37040
D-(+)-Digitoxose
≥99.0% (TLC)
Sinonimo/i:
2,6-Dideoxy-D-ribohexose
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About This Item
Saggio
≥99.0% (TLC)
Attività ottica
[α]20/D +48±2°, c = 1% in H2O
Punto di fusione
98-100 °C
Stringa SMILE
C[C@H]1OC(O)C[C@H](O)[C@@H]1O
InChI
1S/C6H12O4/c1-3-6(9)4(7)2-5(8)10-3/h3-9H,2H2,1H3/t3-,4+,5?,6-/m1/s1
FDWRIIDFYSUTDP-WGDKFINWSA-N
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Azioni biochim/fisiol
The natural glycoside digitoxin contains a trisaccharide component made up of digitoxose monosaccharides. A modified monosaccharide digitoxin (with a single digitoxose moiety) was found to have greater anti-proliferative effects on various human non-small cell lung cancer cell lines than intact digitoxin.
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Biological & pharmaceutical bulletin, 17(4), 467-471 (1994-04-01)
In order to obtain specific antisera to digitoxin, four new types of hapten-bovine serum albumin (BSA) conjugates were synthesized from digitoxin. The haptens were linked to the carrier protein through hemisuccinate and hemisuccinylglycine bridges at the C-3' and C-3" positions
Biochemical and biophysical research communications, 129(2), 358-367 (1985-06-14)
Digitoxose specifically and competitively inhibited glucose stimulated insulin release from islets of both lean and obese mice without affecting either the rate of glucose oxidation or the rate of glucose stimulated oxygen consumption. Obese mouse islets were marginally more resistant
Molecular microbiology, 58(1), 17-27 (2005-09-17)
The indolocarbazole staurosporine is a potent inhibitor of a variety of protein kinases. It contains a sugar moiety attached through C-N linkages to both indole nitrogen atoms of the indolocarbazole core. Staurosporine biosynthesis was reconstituted in vivo in a heterologous
Chemical communications (Cambridge, England), (35)(35), 3738-3740 (2006-10-19)
We report the first 2,6-dideoxysugar-O-glycosyltransferase with substrate flexibility at the 2 position, confirm the function of a putative NDP-hexose 2,3-dehydratase in the jadomycin B biosynthetic gene cluster and deduce the substrate flexibility of downstream enzymes in l-digitoxose assembly, enabling reprogramming
Biochemical pharmacology, 39(4), 655-659 (1990-02-15)
The purpose of this investigation was to define, under controlled in vitro conditions, the processes contributing to the uptake and accumulation of [3H]digoxin by incubated slices of chicken renal cortex. Progressive uptake was evident in time-course experiments with the slice-to-medium
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