UA19149A - Спосіб одержаhhя кристалічhого моhогідратhої форми 1-карбацефалоспориhу - Google Patents
Спосіб одержаhhя кристалічhого моhогідратhої форми 1-карбацефалоспориhуInfo
- Publication number
- UA19149A UA19149A UA4356543A UA4356543A UA19149A UA 19149 A UA19149 A UA 19149A UA 4356543 A UA4356543 A UA 4356543A UA 4356543 A UA4356543 A UA 4356543A UA 19149 A UA19149 A UA 19149A
- Authority
- UA
- Ukraine
- Prior art keywords
- crystalline
- preparation
- carbacephalosporin
- monohydrate form
- cephalosporin
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D463/00—Heterocyclic compounds containing 1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbacephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
- C07D463/10—Heterocyclic compounds containing 1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbacephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring with a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2
- C07D463/14—Heterocyclic compounds containing 1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbacephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring with a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2 with hetero atoms directly attached in position 7
- C07D463/16—Nitrogen atoms
- C07D463/18—Nitrogen atoms further acylated by radicals derived from carboxylic acids or by nitrogen or sulfur analogues thereof
- C07D463/20—Nitrogen atoms further acylated by radicals derived from carboxylic acids or by nitrogen or sulfur analogues thereof with the acylating radicals further substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D463/22—Nitrogen atoms further acylated by radicals derived from carboxylic acids or by nitrogen or sulfur analogues thereof with the acylating radicals further substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen further substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
-
- 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)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Cephalosporin Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Винахід відноситься до способу одержання нової кристалічної форми антибіотика цефалоспоринового ряду, а саме кристалічного моногідрата 1-карбаце-фалоспорину формули , який знаходить застосування в медицині. Метою винаходу є створення нової кристалічної форми цефалоспорину, який має вищу стійкість в умовах вологості.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10576687A | 1987-10-06 | 1987-10-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
UA19149A true UA19149A (uk) | 1997-12-25 |
Family
ID=22307671
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UA4356543A UA19149A (uk) | 1987-10-06 | 1988-10-05 | Спосіб одержаhhя кристалічhого моhогідратhої форми 1-карбацефалоспориhу |
Country Status (32)
Country | Link |
---|---|
EP (1) | EP0311366B1 (uk) |
JP (1) | JP2641745B2 (uk) |
KR (1) | KR970002637B1 (uk) |
CN (1) | CN1029966C (uk) |
AR (1) | AR248407A1 (uk) |
AT (1) | ATE103916T1 (uk) |
AU (1) | AU598155B2 (uk) |
BG (1) | BG47036A3 (uk) |
CA (1) | CA1334970C (uk) |
CS (1) | CS270594B2 (uk) |
DD (1) | DD273634A5 (uk) |
DE (1) | DE3888913T2 (uk) |
DK (1) | DK170070B1 (uk) |
EG (1) | EG18529A (uk) |
ES (1) | ES2063049T3 (uk) |
FI (1) | FI884554A (uk) |
HK (1) | HK15497A (uk) |
HU (1) | HU206348B (uk) |
IE (1) | IE62108B1 (uk) |
IL (1) | IL87905A (uk) |
MX (1) | MX13277A (uk) |
MY (1) | MY104063A (uk) |
NO (1) | NO884416L (uk) |
NZ (1) | NZ226450A (uk) |
OA (1) | OA08958A (uk) |
PH (1) | PH31002A (uk) |
PL (1) | PL152022B1 (uk) |
PT (1) | PT88662B (uk) |
SU (1) | SU1731058A3 (uk) |
UA (1) | UA19149A (uk) |
YU (1) | YU46699B (uk) |
ZA (1) | ZA887409B (uk) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
YU46700B (sh) * | 1987-10-07 | 1994-04-05 | Eli Lilly And Co. | Kristalni monohidrat i kristalni mono- i bis (n-n'-dimetilformamid) solvati beta-laktamskog antibiotika |
CA2002596A1 (en) * | 1988-11-14 | 1990-05-14 | Thomas M. Eckrich | Hydrates of b-lactam antibiotic |
CA2002597C (en) * | 1988-11-14 | 1999-03-23 | Thomas M. Eckrich | Solvates of b-lactam antibiotic |
CA2034592C (en) * | 1990-01-26 | 2001-06-05 | Ralph R. Pfeiffer | Crystalline hydrochloride of new beta-lactam antibiotic and process therefor |
US5374719A (en) * | 1993-06-04 | 1994-12-20 | Eli Lilly And Company | Process for converting loracarbef dihydrate to loracarbef monohydrate |
US5352782A (en) * | 1993-06-04 | 1994-10-04 | Eli Lilly And Company | Process for preparing crystalline β-lactam monohydrate |
US5399686A (en) * | 1993-06-04 | 1995-03-21 | Eli Lilly And Company | Loracarbef isopropanolate and a process for converting loracarbef isopropanolate to loracarbef monohydrate |
US5550231A (en) * | 1993-06-15 | 1996-08-27 | Eli Lilly And Company | Loracarbef hydrochloride C1-C3 alcohol solvates and uses thereof |
US5412094A (en) * | 1993-06-28 | 1995-05-02 | Eli Lilly And Company | Bicyclic beta-lactam/paraben complexes |
US5580977A (en) * | 1995-03-01 | 1996-12-03 | Eli Lilly And Company | Process for preparing loracarbef monohydrate |
US6001996A (en) * | 1995-05-11 | 1999-12-14 | Eli Lilly And Company | Complexes of cephalosporins and carbacephalosporins with parabens |
US7056906B2 (en) | 2001-09-21 | 2006-06-06 | Schering Corporation | Combinations of hormone replacement therapy composition(s) and sterol absorption inhibitor(s) and treatments for vascular conditions in post-menopausal women |
DE602004018617D1 (de) | 2003-03-07 | 2009-02-05 | Schering Corp | Substituierte azetidinon-derivate, deren pharmazeutische formulierungen und deren verwendung zur behandlung von hypercholesterolemia |
MXPA05009503A (es) | 2003-03-07 | 2005-10-18 | Schering Corp | Compuestos de azetidinona sustituidos, formulaciones y usos de los mismos para el tratamiento de hipercolesterolemia. |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3655656A (en) * | 1970-06-04 | 1972-04-11 | Lilly Co Eli | Crystalline cephalexin monohydrate |
JPS5672698A (en) * | 1979-11-14 | 1981-06-16 | Kyowa Hakko Kogyo Co Ltd | Preparation of optically active cephalosporin analogue |
YU46700B (sh) * | 1987-10-07 | 1994-04-05 | Eli Lilly And Co. | Kristalni monohidrat i kristalni mono- i bis (n-n'-dimetilformamid) solvati beta-laktamskog antibiotika |
-
1988
- 1988-10-03 DD DD88320417A patent/DD273634A5/de unknown
- 1988-10-03 MY MYPI88001103A patent/MY104063A/en unknown
- 1988-10-03 CA CA000579158A patent/CA1334970C/en not_active Expired - Fee Related
- 1988-10-03 ZA ZA887409A patent/ZA887409B/xx unknown
- 1988-10-03 EG EG506/88A patent/EG18529A/xx active
- 1988-10-03 YU YU184588A patent/YU46699B/sh unknown
- 1988-10-04 PT PT88662A patent/PT88662B/pt not_active IP Right Cessation
- 1988-10-04 MX MX1327788A patent/MX13277A/es unknown
- 1988-10-04 PH PH37636A patent/PH31002A/en unknown
- 1988-10-04 JP JP63251712A patent/JP2641745B2/ja not_active Expired - Fee Related
- 1988-10-04 AR AR88312109A patent/AR248407A1/es active
- 1988-10-04 BG BG085594A patent/BG47036A3/xx unknown
- 1988-10-04 NZ NZ226450A patent/NZ226450A/xx unknown
- 1988-10-04 DK DK553788A patent/DK170070B1/da active IP Right Grant
- 1988-10-04 AU AU23372/88A patent/AU598155B2/en not_active Expired
- 1988-10-04 FI FI884554A patent/FI884554A/fi not_active Application Discontinuation
- 1988-10-04 IL IL87905A patent/IL87905A/xx active Protection Beyond IP Right Term
- 1988-10-05 HU HU885171A patent/HU206348B/hu unknown
- 1988-10-05 ES ES88309261T patent/ES2063049T3/es not_active Expired - Lifetime
- 1988-10-05 PL PL1988275093A patent/PL152022B1/pl unknown
- 1988-10-05 NO NO88884416A patent/NO884416L/no unknown
- 1988-10-05 CN CN88109140A patent/CN1029966C/zh not_active Expired - Lifetime
- 1988-10-05 UA UA4356543A patent/UA19149A/uk unknown
- 1988-10-05 IE IE301588A patent/IE62108B1/en not_active IP Right Cessation
- 1988-10-05 KR KR1019880012961A patent/KR970002637B1/ko not_active IP Right Cessation
- 1988-10-05 OA OA59444A patent/OA08958A/xx unknown
- 1988-10-05 EP EP88309261A patent/EP0311366B1/en not_active Expired - Lifetime
- 1988-10-05 SU SU884356543A patent/SU1731058A3/ru active
- 1988-10-05 AT AT88309261T patent/ATE103916T1/de not_active IP Right Cessation
- 1988-10-05 DE DE3888913T patent/DE3888913T2/de not_active Expired - Lifetime
- 1988-10-06 CS CS886666A patent/CS270594B2/cs not_active IP Right Cessation
-
1997
- 1997-02-05 HK HK15497A patent/HK15497A/xx not_active IP Right Cessation
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
UA19149A (uk) | Спосіб одержаhhя кристалічhого моhогідратhої форми 1-карбацефалоспориhу | |
FI882253A (fi) | Menetelmä kefuroksiimiaksetiilikoostumuksen valmistamiseksi | |
GB1405886A (en) | Synergistic compositions comprising penicillin and cephalosporin antibiotics | |
HUT51485A (en) | Process for production of immune-hindering, monoquin, especially internuclein-1-hindering medical compositions | |
GR862517B (en) | Macrolide antibiotic derivatives | |
YU54189A (en) | Process for obtaining cephem derivatives and midproducts for the same | |
PT81840A (en) | Process for the production of cephem derivatives useful as antibacterial agents | |
UA6330A1 (uk) | Спосіб одержання похідних бензаміда | |
ES434976A1 (es) | Un procedimiento para la preparacion de un medicamento an- tibiotico. | |
GR3017917T3 (en) | Crystalline addition salts of cephem compounds and process for their preparation. | |
IL113744A0 (en) | 3-Cephem derivatives and their preparation | |
GR1002384B (el) | Μεθοδος παρασκευης παραγωγων υποκατεστημενου στυρολιου. | |
MY104109A (en) | Antibacterial 9-deoxo-9a-allyl and propargyl-9a-aza-9a-homoerythromycin a derivatives. | |
FI864970A0 (fi) | Nya kristallina salter av aryloxi-propanolaminer, foerfarande foer deras framstaellning och deras anvaendning. | |
AU3285989A (en) | Treatment of infections caused by a primary immunodeficiency with interleukin-2 | |
EP0453574A4 (en) | Cephalosporin derivative | |
DE3463050D1 (en) | Novel penem compounds, pharmaceutical compositions containing them, processes for their preparation | |
ES423024A1 (es) | Procedimiento para la preparacion de derivados de acidos penicilanico y cefalosporanico. | |
DE3480542D1 (en) | Cephem compounds | |
ZA841850B (en) | 2'-desoxyoxanosine,a process for the preparation thereof and its use as a medicament | |
NZ220122A (en) | Crystalline (5r,6s)-2-aminomethyl- -2-penem-3-carboxylic acid monohydrate, derivatives thereof, and pharmaceutical compositions | |
AU1009688A (en) | Methods for the production of crystalline amino-protected-beta-benzyl-l-aspartic acid | |
HRP940557B1 (en) | Process for the preparation of ceruroxime axetil as pharmaceutical preparation | |
IE46280L (en) | Acetoxyazetidin-2-one compounds. |