E32754
4,6-O-Ethylidene-α-D-glucose
Sinónimos:
4,6-O-Ethylidene α-D-glucopyranose, Ethylidene glucose, NSC 89726
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1 G
MXP 2,264.00
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1 G
MXP 2,264.00
About This Item
Fórmula empírica (notación de Hill):
C8H14O6
Número de CAS:
Peso molecular:
206.19
Número CE:
Número MDL:
Código UNSPSC:
12352200
ID de la sustancia en PubChem:
NACRES:
NA.22
Productos recomendados
mp
168-170 °C (lit.)
cadena SMILES
CC1OC[C@H]2O[C@H](O)[C@H](O)[C@@H](O)[C@@H]2O1
InChI
1S/C8H14O6/c1-3-12-2-4-7(13-3)5(9)6(10)8(11)14-4/h3-11H,2H2,1H3/t3?,4-,5-,6-,7-,8+/m1/s1
Clave InChI
VZPBLPQAMPVTFO-NKWOADHPSA-N
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Equipo de protección personal
Eyeshields, Gloves, type N95 (US)
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J Kawada et al.
The Journal of endocrinology, 112(3), 375-378 (1987-03-01)
Ethylidene glucose (4,6-O-ethylidene glucose; EG) is known to bind the outer surface of the glucose transporter in the membranes of human erythrocytes and other mammalian cells. If a glucose transport system is present on pancreatic beta cells and recognizes the
M Wellner et al.
FEBS letters, 370(1-2), 19-22 (1995-08-14)
Two triple cysteine mutants containing Cys-less N- or C-terminal halves and the Cys-less GLUT1 were generated by site-directed mutagenesis. Following expression in Xenopus oocytes, the intrinsic transport activities of the multiple cysteine mutants were slightly decreased when either the cysteine
A Janoshazi et al.
The Journal of membrane biology, 123(3), 191-207 (1991-09-01)
We have previously shown that the human red cell glucose transport protein and the anion exchange protein, band 3, are in close enough contact that information can be transmitted from the glucose transport protein to band 3. The present experiments
J Kawada et al.
Molecular and cellular endocrinology, 62(2), 153-159 (1989-04-01)
4,6-O-Ethylidene glucose (ethylidene glucose), a specific inhibitor at the outer surface of a glucose transporter in the cell membranes, substituted analogue of streptozotocin was newly synthesized. This compound did not induce diabetes in rats and also did not show cytotoxic
J R Appleman et al.
The Journal of biological chemistry, 260(8), 4575-4578 (1985-04-25)
The stopped flow method combined with fluorescence detection has been employed to study the rapid kinetics of the glucose transporter from human erythrocytes. Upon mixing the purified transporter reconstituted into unsealed membranes of erythrocyte lipids with 4,6-ethylidene D-glucose, a derivative
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