52035
n-Heptyl β-D-thioglucopyranoside
≥99.0% (TLC)
Synonym(s):
Heptyl thioglucoside, Heptyl-β-D-1-thioglucopyranoside
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About This Item
Empirical Formula (Hill Notation):
C13H26O5S
CAS Number:
Molecular Weight:
294.41
UNSPSC Code:
12161900
Beilstein/REAXYS Number:
6057483
MDL number:
description
non-ionic
assay
≥99.0% (TLC)
solubility
methanol: 0.1 g/mL, clear, yellow
SMILES string
CCCCCCCS[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
InChI
1S/C13H26O5S/c1-2-3-4-5-6-7-19-13-12(17)11(16)10(15)9(8-14)18-13/h9-17H,2-8H2,1H3/t9-,10-,11+,12-,13+/m1/s1
InChI key
HPEGNLMTTNTJSP-LBELIVKGSA-N
Other Notes
Non-ionic detergent useful for the solubilization and reconstitution of membrane proteins
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N Sone
Journal of biochemistry, 100(6), 1465-1470 (1986-12-01)
It is possible to prepare liposomal vesicles by solubilization of total bacterial membranes with n-heptyl beta-D-thioglucoside followed by reconstitution into proteoliposomes by a freeze-thaw-sonication procedure with soybean phospholipids. The resulting proteoliposomes from total membrane fraction of sufficiently aerated cells of
T Ohyashiki et al.
Biochimica et biophysica acta, 902(1), 46-52 (1987-08-07)
The brush-border membrane from the porcine small intestine possesses Ca2+-dependent ATPase activity. The Ca2+ stimulation of ATP hydrolysis by the membranes is biphasic with a high affinity (Km = 0.38 microM) and a low affinity (Km = 98.3 microM). Treatment
T Shimamoto et al.
Journal of biochemistry, 97(6), 1807-1810 (1985-06-01)
A new nonionic detergent, heptylthioglucoside, was synthesized and found to be more soluble than octylthioglucoside in water at low temperatures. Use of this detergent for solubilization and reconstitution of membrane proteins of Escherichia coli was examined. Heptylthioglucoside was as effective
K Nagai et al.
Journal of biochemistry, 101(5), 1115-1127 (1987-05-01)
Some properties of the enzyme activity that catalyzes the transfer of N-acetylgalactosamine from UDP-N-acetylgalactosamine to exogenous lactosylceramide-II3-sulfate (SM3) and N-acetylneuraminosyllactosylceramide (GM3) were studied using the enzyme preparation solubilized from the 100,000 X g pellet of 6-day-old rat brain. The products
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