CA2115807A1 - Forme purifiee de streptogramines, sa preparation et les compositions pharmaceutiques qui la contiennent - Google Patents
Forme purifiee de streptogramines, sa preparation et les compositions pharmaceutiques qui la contiennentInfo
- Publication number
- CA2115807A1 CA2115807A1 CA002115807A CA2115807A CA2115807A1 CA 2115807 A1 CA2115807 A1 CA 2115807A1 CA 002115807 A CA002115807 A CA 002115807A CA 2115807 A CA2115807 A CA 2115807A CA 2115807 A1 CA2115807 A1 CA 2115807A1
- Authority
- CA
- Canada
- Prior art keywords
- radical
- hydrogen atom
- streptogramins
- group
- general formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
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- 229940041030 streptogramins Drugs 0.000 title claims abstract description 34
- 238000002360 preparation method Methods 0.000 title claims abstract description 16
- 239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 4
- 150000003254 radicals Chemical class 0.000 claims abstract description 30
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 15
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical group C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 claims abstract description 12
- YKPQUSLRUFLVDA-UHFFFAOYSA-N $l^{2}-azanylmethane Chemical compound [NH]C YKPQUSLRUFLVDA-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000000843 powder Substances 0.000 claims abstract description 8
- 239000006069 physical mixture Substances 0.000 claims abstract description 4
- KTOQRRDVVIDEAA-UHFFFAOYSA-N 2-methylpropane Chemical group [CH2]C(C)C KTOQRRDVVIDEAA-UHFFFAOYSA-N 0.000 claims abstract 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 50
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- 238000011282 treatment Methods 0.000 claims description 14
- 239000013078 crystal Substances 0.000 claims description 13
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical group [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 12
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- 241000699670 Mus sp. Species 0.000 description 1
- 241000204031 Mycoplasma Species 0.000 description 1
- 241000202934 Mycoplasma pneumoniae Species 0.000 description 1
- VZUNGTLZRAYYDE-UHFFFAOYSA-N N-methyl-N'-nitro-N-nitrosoguanidine Chemical compound O=NN(C)C(=N)N[N+]([O-])=O VZUNGTLZRAYYDE-UHFFFAOYSA-N 0.000 description 1
- 241000588652 Neisseria gonorrhoeae Species 0.000 description 1
- 208000030852 Parasitic disease Diseases 0.000 description 1
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- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 1
- 241000015473 Schizothorax griseus Species 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 241000295644 Staphylococcaceae Species 0.000 description 1
- 241000193985 Streptococcus agalactiae Species 0.000 description 1
- 241000936762 Streptomyces daghestanicus Species 0.000 description 1
- 241000187389 Streptomyces lavendulae Species 0.000 description 1
- 241001518258 Streptomyces pristinaespiralis Species 0.000 description 1
- 241000187122 Streptomyces virginiae Species 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 241000202898 Ureaplasma Species 0.000 description 1
- PBCJIPOGFJYBJE-UHFFFAOYSA-N acetonitrile;hydrate Chemical compound O.CC#N PBCJIPOGFJYBJE-UHFFFAOYSA-N 0.000 description 1
- 206010000496 acne Diseases 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- 230000007815 allergy Effects 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000001668 ameliorated effect Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 230000003385 bacteriostatic effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000006696 biosynthetic metabolic pathway Effects 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 238000002512 chemotherapy Methods 0.000 description 1
- 229940038705 chlamydia trachomatis Drugs 0.000 description 1
- 238000007813 chromatographic assay Methods 0.000 description 1
- 238000000975 co-precipitation Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 239000013066 combination product Substances 0.000 description 1
- 229940127555 combination product Drugs 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 206010014665 endocarditis Diseases 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000012239 gene modification Methods 0.000 description 1
- 230000005017 genetic modification Effects 0.000 description 1
- 235000013617 genetically modified food Nutrition 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 239000000138 intercalating agent Substances 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 1
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 238000011866 long-term treatment Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000003120 macrolide antibiotic agent Substances 0.000 description 1
- 229940041033 macrolides Drugs 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 231100000350 mutagenesis Toxicity 0.000 description 1
- 229940013390 mycoplasma pneumoniae Drugs 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 229940049954 penicillin Drugs 0.000 description 1
- 238000005325 percolation Methods 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 239000013612 plasmid Substances 0.000 description 1
- 230000001323 posttranslational effect Effects 0.000 description 1
- 210000001938 protoplast Anatomy 0.000 description 1
- 230000002685 pulmonary effect Effects 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 231100000161 signs of toxicity Toxicity 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 206010040872 skin infection Diseases 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
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- 230000000699 topical effect Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
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Classifications
-
- 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
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
- C07K5/06182—Dipeptides with the first amino acid being heterocyclic and Pristinamycin II; Derivatives thereof
-
- 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
- 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
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9301787A FR2701709B1 (fr) | 1993-02-17 | 1993-02-17 | Forme purifiée de streptograminés, sa préparation et les compositions pharmaceutiques qui la contiennent. |
| FR9301787 | 1993-02-17 | ||
| APAP/P/1994/000660A AP520A (en) | 1993-02-17 | 1994-08-01 | Purified form of streptogramins, its preparation and pharmaceutical compositions containing it. |
| PCT/FR1994/001006 WO1996005219A1 (fr) | 1993-02-17 | 1994-08-12 | Forme purifiee de streptogramines, sa preparation et les compositions pharmaceutiques qui la contiennent |
| CN94195158A CN1159197A (zh) | 1993-02-17 | 1994-08-12 | 链阳菌素的纯化形式、其制备和含有它的药物组合物 |
| OA60964A OA10400A (fr) | 1993-02-17 | 1997-02-07 | Forme purifiée de streptogramines sa préparation et les compositions pharmaceutiques qui la contiennent |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2115807A1 true CA2115807A1 (fr) | 1994-08-18 |
Family
ID=33437085
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002115807A Abandoned CA2115807A1 (fr) | 1993-02-17 | 1994-02-16 | Forme purifiee de streptogramines, sa preparation et les compositions pharmaceutiques qui la contiennent |
Country Status (21)
| Country | Link |
|---|---|
| JP (1) | JPH06298664A (cs) |
| AU (1) | AU678785B2 (cs) |
| BE (1) | BE1006554A3 (cs) |
| BR (1) | BR9408613A (cs) |
| CA (1) | CA2115807A1 (cs) |
| CZ (1) | CZ285541B6 (cs) |
| ES (1) | ES2081763B1 (cs) |
| FI (1) | FI111009B (cs) |
| FR (1) | FR2701709B1 (cs) |
| GB (1) | GB2275269B (cs) |
| GR (1) | GR1002385B (cs) |
| HU (1) | HUT66821A (cs) |
| IL (1) | IL108641A (cs) |
| IT (1) | IT1269214B (cs) |
| LU (1) | LU88454A1 (cs) |
| NO (1) | NO940533D0 (cs) |
| NZ (1) | NZ250884A (cs) |
| PL (1) | PL174835B1 (cs) |
| PT (1) | PT101460B (cs) |
| SK (1) | SK18494A3 (cs) |
| ZA (1) | ZA941024B (cs) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2723373B1 (fr) | 1994-08-02 | 1996-09-13 | Rhone Poulenc Rorer Sa | Forme purifiee de streptogramines, sa preparation et les compositions pharmaceutiques qui la contiennent |
| FR2841563B1 (fr) * | 2002-06-28 | 2006-09-01 | Aventis Pharma Sa | Nouveaux variants du polypeptide papm de bacteries du genre streptomyces |
| ITUB20169994A1 (it) * | 2016-01-14 | 2017-07-14 | Phf Sa | Nuove forme cristalline di farmaci immunomodulatori |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2549065B1 (fr) * | 1983-07-13 | 1985-10-25 | Rhone Poulenc Sante | Nouveaux derives de synergistines, leur preparation et les compositions pharmaceutiques qui les contiennent |
| FR2619008B1 (fr) * | 1987-08-03 | 1990-06-29 | Cird | Utilisation de synergistines dans des compositions pharmaceutiques ou cosmetiques anti-acneiques |
| FR2674539B1 (fr) * | 1991-03-28 | 1993-05-21 | Rhone Poulenc Rorer Sa | Procede de preparation enzymatique de macrolactone. |
| FR2689518B1 (fr) * | 1992-04-01 | 1995-04-07 | Rhone Poulenc Rorer Sa | Microorganismes, procédé de préparation et utilisation. |
-
1993
- 1993-02-17 FR FR9301787A patent/FR2701709B1/fr not_active Expired - Fee Related
-
1994
- 1994-01-20 LU LU88454A patent/LU88454A1/fr unknown
- 1994-02-03 IT ITMI940192A patent/IT1269214B/it active IP Right Grant
- 1994-02-14 AU AU55100/94A patent/AU678785B2/en not_active Ceased
- 1994-02-14 IL IL10864194A patent/IL108641A/en not_active IP Right Cessation
- 1994-02-14 PT PT101460A patent/PT101460B/pt not_active IP Right Cessation
- 1994-02-15 SK SK184-94A patent/SK18494A3/sk unknown
- 1994-02-15 CZ CZ94326A patent/CZ285541B6/cs not_active IP Right Cessation
- 1994-02-15 GR GR940100078A patent/GR1002385B/el not_active IP Right Cessation
- 1994-02-15 ZA ZA941024A patent/ZA941024B/xx unknown
- 1994-02-15 NZ NZ250884A patent/NZ250884A/en unknown
- 1994-02-16 ES ES09400294A patent/ES2081763B1/es not_active Expired - Fee Related
- 1994-02-16 HU HU9400447A patent/HUT66821A/hu unknown
- 1994-02-16 JP JP6040579A patent/JPH06298664A/ja active Pending
- 1994-02-16 CA CA002115807A patent/CA2115807A1/fr not_active Abandoned
- 1994-02-16 BE BE9400182A patent/BE1006554A3/fr not_active IP Right Cessation
- 1994-02-16 FI FI940717A patent/FI111009B/fi not_active IP Right Cessation
- 1994-02-16 PL PL94302250A patent/PL174835B1/pl unknown
- 1994-02-16 NO NO940533A patent/NO940533D0/no unknown
- 1994-02-17 GB GB9403057A patent/GB2275269B/en not_active Expired - Fee Related
- 1994-08-12 BR BR9408613A patent/BR9408613A/pt not_active Application Discontinuation
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |