Matsuda et al., 1987 - Google Patents
Studies on antiviral agents V. Synthesis and in vitro antiviral activity of new aminoglycoside derivatives having palmitoyl groupMatsuda et al., 1987
View PDF- Document ID
- 8147640455584697123
- Author
- Matsuda K
- Yasuda N
- Tsutsumi H
- Takaya T
- Publication year
- Publication venue
- The Journal of Antibiotics
External Links
Snippet
and influenza virus (A/PR8). Among these derivatives, 1-JV-palmitoy1-3"-JV-(trifluoroacety^ kana-mycin Adihydrochloride (PTKA) showed especially potent antiviral activity as well as cytotoxicity. Wehave also reported that the positional isomers of iV-palmitoyl-and iV …
- 230000000840 anti-viral 0 title abstract description 32
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/20—Carbocyclic rings
- C07H15/22—Cyclohexane rings, substituted by nitrogen atoms
- C07H15/222—Cyclohexane rings substituted by at least two nitrogen atoms
- C07H15/224—Cyclohexane rings substituted by at least two nitrogen atoms with only one saccharide radical directly attached to the cyclohexyl radical, e.g. destomycin, fortimicin, neamine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/02—Acyclic radicals, not substituted by cyclic structures
- C07H15/04—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/20—Carbocyclic rings
- C07H15/24—Condensed ring systems having three or more rings
- C07H15/244—Anthraquinone radicals, e.g. sennosides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/20—Carbocyclic rings
- C07H15/24—Condensed ring systems having three or more rings
- C07H15/252—Naphthacene radicals, e.g. daunomycins, adriamycins
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/02—Acyclic radicals, not substituted by cyclic structures
- C07H15/14—Acyclic radicals, not substituted by cyclic structures attached to a sulfur, selenium or tellurium atom of a saccharide radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2103/00—Systems containing at least three condensed rings
- C07C2103/02—Ortho- or ortho- and peri-condensed systems
- C07C2103/04—Ortho- or ortho- and peri-condensed systems containing three rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H5/00—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA1089851A (en) | 3-de-o-methylfortimicins | |
CA1114809A (en) | 4-n-acylfortimicin b derivatives and the chemical conversion of fortimicin b to fortimicin a | |
Sparks et al. | Synthesis of potential inhibitors of hemagglutination by influenza virus: chemoenzymic preparation of N-5 analogs of N-acetylneuraminic acid. | |
Bobek et al. | Synthesis and biological activity of 4'-thio analogs of the antibiotic toyocamycin | |
EP0105193B1 (en) | Spergualin-related compounds, processes for the preparation thereof and their use as medicaments | |
US4117221A (en) | Aminoacyl derivatives of aminoglycoside antibiotics | |
US4525299A (en) | (-)-15-Deoxyspergualin, process for the preparation thereof, and intermediate of the same | |
SI9620099A (en) | Diglycosylated 1,2-diols as mimetics of sialyl-lewis x and sialyl-lewis a | |
US3796699A (en) | Antibiotic derivatives of gentamicin c1a | |
Matsuda et al. | Studies on antiviral agents V. Synthesis and in vitro antiviral activity of new aminoglycoside derivatives having palmitoyl group | |
US3651045A (en) | 9-(beta-d-arabinofuranosyl)adenine esters and methods for their production | |
EP0094632B1 (en) | (-)-15-deoxyspergualin, a process for the preparation of the same, and a pharmaceutical composition containing the same | |
Umezawa et al. | Studies of Aminosugars. XIV. Syntheses of 6, 6′-Diamino-6, 6′-dideoxymaltosylamine, 1′, 6, 6′-Triamino-, 1′, 6, 6′-trideoxysucrose and 6, 6′-Diamino-6, 6′-dideoxytrehalose | |
US4170641A (en) | 1-N-(ω-aminoalkanesulfonyl) derivative of aminoglycosidic antibiotic and process for preparation thereof | |
US3886138A (en) | 4{40 -Deoxykanamycin A | |
Ohba et al. | Studies on a new aminoglycoside antibiotic, dactimicin II. Isolation, structure and chemical degradation | |
EP0071251A1 (en) | Novel aminoglycosides and use thereof | |
KR840001622B1 (en) | Method of preparing for 3-0-demethyl istamycine b | |
GB2090831A (en) | A process for preparing n-acylcarnosine | |
Vince et al. | Carbocyclic purmocyin: Synthesis and inhibition of protein biosynthesis | |
EP0096392A1 (en) | Novel aminoglycosides, process for production thereof and use thereof | |
EP0040764B1 (en) | Novel aminoglycosides, and antibiotic use thereof | |
DELAWARE et al. | AMINOGLYCOSIDE ANTIBIOTICS 7. DIHYDROSTREPTOMYCIN ANALOGUES | |
US4298727A (en) | 3',4'-Dideoxykanamycin A and 1-N-(S)-α-hydroxy-ω-aminoalkanoyl) derivatives thereof | |
US4252972A (en) | Fortimicin B-1,2:4,5-bis-carbamates |