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E32754

Sigma-Aldrich

4,6-O-Ethylidene-α-D-glucose

Synonym(s):

4,6-O-Ethylidene α-D-glucopyranose, Ethylidene glucose, NSC 89726

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About This Item

Empirical Formula (Hill Notation):
C8H14O6
CAS Number:
13224-99-2
Molecular Weight:
206.19
EC Number:
236-198-2
MDL number:
MFCD00006820
UNSPSC Code:
12352200
PubChem Substance ID:
24894503
NACRES:
NA.22

mp

168-170 °C (lit.)

SMILES string

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

InChI key

VZPBLPQAMPVTFO-NKWOADHPSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Y Yano et al.
The Biochemical journal, 295 ( Pt 1), 183-188 (1993-10-01)
The transport conformation of the human erythrocyte glucose transporter (GLUT1) modifies rates of proteolytic cleavage of this protein by a variety of enzymes. We investigated the effects of ligand-induced conformational change on the susceptibility to enzymic cleavage of the insulin-sensitive
A F Gibbs et al.
The Biochemical journal, 256(2), 421-427 (1988-12-01)
Tryptic digestion has been used to investigate the conformational changes associated with substrate translocation by the human erythrocyte glucose transporter. The effects of substrates and inhibitors of transport on the rates of tryptic cleavage at the cytoplasmic surface of the
M Hashiramoto et al.
The Journal of biological chemistry, 267(25), 17502-17507 (1992-09-05)
The structure-function relationship of the HepG2/erythrocyte-type glucose transporter (GLUT1) has been studied by in vitro site-directed mutagenesis. Chinese hamster ovary clones in which glucose transporters were transfected were shown by Western blotting with a GLUT1 anti-COOH-terminal peptide antibody to have
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
P D Wheeler et al.
Journal of developmental physiology, 11(3), 159-169 (1989-03-01)
The effects of insulin, prostaglandin E1 (PGE1) and uptake inhibitors on unidirectional D-glucose influx at brush border (maternal) and basal (fetal) sides of the guinea-pig syncytotrophoblast were investigated in the intact, perfused guinea-pig placenta by rapid, paired-tracer dilution. Experiments were
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