HK65793A - Antiparasitic avermectin and milbemycin derivatives and process for their preparation - Google Patents
Antiparasitic avermectin and milbemycin derivatives and process for their preparation Download PDFInfo
- Publication number
- HK65793A HK65793A HK657/93A HK65793A HK65793A HK 65793 A HK65793 A HK 65793A HK 657/93 A HK657/93 A HK 657/93A HK 65793 A HK65793 A HK 65793A HK 65793 A HK65793 A HK 65793A
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/01—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing oxygen
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/195—Antibiotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/20—Bacteria; Culture media therefor
- C12N1/205—Bacterial isolates
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
- C12P17/18—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing at least two hetero rings condensed among themselves or condensed with a common carbocyclic ring system, e.g. rifamycin
- C12P17/181—Heterocyclic compounds containing oxygen atoms as the only ring heteroatoms in the condensed system, e.g. Salinomycin, Septamycin
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/44—Preparation of O-glycosides, e.g. glucosides
- C12P19/60—Preparation of O-glycosides, e.g. glucosides having an oxygen of the saccharide radical directly bound to a non-saccharide heterocyclic ring or a condensed ring system containing a non-saccharide heterocyclic ring, e.g. coumermycin, novobiocin
- C12P19/62—Preparation of O-glycosides, e.g. glucosides having an oxygen of the saccharide radical directly bound to a non-saccharide heterocyclic ring or a condensed ring system containing a non-saccharide heterocyclic ring, e.g. coumermycin, novobiocin the hetero ring having eight or more ring members and only oxygen as ring hetero atoms, e.g. erythromycin, spiramycin, nystatin
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/01—Bacteria or Actinomycetales ; using bacteria or Actinomycetales
- C12R2001/465—Streptomyces
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/822—Microorganisms using bacteria or actinomycetales
- Y10S435/886—Streptomyces
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Veterinary Medicine (AREA)
- Tropical Medicine & Parasitology (AREA)
- Food Science & Technology (AREA)
- Plant Pathology (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Animal Husbandry (AREA)
- Dentistry (AREA)
- Environmental Sciences (AREA)
- Virology (AREA)
- Biomedical Technology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Saccharide Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Claims (18)
1. Composé de formule:
dans laquelle la ligne en pointillés en position 22-23 représente une double liaison facultative et dans laquelle soit R1 représente H ou OH, auquel cas la double liaison n'existe pas, soit la double liaison existe et R1 n'existe pas;
R2 est un groupe alkyle, alkényle, alcoxyalkyle ou alkylthioalkyle en C3―C8 ramifié en alpha; un groupe alkynyle en C4―C8 ramifié en alpha; un groupe alkyl(cycloalkyl en C5―C8) dans lequel le groupe alkyle est un groupe alkyle en C2―C5 ramifié en alpha; un groupe cycloalkyle en C3―C8 ou cycloalkényle en C5―C8, l'un ou l'autre pouvant être éventuellement substitués par un groupe méthylène ou un ou plusieurs groupes alkyle en C1―C4 ou atomes d'halogène; ou un noyau hétérocyclique ayant de 3 à 6 chaînons et contenant de l'oxygène ou du soufre, lequel noyau peut être saturé ou totalement ou partiellement insaturé et qui peut être éventuellement substitué par un ou plusieurs groupes alkyle en C1―C4 ou atomes d'halogène;
R3 représente l'hydrogène ou un groupe méthyle;
R4 représente H ou un groupe 4'-(alpha-L-oléandrosyl)-alpha-L-oléandrosyloxy de formule:
étant entendu que lorsque R2 représente un groupe alkyle, il ne s'agit pas d'un groupe isopropyle ou sec- butyle, et lorsque R4 représente H, R2 ne représente pas un groupe 2-butèn-2-yle, 2-pentèn-2-yle ou 4-méthyl-2-pentèn-2-yle.
2. Composé de formule (I) selon la revendication 1, dans laquelle R4 est un groupe 4'-(alpha-L-oléandrosyl)-alpha-L-oléandrosyloxy.
3. Composé selon la revendication 2, dans lequel R2 est un groupe cycloalkyle ou cycloalkényle en Cs ou C6 qui peut être éventuellement substitué par un ou plusieurs groupes alkyle en C1―C4.
4. Composé selon la revendication 3, dans lequel R2 est un groupe cyclopentyle.
5. Composé selon la revendication 3, dans lequel R2 est un groupe cyclohexyle.
6. Composé selon la revendication 2, dans lequel R2 est un groupe cyclobutyle.
7. Composé selon la revendication 2, dans lequel R2 est un noyau hétérocyclique à 5 ou 6 chaînons contenant de l'oxygène ou du soufre qui peut être éventuellement substitué par un ou plusieurs groupes alkyle en C1―C4 ou atomes d'halogène.
8. Composé selon la revendication 7, dans lequel R2 est un groupe 3-thiényle.
9. Composé selon la revendication 2, dans lequel R2 est un groupe alkylthioalkyle en C3-C8.
10. Composé selon la revendication 9, dans lequel R2 est un groupe 1-méthylthioéthyle.
11. Procédé de production d'un nouveau dérivé de l'avermectine ayant un groupe substituant artificiel en position-25 qui consiste à ajouter un acide carboxylique, ou un sel, ester ou amide ou précurseur oxydatif de celui-ci, à un milieu de fermentation d'une souche de l'organisme Streptomyces avermitilis produisant l'avermectine et à isoler le nouveau dérivé de l'avermectine.
12. Procédé de production d'un composé de formule (1) selon la revendication 1, qui consiste à faire fermenter une souche productrice d'avermectine de l'organisme Streptomyces avermitilis en présence d'un acide carboxylique de formule R2CO2H dans laquelle R2 est tel que défini dans la revendication 1, ou un sel, ester ou amide ou précurseur oxydatif d'un tel composé, et à isoler le composé de formule (I) dans lequel soit R' représente OH auquel cas la double liaison n'existe pas, soit la double liaison existe et R' n'existe pas, et R4 est un groupe 4'-(alpha-L-oléandrosyl)-alpha-L-oléandrosyloxy et, si désiré, à réduire le composé lorsqu'il présente une double liaison et que R' n'existe pas pour obtenir le composé de formule (I) dans lequel R' représente H et la double liaison est inexistante ou, si on le souhaite, à éliminer le groupe 4-(alpha-L-oléandrosyl)-alpha-L-oléandrosyloxy par hydrolyse suivie d'une halogénation et d'une réduction pour donner le composé de formule (I) dans lequel R4 représente H.
13. Procédé selon la revendication 12, dans lequel l'organisme est Streptomyces avermitilis NCIB 12121.
14. Composition pour le traitement et la prévention d'infections à parasites chez l'homme et l'animal, comprenant les compositions ectoparasiticides, insecticides, acaricides et anthelmintiques qui renferment un composé de formule (I) selon l'une quelconque des revendications 1 à 10 avec un diluant ou un véhicule inerte.
15. Composition selon la revendication 14, sous la forme d'un breuvage liquide ou d'une formulation pour l'administration par voie orale ou injectable.
16. Composition selon la revendication 14 sous la forme d'un aliment pour animaux ou sous la forme d'un prémélange ou d'un supplément pour l'adjonction à l'alimentation animale.
17. Composé de formule (I) selon l'une quelconque des revendications 1 à 10, ou composition d'un tel composé selon les revendications 14 à 16, destinés au traitement ou à la prévention d'infections à parasites chez l'homme et l'animal.
18. Procédé de lutte contre les infections et les infestations par les insectes ou les parasites, y compris les infections par les parasites chez les animaux, l'homme excepté, et les infections par les parasites agricoles ou horticoles, qui consiste à appliquer une quantité efficace d'un composé de formule (I) selon l'une quelconque des revendications 1 à 10 sur l'organisme responsable de ladite infection ou infestation ou de son lieu de manifestation.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB858518999A GB8518999D0 (en) | 1985-07-27 | 1985-07-27 | Antiparasitic agents |
| GB858520069A GB8520069D0 (en) | 1985-08-09 | 1985-08-09 | Anti-parasitic agents |
| GB868610063A GB8610063D0 (en) | 1986-04-24 | 1986-04-24 | Antiparasitic agents |
| GB868610862A GB8610862D0 (en) | 1986-05-02 | 1986-05-02 | Antiparasitic agents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HK65793A true HK65793A (en) | 1993-07-16 |
Family
ID=27449680
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HK657/93A HK65793A (en) | 1985-07-27 | 1993-07-08 | Antiparasitic avermectin and milbemycin derivatives and process for their preparation |
Country Status (31)
| Country | Link |
|---|---|
| US (2) | US5089480A (fr) |
| EP (1) | EP0214731B1 (fr) |
| JP (1) | JPH0637501B2 (fr) |
| CN (1) | CN1007266B (fr) |
| AP (1) | AP37A (fr) |
| AU (1) | AU572402B2 (fr) |
| BG (1) | BG46601A3 (fr) |
| CA (1) | CA1339480C (fr) |
| CY (1) | CY1719A (fr) |
| DE (1) | DE3676396D1 (fr) |
| DK (1) | DK169036B1 (fr) |
| ES (1) | ES8800986A1 (fr) |
| FI (1) | FI87367C (fr) |
| GR (1) | GR861965B (fr) |
| HK (1) | HK65793A (fr) |
| HU (1) | HU195856B (fr) |
| IE (1) | IE58640B1 (fr) |
| IL (1) | IL79523A (fr) |
| LU (1) | LU88788I2 (fr) |
| MA (1) | MA20746A1 (fr) |
| NL (1) | NL950011I2 (fr) |
| NO (2) | NO165881C (fr) |
| NZ (1) | NZ216980A (fr) |
| OA (1) | OA08370A (fr) |
| PH (1) | PH23081A (fr) |
| PL (1) | PL153429B1 (fr) |
| PT (1) | PT83070B (fr) |
| SK (1) | SK278513B6 (fr) |
| SU (1) | SU1560059A3 (fr) |
| UA (1) | UA6345A1 (fr) |
| YU (1) | YU44294B (fr) |
Families Citing this family (104)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3532794A1 (de) * | 1984-09-14 | 1986-04-17 | Glaxo Group Ltd., London | Antibiotika, verfahren zu deren herstellung und diese verbindungen enthaltende mittel |
| ES8802229A1 (es) * | 1985-04-30 | 1988-04-16 | Glaxo Group Ltd | Un procedimiento para preparar nuevos derivados lactonicos macrociclicos. |
| IE67373B1 (en) * | 1985-09-13 | 1996-03-20 | American Cyanamid Co | Macrolide antibiotics and their preparation |
| ES2054664T3 (es) * | 1986-03-12 | 1994-08-16 | American Cyanamid Co | Compuestos macrolidos. |
| JP2587241B2 (ja) * | 1986-07-24 | 1997-03-05 | ビ−チヤム・グル−プ・ピ−エルシ− | 新規化合物、その製法及びそれを含む医薬組成物 |
| US5019589A (en) * | 1986-09-12 | 1991-05-28 | American Cyanamid Company | Δ23 -LL-F28249 compounds |
| US4886828A (en) * | 1986-09-12 | 1989-12-12 | American Cyanamid Company | Δ22 -derivatives of LL-F28249 compounds |
| DE3782481T2 (de) * | 1986-09-12 | 1993-05-19 | American Cyanamid Co | 23-deoxy-derivate von ll-f28249-verbindungen. |
| US5149832A (en) * | 1986-09-12 | 1992-09-22 | American Cyanamid Company | Mono and diacyl derivatives of ll-f28249 compounds |
| EP0260537A1 (fr) * | 1986-09-12 | 1988-03-23 | American Cyanamid Company | Dérivés 13-déoxy-23-oxo(céto) et 23-imino des composés de 13-déoxy-C-076-aglycone |
| IL85119A (en) * | 1987-01-23 | 1993-01-14 | Pfizer | Streptomyces avermitilis strains, their preparation and use in production of avermectins |
| IN167980B (fr) * | 1987-01-23 | 1991-01-19 | Pfizer | |
| US5234831A (en) * | 1987-01-23 | 1993-08-10 | Pfizer Inc | Cultures for production of B avermectins |
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| US4956479A (en) * | 1987-03-06 | 1990-09-11 | American Cyanamid Company | 23-deoxy-27-chloro derivatives of LL-F28249 compounds |
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- 1986-07-22 DE DE8686305604T patent/DE3676396D1/de not_active Expired - Lifetime
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- 1986-07-25 MA MA20974A patent/MA20746A1/fr unknown
- 1986-07-25 DK DK353486A patent/DK169036B1/da not_active IP Right Cessation
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- 1986-07-25 NZ NZ216980A patent/NZ216980A/xx unknown
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