MY111735A - Novel antimicrobial lactam-quinolones. - Google Patents
Novel antimicrobial lactam-quinolones.Info
- Publication number
- MY111735A MY111735A MYPI89001466A MYPI19891466A MY111735A MY 111735 A MY111735 A MY 111735A MY PI89001466 A MYPI89001466 A MY PI89001466A MY PI19891466 A MYPI19891466 A MY PI19891466A MY 111735 A MY111735 A MY 111735A
- Authority
- MY
- Malaysia
- Prior art keywords
- lactam
- moiety
- reversed
- quinolone
- linking
- Prior art date
Links
- 230000000845 anti-microbial effect Effects 0.000 title abstract 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 5
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 abstract 4
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical group C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 abstract 3
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 abstract 2
- 239000012990 dithiocarbamate Substances 0.000 abstract 2
- FTWHMBSUYWGHMM-UHFFFAOYSA-N (diaminophosphorylamino)phosphonic acid Chemical compound NP(N)(=O)NP(O)(O)=O FTWHMBSUYWGHMM-UHFFFAOYSA-N 0.000 abstract 1
- FLBAYUMRQUHISI-UHFFFAOYSA-N 1,8-naphthyridine Chemical compound N1=CC=CC2=CC=CN=C21 FLBAYUMRQUHISI-UHFFFAOYSA-N 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- -1 HETEROARYLIUM Chemical compound 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 239000004202 carbamide Substances 0.000 abstract 1
- STIAPHVBRDNOAJ-UHFFFAOYSA-N carbamimidoylazanium;carbonate Chemical compound NC(N)=N.NC(N)=N.OC(O)=O STIAPHVBRDNOAJ-UHFFFAOYSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 abstract 1
- 150000002466 imines Chemical class 0.000 abstract 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- 229940124530 sulfonamide Drugs 0.000 abstract 1
- 150000003456 sulfonamides Chemical class 0.000 abstract 1
- 150000007970 thio esters Chemical class 0.000 abstract 1
- 150000003568 thioethers Chemical class 0.000 abstract 1
- HIZCIEIDIFGZSS-UHFFFAOYSA-L trithiocarbonate Chemical compound [S-]C([S-])=S HIZCIEIDIFGZSS-UHFFFAOYSA-L 0.000 abstract 1
- 239000012989 trithiocarbonate Substances 0.000 abstract 1
- 239000012991 xanthate Substances 0.000 abstract 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
ANTIMICROBIAL LACTAM-QUINOLONE COMPOUNDS COMPRISING A LACTAM-CONTAINING MOIETY LINKED TO A QUINOLONE MOIETY, OF THE FORMULA:WHEREIN (I) A1, A2, A3, R1, R4 AND R6 GENERALLY FORM ANY OF A VARIETY OF QUINOLONE, NAPHTHYRIDINE OR RELATED CYCLIC MOIETIES KNOWN IN THE ART TO HAVE ANTIMICROBIAL ACTIVITY;AND (2) R1 OR R3 CONTAIN A LINKING MOIETY, LINKING THE QUINOLONE MOIETY TO A LACTAM-CONTAINING MOIETY HAVING THE FORMULA:WHEREIN (3) R10, R11, R12, R13, AND R14, TOGETHER WITH BONDS "A" AND "B" , FORM ANY OF A VARIETY OF LACTAM-CONTAINING MOIETIES KNOWN IN THE ART TO HAVE ANTIMICROBIAL ACTIVITY;AND (4) THE LINKING MOIETY INCLUDES (FOR EXAMPLE) CARBAMATE, DITHIOCARBAMATE, UREA, THIOUREA, ISOURONIUM, ISOTHIOURONIUM, GUANIDINE, CARBONATE, TRITHIOCARBONATE, REVERSED CARBAMATE, XANTHATE, REVERSED ISOURONIUM, REVERSED DITHIOCARBAMATE, REVERSED ISOTHIOURONIUM, AMINE, IMINE, AMMONIUM, HETEROARYLIUM, ETHER, THIOETHER, PHOSPHONO, PHOSPHORAMIDE, PHOSPHATE, SULFONAMIDE, ESTER, THIOESTER, AMIDE, AND HYDRAZIDE GROUPS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26194888A | 1988-10-24 | 1988-10-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MY111735A true MY111735A (en) | 2000-12-30 |
Family
ID=22995566
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MYPI89001466A MY111735A (en) | 1988-10-24 | 1989-10-21 | Novel antimicrobial lactam-quinolones. |
Country Status (3)
| Country | Link |
|---|---|
| IL (1) | IL92032A (en) |
| MY (1) | MY111735A (en) |
| ZA (2) | ZA898008B (en) |
-
1989
- 1989-10-17 IL IL9203289A patent/IL92032A/en not_active IP Right Cessation
- 1989-10-21 MY MYPI89001466A patent/MY111735A/en unknown
- 1989-10-23 ZA ZA898008A patent/ZA898008B/en unknown
- 1989-10-24 ZA ZA898045A patent/ZA898045B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IL92032A (en) | 1995-10-31 |
| IL92032A0 (en) | 1990-07-12 |
| ZA898045B (en) | 1990-08-29 |
| ZA898008B (en) | 1990-08-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2001225A1 (en) | Antimicrobial lactam-quinolones | |
| DK0525057T3 (en) | Antimicrobial quinolonyllactams | |
| AU666702B2 (en) | Morphinan derivative and medicinal use | |
| IL99161A0 (en) | Novel substituted guanidine derivatives,their preparation and use | |
| DE69014490D1 (en) | Piperaziniocephalosporins. | |
| FI911763A7 (en) | Ammonium salts of N5-methyl-5,6,7,8-tetrahydrofolic acid | |
| EP0475418A3 (en) | Self-extinguishing polymeric compositions | |
| IT1244869B (en) | SELF-EXTINGUISHING POLYMERIC COMPOSITIONS. | |
| HUT50345A (en) | Process for production of cefem-derivatives and their intermediers | |
| TR200001010T2 (en) | Isoquinolins with urokinase inhibitors. | |
| HUT43329A (en) | Process for preparing n-substituted aminomethyl phosphonic acid derivatives | |
| GR3019351T3 (en) | Diaminoethylene compounds | |
| MY106904A (en) | Herbicidal composition. | |
| HUP9902465A1 (en) | New amidinium derivatives, pharmaceutical compositions containing same, and uses thereof | |
| CA2343002A1 (en) | Ammonia salts of amides of alkylphosphonic acid with ammonium choloride and use as combustion retardant for polymeric materials | |
| EP0882721A4 (en) | 4-SUBSTITUTED 2,7-DIDEOXY-7-FLUORO-2,3-DIDEHYDRO SIAL ACIDS | |
| FR2539417B1 (en) | ||
| HUP9902149A2 (en) | 1-methylcarbapenem derivatives with antibacterial activity, use thereof, pharmaceutical compositions containing these compounds | |
| JPS6438091A (en) | Condensed heterocyclic sulfonylurea | |
| ATE247638T1 (en) | METHOD FOR PRODUCING N-ALKYL-N'-NITROGUANIDINE | |
| IE821192L (en) | N-(aryloxyalkyl)-n'-(aminoalkyl) ureas | |
| EP0255366A3 (en) | Nitrogen- and sulfur-containing lipid compound, their production and use | |
| IE832664L (en) | Penems. | |
| AU6176686A (en) | Amides of N-acylated amino acids as anticonvulsants | |
| MY101610A (en) | Penems, pharmaceutical compositions containing them , process for preparing them. |