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1.
Biochem Syst Ecol ; 29(5): 531-533, 2001 May.
Artigo em Inglês | MEDLINE | ID: mdl-11274773
2.
3.
Experientia ; 51(4): 368-9, 1995 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-7729504

RESUMO

(E)-3-tridecen-2-one, the major volatile component of interdigital gland extracts from the black-tailed deer, Odocoileus hemionus columbianus, inhibited the growth of gram-positive bacteria and fungi. The bacteria, Propionibacterium acnes, and the fungi, Trichophyton mentagrophytes had a minimum inhibitory concentration (MIC) of 12.5 micrograms/mL and 25 micrograms/mL, respectively.


Assuntos
Alcenos/farmacologia , Cervos/metabolismo , Glândulas Exócrinas/metabolismo , Fungos/efeitos dos fármacos , Bactérias Gram-Positivas/efeitos dos fármacos , Alcenos/química , Animais , Cromatografia Gasosa-Espectrometria de Massas , Espectroscopia de Ressonância Magnética , Espectroscopia de Infravermelho com Transformada de Fourier
4.
J Chem Ecol ; 21(10): 1401-8, 1995 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-24233672

RESUMO

Three volatile ketones, 2-tridecanone, (E)-3-tridecen-2-one and (E)-4-tridecen-2-one were identified in interdigital gland extracts from black-tailed deer,Odocoileus hemionus columbianus. The major compound, (E)-3-tridecen-2-one, inhibited the growth of several species of fungi and grampositive bacteria. The bacterium,Propionibacterium acnes, and the fungus,Trichophyton mentagrophytes required a minimum concentration (MIC) of 12.5 µg/ml and 25 µg/ml, respectively, for inhibition, (E)-3-Tridecen-2-one represents a new class of lipid antibiotics found on animal skin. The second major compound is this secretion, 2-tridecanone, was not active against any of the organisms tested.

5.
J Chem Ecol ; 21(2): 213-9, 1995 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24234020

RESUMO

Previous analyses of the scent gland secretions of snakes have focused on the nonvolatile components. Gas chromatography-mass spectrometry of secretions from North American garter snakes (Thamnophis butleri, T. couchi, T. elegans, T. melanogaster, andT. sirtalis) indicated the following seven major volatile components: acetic, propanoic, 2-methylpropanoic, butanoic, and 3-methylbutanoic acids, trimethylamine, and 2-piperidone. Five or more of these compounds were observed in secretions of select boid, colubrid, pythonid, and viperid snakes, suggesting that they are widespread scent gland products. 3-Methylbutanal also was detected in some snake species.

6.
J Chem Ecol ; 19(4): 837-41, 1993 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24249022

RESUMO

GC-MS analysis of the anal sac secretion from the hog-nosed skunk,Conepatus mesoleucus, showed two major volatile components, (E)-2-butene-1-thiol and (E)-S-2-butenyl thioacetate. Minor volatile components identified from this secretion were phenylmethanethiol, 2-methylquinoline, 2-quinolinemethanethiol, and bis[(E)-2-butenyl] disulfide. 3-Methyl-1-butanethiol, a major component in the defensive spray of the striped skunk,Mephitis mephitis, and the spotted skunk,Spilogale putorius, was absent from this secretion.

7.
Photosynth Res ; 36(1): 17-23, 1993 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24318794

RESUMO

Several species of marine benthic algae, four species of phytoplankton and two species of seagrass have been subjected to ultraviolet B irradiation for varying lengths of time and the effects on respiration, photosynthesis and fluorescence rise kinetics studied. No effect on respiration was found. Photosynthesis was inhibited to a variable degree in all groups of plants after irradiation over periods of up to 1 h and variable fluorescence was also inhibited in a similar way. The most sensitive plants were phytoplankton and deep-water benthic algae. Intertidal benthic algae were the least sensitive to UV-B irradiation and this may be related to adaptation, through the accumulation of UV-B screening compounds, to high light/high UV-B levels. Inhibition of variable fluorescence (Fv) of the fluorescence rise curve was a fast and sensitive indicator of UV-B damage. Two plants studied, a brown alga and a seagrass, showed very poor recovery of Fv over a period of 32 h.

8.
J Chem Ecol ; 17(7): 1415-20, 1991 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-24257801

RESUMO

GC-MS analysis of the anal sac secretion from the spotted skunk,Spilogale putorius, showed three major volatile components: (E)-2-butene-1-thiol, 3-methyl-1-butanethiol, and 2-phenylethanethiol. Minor volatile components identified from this secretion were: phenylmethanethiol, 2-methylquinoline, 2-quinolinemethanethiol, bis[(E)-2-butenyl] disulfide, (E)-2-butenyl 3-methylbufyl disulfide, bis(3-methylbutyl) disulfide. All of these compounds except 2-phenylethanethioi have been identified previously from the striped skunk,Mephitis mephitis. The thioacetate derivativesS- (E)-2-butenyl thioacetate,S-3-methylbutanyl thioacetate, andS-2-quinolinemethyl thioacetate found in the striped skunk were not seen in this species.

9.
J Chem Ecol ; 16(6): 2057-65, 1990 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24264006

RESUMO

GC-MS analysis of the anal sac secretion of the striped skunk (Mephitis mephitis), shows seven major components: (E)-2-butene-1-thiol, 3-methyl-1-butanethiol, S-(E)-2-butenyl thioacetate,S-3-methylbutanyl thioacetate, 2-methylquinoline, 2-quinolinemethanethiol, andS-2-quinolinemethyl thioacetate. The following compounds previously reported from this secretion could not be confirmed: bis(2-butenyl) sulfide, (E)-2-Butenyl methyl disuffide, (E)-2-butenyl propyl sulfide, butyl 3-methylbutyl disulfide, and 2-butenyl butyl disulfide.

11.
J Med Chem ; 19(5): 643-7, 1976 May.
Artigo em Inglês | MEDLINE | ID: mdl-178870

RESUMO

Reaction of the trimethylsilyl derivative of 2,3-dihydro-6H-1,3-oxazine-2,6-dione (2, "uracil anhydride") with protected 1-O-acetylribofuranoses in the presence of stannic chloride gave the corresponding block nucleosides. 3-(2,3-5-Tri-O-2',2',2'-trichloroethoxycarbonyl-beta-d-ribofuranosyl)-2,3-dihydro-6H-1,3-oxazine-2,6-dione (4c) thus prepared from the protected sugar 3c, 1-O-acetyl-2,3,5-tri-O-(2,2,2-trichloroethoxycarbonyl)ribofuranose, gave, on removal of the protecting groups with zinc dust,3-(beta-d-ribofuranosyl)-2,3-dihydro-6H-1,3-oxazine-2,6-dione (1). The structure of 1 was confirmed by uv, ir, NMR, and CD spectral data and was shown to be an N nucleoside. Uracil anhydride, 2, and, to a lesser extent, its ribonucleoside 1 exert a moderate growth inhibition of mouse leukemia L5178Y, HeLa, and Novikoff hepatoma cells i- culture. Both compounds produce weak inhibition of vaccinia viral replication in HeLa cells.


Assuntos
Oxazinas/síntese química , Ribonucleosídeos/síntese química , Uridina/análogos & derivados , Animais , Carcinoma Hepatocelular/metabolismo , Linhagem Celular , Escherichia coli/efeitos dos fármacos , Escherichia coli/crescimento & desenvolvimento , Leucemia L1210/metabolismo , Leucemia Experimental/metabolismo , Neoplasias Hepáticas/metabolismo , Camundongos , Neoplasias Experimentais/metabolismo , Oxazinas/farmacologia , Ratos , Ribonucleosídeos/farmacologia , Vaccinia virus/metabolismo , Replicação Viral/efeitos dos fármacos
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