IL57798A - Antibacterial compositions comprising a combination of a thienamycin-type compound and a dipeptidase inhibitor - Google Patents
Antibacterial compositions comprising a combination of a thienamycin-type compound and a dipeptidase inhibitorInfo
- Publication number
- IL57798A IL57798A IL57798A IL5779879A IL57798A IL 57798 A IL57798 A IL 57798A IL 57798 A IL57798 A IL 57798A IL 5779879 A IL5779879 A IL 5779879A IL 57798 A IL57798 A IL 57798A
- Authority
- IL
- Israel
- Prior art keywords
- thienamycin
- combination
- type compound
- antibacterial compositions
- dipeptidase inhibitor
- Prior art date
Links
- 229940090955 Dipeptidase inhibitor Drugs 0.000 title 1
- 230000000844 anti-bacterial effect Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D477/00—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring
- C07D477/10—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 4, and 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
- C07D477/12—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 4, and 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 hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached in position 6
- C07D477/16—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 4, and 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 hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached in position 6 with hetero atoms or carbon atoms 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 3
- C07D477/20—Sulfur atoms
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3808—Acyclic saturated acids which can have further substituents on alkyl
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Biochemistry (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IL6644882A IL66448A (en) | 1979-07-13 | 1982-08-02 | Antibacterial compositions containing combinations of 2-substituted penems with dipeptidase inhibitors |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US92721378A | 1978-07-24 | 1978-07-24 | |
US5023279A | 1979-06-22 | 1979-06-22 |
Publications (2)
Publication Number | Publication Date |
---|---|
IL57798A0 IL57798A0 (en) | 1979-11-30 |
IL57798A true IL57798A (en) | 1986-11-30 |
Family
ID=26728043
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IL57798A IL57798A (en) | 1978-07-24 | 1979-07-13 | Antibacterial compositions comprising a combination of a thienamycin-type compound and a dipeptidase inhibitor |
Country Status (19)
Country | Link |
---|---|
EP (1) | EP0007614B1 (xx) |
AR (1) | AR244550A1 (xx) |
AU (1) | AU529315B2 (xx) |
CA (1) | CA1136549A (xx) |
CZ (1) | CZ280583B6 (xx) |
DD (1) | DD145059A5 (xx) |
DE (1) | DE2964609D1 (xx) |
EG (1) | EG14367A (xx) |
ES (1) | ES482774A1 (xx) |
FI (1) | FI792282A (xx) |
GR (1) | GR69997B (xx) |
HK (1) | HK23286A (xx) |
HU (1) | HU182973B (xx) |
IE (1) | IE51691B1 (xx) |
IL (1) | IL57798A (xx) |
NZ (1) | NZ190993A (xx) |
PH (1) | PH16620A (xx) |
PT (1) | PT69955B (xx) |
SK (1) | SK278357B6 (xx) |
Families Citing this family (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5071843A (en) * | 1978-07-24 | 1991-12-10 | Merck & Co., Inc. | Combination of 2-substituted carbapenems with dipeptidase inhibitors |
US4880793A (en) * | 1978-07-24 | 1989-11-14 | Merck & Co., Inc. | Combination of thienamycin-type antibiotics with dipeptidase inhibitors |
IE50333B1 (en) * | 1979-11-02 | 1986-04-02 | Merck & Co Inc | Antibacterial compositions comprising a beta-lactam-type compound and a 3-substituted propenoate |
EP0048025B1 (en) * | 1980-09-17 | 1986-01-15 | Merck & Co. Inc. | Antibacterial composition of thienamycin type compound and a dipeptidase inhibitor |
PT73640B (en) * | 1980-09-17 | 1983-10-19 | Merck & Co Inc | Process for preparing chemical compounds selectively inhibit the metabolism of dipeptidase |
EP0048301A1 (en) * | 1980-09-24 | 1982-03-31 | Merck & Co. Inc. | 2-(Cyclopropane-carboxamido)-2-alkenoic acids, their esters and salts, and antibacterial compositions comprising the same and a thienamycin-type compound |
NZ201471A (en) * | 1981-08-10 | 1985-09-13 | Merck & Co Inc | Antibacterial compositions containing penems and dipeptidase inhibitors |
JPS6025952A (ja) * | 1983-07-20 | 1985-02-08 | Sumitomo Chem Co Ltd | 光学活性2,2−ジメチルシクロプロパン−1−カルボン酸誘導体の製造法 |
EP0161546B1 (en) * | 1984-04-30 | 1989-12-13 | Merck & Co. Inc. | Combination of 2-substituted carbapenems with dipeptidase inhibitors |
CA1273012A (en) * | 1984-07-02 | 1990-08-21 | Burton G. Christensen | 1-methylcarbapenems having an externally alkylated mono- of bicyclic 2-quarternary heteroarylalkylthio substituent |
CA1273011A (en) * | 1984-07-02 | 1990-08-21 | Susan M. Schmitt | Carbapenems having an externally alkylated mono- or bicyclic 2-quaternary heteroarylalkylthio substituent |
IE851586L (en) * | 1984-07-02 | 1986-01-02 | Interchem Internat S A | I methylcarbapenems having a 2-quaternary¹heteroarylalkylthio substituent |
NO172099C (no) * | 1984-10-15 | 1993-06-09 | Sankyo Co | Fremgangsmaate til fremstilling av et preparat som inneholder et penem -eller karbapenemantibiotikum og en n-acetylert aminosyre |
US4680292A (en) * | 1984-12-13 | 1987-07-14 | Merck & Co., Inc. | Carbapenems and 1-methylcarbapenems having a 2-heteroaryliumaliphatic substituent |
US4739113A (en) * | 1986-05-30 | 1988-04-19 | Merck & Co., Inc. | Bis(cyclopropanecarboxamido)alkadienedioic acids as renal dipeptidase inhibitors |
EP0464900A3 (en) | 1990-06-26 | 1992-07-22 | Merck & Co. Inc. | 2-biphenyl-carbapenems |
CA2052730A1 (en) | 1990-10-11 | 1992-04-12 | Frank P. Dininno | 2-(substituted-dibenzofuranyl and dibenzothienyl) carbapenem antibacterial agents |
ES2244529T3 (es) * | 1991-02-01 | 2005-12-16 | Daiichi Suntory Pharma Co., Ltd. | Composiciones antibacterianas orales y metodo para la mejora de la absorcion gastrointestinal de los antibioticos de penemo o carbapenemo. |
US6297231B1 (en) | 1996-10-28 | 2001-10-02 | Merck & Co., Inc. | Stabilized carbapenem antibiotic compositions and method of making |
US6255300B1 (en) | 1997-09-09 | 2001-07-03 | Merck & Co., Inc. | Carbapenem antibacterial compounds, compositions containing such compounds and methods of treatment |
US6277843B1 (en) | 1997-09-17 | 2001-08-21 | Merck & Co., Inc. | Carbapenem antibacterial compounds, compositions containing such compounds and methods of treatment |
US6271222B1 (en) | 1998-05-28 | 2001-08-07 | Merck & Co., Inc. | Penem antibacterial compounds, compositions and methods of treatment |
US6284753B2 (en) | 1998-06-02 | 2001-09-04 | Merck & Co., Inc. | Carbapenem antibacterial compounds, compositions containing such compounds and methods of treatment |
US6310055B2 (en) | 1998-06-02 | 2001-10-30 | Merck & Co., Inc. | Halophenoxy substituted carbapenem antibacterial compounds |
US6288054B1 (en) | 1998-06-02 | 2001-09-11 | Merck & Co., Inc. | Carbapenem antibacterial compounds, compositions containing such compounds and methods of treatment |
US6265395B1 (en) | 1998-06-25 | 2001-07-24 | Merck & Co., Inc. | Carbapenem antibacterial compounds, compositions containing such compounds and methods of treatment |
EP1090000A4 (en) | 1998-06-25 | 2002-11-27 | Merck & Co Inc | ANTIBACTERIAL NAPHTHO [1,8-DE] THIASIN-2-YL-METHYL-CARBAPENEM COMPOUNDS |
CA2335571A1 (en) | 1998-06-25 | 1999-12-29 | Merck & Co. Inc. | (heterocyclic) methyl substituted carbapenem antibacterials |
WO1999066928A1 (en) | 1998-06-25 | 1999-12-29 | Merck & Co., Inc. | Carbapenem antibacterial compounds, compositions containing such compounds and methods of treatment |
AU4828999A (en) | 1998-06-25 | 2000-01-10 | Merck & Co., Inc. | (heterocyclic)methyl substituted carbapenem antibacterials |
US6316488B1 (en) | 1999-06-17 | 2001-11-13 | Merck & Co., Inc. | Antibiotic compound |
US6221859B1 (en) | 1999-08-27 | 2001-04-24 | Merck & Co., Inc. | Carbapenem antibacterial compositions and methods of the treatment |
WO2012104793A1 (en) * | 2011-02-02 | 2012-08-09 | Indian Council Of Medical Research | An antibacterial and antiviral compound |
CA2840060A1 (en) | 2011-06-27 | 2013-01-03 | Kyorin Pharmaceutical Co., Ltd. | Bridged bicyclic compounds for the treatment of bacterial infections |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2272684A1 (en) * | 1975-01-07 | 1975-12-26 | Ito Shojiro | Antibiotic-unsaturated acid compsns. - having a synergistic effect against gram positive and negative bacteria |
-
1979
- 1979-07-04 AR AR79277427A patent/AR244550A1/es active
- 1979-07-12 NZ NZ190993A patent/NZ190993A/xx unknown
- 1979-07-12 PH PH22771A patent/PH16620A/en unknown
- 1979-07-13 IL IL57798A patent/IL57798A/xx unknown
- 1979-07-16 AU AU48932/79A patent/AU529315B2/en not_active Expired
- 1979-07-20 GR GR59656A patent/GR69997B/el unknown
- 1979-07-20 FI FI792282A patent/FI792282A/fi not_active Application Discontinuation
- 1979-07-20 CA CA000332316A patent/CA1136549A/en not_active Expired
- 1979-07-20 PT PT69955A patent/PT69955B/pt unknown
- 1979-07-20 HU HU79ME2286A patent/HU182973B/hu unknown
- 1979-07-23 CZ CS795137A patent/CZ280583B6/cs unknown
- 1979-07-23 SK SK5137-79A patent/SK278357B6/sk unknown
- 1979-07-23 ES ES482774A patent/ES482774A1/es not_active Expired
- 1979-07-24 DE DE7979102615T patent/DE2964609D1/de not_active Expired
- 1979-07-24 EP EP79102615A patent/EP0007614B1/en not_active Expired
- 1979-07-24 EG EG443/79A patent/EG14367A/xx active
- 1979-07-24 DD DD79214580A patent/DD145059A5/de unknown
- 1979-08-08 IE IE1388/79A patent/IE51691B1/en not_active IP Right Cessation
-
1986
- 1986-04-03 HK HK232/86A patent/HK23286A/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
EG14367A (en) | 1984-09-30 |
DD145059A5 (de) | 1980-11-19 |
FI792282A (fi) | 1980-01-25 |
SK513779A3 (en) | 1997-01-08 |
SK278357B6 (en) | 1997-01-08 |
PT69955A (en) | 1979-08-01 |
IE791388L (en) | 1980-01-24 |
NZ190993A (en) | 1981-10-19 |
EP0007614A1 (en) | 1980-02-06 |
AU4893279A (en) | 1980-01-31 |
AU529315B2 (en) | 1983-06-02 |
GR69997B (xx) | 1982-07-23 |
PH16620A (en) | 1983-11-28 |
EP0007614B1 (en) | 1983-01-26 |
DE2964609D1 (en) | 1983-03-03 |
CA1136549A (en) | 1982-11-30 |
CZ513779A3 (en) | 1995-10-18 |
CZ280583B6 (cs) | 1996-02-14 |
PT69955B (pt) | 1981-06-11 |
HK23286A (en) | 1986-04-11 |
AR244550A1 (es) | 1993-11-30 |
IE51691B1 (en) | 1987-02-18 |
IL57798A0 (en) | 1979-11-30 |
HU182973B (en) | 1984-03-28 |
ES482774A1 (es) | 1980-09-01 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
KB | Patent renewed |