[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Rabbani et al., 2020 - Google Patents

Synthesis and Characterization of Some NH-Analogues of Ciprofloxacin on Antibacterial, Antifungal, and Cytotoxic Activities.

Rabbani et al., 2020

View PDF
Document ID
5065556352213670354
Author
Rabbani M
Islam M
Publication year
Publication venue
Journal of Scientific Research

External Links

Snippet

Present work includes synthesis of five NH-analogues of ciprofloxacin, 2-6 have been prepared to find out their medicinal assessment, for instance, antibacterial, antifungal, and cytotoxicity. The structure of the analogues has been confirmed by FT-IR, 1H-NMR, 13C …
Continue reading at pdfs.semanticscholar.org (PDF) (other versions)

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/20—Oxygen atoms
    • C07D215/22—Oxygen atoms attached in position 2 or 4
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/06—Peri-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/06—Peri-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O-metal, -CHO, keto, ether, groups, groups, or groups
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients

Similar Documents

Publication Publication Date Title
Mungra et al. Synthesis and identification of β-aryloxyquinolines and their pyrano [3, 2-c] chromene derivatives as a new class of antimicrobial and antituberculosis agents
US9493419B2 (en) Quinoline derivatives as anti-cancer agents
US20220380285A1 (en) Prenylated hydroxystilbenes
Kathrotiya et al. Synthesis and identification of β-aryloxyquinoline based diversely fluorine substituted N-aryl quinolone derivatives as a new class of antimicrobial, antituberculosis and antioxidant agents
Carta et al. Quinoxalin-2-ones: Part 5. Synthesis and antimicrobial evaluation of 3-alkyl-, 3-halomethyl-and 3-carboxyethylquinoxaline-2-ones variously substituted on the benzo-moiety
Aridoss et al. Synthesis and spectral characterization of a new class of N-(N-methylpiperazinoacetyl)-2, 6-diarylpiperidin-4-ones: Antimicrobial, analgesic and antipyretic studies
Arendt-Pindel et al. Design and functionalization of bioactive benzoxazines. An unexpected ortho-substitution effect
Rabbani et al. Synthesis and Characterization of Some NH-Analogues of Ciprofloxacin on Antibacterial, Antifungal, and Cytotoxic Activities.
Dave et al. Syntheses and anti-microbial evaluation of new quinoline scaffold derived pyrimidine derivatives
Das et al. Synthesis and assessment of antitubercular and antimicrobial activity of some novel triazolo and tetrazolo-fused 1, 3, 4-oxadiazole molecules containing pyrazine moiety
Rabbani et al. Synthesis and Characterization of Some Mannich Base Analogues of Ciprofloxacin: Antibacterial, Antifungal, and Cytotoxic Activities.
Kanani et al. Synthesis and in vitro antimicrobial evaluation of novel 2-amino-6-(phenylthio)-4-(2-(phenylthio) quinolin-3-yl) pyridine-3, 5-dicarbonitriles
EP3260445A1 (en) Compounds for use as an anti-bacterial or anti-fungal agent and as a zinc sensor
Georgieva et al. Synthesis and properties of several Betti bases as potential drugs
Patel et al. Synthesis and characterization of some new thiazolidinones containing coumarin moiety and their antimicrobial study
Rabbani et al. Synthesis, Characterization and Biological Evaluation of Ciprofloxacin-pnitrobenzoylated and Its Transition Metal Analogues.
Ashok et al. Microwave assisted synthesis of substituted (Z)-2-{[1-phenyl-3-(thiophen-2-yl)-1 H-pyrazol-4-yl] methylene} benzofuran-3 (2 H)-ones and their antimicrobial activity
Kavitha et al. Design, Synthesis, Characterization of Antimicrobial activity of Schiff bases of novel Quinazolin-4-one Derivatives
US9388209B2 (en) 2′, 3′-dideoxy-5-fluorouridine derivatives, a process for the manufacture thereof and application thereof
Ashok et al. Microwave assisted synthesis of 1H-tetrazole-based flavonoid derivatives and their antimicrobial activity
Jadhav et al. MICROWAVE ASSISTED SOLVENT FREE SYNTHESIS AND EVALUATION OF ANTIMICROBIAL AND ANTIOXIDANT ACTIVITIES OF SOME NOVEL 3, 4-BIS (SUBSTITUTED PHENYL)-7-(6-METHYL PYRIDIN-2-YL)-3, 3A, 3B, 4-TETRAHYDRO7H-PYRROLO [2, 3-C: 5, 4-C'] DIISOXAZOLE
Mohan et al. Novel bridgehead nitrogen bisheterocyclic systems: Synthesis, stereochemistry and antimicrobial activity of p-bis [2H, 5H-4-oxo-thiazol-3-yl] phenylenes and p-bis [cis-5H-3, 3a-dihydropyrazolo [3, 4-d] thiazol-6-yl] phenylenes
CN114763357B (en) Indolopyrimidine tricyclic compound and preparation method and application thereof
DE4339134A1 (en) 1- (2-fluorocyclopropyl) quinolone and naphthyridonecarboxylic acid derivatives
Saglani et al. Rapid and greener ultrasound assisted synthesis of series (2-((substituted 2-Chloroquinolin-3-yl) methylene)-3, 4-dihydronaphthalen-1 (2h)-one) derivatives and their biological activity