ES2071036T3 - Derivados de 6-o-metileritromicina a oxima. - Google Patents
Derivados de 6-o-metileritromicina a oxima.Info
- Publication number
- ES2071036T3 ES2071036T3 ES90310923T ES90310923T ES2071036T3 ES 2071036 T3 ES2071036 T3 ES 2071036T3 ES 90310923 T ES90310923 T ES 90310923T ES 90310923 T ES90310923 T ES 90310923T ES 2071036 T3 ES2071036 T3 ES 2071036T3
- Authority
- ES
- Spain
- Prior art keywords
- group
- halogen
- groups
- substituted
- phenyltius
- 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.)
- Expired - Lifetime
Links
- 150000002923 oximes Chemical class 0.000 title abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- ULGZDMOVFRHVEP-RWJQBGPGSA-N Erythromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)C(=O)[C@H](C)C[C@@](C)(O)[C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 ULGZDMOVFRHVEP-RWJQBGPGSA-N 0.000 abstract 2
- 241000894006 Bacteria Species 0.000 abstract 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical group C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical class O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- 230000000844 anti-bacterial effect Effects 0.000 abstract 1
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical group C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 abstract 1
- 229960003276 erythromycin Drugs 0.000 abstract 1
- WCMIIGXFCMNQDS-IDYPWDAWSA-M piperacillin sodium Chemical compound [Na+].O=C1C(=O)N(CC)CCN1C(=O)N[C@H](C=1C=CC=CC=1)C(=O)N[C@@H]1C(=O)N2[C@@H](C([O-])=O)C(C)(C)S[C@@H]21 WCMIIGXFCMNQDS-IDYPWDAWSA-M 0.000 abstract 1
- XMVJITFPVVRMHC-UHFFFAOYSA-N roxarsone Chemical group OC1=CC=C([As](O)(O)=O)C=C1[N+]([O-])=O XMVJITFPVVRMHC-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
- C07H17/04—Heterocyclic radicals containing only oxygen as ring hetero atoms
- C07H17/08—Hetero rings containing eight or more ring members, e.g. erythromycins
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Genetics & Genomics (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Oncology (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Communicable Diseases (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
EL INVENTO PROVEE DERIVADOS OXIME A METILERITROMICIN-6-0 DE LA FORMULA: EN LA QUE X ES UN GRUPO BENCIL SUSTITUIDO EN EL ANILLO BENCENO POR 1 A 5 SUSTITUYENTES SELECCIONADOS DE HALOGENO Y ALQUIL C1-C5, NITRO, TRIFLUOROMETIL, FENIL, BENZIL, ESTIRIL, CLOROBENZILOXI-2, IL-5-OXADIAZOL-1,2,4-(CLOROFENIL-4)-3, Y GRUPOS METOXICARBONILBENZOIL-2; UN GRUPO FENIL SUSTITUIDO POR 1 A 3 GRUPOS NITRO; UN GRUPO METILBENZIL-A; UN GRUPO METILFENETIL-A; UN GRUPO DIFENILMETIL; UN GRUPO TRITIL; UN GRUPO DIBENZOSUBERANIL; O UN GRUPO DE LA FORMULA -(CH2)N-R (EN EL QUE R ES UN GRUPO BENZIL, UN GRUPO FENILTIO, UN GRUPO FENILTIO SUSTITUIDO POR UN HALOGENO, UN GRUPO CICLOALQUIL C6 O C5, UN GRUPO NAFTIL, UN GRUPO ANTRACENIL, UN GRUPO QUINOLIL, UN GRUPO IL-4-TIAZOL-BENZILOXICARBONILAMINO-2, UN GRUPO FTALIMIDA, UN GRUPO FLUOROENIL-9-BROMO-9, UN GRUPO IL-1-METILINDOL-ALCOXICARBONIL-1 CUYO GRUPO ALCOXI TIENE 1 A 3 CARBONOS, UN GRUPO PIPERACIL(PIRID-IL)-4 O UN GRUPO PIRIDIL SUSTITUIDO POR 1 O 2 MIEMBROS SELECCIONADOS DE HALOGENO Y GRUPOS TRIFLUOROETIOXI-2,2,2; Y N ES UN ENTERO DE 1 A 6); ESOS COMPONENTES TIENEN ACTIVIDAD ANTIBACTERIAL CONTRA LA BACTERIA RESISTENTE DE ERITROMICIN.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26279789 | 1989-10-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2071036T3 true ES2071036T3 (es) | 1995-06-16 |
Family
ID=17380743
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES90310923T Expired - Lifetime ES2071036T3 (es) | 1989-10-07 | 1990-10-04 | Derivados de 6-o-metileritromicina a oxima. |
Country Status (10)
Country | Link |
---|---|
US (1) | US5302705A (es) |
EP (1) | EP0422843B1 (es) |
JP (1) | JPH03204893A (es) |
KR (1) | KR910007953A (es) |
AT (1) | ATE118503T1 (es) |
CA (1) | CA2027074A1 (es) |
DE (1) | DE69016912T2 (es) |
DK (1) | DK0422843T3 (es) |
ES (1) | ES2071036T3 (es) |
TW (1) | TW199098B (es) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3782994T2 (de) | 1986-09-18 | 1993-04-08 | Taisho Pharmaceutical Co Ltd | Erythromycin-a-derivate und verfahren zu ihrer herstellung. |
WO1996004920A1 (fr) * | 1994-08-12 | 1996-02-22 | Taisho Pharmaceutical Co., Ltd. | Inhibiteur de production de l'interleukine-5 |
IT1276901B1 (it) * | 1994-12-13 | 1997-11-03 | Zambon Spa | Derivati dell'eritromicina a 9-0-ossina dotati di attivita' antibiotica |
US5872229A (en) | 1995-11-21 | 1999-02-16 | Abbott Laboratories | Process for 6-O-alkylation of erythromycin derivatives |
US5929219A (en) | 1997-09-10 | 1999-07-27 | Abbott Laboratories | 9-hydrazone and 9-azine erythromycin derivatives and a process of making the same |
PT941998E (pt) * | 1998-03-03 | 2004-12-31 | Pfizer Prod Inc | Antibioticos macrolidos do tipo 3,6-cetal |
HRP980189B1 (en) * | 1998-04-06 | 2004-04-30 | Pliva Pharm & Chem Works | Novel 15-membered lactams ketolides |
CA2411293A1 (en) | 1999-01-28 | 2000-07-28 | Pfizer Products Inc. | Novel azalides and methods of making same |
AR023264A1 (es) * | 1999-04-08 | 2002-09-04 | Hokuriku Pharmaceutical | Derivados de eritromicina |
KR100428703B1 (ko) * | 2000-02-02 | 2004-04-30 | 한국과학기술연구원 | 헬리코박터 파이로리의 성장 억제 효과를 지닌 신규 마크로라이드 화합물 |
US20090054634A1 (en) * | 2007-08-09 | 2009-02-26 | Vinod Kumar Kansal | Process for the preparation of clarithromycin |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2473525A1 (fr) * | 1980-01-11 | 1981-07-17 | Roussel Uclaf | Nouvelles oximes derivees de l'erythromycine, leur procede de preparation et leur application comme medicaments |
US4331803A (en) * | 1980-06-04 | 1982-05-25 | Taisho Pharmaceutical Co., Ltd. | Novel erythromycin compounds |
JPS60214796A (ja) * | 1984-04-06 | 1985-10-28 | Taisho Pharmaceut Co Ltd | 6−0−メチルエリスロマイシン類の製法 |
JPS61103890A (ja) * | 1984-10-26 | 1986-05-22 | Taisho Pharmaceut Co Ltd | 6−0−メチルエリスロマイシンa誘導体 |
GB8506380D0 (en) * | 1985-03-12 | 1985-04-11 | Beecham Group Plc | Chemical compounds |
GR860655B (en) * | 1985-03-12 | 1986-07-11 | Beecham Group Plc | Chemical compounds |
US4670549A (en) * | 1985-03-18 | 1987-06-02 | Taisho Pharmaceutical Co., Ltd. | Method for selective methylation of erythromycin a derivatives |
US4833236A (en) * | 1986-05-02 | 1989-05-23 | Taisho Pharmaceutical Co., Ltd. | Erythromycin derivatives |
US4740502A (en) * | 1986-06-20 | 1988-04-26 | Abbott Laboratories | Semisynthetic erythromycin antibiotics |
DE3782994T2 (de) * | 1986-09-18 | 1993-04-08 | Taisho Pharmaceutical Co Ltd | Erythromycin-a-derivate und verfahren zu ihrer herstellung. |
AU1204288A (en) * | 1987-02-24 | 1988-08-25 | Beecham Group Plc | Erythromycins |
-
1990
- 1990-10-01 US US07/590,805 patent/US5302705A/en not_active Expired - Fee Related
- 1990-10-02 TW TW079108273A patent/TW199098B/zh active
- 1990-10-03 JP JP2265812A patent/JPH03204893A/ja active Pending
- 1990-10-04 DE DE69016912T patent/DE69016912T2/de not_active Expired - Fee Related
- 1990-10-04 EP EP90310923A patent/EP0422843B1/en not_active Expired - Lifetime
- 1990-10-04 DK DK90310923.9T patent/DK0422843T3/da active
- 1990-10-04 ES ES90310923T patent/ES2071036T3/es not_active Expired - Lifetime
- 1990-10-04 AT AT90310923T patent/ATE118503T1/de not_active IP Right Cessation
- 1990-10-05 CA CA002027074A patent/CA2027074A1/en not_active Abandoned
- 1990-10-06 KR KR1019900015911A patent/KR910007953A/ko not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
DE69016912D1 (de) | 1995-03-23 |
EP0422843A3 (en) | 1991-09-18 |
DE69016912T2 (de) | 1995-07-06 |
EP0422843B1 (en) | 1995-02-15 |
KR910007953A (ko) | 1991-05-30 |
DK0422843T3 (da) | 1995-04-03 |
JPH03204893A (ja) | 1991-09-06 |
CA2027074A1 (en) | 1991-04-08 |
US5302705A (en) | 1994-04-12 |
EP0422843A2 (en) | 1991-04-17 |
TW199098B (es) | 1993-02-01 |
ATE118503T1 (de) | 1995-03-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG2A | Definitive protection |
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