HUT42493A - Process for producing new conjugates and derivatives of vinblastine and pharmaceutical compositions containing them - Google Patents
Process for producing new conjugates and derivatives of vinblastine and pharmaceutical compositions containing themInfo
- Publication number
- HUT42493A HUT42493A HU864190A HU419086A HUT42493A HU T42493 A HUT42493 A HU T42493A HU 864190 A HU864190 A HU 864190A HU 419086 A HU419086 A HU 419086A HU T42493 A HUT42493 A HU T42493A
- Authority
- HU
- Hungary
- Prior art keywords
- vinblastine
- derivatives
- image
- group
- conjugates
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
- C07D519/04—Dimeric indole alkaloids, e.g. vincaleucoblastine
-
- 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
- A61K47/6805—Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates the drug being a vinca alkaloid
Landscapes
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicinal Preparation (AREA)
- Peptides Or Proteins (AREA)
Abstract
Previously unknown conjugates of vinblastine, or derivatives thereof, have the general formula <IMAGE> where A denotes an "arm" such as <IMAGE> or <IMAGE> where n is an integer from 1-5 and R is a hydrogen atom or an acyl group, R1 is an optionally modified protein radical, R2 is a methoxy group, an amino group or an α-amino acid ester which is bonded using a bond of the amide type and where the ester group contains 1-6 carbon atoms, and where R3 is a hydrogen atom or an hydroxyl group and is in all cases in the two possible configurations. These conjugates have a powerful effect when treating leukaemias, lymphosarcomas and other malignant tumours, including the so-called "solid" tumours, and when treating Hodgkin's disease.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
LU86157A LU86157A1 (en) | 1985-11-12 | 1985-11-12 | NEW PROCESS FOR THE MANUFACTURE OF VINBLASTIN CONJUGATES AND DERIVATIVES THEREOF |
EP86870042A EP0222722B1 (en) | 1985-11-12 | 1986-04-08 | Conjugates of vinblastine and its derivatives, process for preparing them and pharmaceutical compositions containing these conjugates |
Publications (2)
Publication Number | Publication Date |
---|---|
HUT42493A true HUT42493A (en) | 1987-07-28 |
HU196217B HU196217B (en) | 1988-10-28 |
Family
ID=26106792
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU864190A HU196217B (en) | 1985-11-12 | 1986-10-06 | Process for production of new vinblastin-ensime-conjugates and their derivatives and medical compounds containing such substances |
Country Status (6)
Country | Link |
---|---|
AT (1) | ATE89567T1 (en) |
AU (1) | AU577206B2 (en) |
DK (1) | DK164107C (en) |
GR (1) | GR862436B (en) |
HU (1) | HU196217B (en) |
OA (1) | OA08424A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2508905B1 (en) * | 1981-07-01 | 1984-01-27 | Roussel Uclaf | |
CA1285866C (en) * | 1984-10-19 | 1991-07-09 | Akiko Kubodera | Immunoassay for estriol-3-sulfate |
ZA873600B (en) * | 1986-05-27 | 1988-12-28 | Lilly Co Eli | Immunoglobulin conjugates |
US5094849A (en) * | 1988-08-08 | 1992-03-10 | Eli Lilly And Company | Cytotoxic antibody conjugates of hydrazide derivatized vinca analogs via simple organic linkers |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GR81790B (en) * | 1983-04-29 | 1984-12-12 | Omnichem Sa |
-
1986
- 1986-04-08 AT AT86870042T patent/ATE89567T1/en not_active IP Right Cessation
- 1986-09-24 GR GR862436A patent/GR862436B/en unknown
- 1986-09-30 AU AU63401/86A patent/AU577206B2/en not_active Ceased
- 1986-10-03 DK DK473286A patent/DK164107C/en not_active IP Right Cessation
- 1986-10-06 HU HU864190A patent/HU196217B/en not_active IP Right Cessation
- 1986-10-07 OA OA58971A patent/OA08424A/en unknown
Also Published As
Publication number | Publication date |
---|---|
GR862436B (en) | 1986-12-23 |
AU6340186A (en) | 1988-04-14 |
DK164107C (en) | 1992-10-05 |
HU196217B (en) | 1988-10-28 |
DK473286A (en) | 1987-05-13 |
OA08424A (en) | 1988-06-30 |
ATE89567T1 (en) | 1993-06-15 |
DK164107B (en) | 1992-05-11 |
DK473286D0 (en) | 1986-10-03 |
AU577206B2 (en) | 1988-09-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0124502A3 (en) | Conjugates of vinblastine and its derivatives, process for their preparation and pharmaceutical compositions containing these conjugates | |
AU579387B2 (en) | New tetrapyrrole therapeutic agents | |
DE3683528D1 (en) | TETRAPYRROL THERAPY AGENT. | |
IL76457A0 (en) | Tetralin derivatives,their preparation and pharmaceutical compositions containing them | |
AU578781B2 (en) | Novel peptide derivatives having a nitrogenous polycyclic structure, process for the preparation thereof and pharmaceutical compositions containing them | |
OA06421A (en) | Process for the preparation of N- (vinblastinoyl-23) derivatives of amino acids and peptides. | |
GR3001889T3 (en) | Prodrug compounds, process for the preparation thereof and sustained release preparation comprising the same | |
DE3869173D1 (en) | AMINO 5,6,7,8-TETRAHYDRONAPHTHO (2,3B) FURANDERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND MEDICINAL PRODUCTS CONTAINING THEM. | |
DE3570437D1 (en) | 1-hydroxy-1,1-diphosphonic-acid derivatives, process for their preparation and pharmaceutical preparations, especially for the treatment of bone tumours | |
HUT42493A (en) | Process for producing new conjugates and derivatives of vinblastine and pharmaceutical compositions containing them | |
DE3362009D1 (en) | L-alanyl-d-isoglutaminyl-adamantyl amide, process for its preparation and pharmaceutical compositions containing this compound | |
GR3005533T3 (en) | ||
ES8602676A1 (en) | Hexahydropyrrolo (2,1-a) isoquinoline derivatives. | |
IL85231A0 (en) | Substituted 3-phenyl-7h-thiazolo(3,2-b)(1,2,4)triazin-7-ones,a process for the preparation thereof,pharmaceutical compositions containing same and the use thereof | |
EP0418990A3 (en) | 13-bromo and 13,14-dibromo ergoline, their preparation and their use | |
GR3015706T3 (en) | Benzylselenobenzamides of aminopyridines and picolylamines. | |
NZ223664A (en) | 2,3-dihydro-3-phenyl-2-oxo-benzofuranylacetic acid amide derivatives and pharmaceutical compositions | |
MX4658E (en) | PROCEDURE FOR PREPARING 3-CEFEM-4-CARBOXYLIC ACID COMPOUNDS 3.7 DISUBSTITUTED | |
IT1251979B (en) | Diazacyclic derivatives |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
HU90 | Patent valid on 900628 | ||
HMM4 | Cancellation of final prot. due to non-payment of fee |