AR002280A1 - Un compuesto derivado del acido poli-pirrol-carboxamidonaftalenico, un procedimiento para su preparacion, una composicion farmaceutica que lo contieney un procedimiento para mejorar la biodisponibilidad sistemica de un compuesto biologicamente activo. - Google Patents
Un compuesto derivado del acido poli-pirrol-carboxamidonaftalenico, un procedimiento para su preparacion, una composicion farmaceutica que lo contieney un procedimiento para mejorar la biodisponibilidad sistemica de un compuesto biologicamente activo.Info
- Publication number
- AR002280A1 AR002280A1 ARP960101576A AR10157696A AR002280A1 AR 002280 A1 AR002280 A1 AR 002280A1 AR P960101576 A ARP960101576 A AR P960101576A AR 10157696 A AR10157696 A AR 10157696A AR 002280 A1 AR002280 A1 AR 002280A1
- Authority
- AR
- Argentina
- Prior art keywords
- procedure
- biologically active
- acid
- poly
- active compound
- 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)
- Proteomics, Peptides & Aminoacids (AREA)
- Biophysics (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
Se provee un compuesto derivado del ácido ácido-poli-pirrol-carboxamidonaftalénico de fórmula (II); en donde R es ungrupo ácido; m es un entero de 1 a 3; n es cero o un entero de 1 a 3; A es un espaciador enzimáticamente hidrolizable; y X es un compuesto biológicamenteactivo; o una sal farmacéuticamente aceptable del mismo, para usar como un agente antiproliferativo, en particular antitumoral y antiangiogénico y como unagente antiinflamatorio. Además se provee un procedimiento para su preparación, una composición farmacéutica que lo contiene y un procedimiento para mejorarla biodisponibilidad sistémica de un compuesto X biológicamente activo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB9504065.5A GB9504065D0 (en) | 1995-03-01 | 1995-03-01 | Poly-pyrrolecarboxamidonaphthalenic acid derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
AR002280A1 true AR002280A1 (es) | 1998-03-11 |
Family
ID=10770421
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP960101576A AR002280A1 (es) | 1995-03-01 | 1996-02-29 | Un compuesto derivado del acido poli-pirrol-carboxamidonaftalenico, un procedimiento para su preparacion, una composicion farmaceutica que lo contieney un procedimiento para mejorar la biodisponibilidad sistemica de un compuesto biologicamente activo. |
Country Status (18)
Country | Link |
---|---|
EP (1) | EP0758339A1 (es) |
JP (1) | JPH10504319A (es) |
KR (1) | KR970702868A (es) |
CN (1) | CN1148391A (es) |
AR (1) | AR002280A1 (es) |
AU (1) | AU696470B2 (es) |
CA (1) | CA2189358A1 (es) |
EA (1) | EA000006B1 (es) |
FI (1) | FI964331A (es) |
GB (1) | GB9504065D0 (es) |
HU (1) | HUP9603305A3 (es) |
IL (1) | IL117193A0 (es) |
MX (1) | MX9605089A (es) |
NO (1) | NO964610L (es) |
NZ (1) | NZ302267A (es) |
PL (1) | PL317094A1 (es) |
WO (1) | WO1996026950A1 (es) |
ZA (1) | ZA961636B (es) |
Families Citing this family (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998014459A1 (de) * | 1996-09-30 | 1998-04-09 | Bayer Aktiengesellschaft | Glycokonjugate von modifizierten camptothecin-derivaten (20-o-verknüpfung) |
DE19640969A1 (de) * | 1996-10-04 | 1998-04-16 | Bayer Ag | 20-0-verknüpfte Glycokonjugate von Camptothecin |
ID23424A (id) * | 1997-05-14 | 2000-04-20 | Bayer Ag | Glikokonjugat dari 20(s)-kamptotesin |
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 |
US6403604B1 (en) | 2001-03-01 | 2002-06-11 | California Pacific Medical Center | Nitrogen-based camptothecin derivatives |
US6855720B2 (en) | 2001-03-01 | 2005-02-15 | California Pacific Medical Center | Nitrogen-based camptothecin derivatives |
JP2005505507A (ja) | 2001-06-13 | 2005-02-24 | ジーンソフト ファーマシューティカルズ インコーポレイテッド | 抗感染活性を有するイソキノリン化合物 |
CA2486106C (en) * | 2002-05-16 | 2013-07-16 | Glycomimetics, Inc. | Compounds and methods for inhibiting selectin-mediated function |
AU2003243380A1 (en) | 2002-06-03 | 2003-12-19 | California Pacific Medical Center | Nitrogen-based homo-camptothecin derivatives |
DE60326735D1 (de) | 2002-08-02 | 2009-04-30 | Genesoft Pharmaceuticals Inc | Biaryl-verbindungen mit antiinfektiver wirkung |
WO2004039318A2 (en) | 2002-10-25 | 2004-05-13 | Genesoft Pharmaceuticals, Inc. | Anti-infective biaryl compounds |
JP2006509027A (ja) | 2002-12-10 | 2006-03-16 | オーシェント ファーマシューティカルズ コーポレーション | (ピロールカルボキサミド)−(ベンズアミド)−(イミダゾールカルボキサミド)モチーフを有する抗菌化合物 |
AU2006284578B2 (en) | 2005-09-02 | 2011-01-27 | 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 |
WO2011163568A1 (en) * | 2010-06-24 | 2011-12-29 | University Of Kansas | Conjugates comprising an n-oxime bond and associated methods |
WO2012037034A1 (en) | 2010-09-14 | 2012-03-22 | Glycomimetics, Inc. | E-selectin antagonists |
JP2015500887A (ja) | 2011-12-22 | 2015-01-08 | グリコミメティクス, インコーポレイテッド | E−セレクチンアンタゴニスト化合物、組成物および使用方法 |
AU2013355238B2 (en) | 2012-12-07 | 2017-12-14 | Glycomimetics, Inc. | Compounds, compositions and methods using E-selectin antagonists for mobilization of hematopoietic cells |
SI3227310T1 (sl) | 2014-12-03 | 2019-11-29 | Glycomimetics Inc | Heterobifunkcionalni inhibitorji e-selektinov in receptorjev kemokina CXCR4 |
CA3009836A1 (en) | 2016-01-22 | 2017-07-27 | Glycomimetics, Inc. | Glycomimetic inhibitors of pa-il and pa-iil lectins |
US11291678B2 (en) | 2016-03-02 | 2022-04-05 | Glycomimetics, Inc | Methods for the treatment and/or prevention of cardiovascular disease by inhibition of E-selectin |
WO2018031445A1 (en) | 2016-08-08 | 2018-02-15 | Glycomimetics, Inc. | Combination of t-cell checkpoint inhibitors with inhibitors of e-selectin or cxcr4, or with heterobifunctional inhibitors of both e-selectin and cxcr4 |
JP7069136B2 (ja) | 2016-10-07 | 2022-05-17 | グリコミメティクス, インコーポレイテッド | 極めて強力な多量体e-セレクチンアンタゴニスト |
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 |
JP7275131B2 (ja) | 2017-11-30 | 2023-05-17 | グリコミメティクス, インコーポレイテッド | 骨髄浸潤リンパ球を動員する方法、およびその使用 |
CN111566117A (zh) | 2017-12-29 | 2020-08-21 | 糖模拟物有限公司 | E-选择蛋白和半乳凝素-3的异双功能抑制剂 |
JP7455064B2 (ja) | 2018-03-05 | 2024-03-25 | グリコミメティクス, インコーポレイテッド | 急性骨髄性白血病および関連状態を処置する方法 |
WO2020139962A1 (en) | 2018-12-27 | 2020-07-02 | 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 |
CN114933569A (zh) * | 2022-04-07 | 2022-08-23 | 澳门科技大学 | 鞘脂类化合物、含有鞘脂类化合物的脂质体和应用 |
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 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 CN CN96190152A patent/CN1148391A/zh active Pending
- 1996-02-08 EP EP96904024A patent/EP0758339A1/en not_active Withdrawn
- 1996-02-08 HU HU9603305A patent/HUP9603305A3/hu unknown
- 1996-02-08 MX MX9605089A patent/MX9605089A/es unknown
- 1996-02-08 AU AU48698/96A patent/AU696470B2/en not_active Ceased
- 1996-02-08 EA EA199600104A patent/EA000006B1/ru not_active IP Right Cessation
- 1996-02-08 PL PL96317094A patent/PL317094A1/xx unknown
- 1996-02-08 NZ NZ302267A patent/NZ302267A/en unknown
- 1996-02-08 JP JP8525980A patent/JPH10504319A/ja active Pending
- 1996-02-20 IL IL11719396A patent/IL117193A0/xx unknown
- 1996-02-29 ZA ZA961636A patent/ZA961636B/xx unknown
- 1996-02-29 AR ARP960101576A patent/AR002280A1/es unknown
- 1996-10-28 FI FI964331A patent/FI964331A/fi unknown
- 1996-10-31 NO NO964610A patent/NO964610L/no unknown
- 1996-11-01 KR KR1019960706263A patent/KR970702868A/ko not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
EP0758339A1 (en) | 1997-02-19 |
EA199600104A1 (ru) | 1997-09-30 |
PL317094A1 (en) | 1997-03-17 |
CA2189358A1 (en) | 1996-09-06 |
HUP9603305A2 (en) | 1997-08-28 |
GB9504065D0 (en) | 1995-04-19 |
ZA961636B (en) | 1996-09-06 |
KR970702868A (ko) | 1997-06-10 |
FI964331A (fi) | 1996-11-01 |
AU696470B2 (en) | 1998-09-10 |
FI964331A0 (fi) | 1996-10-28 |
NO964610D0 (no) | 1996-10-31 |
MX9605089A (es) | 1997-12-31 |
WO1996026950A1 (en) | 1996-09-06 |
NO964610L (no) | 1996-10-31 |
IL117193A0 (en) | 1996-06-18 |
NZ302267A (en) | 1997-10-24 |
AU4869896A (en) | 1996-09-18 |
JPH10504319A (ja) | 1998-04-28 |
HUP9603305A3 (en) | 1998-01-28 |
CN1148391A (zh) | 1997-04-23 |
EA000006B1 (ru) | 1997-12-30 |
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