RESUMEN
Synthesis and resolution of the antibiotic phosphonomycin are described. The structure is (-)(IR, 2S)-1,2-epoxypropylphosphonic acid.
Asunto(s)
Antibacterianos/aislamiento & purificación , Antibacterianos/síntesis química , Espectroscopía de Resonancia MagnéticaRESUMEN
Incubation of rat adrenal homogenates with tritiated and unlabeled 19-nor-deoxycorticosterone yielded, in addition to unconverted starting substrate, two major radioactive conversion products. These two products were purified by TLC and HPLC and subjected to mass spectrometry and nuclear magnetic resonance analysis. The interpretation of the spectra was consistent with the structures to be 19-nor-corticosterone and 19-nor-18-hydroxydeoxycorticosterone. The possible biological significance of these two compounds is discussed.
Asunto(s)
Glándulas Suprarrenales/metabolismo , Corticosterona/análogos & derivados , Desoxicorticosterona/análogos & derivados , Animales , Cromatografía Líquida de Alta Presión , Corticosterona/metabolismo , Desoxicorticosterona/metabolismo , Espectroscopía de Resonancia Magnética , Masculino , Espectrometría de Masas , Ratas , Ratas EndogámicasRESUMEN
Analysis of polyol extracts from various stages of Eimeria tenella has revealed the presence of mannitol and 2-O-methyl-chiro-inositol (quebrachitol). Previously, both compounds had been found almost exclusively in plants, and in the case of mannitol in a few species of bacteria. Identification was achieved by various analytical techniques including nuclear magnetic resonance (NMR), capillary gas-liquid chromatography (GLC), and GLC-mass spectrometry. Unsporulated oocysts contain a high level of mannitol (300 mM) which diminished during sporulation to 10 mM in sporulated oocysts.
Asunto(s)
Eimeria/análisis , Inositol/análogos & derivados , Manitol/análisis , Animales , Fenómenos Químicos , Química , Cromatografía de Gases , Cromatografía de Gases y Espectrometría de Masas , Inositol/análisis , Espectroscopía de Resonancia Magnética , Manitol/metabolismoRESUMEN
Thyrotropin-releasing hormone (TRH) analogues which show relative selectivity for action in the central nervous system have been recognized. Practical syntheses for three of these TRH analogues which show the greatest selectivity, less than Aad-His-Tzl-NH2 (5), less than Glu-His-Pip-OMe (2), and less than Aad-His-Pro-NH2 (6), are described. The first two were prepared by solution methods of peptide synthesis. Compound 6 was prepared by the solid-phase method. Problems of histidine racemization, facile diketopiperazine formation, and instability of acylated thiazolidine carboxylic acid derivatives under acidic conditions have been minimized in order to attain optimal yields. Physical properties such as pK, NMR shifts, and circular dichroism have been examined as they might relate to biological activity and peptide conformation.
Asunto(s)
Sistema Nervioso Central/efectos de los fármacos , Hormona Liberadora de Tirotropina/análogos & derivados , Ácido Pirrolidona Carboxílico/análogos & derivados , Relación Estructura-Actividad , Tiazolidinas , Hormona Liberadora de Tirotropina/síntesis química , Hormona Liberadora de Tirotropina/farmacología , Tiroxina/metabolismo , Triyodotironina/metabolismoRESUMEN
Syntheses are reported for three metabolites (2-4) of timolol (1) formed by oxidative metabolism of the morpholine ring. GLC-MS comparisons are presented which establish that the two metabolites whose structures were previously in question are identical with their synthetic counterparts 2 and 3. In 2, metabolic oxidation of the 4-morpholinyl group of 1 had occurred at the carbon next to oxygen to give the 2-hydroxy-4-morpholinyl moiety, whereas in 3, the morpholine of 1 has been oxidized one step further and then ring opened to produce the N-(2-hydroxyethyl)glycine substituent. Biological testing of synthetic samples of the three major metabolites from human urine (3, 4, and 6) indicated that only 4, in which the morpholine moiety has been degraded to a 2-hydroxyethylamino group, had significant beta-adrenergic blocking activity (one-seventh that of timolol in anesthetized dogs).
Asunto(s)
Propanolaminas/orina , Timolol/orina , Antagonistas Adrenérgicos beta , Animales , Perros , Femenino , Cromatografía de Gases y Espectrometría de Masas , Humanos , Isoproterenol/antagonistas & inhibidores , Masculino , Timolol/análogos & derivados , Timolol/síntesis química , Timolol/farmacologíaRESUMEN
The synthesis and resolution of 3-iodocyproheptadine [(+/-)-5a] and 1-cyclopropylmethyl-4-(3-iodo-5H-dibenzo-[a,d]cyclohepten-5-ylidene)piperidine [(+/-)-5b] are described. The resulting atropisomers undergo reaction with trifluoromethylthiocopper to give optically active products without extensive racemization. In this manner, optically pure (+)- and (-)-3-trifluoromethylthiocyproheptadine [(+)-6a and (-)-6a, respectively] and (+)- and (-)-1-cyclopropylmethyl-4-(3-trifluoromethylthio-5H-dibenzo[a,d]cyclohepten-5-ylidene)piperidine [(+)-6b and (-)-6b, respectively] have been prepared. The influence of a chiral europium shift reagent on the proton and fluorine resonance signals as a diagnostic tool for the determination of the optical purities of these atropisomers is discussed. The four compounds, (+)-6a, (-)-6a, (+)-6b, and (-)-6b, were studied in squirrel monkeys for their ability to block conditioned avoidance responding. All of the antiavoidance activity was found to reside solely in the levorotatory compounds (-)-6a and (-)-6b. Further comparison of the enantiomers (-)-6b and (+)-6b showed that the ability to antagonize apomorphine-induced stereotyped behavior is confined to the levorotatory isomer (-)-6b while weak central anticholinergic activity resides solely in the dextrorotatory isomer (+)-6b. Neither (-)-6b has significant peripheral anticholinergic activity.
Asunto(s)
Antipsicóticos/síntesis química , Ciproheptadina/análogos & derivados , Animales , Reacción de Prevención/efectos de los fármacos , Ciproheptadina/síntesis química , Ciproheptadina/farmacología , Interacciones Farmacológicas , Haplorrinos , Humanos , Espectroscopía de Resonancia Magnética , Parasimpatolíticos/síntesis química , Parasimpatolíticos/farmacología , Saimiri , Estereoisomerismo , Conducta Estereotipada/efectos de los fármacosRESUMEN
11 beta-Hydroxy dehydrogenation of cortisol to cortisone is specifically impaired in the syndrome of apparent mineralocorticoid excess. This defect bears on the pathogenesis of the disorder by unmasking the potential mineralocorticoid agonism of unmetabolized cortisol at or near mineralocorticoid target tissues. A specific index of this defect is provided by measurement of the formation of tritiated water following the administration of [3H]11 alpha-cortisol. We have explored the use of a non-radioactive tracer to follow this unidirectional dehydrogenation reaction but because of the relatively lower sensitivity of measurement of 2H2O compared to 3H2O in body fluids, use of the corresponding [2H]11 alpha-cortisol was not feasible. We have devised instead a method incorporating additional deuterium atoms into cortisol to measure unidirectional 11 beta-hydroxy dehydrogenation not by the formation of labeled water but by the determination of the dehydrogenated cortisol product from its residual deuterium content. Cortisol-d4 metabolized to cortisone-d3 is conveniently measured by the techniques of organic mass spectrometry. The synthesis of cortisol-9 alpha, 11 alpha, 12 alpha 12 beta-d4 and the validation of its isotopic distribution by mass spectrometry and nuclear magnetic resonance is described.
Asunto(s)
Hidrocortisona/síntesis química , Cortisona/química , Deuterio , Humanos , Hidrocortisona/química , Hidrogenación , Espectroscopía de Resonancia Magnética , Espectrometría de MasasRESUMEN
Finasteride (MK-0906), a drug used for the treatment of benign prostatic hyperplasia, is a highly specific inhibitor of steroid 5 alpha-reductase, an enzyme that converts testosterone (T) to dihydrotestosterone (DHT) in animals and humans. In a study to evaluate the effect of finasteride on the growth of green alga, Selenastrum capricornutum, the parent drug was not detected by HPLC in the posttreatment (14 day) samples, suggesting complete biotransformation. Thermospray LC/MS, followed by NMR analysis, indicated that the major algal metabolite was 11 alpha-hydroxy-finasteride. This metabolite has negligible in vitro bioactivity against human prostatic 5 alpha-reductase; its potency is only 2% that of finasteride. The primary metabolite of finasteride produced by the green alga involved a biotransformation not previously observed in mammalian and human studies. The green alga effectively deactivates the drug, thereby mitigating any potential environmental impact.
Asunto(s)
Chlorophyta/metabolismo , Finasterida/análogos & derivados , Finasterida/metabolismo , Inhibidores de 5-alfa-Reductasa , Biotransformación , Chlorophyta/efectos de los fármacos , Chlorophyta/crecimiento & desarrollo , Cromatografía Líquida de Alta Presión , Finasterida/farmacología , Finasterida/toxicidad , Cromatografía de Gases y Espectrometría de Masas , Humanos , Espectroscopía de Resonancia Magnética , Masculino , Próstata/enzimologíaRESUMEN
Marked variations in the 3beta-hydroxysterol content of hamster spermatozoa were observed as they progress through the epididymis. Cholesterol is the major sterol of caputal spermatozoa while the concentration of precursors of cholesterol was higher than that of cholesterol in caudal spermatozoa. One of these precursors has been identified as desmosterol. A second sterol has now been identified as 5alpha-cholestra-7,24-dien-3beta-ol by GLC-MS and by NMR. Its concentration is approximately 3-fold higher than that of cholesterol. This 3beta-hydroxysterol is also found in epididymal tissue.
Asunto(s)
Colestadienoles/biosíntesis , Genitales Masculinos/metabolismo , Animales , Colesterol/biosíntesis , Cromatografía de Gases , Cricetinae , Desmosterol/biosíntesis , Epidídimo/metabolismo , Espectroscopía de Resonancia Magnética , Masculino , Espectrometría de Masas , Mesocricetus , Espermatozoides/metabolismoRESUMEN
When ronidazole (1-methyl-5-nitroimidazole-2-methanol carbamate) is reduced by either dithionite or rat liver microsomal enzymes in the presence of cysteine, ronidazole-cysteine adducts can be isolated. Upon reduction with dithionite ronidazole can react with either one or two molecules of cysteine to yield either a monosubstituted ronidazole-cysteine adduct substituted at the 4-position or a disubstituted ronidazole-cysteine adduct substituted at both the 4-position and the 2-methylene position. In both products the carbamoyl group of ronidazole has been lost. The use of rat liver microsomes to reduce ronidazole led to the formation of the disubstituted ronidazole-cysteine adduct. These data indicate that upon the reduction of ronidazole one or more reactive species can be formed which can bind covalently to cysteine. The proposed reactive intermediates formed under these conditions may account for the observed binding of ronidazole to microsomal protein and the presence of intractable drug residues in the tissues of animals treated with this compound. They may also account for the mutagenicity of this compound in bacteria.
Asunto(s)
Cisteína , Ditionita , Microsomas Hepáticos/enzimología , Nitroimidazoles/metabolismo , Ronidazol/metabolismo , Sulfitos , Animales , Fenómenos Químicos , Química , Espectroscopía de Resonancia Magnética , Espectrometría de Masas , Oxidación-Reducción , RatasRESUMEN
Twelve in vitro oxygenated metabolites of 3a,4,5,6,7,7a-hexahydro-3-(1-methyl-5-nitro-1H-imidazol-2-yl)-1,2-benzisoxazole (MK-0436) were produced by incubation of this antiprotozoal agent with the postmitochondrial supernatant (S9) fraction isolated from the livers of rats treated with phenobarbital. Metabolite structure elucidation was achieved using NMR and mass spectrometry. Seven monohydroxy and two dihydroxy metabolites were fully characterized; two other metabolites were partially characterized as dihydroxy derivatives of the drug. The major in vitro metabolite is the 5 axial hydroxy compound, and a minor metabolite is the corresponding ketone. In all cases metabolite formation involved biotransformation on the hexahydrobenzisoxazole ring.
Asunto(s)
Antiprotozoarios/metabolismo , Hígado/metabolismo , Nitroimidazoles/metabolismo , Animales , Biotransformación , Técnicas In Vitro , Espectroscopía de Resonancia Magnética , Espectrometría de Masas , RatasRESUMEN
The reaction of 17 alpha-benzoyloxy-11 beta-hydroxy-3,20-dioxo-1, 4-pregnadien-21-al as the hemiacetal (1) with methanol:acetic acid:potassium cyanide:manganese dioxide followed by acetylation and preparative HPLC of the reaction mixture afforded 11 crystalline products. These products can be conveniently divided into three categories representing side-chain cleavage and oxidative esterification with or without elimination of the benzoyloxy group. Of special interest was the stereospecific formation of the C-17 cyanohydrin acetate 4a and the cis delta 17(20) enol acetate methyl ester 5. On the other hand, nonstereospecific addition of HCN to the side chain gave the C-20 epimeric cyanohydrin acetates 7a and 7b. The use of activated versus nonactivated MnO2 plays a major role in determining the quantitative distribution of the products. It was also discovered that even in the absence of MnO2, the reaction goes to completion. A proposed mechanism which explains the formation of all products is presented.
Asunto(s)
Pregnadienos , Fenómenos Químicos , Química , EsterificaciónRESUMEN
Metabolite fractions from the urine of a dog dosed with 3a,4,5,6,7a-hexahydro-3-(1-methyl-5-nitro-1H-imidazol-2-yl)-1,2-benzisoxazole (MK-0436) were obtained by the use of high-performance liquid chromatography. These fractions were of suitable purity for structural elucidation. Data obtained by mass spectrometry and NMR spectroscopy allowed the identification of seven major metabolites of this drug. Biotransformation in each case involved hydroxylation (mono or di) of the hexahydrobenzisoxazole ring.
Asunto(s)
Antiprotozoarios/orina , Isoxazoles/orina , Nitroimidazoles/orina , Oxazoles/orina , Animales , Antiprotozoarios/metabolismo , Cromatografía de Gases , Cromatografía Líquida de Alta Presión , Perros , Cromatografía de Gases y Espectrometría de Masas , Isoxazoles/metabolismo , Espectroscopía de Resonancia Magnética , Nitroimidazoles/metabolismoRESUMEN
1H-NMR and MS were employed to identify 13 rat urinary metabolites of 14C-labeled cis-3a,4,5,6,7,7a- hexahydro-3-(1-methyl-5-nitro-1H-imidazol-2-yl)-1,2-benzisoxazole (MK-0436). The major free (unconjugated) metabolite was cis-3a,4,5,6,7, 7a-hexahydro-3-carboxamido-1,2-benzisoxazole; it was also the second most abundant metabolite released during hydrolysis of the conjugated fraction. All other identified metabolites were hydroxylated analogues substituted at C(4)-C(7a) of the cyclohexane ring. the 4-equatorial,5-axial,7a-triol was the second most abundant metabolite excreted in an unconjugated form. Four monohydroxy (5-axial, 6-axial, 6-equatorial, 7-equatorial) metabolites of the drug were identified; they were found in the conjugated fraction only and were released by hydrolysis. The 5-axial hydroxy compound is the major conjugated metabolite and is overall the most abundant of all the metabolites. Six dihydroxy metabolites were identified: one was found exclusively in the free state, three as conjugates only (including the 7-axial,7a-diol, which is the major dihydroxy species), and two both free and conjugated. A second triol was found both free and conjugated.
Asunto(s)
Antiprotozoarios/orina , Nitroimidazoles/orina , Animales , Antiprotozoarios/metabolismo , Biotransformación , Hidrólisis , Espectrometría de Masas , Nitroimidazoles/metabolismo , Ratas , Ratas EndogámicasRESUMEN
The antiprotozoal drug 3a,4,5,6,7,7a-hexahydro-3-(1-methyl-5-nitro-1H-imidazol-2-yl)-1,2-benzisoxazole (I), which exhibits activity against trypanosomiasis, is also antibacterial in vivo. Since the urine from a dog dosed with I showed a broader spectrum of antibacterial activity than I itself, metabolites from this urine were isolated and partially characterized. The metabolites were mono- and dihydroxy-substituted species with the hydroxyl groups on carbons 4--7 of the hexahydrobenzisoxazole ring. These observations led to the synthesis of several such hydroxy derivatives of I, and their properties fully supported the proposed positions of metabolic hydroxylation. One synthetic compound, the 6,7-cis-dihydroxy compound, exhibited higher antibacterial activity against Salmonella schottmuelleri in mice and greater trypanocidal activity in vivo against Trypanosoma cruzi (Brazil strain) than I.
Asunto(s)
Antiprotozoarios/orina , Isoxazoles/orina , Nitroimidazoles/orina , Oxazoles/orina , Animales , Antiprotozoarios/farmacología , Biotransformación , Enfermedad de Chagas/tratamiento farmacológico , Cromatografía de Gases , Perros , Femenino , Isoxazoles/farmacología , Espectrometría de Masas , Ratones , Nitroimidazoles/farmacología , Salmonella/efectos de los fármacosRESUMEN
3-Methylpseudouridine (beta isomer) has been identified in fermentation broths of Nocardia lactamdurans. It accumulates at quite high levels following the accumulation of extracellular uracil in strains exhibiting increased levels of de novo pyrimidine biosynthetic enzymes. It is labeled by exogenous uracil, and appears to result from an irreversible modification of one of the components of the elevated pyrimidine pool. Its methyl group is labeled efficiently by [methyl-14C]methionine.
Asunto(s)
Nocardia/metabolismo , Seudouridina/análogos & derivados , Uridina/análogos & derivados , Antibacterianos/biosíntesis , Fermentación , Espectroscopía de Resonancia Magnética , Espectrometría de Masas , Metionina/metabolismo , Seudouridina/biosíntesis , Piridonas/biosíntesis , Espectrofotometría Ultravioleta , Uracilo/metabolismoRESUMEN
The antibiotic efrotomycin (I), C59H88N2O20, was isolated from cultures of Nocardia lactamdurans as an amorphous yellow powder. Mass spectral and NMR analyses show that the compound is a glycoside of the known antibiotic aurodox (II), C44H62N2O12. Ozonolysis and hydrolysis of I produced the disaccharide V, 6-deoxy-4-O-(6-deoxy-2,4-di-O-methyl-alpha -L-mannopyranosyl)-3-O-methyl-beta-D-allopyranose. This disaccharide is attached to the 4-hydroxyl group of the hexahydropyran substructure of aurodox via a beta-linkage to C-1 of the allose.
Asunto(s)
Antibacterianos , Espectroscopía de Resonancia Magnética , Espectrometría de Masas , Conformación Molecular , PiridonasRESUMEN
The immunosuppressants FK506 and FR 900520 were desmethylated by Actinoplanes sp. ATCC 53771 to yield various O-desmethylated products. The products were isolated and purified by solvent extraction and HPLC chromatography, and identified by NMR and MS spectroscopy.
Asunto(s)
Actinomycetales/metabolismo , Inmunosupresores/metabolismo , Piperidinas/metabolismo , Tacrolimus/metabolismo , Animales , Células Cultivadas , Cromatografía Líquida de Alta Presión , Fermentación , Inmunosupresores/química , Espectroscopía de Resonancia Magnética , Espectrometría de Masas , Cloruro de Metileno , Ratones , Conformación Molecular , Estructura Molecular , Piperidinas/química , Espectrometría de Masa Bombardeada por Átomos Veloces , Linfocitos T/efectos de los fármacos , Tacrolimus/químicaRESUMEN
Two new carbapenem antibiotics, northienamycin and 8-epi-thienamycin have been isolated from culture broth of Streptomyces cattleya grown under conditions for thienamycin production. The isolation, structure elucidation and in vitro antibacterial spectra of the new carbapenems are reported. In addition, comparison of the in vitro potency of the corresponding formamidine derivatives to that of MK787 is presented.
Asunto(s)
Antibacterianos/aislamiento & purificación , Streptomyces/crecimiento & desarrollo , Tienamicinas/aislamiento & purificación , Bacterias/efectos de los fármacos , Cromatografía Líquida de Alta Presión , Espectroscopía de Resonancia Magnética , Pruebas de Sensibilidad Microbiana , Relación Estructura-Actividad , Tienamicinas/toxicidadRESUMEN
Two antibiotics isolated from a culture MA-2465 were identified as aureothin and labilomycin, the chemical structures of which had been reported previously. It was also concluded that mycolutein and pulvomycin isolated as antibiotics in 1955 and 1957 respectively are also identical with aureothin and labilomycin. A cursory study of MA-2465 indicates that it is distinctly different from the culture which was first observed to produce labilomycin and is probably different from the organism first noted to produce aureothin.