Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 9 de 9
Filtrar
Más filtros










Base de datos
Intervalo de año de publicación
1.
J Nat Prod ; 63(10): 1349-55, 2000 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-11076550

RESUMEN

Three new triterpene glycosides, calcigerosides D(1) (1), D(2) (2), and E (3), have been isolated from the sea cucumber Pentamera calcigera. Their structures have been deduced from extensive spectral analysis (NMR and MS) and chemical evidence. All the compounds are disulfated pentaosides differing in aglycon structure and position of sulfate group, which were determined by the measurement of NT(1) values in the cases of glycosides 1 and 2. Glycoside 1 is a nonholostane derivative, that is, it lacks an 18(20)-lactone, which is very rare among the sea cucumber glycosides.


Asunto(s)
Glicósidos/aislamiento & purificación , Pepinos de Mar/química , Triterpenos/aislamiento & purificación , Animales , Glicósidos/química , Espectroscopía de Resonancia Magnética , Triterpenos/química
2.
J Nat Prod ; 63(1): 65-71, 2000 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-10650081

RESUMEN

Three new monosulfated triterpene glycosides, calcigerosides B (2), C(1) (3), and C(2) (4), along with the known cucumarioside G(2) (1), have been isolated from the sea cucumber Pentamera calcigera. Their structures have been deduced from extensive spectral analysis (NMR and MS) and chemical evidence. Compounds 2-4 present a novel pentasacharide chain never reported before in sea cucumber triterpene glycosides. The desulfated derivatives of calcigerosides B, C(1), and C(2) (5, 7, and 9, respectively) showed moderate cytotoxicity (IC(50) = 5 microg/mL) against a selection of four human and mouse tumor cell lines.


Asunto(s)
Glicósidos/aislamiento & purificación , Pepinos de Mar/química , Triterpenos/aislamiento & purificación , Animales , Ensayos de Selección de Medicamentos Antitumorales , Glicósidos/química , Glicósidos/farmacología , Humanos , Ratones , Estructura Molecular , Triterpenos/química , Triterpenos/farmacología , Células Tumorales Cultivadas
3.
Toxicon ; 34(4): 475-83, 1996 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-8735247

RESUMEN

Hemolysis and K+ loss from mouse erythrocytes, induced by triterpene glycosides and their derivatives from this order of sea cucumbers were studied. Sulfate groups, attached to position 4 of the first xylose residue and to position 6 of the third glucose residue of the branched pentaosides, having 3-O-methyl-groups in terminal monosaccharide moieties increase K+ loss. A sulfate group at C-4 of the first xylose residue increases the hemolytic activity while a sulfate at C-6 of the third monosaccharide unit decreases it. A sulfate group at C-6 of terminal 3-O-methylglucose drastically decreases the hemolytic activity and rate of K+ loss. The presence of a sulfate group at the first xylose residue in glycosides having no 3-O-methyl group at the terminal monosaccharide decreases hemolytic activity and rate of K+ loss. The presence of the 16-ketone group in aglycones having the 7(8)-double bond significantly decreases activity. These results correlate with the previously proposed trends in evolution of sea cucumber glycosides from substances having sulfate groups at C-6 of glucose and 3-O-methylglucose units to substances sulfated at C-4 of the first xylose or having no sulfate groups, and from substances with aglycone 16-ketone to substances having no oxygen functions in this position.


Asunto(s)
Eritrocitos/efectos de los fármacos , Glicósidos/toxicidad , Toxinas Marinas/toxicidad , Pepinos de Mar/metabolismo , Triterpenos/toxicidad , 3-O-Metilglucosa/metabolismo , Animales , Cromatografía en Capa Delgada , Relación Dosis-Respuesta a Droga , Eritrocitos/citología , Glicósidos/química , Hemólisis/efectos de los fármacos , Holoturina/química , Holoturina/toxicidad , Dosificación Letal Mediana , Espectroscopía de Resonancia Magnética , Toxinas Marinas/química , Ratones , Potasio/metabolismo , Relación Estructura-Actividad , Sulfatos/metabolismo , Triterpenos/química
5.
Tsitol Genet ; 16(1): 14-8, 1982.
Artículo en Ruso | MEDLINE | ID: mdl-7064219

RESUMEN

The agar culture method was used to state that colony-forming units responsible for cell structures of a hemopoietic series remained undamaged after cryopreservation (-196 degrees) in a suspension of mouse and human donor bone marrow. Cultivation of cryopreserved bone marrow revealed the inhibition of proliferative activity of cells growing in agar as compared with native ones. The inhibition of DNA synthesis was the basis of this process.


Asunto(s)
Células de la Médula Ósea , Animales , Médula Ósea/efectos de los fármacos , Médula Ósea/metabolismo , División Celular/efectos de los fármacos , Ensayo de Unidades Formadoras de Colonias , Crioprotectores/farmacología , ADN/metabolismo , Congelación , Humanos , Ratones , Ratones Endogámicos BALB C , Polietilenglicoles/farmacología , Factores de Tiempo
7.
Tsitologiia ; 22(10): 1220-5, 1980 Oct.
Artículo en Ruso | MEDLINE | ID: mdl-7445086

RESUMEN

The growth-enhancing effect and the differentiation of colonies formed by native and frozen-thawed myelokaryocytes in semiliquid agar were observed over a period from the 2nd to the 28th day. The cultivation of bone marrow in agar was shown to form colonies consisting of haemopoietic cells as well as of stromal elements. Under the cultivation of frozen-thawed bone marrow, the retardation of proliferative activity of growing cells was observed within up to 4 days. Later on the proliferative character and the rate of the myelokaryocytes of both the types were seen identical. The question of a possible existence of haemopoietic tissue and stromal elements in the progenitor cells of normal bone marrow is being discussed.


Asunto(s)
Células de la Médula Ósea , Agar , Animales , Diferenciación Celular , División Celular , Células Cultivadas , Ensayo de Unidades Formadoras de Colonias , Medios de Cultivo , Humanos , Ratones , Ratones Endogámicos CBA , Factores de Tiempo
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA