regeneron Pharmaceuticals, Inc. Dérivés de verrucarine a et conjugués anticorps-médicament de ceux-ci

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US4631190A (en) * 1981-06-26 1986-12-23 Shen Wei C Acidity-sensitive spacer molecule to control the release of pharmaceuticals from molecular carriers
US4542225A (en) * 1984-08-29 1985-09-17 Dana-Farber Cancer Institute, Inc. Acid-cleavable compound
US4744981A (en) * 1985-10-17 1988-05-17 Neorx Corporation Trichothecene antibody conjugates
US4997913A (en) * 1986-06-30 1991-03-05 Oncogen pH-sensitive immunoconjugates and methods for their use in tumor therapy
US5140013A (en) * 1989-11-28 1992-08-18 Universite Laval Maleic anhydride derivatives used as conjugation agents of anti-tumor agents on desired carriers

Also Published As

Publication number Publication date
DE69103255T2 (de) 1994-12-08
PT99954A (pt) 1993-06-30
ATE109476T1 (de) 1994-08-15
FI916131A (fi) 1992-07-01
NO180417B (no) 1997-01-06
PT99954B (pt) 1999-06-30
NZ241217A (en) 1993-12-23
IE65406B1 (en) 1995-10-18
JPH04334377A (ja) 1992-11-20
DK0495265T3 (da) 1995-01-02
CA2058595A1 (fr) 1992-07-01
IE914567A1 (en) 1992-07-01
HU914133D0 (en) 1992-03-30
NO920040L (no) 1992-07-01
US5306809A (en) 1994-04-26
FI916131A0 (fi) 1991-12-27
AU646121B2 (en) 1994-02-10
EP0495265A1 (fr) 1992-07-22
EP0495265B1 (fr) 1994-08-03
FI101678B (fi) 1998-08-14
HUT60484A (en) 1992-09-28
FI101678B1 (fi) 1998-08-14
DE69103255D1 (de) 1994-09-08
KR920012063A (ko) 1992-07-25
ES2061166T3 (es) 1994-12-01
AU9009891A (en) 1993-01-28
ZA9110203B (en) 1993-01-27
NO920040D0 (no) 1992-01-02

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