ZA9110203B - Acid-labile linker molecules - Google Patents
Acid-labile linker moleculesInfo
- Publication number
- ZA9110203B ZA9110203B ZA9110203A ZA9110203A ZA9110203B ZA 9110203 B ZA9110203 B ZA 9110203B ZA 9110203 A ZA9110203 A ZA 9110203A ZA 9110203 A ZA9110203 A ZA 9110203A ZA 9110203 B ZA9110203 B ZA 9110203B
- Authority
- ZA
- South Africa
- Prior art keywords
- aralkyl
- aryl
- lower alkyl
- acid
- alkylene
- Prior art date
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
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP90203526 | 1990-12-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA9110203B true ZA9110203B (en) | 1993-01-27 |
Family
ID=8205218
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA9110203A ZA9110203B (en) | 1990-12-31 | 1991-12-30 | Acid-labile linker molecules |
Country Status (17)
Country | Link |
---|---|
US (1) | US5306809A (xx) |
EP (1) | EP0495265B1 (xx) |
JP (1) | JPH04334377A (xx) |
KR (1) | KR920012063A (xx) |
AT (1) | ATE109476T1 (xx) |
AU (1) | AU646121B2 (xx) |
CA (1) | CA2058595A1 (xx) |
DE (1) | DE69103255T2 (xx) |
DK (1) | DK0495265T3 (xx) |
ES (1) | ES2061166T3 (xx) |
FI (1) | FI101678B (xx) |
HU (1) | HUT60484A (xx) |
IE (1) | IE65406B1 (xx) |
NO (1) | NO180417C (xx) |
NZ (1) | NZ241217A (xx) |
PT (1) | PT99954B (xx) |
ZA (1) | ZA9110203B (xx) |
Families Citing this family (54)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 (en) * | 1993-08-13 | 1995-02-15 | Hoechst Aktiengesellschaft | Aminosugar active substances, a process for their preparation and use as pharmaceuticals |
DE4433890C2 (de) * | 1994-09-22 | 1999-02-18 | Deutsches Krebsforsch | Konjugat aus einem Wirkstoff und einem nicht als körperfremd angesehenen, nativen Protein |
WO1997023243A1 (en) * | 1995-12-22 | 1997-07-03 | Bristol-Myers Squibb Company | Branched hydrazone linkers |
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 (en) * | 1998-08-31 | 2000-02-29 | Christopher D. Batich | Microspheres for use in the treatment of cancer |
TWI242000B (en) * | 1998-12-10 | 2005-10-21 | Univ Southern California | Reversible aqueous pH sensitive lipidizing reagents, compositions and methods of use |
US6140015A (en) * | 1998-12-10 | 2000-10-31 | International Business Machines Corporation | Photoresist compositions with pendant polar-functionalized aromatic groups and acid-labile branching |
EP1159756B1 (en) * | 1999-03-11 | 2006-06-28 | Ardenia Investments Ltd. | Compounds for the treatment of cancer |
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 |
WO2002092771A2 (en) | 2001-05-11 | 2002-11-21 | Ludwig Institute For Cancer Research | Specific binding proteins and uses 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 |
CA2822457C (en) | 2001-12-14 | 2016-03-08 | The University Of Wyoming | Methods and compositions for controlled resease of drugs |
US8361464B2 (en) | 2002-03-01 | 2013-01-29 | Immunomedics, Inc. | Anthracycline-Antibody Conjugates for Cancer Therapy |
US20050069551A1 (en) * | 2002-03-08 | 2005-03-31 | Emory University | Cytotoxic compound-protein conjugates as suppressors of tumor growth and angiogenesis |
US20060229239A9 (en) * | 2002-03-08 | 2006-10-12 | Mamoru Shoji | Novel curcuminoid-factor VIIa constructs as suppressors of tumor growth and angiogenesis |
EP1506218B1 (en) * | 2002-05-24 | 2017-04-12 | Arrowhead Pharmaceuticals, Inc. | Reversible modification of membrane interaction |
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 |
ES2408704T3 (es) | 2005-01-05 | 2013-06-21 | Biogen Idec Ma Inc. | Moléculas de unión a Cripto |
JP2010508271A (ja) | 2006-10-27 | 2010-03-18 | ウェイ‐チャン シェン | 脂質化インターフェロンおよびその使用 |
MX2009007987A (es) * | 2007-01-25 | 2010-03-01 | Dana Farber Cancer Inst Inc | Uso de anticuerpos anti-egfr en el tratamiento de enfermedad mediada por egfr mutante. |
US9023356B2 (en) * | 2007-03-15 | 2015-05-05 | Ludwig Institute For Cancer Research Ltd | Treatment method using EGFR antibodies and SRC inhibitors and related formulations |
JP5532486B2 (ja) | 2007-08-14 | 2014-06-25 | ルードヴィッヒ インスティテュート フォー キャンサー リサーチ | Egf受容体を標的とするモノクローナル抗体175ならびにその誘導体および用途 |
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 |
US9051354B2 (en) | 2009-03-17 | 2015-06-09 | The University Of Tokyo | Protein charge regulator and protein-encapsulating polymer micelle complex |
US8535948B2 (en) * | 2009-03-26 | 2013-09-17 | Institute For Systems Biology | Method to determine protein interaction sites |
JP2012531212A (ja) | 2009-07-03 | 2012-12-10 | アビペップ ピーティーワイ リミテッド | イムノコンジュゲート及びその作製方法 |
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 |
US9738707B2 (en) | 2011-07-15 | 2017-08-22 | Biogen Ma Inc. | Heterodimeric Fc regions, binding molecules comprising same, and methods relating thereto |
EP2744931B1 (en) | 2011-08-18 | 2018-05-02 | Affinity Biosciences Pty Ltd | Soluble polypeptides |
PL2802606T3 (pl) | 2012-01-10 | 2018-09-28 | Biogen Ma Inc. | Udoskonalenie transportu cząsteczek terapeutycznych przez barierę krew-mózg |
GB201202268D0 (en) | 2012-02-09 | 2012-03-28 | Medical Res Council | Intracellular immunity |
WO2014057436A2 (en) | 2012-10-10 | 2014-04-17 | Adamed Sp. Z O.O. | Anticancer conjugate |
CA2895284A1 (en) | 2013-02-07 | 2014-08-14 | Immunomedics, Inc. | Pro-drug form (p2pdox) of the highly potent 2-pyrrolinodoxorubicin conjugated to antibodies for targeted therapy of cancer |
WO2014141094A1 (en) | 2013-03-14 | 2014-09-18 | Adamed Sp. Z O.O. | Anticancer conjugate |
WO2015123595A1 (en) | 2014-02-14 | 2015-08-20 | The Regents Of The University Of California | Cyclic peroxides as prodrugs for selective delivery of agents |
EP3200765A4 (en) | 2014-10-03 | 2018-05-30 | 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 |
BR102016018074A2 (pt) | 2015-08-07 | 2021-11-16 | ALX Oncology Inc. | Construção variante de sirp-alfa, seu método de preparação e seus usos, molécula de ácido nucleico, vetor, célula hospedeira, e composição farmacêutica |
SI3380495T1 (sl) | 2015-11-24 | 2022-01-31 | Transfert Plus, S.E.C. | Peptidne spojine in peptidni konjugati za zdravljenje raka z receptorsko posredovano kemoterapijo |
EP3554638B1 (en) | 2016-12-19 | 2022-02-02 | Morehouse School of Medicine | Compositions and methods for treating diseases by inhibiting exosome release |
US10800817B2 (en) | 2016-12-19 | 2020-10-13 | Morehouse School Of Medicine | Compositions and methods for treating diseases by inhibiting exosome release |
WO2020243338A1 (en) | 2019-05-31 | 2020-12-03 | ALX Oncology Inc. | Methods of treating cancer with sirp alpha fc fusion in combination with an immune checkpoint inhibitor |
US11180534B1 (en) | 2021-06-04 | 2021-11-23 | Morehouse School Of Medicine | Compositions and methods for treating SARS-CoV-2 infections |
WO2023137443A1 (en) * | 2022-01-14 | 2023-07-20 | Regeneron Pharmaceuticals, Inc. | Verrucarin a derivatives and antibody drug conjugates thereof |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
-
1991
- 1991-12-27 JP JP3361486A patent/JPH04334377A/ja active Pending
- 1991-12-27 FI FI916131A patent/FI101678B/fi active
- 1991-12-28 HU HU914133A patent/HUT60484A/hu unknown
- 1991-12-30 PT PT99954A patent/PT99954B/pt not_active IP Right Cessation
- 1991-12-30 KR KR1019910025982A patent/KR920012063A/ko not_active Application Discontinuation
- 1991-12-30 ZA ZA9110203A patent/ZA9110203B/xx unknown
- 1991-12-30 DK DK91203439.4T patent/DK0495265T3/da active
- 1991-12-30 AU AU90098/91A patent/AU646121B2/en not_active Ceased
- 1991-12-30 AT AT91203439T patent/ATE109476T1/de active
- 1991-12-30 IE IE456791A patent/IE65406B1/en not_active IP Right Cessation
- 1991-12-30 ES ES91203439T patent/ES2061166T3/es not_active Expired - Lifetime
- 1991-12-30 EP EP91203439A patent/EP0495265B1/en not_active Expired - Lifetime
- 1991-12-30 DE DE69103255T patent/DE69103255T2/de not_active Expired - Fee Related
- 1991-12-30 CA CA002058595A patent/CA2058595A1/en not_active Abandoned
- 1991-12-31 US US07/815,671 patent/US5306809A/en not_active Expired - Fee Related
-
1992
- 1992-01-02 NO NO920040A patent/NO180417C/no unknown
- 1992-01-06 NZ NZ241217A patent/NZ241217A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
PT99954A (pt) | 1993-06-30 |
PT99954B (pt) | 1999-06-30 |
JPH04334377A (ja) | 1992-11-20 |
HU914133D0 (en) | 1992-03-30 |
IE914567A1 (en) | 1992-07-01 |
AU646121B2 (en) | 1994-02-10 |
DE69103255D1 (de) | 1994-09-08 |
IE65406B1 (en) | 1995-10-18 |
US5306809A (en) | 1994-04-26 |
ES2061166T3 (es) | 1994-12-01 |
DE69103255T2 (de) | 1994-12-08 |
FI101678B1 (fi) | 1998-08-14 |
KR920012063A (ko) | 1992-07-25 |
FI916131A0 (fi) | 1991-12-27 |
NZ241217A (en) | 1993-12-23 |
EP0495265B1 (en) | 1994-08-03 |
EP0495265A1 (en) | 1992-07-22 |
AU9009891A (en) | 1993-01-28 |
CA2058595A1 (en) | 1992-07-01 |
ATE109476T1 (de) | 1994-08-15 |
DK0495265T3 (da) | 1995-01-02 |
NO180417C (no) | 1997-04-16 |
HUT60484A (en) | 1992-09-28 |
NO180417B (no) | 1997-01-06 |
FI101678B (fi) | 1998-08-14 |
FI916131A (fi) | 1992-07-01 |
NO920040L (no) | 1992-07-01 |
NO920040D0 (no) | 1992-01-02 |
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