NO320138B1 - Haloderivater av 9-deoksy-9a-aza-9a-homoerytromycin A, fremgangsmate for fremstilling derav, farmasoytiske preparater omfattende dem, samt anvendelse derav. - Google Patents
Haloderivater av 9-deoksy-9a-aza-9a-homoerytromycin A, fremgangsmate for fremstilling derav, farmasoytiske preparater omfattende dem, samt anvendelse derav. Download PDFInfo
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- NO320138B1 NO320138B1 NO20015346A NO20015346A NO320138B1 NO 320138 B1 NO320138 B1 NO 320138B1 NO 20015346 A NO20015346 A NO 20015346A NO 20015346 A NO20015346 A NO 20015346A NO 320138 B1 NO320138 B1 NO 320138B1
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- 239000008272 agar Substances 0.000 description 1
- 125000005115 alkyl carbamoyl group Chemical group 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
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- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- LSPHULWDVZXLIL-QUBYGPBYSA-N camphoric acid Chemical compound CC1(C)[C@H](C(O)=O)CC[C@]1(C)C(O)=O LSPHULWDVZXLIL-QUBYGPBYSA-N 0.000 description 1
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- 229920002678 cellulose Polymers 0.000 description 1
- AJSDVNKVGFVAQU-BIIVOSGPSA-N cladinose Chemical compound O=CC[C@@](C)(OC)[C@@H](O)[C@H](C)O AJSDVNKVGFVAQU-BIIVOSGPSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- VTJCSBJRQLZNHE-CSMHCCOUSA-N desosamine Chemical compound C[C@@H](O)C[C@H](N(C)C)[C@@H](O)C=O VTJCSBJRQLZNHE-CSMHCCOUSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000006345 epimerization reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
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- 125000003106 haloaryl group Chemical group 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 229940071870 hydroiodic acid Drugs 0.000 description 1
- 230000001976 improved effect Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
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- 229940099563 lactobionic acid Drugs 0.000 description 1
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- 239000008101 lactose Substances 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N methyl pentane Natural products CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- 239000004530 micro-emulsion Substances 0.000 description 1
- 244000000010 microbial pathogen Species 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- ODUCDPQEXGNKDN-UHFFFAOYSA-N nitroxyl Chemical compound O=N ODUCDPQEXGNKDN-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
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- 230000003647 oxidation Effects 0.000 description 1
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- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
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- 238000000746 purification Methods 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
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- 238000006722 reduction reaction Methods 0.000 description 1
- 238000006485 reductive methylation reaction Methods 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
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- 239000008117 stearic acid Substances 0.000 description 1
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- 239000005720 sucrose Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- DKVBOUDTNWVDEP-NJCHZNEYSA-N teicoplanin aglycone Chemical group N([C@H](C(N[C@@H](C1=CC(O)=CC(O)=C1C=1C(O)=CC=C2C=1)C(O)=O)=O)[C@H](O)C1=CC=C(C(=C1)Cl)OC=1C=C3C=C(C=1O)OC1=CC=C(C=C1Cl)C[C@H](C(=O)N1)NC([C@H](N)C=4C=C(O5)C(O)=CC=4)=O)C(=O)[C@@H]2NC(=O)[C@@H]3NC(=O)[C@@H]1C1=CC5=CC(O)=C1 DKVBOUDTNWVDEP-NJCHZNEYSA-N 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 238000011269 treatment regimen Methods 0.000 description 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7048—Compounds having saccharide radicals and heterocyclic rings having oxygen as a ring hetero atom, e.g. leucoglucosan, hesperidin, erythromycin, nystatin, digitoxin or digoxin
-
- 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
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H1/00—Processes for the preparation of sugar derivatives
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HR990130A HRP990130B1 (en) | 1999-05-03 | 1999-05-03 | HALOGEN DERIVATIVES 9a-N-(N'-ARYLCARBAMOYL)- AND 9a-N-(N'-ARYLTHIOCARBAMOYL)-9-DEOXO-9a-AZA-9a OF HOMOERYTHROMYCIN A |
PCT/HR2000/000013 WO2000066603A1 (en) | 1999-05-03 | 2000-05-02 | Halo derivatives of 9-deoxo-9a-aza-9a-homerythromycin a |
Publications (3)
Publication Number | Publication Date |
---|---|
NO20015346L NO20015346L (no) | 2001-11-01 |
NO20015346D0 NO20015346D0 (no) | 2001-11-01 |
NO320138B1 true NO320138B1 (no) | 2005-10-31 |
Family
ID=10946916
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20015346A NO320138B1 (no) | 1999-05-03 | 2001-11-01 | Haloderivater av 9-deoksy-9a-aza-9a-homoerytromycin A, fremgangsmate for fremstilling derav, farmasoytiske preparater omfattende dem, samt anvendelse derav. |
Country Status (33)
Country | Link |
---|---|
US (1) | US6872707B1 (ja) |
EP (1) | EP1175429B1 (ja) |
JP (1) | JP2002543213A (ja) |
KR (1) | KR100714740B1 (ja) |
CN (1) | CN1140535C (ja) |
AT (1) | ATE244258T1 (ja) |
AU (1) | AU767681B2 (ja) |
BG (1) | BG106173A (ja) |
BR (1) | BR0010231A (ja) |
CA (1) | CA2372977A1 (ja) |
CZ (1) | CZ20013913A3 (ja) |
DE (1) | DE60003671T2 (ja) |
DK (1) | DK1175429T3 (ja) |
EA (1) | EA005214B1 (ja) |
EE (1) | EE05007B1 (ja) |
ES (1) | ES2202107T3 (ja) |
GE (1) | GEP20032928B (ja) |
HK (1) | HK1045522B (ja) |
HR (1) | HRP990130B1 (ja) |
HU (1) | HUP0201146A3 (ja) |
IL (2) | IL145986A0 (ja) |
IS (1) | IS6115A (ja) |
MX (1) | MXPA01011038A (ja) |
NO (1) | NO320138B1 (ja) |
NZ (1) | NZ515278A (ja) |
PL (1) | PL351402A1 (ja) |
PT (1) | PT1175429E (ja) |
SI (1) | SI1175429T1 (ja) |
SK (1) | SK284513B6 (ja) |
TR (1) | TR200103143T2 (ja) |
UA (1) | UA71962C2 (ja) |
WO (1) | WO2000066603A1 (ja) |
ZA (1) | ZA200108484B (ja) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HRP20010146B1 (en) * | 2001-02-28 | 2005-10-31 | Pliva D.D. | 9a-N-(N'-(PHENYLSULFONYL)CARBAMOYL) DERIVATIVES OF 9-DEOXO-9-DIHYDRO-9a-AZA-9a-HOMOERYTHROMYCIN A AND OF 5-O-DESOSAMINYL-9-DEOXO-9-DIHYDRO-9a-AZA-9a-HOMOERYTHRONOLIDE A |
HRP20020885B1 (en) * | 2002-11-11 | 2007-05-31 | GlaxoSmithKline istra�iva�ki centar Zagreb d.o.o. | SUBSTITUTED 9a-N-{N'-[4-(SULFONYL)PHENYLCARBAMOYL]}DERIVATIVES 9-DEOXO-9-DIHYDRO-9a-AZA-9a-HOMOERITHROMYCIN A AND 5-O-DESOZAMINYL-9-DEOXO-9-DIHYDRO-9a-AZA-9a-HOMOERITHRONOLIDE A |
HRP20020886A2 (en) * | 2002-11-11 | 2005-06-30 | PLIVA-ISTRAŽIVAČKI INSTITUT d.o.o. | SUBSTITUTED 9a-N-[N'-(BENZENSULFONYL)CARBAMOYL-γ-AMINOPROPYL) AND 9a-N(N' -(?-CYANOETHIL)-N' -(b |
HRP20020991A2 (en) * | 2002-12-12 | 2005-02-28 | Pliva-Istra�iva�ki institut d.o.o. | N"-Substituted 9a-N-(N'-carbamoyl-Gamma-aminopropyl), 9a-N-(N'? -thiocarbamoyl-Gamma-aminopropyl), 9a-N-(N'-((Beta-cyanoethyl)-N'-carbamoyl-Gamma? -aminopropyl) and 9a-N-(N'-(Beta-cyanoethyl)-N'-thiocarbamoyl-Gamma? -aminopropyl) derivatives of 9-de |
HRP20030381B1 (en) * | 2003-05-14 | 2007-05-31 | GlaxoSmithKline istra�iva�ki centar Zagreb d.o.o. | 3-DECLADINOZYL 9a-N-CARBAMOYL AND 9a-N-THIOCARBAMOYL DERIVATIVES 9-DEOXO-9-DIHYDRO-9a-AZA-9a-HOMOERYTHROMICYNE A |
ATE429921T1 (de) * | 2005-01-14 | 2009-05-15 | Glaxosmithkline Zagreb | 9a-carbamoyl- und thiocarbamoylazalide mit antimalariawirkung |
MX2010002932A (es) * | 2007-09-17 | 2010-05-27 | Enanta Pharm Inc | Macrolidos de biarilo con puente en 6, 11. |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SI7910768A8 (en) * | 1979-04-02 | 1996-06-30 | Pliva Pharm & Chem Works | Process for pripering 11-aza-4-0-cladinosyl-6-0-desosaminyl-15-ethyl- 7,13,14-trihydroxy-3,5,7,9,12,14-hexamethyl- oxacyclopentadecane-2-one and their derivatives |
WO1992006991A1 (fr) * | 1990-10-15 | 1992-04-30 | Taisho Pharmaceutical Co., Ltd. | Erythromycine modifiee en 2' ou derive de cette substance |
HRP931480B1 (en) * | 1993-12-08 | 1997-08-31 | Sour Pliva | 9a-N-(N'-CARBAMONYL) and 9a-N-(N'-THIOCARBAMONYL) DERIVATES OF 9-DEOXO-9a-HOMOERYTHROMYCIN A |
-
1999
- 1999-05-03 HR HR990130A patent/HRP990130B1/xx not_active IP Right Cessation
-
2000
- 2000-02-05 UA UA2001118221A patent/UA71962C2/uk unknown
- 2000-05-02 KR KR1020017014046A patent/KR100714740B1/ko not_active IP Right Cessation
- 2000-05-02 DK DK00920940T patent/DK1175429T3/da active
- 2000-05-02 HU HU0201146A patent/HUP0201146A3/hu unknown
- 2000-05-02 CA CA002372977A patent/CA2372977A1/en not_active Abandoned
- 2000-05-02 EA EA200101170A patent/EA005214B1/ru not_active IP Right Cessation
- 2000-05-02 DE DE60003671T patent/DE60003671T2/de not_active Expired - Fee Related
- 2000-05-02 PL PL00351402A patent/PL351402A1/xx unknown
- 2000-05-02 CN CNB008071500A patent/CN1140535C/zh not_active Expired - Fee Related
- 2000-05-02 SK SK1570-2001A patent/SK284513B6/sk not_active IP Right Cessation
- 2000-05-02 IL IL14598600A patent/IL145986A0/xx active IP Right Grant
- 2000-05-02 MX MXPA01011038A patent/MXPA01011038A/es active IP Right Grant
- 2000-05-02 JP JP2000615632A patent/JP2002543213A/ja active Pending
- 2000-05-02 PT PT00920940T patent/PT1175429E/pt unknown
- 2000-05-02 EE EEP200100582A patent/EE05007B1/xx not_active IP Right Cessation
- 2000-05-02 TR TR2001/03143T patent/TR200103143T2/xx unknown
- 2000-05-02 WO PCT/HR2000/000013 patent/WO2000066603A1/en active IP Right Grant
- 2000-05-02 NZ NZ515278A patent/NZ515278A/xx unknown
- 2000-05-02 ES ES00920940T patent/ES2202107T3/es not_active Expired - Lifetime
- 2000-05-02 AU AU41350/00A patent/AU767681B2/en not_active Ceased
- 2000-05-02 US US09/959,662 patent/US6872707B1/en not_active Expired - Fee Related
- 2000-05-02 AT AT00920940T patent/ATE244258T1/de not_active IP Right Cessation
- 2000-05-02 BR BR0010231-8A patent/BR0010231A/pt not_active IP Right Cessation
- 2000-05-02 GE GEAP20006227A patent/GEP20032928B/en unknown
- 2000-05-02 CZ CZ20013913A patent/CZ20013913A3/cs unknown
- 2000-05-02 SI SI200030188T patent/SI1175429T1/xx unknown
- 2000-05-02 EP EP00920940A patent/EP1175429B1/en not_active Expired - Lifetime
-
2001
- 2001-10-16 ZA ZA200108484A patent/ZA200108484B/xx unknown
- 2001-10-17 IL IL145986A patent/IL145986A/en unknown
- 2001-10-19 IS IS6115A patent/IS6115A/is unknown
- 2001-11-01 NO NO20015346A patent/NO320138B1/no unknown
- 2001-12-03 BG BG106173A patent/BG106173A/bg unknown
-
2002
- 2002-09-26 HK HK02107027.0A patent/HK1045522B/zh not_active IP Right Cessation
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