NO964610L - Increased bioavailability of biologically active compounds by binding to polypyrrole carboxamidone offset derivatives - Google Patents
Increased bioavailability of biologically active compounds by binding to polypyrrole carboxamidone offset derivativesInfo
- Publication number
- NO964610L NO964610L NO964610A NO964610A NO964610L NO 964610 L NO964610 L NO 964610L NO 964610 A NO964610 A NO 964610A NO 964610 A NO964610 A NO 964610A NO 964610 L NO964610 L NO 964610L
- Authority
- NO
- Norway
- Prior art keywords
- biologically active
- carboxamidone
- polypyrrole
- binding
- active compounds
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Biophysics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biotechnology (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicinal Preparation (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Forbindelse av formel (II) NH--CO¿A-X --CO- N CH, (II) hvor R er en sur gruppe; m er et helt tall fra l til 3; n er O eller et helt tall fra l til 3; A er en enzymatisk hydrolyserbar avstandsgruppe; og X er en biologisk aktiv forbindelse; eller et farmasøytisk akseptabelt salt derav, for bruk som et antiproliferativ, spesielt anti-tumor- og anti-angiogent middel, og anti-inflammatorisk middel.Compound of formula (II) NH - CO COA-X - CO- N CH, (II) wherein R is an acidic group; m is an integer from 1 to 3; n is 0 or an integer from 1 to 3; A is an enzymatic hydrolyzable spacer; and X is a biologically active compound; or a pharmaceutically acceptable salt thereof, for use as an antiproliferative, especially anti-tumor and anti-angiogenic agent, and anti-inflammatory agent.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB9504065.5A GB9504065D0 (en) | 1995-03-01 | 1995-03-01 | Poly-pyrrolecarboxamidonaphthalenic acid derivatives |
PCT/EP1996/000528 WO1996026950A1 (en) | 1995-03-01 | 1996-02-08 | Increased bioavailability of biologically active compounds by linking to polypyrrolecarboxamidonaphthalene derivatives |
Publications (2)
Publication Number | Publication Date |
---|---|
NO964610D0 NO964610D0 (en) | 1996-10-31 |
NO964610L true NO964610L (en) | 1996-10-31 |
Family
ID=10770421
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO964610A NO964610L (en) | 1995-03-01 | 1996-10-31 | Increased bioavailability of biologically active compounds by binding to polypyrrole carboxamidone offset derivatives |
Country Status (18)
Country | Link |
---|---|
EP (1) | EP0758339A1 (en) |
JP (1) | JPH10504319A (en) |
KR (1) | KR970702868A (en) |
CN (1) | CN1148391A (en) |
AR (1) | AR002280A1 (en) |
AU (1) | AU696470B2 (en) |
CA (1) | CA2189358A1 (en) |
EA (1) | EA000006B1 (en) |
FI (1) | FI964331A (en) |
GB (1) | GB9504065D0 (en) |
HU (1) | HUP9603305A3 (en) |
IL (1) | IL117193A0 (en) |
MX (1) | MX9605089A (en) |
NO (1) | NO964610L (en) |
NZ (1) | NZ302267A (en) |
PL (1) | PL317094A1 (en) |
WO (1) | WO1996026950A1 (en) |
ZA (1) | ZA961636B (en) |
Families Citing this family (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PT934329E (en) * | 1996-09-30 | 2002-05-31 | Bayer Ag | GLYCOCONYGATES OF MODIFIED CAMPTOTECIN DERIVATIVES (LIGACAO 20-O) |
DE19640969A1 (en) * | 1996-10-04 | 1998-04-16 | Bayer Ag | 20-0 linked glycoconjugates from camptothecin |
ID23424A (en) * | 1997-05-14 | 2000-04-20 | Bayer Ag | GLIKOKONJUGUS OF 20 (S) -CAMPTOTESIN |
GB9713732D0 (en) * | 1997-06-27 | 1997-09-03 | Pharmacia & Upjohn Spa | Substituted triazinic compounds |
GB9713733D0 (en) * | 1997-06-27 | 1997-09-03 | Pharmacia & Upjohn Spa | Poly-branched polycarboxamido compounds |
US6485514B1 (en) * | 1997-12-12 | 2002-11-26 | Supergen, Inc. | Local delivery of therapeutic agents |
US6288072B1 (en) * | 1999-12-29 | 2001-09-11 | Monroe E. Wall | Camptothecin β-alanine esters with topoisomerase I inhibition |
US6350756B1 (en) | 2001-01-18 | 2002-02-26 | California Pacific Medical Center | Camptothecin derivatives |
US6855720B2 (en) | 2001-03-01 | 2005-02-15 | California Pacific Medical Center | Nitrogen-based camptothecin derivatives |
US6403604B1 (en) | 2001-03-01 | 2002-06-11 | California Pacific Medical Center | Nitrogen-based camptothecin derivatives |
WO2002100832A1 (en) | 2001-06-13 | 2002-12-19 | Genesoft Pharmaceuticals, Inc. | Isoquinoline compounds having antiinfective activity |
WO2003097658A2 (en) * | 2002-05-16 | 2003-11-27 | Glycomimetics, Inc. | Compounds and methods for inhibiting selectin-mediated function |
WO2003101998A1 (en) | 2002-06-03 | 2003-12-11 | California Pacific Medical Center | Nitrogen-based homo-camptothecin derivatives |
DE60326735D1 (en) | 2002-08-02 | 2009-04-30 | Genesoft Pharmaceuticals Inc | BIARYL COMPOUNDS WITH ANTI-INFECTIVE EFFECT |
US7265129B2 (en) | 2002-10-25 | 2007-09-04 | Genesoft Pharmaceuticals, Inc. | Anti-infective biaryl compounds |
EP1587529A4 (en) | 2002-12-10 | 2009-08-12 | Oscient Pharmaceuticals Corp | Antibacterial compounds having a (pyrrole carboxamide)-(benzamide)-(imidazole carboxamide) motif |
ES2651929T3 (en) | 2005-09-02 | 2018-01-30 | Glycomimetics, Inc. | Heterobifunctional pan-selectin inhibitors |
US7875602B2 (en) * | 2005-10-21 | 2011-01-25 | Sutter West Bay Hospitals | Camptothecin derivatives as chemoradiosensitizing agents |
WO2009126556A1 (en) | 2008-04-08 | 2009-10-15 | Glycomimetics, Inc. | Pan-selectin inhibitor with enhanced pharmacokinetic activity |
EP2585096B1 (en) * | 2010-06-24 | 2021-05-05 | University Of Kansas | Bifunctional conjugate compositions and associated methods |
WO2012037034A1 (en) | 2010-09-14 | 2012-03-22 | Glycomimetics, Inc. | E-selectin antagonists |
KR102055958B1 (en) | 2011-12-22 | 2019-12-13 | 글리코미메틱스, 인크. | E-selectin antagonist compounds, compositions, and methods of use |
SI2928476T1 (en) | 2012-12-07 | 2018-06-29 | Glycomimetics, Inc. | Compounds, compositions and methods using e-selectin antagonists for mobilization of hematopoietic cells |
PT3227310T (en) | 2014-12-03 | 2019-11-06 | Glycomimetics Inc | Heterobifunctional inhibitors of e-selectins and cxcr4 chemokine receptors |
WO2017127422A1 (en) | 2016-01-22 | 2017-07-27 | Glycomimetics, Inc. | Glycomimetic inhibitors of pa-il and pa-iil lectins |
WO2017151708A1 (en) | 2016-03-02 | 2017-09-08 | Glycomimetics, Inc. | Methods for the treatment and/or prevention of cardiovescular disease by inhibition of e-selectin |
JP2019524791A (en) | 2016-08-08 | 2019-09-05 | グリコミメティクス, インコーポレイテッド | Combinations of T cell checkpoint inhibitors with inhibitors of E-selectin or inhibitors of CXCR4 or with heterobifunctional inhibitors of both E-selectin and CXCR4 |
BR112019006642A2 (en) | 2016-10-07 | 2019-07-02 | Glycomimetics Inc | highly potent multimeric e-selectin antagonists |
EP3596096A1 (en) | 2017-03-15 | 2020-01-22 | GlycoMimetics, Inc. | Galactopyranosyl-cyclohexyl derivatives as e-selectin antagonists |
EP3381897A1 (en) | 2017-03-27 | 2018-10-03 | Leadiant Biosciences SA | Derivatives of the disodium 2,2'-{carbonylbis[imino-3,1-phenylenecarbonylimino(1-methyl-1h-pyrrole-4,2-diyl)carbonylimino]}dinaphthalene-1,5-disulfonate salt and related compounds as heparanase inhibitors for the treatment of cancer |
WO2019108750A1 (en) | 2017-11-30 | 2019-06-06 | Glycomimetics, Inc. | Methods of mobilizing marrow infiltrating lymphocytes and uses thereof |
KR20200104889A (en) | 2017-12-29 | 2020-09-04 | 글리코미메틱스, 인크. | E-selectin and heterobifunctional inhibitors of galectin-3 |
WO2019173229A1 (en) | 2018-03-05 | 2019-09-12 | Glycomimetics, Inc. | Methods for treating acute myeloid leukemia and related conditions |
US11845771B2 (en) | 2018-12-27 | 2023-12-19 | Glycomimetics, Inc. | Heterobifunctional inhibitors of E-selectin and galectin-3 |
WO2021118927A1 (en) | 2019-12-13 | 2021-06-17 | Insideoutbio, Inc. | Methods and compositions for targeted delivery of nucleic acid therapeutics |
CN114933569B (en) * | 2022-04-07 | 2024-07-23 | 澳门科技大学 | Sphingolipid compound, liposome containing sphingolipid compound and application |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9000644D0 (en) * | 1990-01-11 | 1990-03-14 | Erba Carlo Spa | New ureido derivatives of poly-4-amino-2-carboxy-1-methyl compounds |
GB9216962D0 (en) * | 1992-08-11 | 1992-09-23 | Erba Carlo Spa | Therapeutically active naphthalenesulfonic-pyrrolecarboxamido derivatives |
GB9304589D0 (en) * | 1993-03-05 | 1993-04-21 | Erba Carlo Spa | Biologically active ureido derivatives useful as antimetastic agents |
GB9307948D0 (en) * | 1993-04-16 | 1993-06-02 | Erba Carlo Spa | Biologically active ureido derivatives useful in the treatment of lentivirus-induced disease |
GB9403909D0 (en) * | 1994-03-01 | 1994-04-20 | Erba Carlo Spa | Ureido derivatives of naphthalenephosphonic acids and process for their preparation |
-
1995
- 1995-03-01 GB GBGB9504065.5A patent/GB9504065D0/en active Pending
-
1996
- 1996-02-08 MX MX9605089A patent/MX9605089A/en unknown
- 1996-02-08 EP EP96904024A patent/EP0758339A1/en not_active Withdrawn
- 1996-02-08 HU HU9603305A patent/HUP9603305A3/en unknown
- 1996-02-08 WO PCT/EP1996/000528 patent/WO1996026950A1/en not_active Application Discontinuation
- 1996-02-08 CA CA002189358A patent/CA2189358A1/en not_active Abandoned
- 1996-02-08 AU AU48698/96A patent/AU696470B2/en not_active Ceased
- 1996-02-08 NZ NZ302267A patent/NZ302267A/en unknown
- 1996-02-08 PL PL96317094A patent/PL317094A1/en unknown
- 1996-02-08 EA EA199600104A patent/EA000006B1/en not_active IP Right Cessation
- 1996-02-08 JP JP8525980A patent/JPH10504319A/en active Pending
- 1996-02-08 CN CN96190152A patent/CN1148391A/en active Pending
- 1996-02-20 IL IL11719396A patent/IL117193A0/en unknown
- 1996-02-29 AR ARP960101576A patent/AR002280A1/en unknown
- 1996-02-29 ZA ZA961636A patent/ZA961636B/en unknown
- 1996-10-28 FI FI964331A patent/FI964331A/en unknown
- 1996-10-31 NO NO964610A patent/NO964610L/en unknown
- 1996-11-01 KR KR1019960706263A patent/KR970702868A/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
NZ302267A (en) | 1997-10-24 |
AU696470B2 (en) | 1998-09-10 |
HUP9603305A3 (en) | 1998-01-28 |
NO964610D0 (en) | 1996-10-31 |
FI964331A0 (en) | 1996-10-28 |
CA2189358A1 (en) | 1996-09-06 |
ZA961636B (en) | 1996-09-06 |
HUP9603305A2 (en) | 1997-08-28 |
AU4869896A (en) | 1996-09-18 |
EP0758339A1 (en) | 1997-02-19 |
KR970702868A (en) | 1997-06-10 |
CN1148391A (en) | 1997-04-23 |
EA199600104A1 (en) | 1997-09-30 |
FI964331A (en) | 1996-11-01 |
WO1996026950A1 (en) | 1996-09-06 |
IL117193A0 (en) | 1996-06-18 |
MX9605089A (en) | 1997-12-31 |
GB9504065D0 (en) | 1995-04-19 |
EA000006B1 (en) | 1997-12-30 |
AR002280A1 (en) | 1998-03-11 |
JPH10504319A (en) | 1998-04-28 |
PL317094A1 (en) | 1997-03-17 |
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