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1 In reality, they contain little sugar alcohol.
2 ine) is a dipeptide, and 1 (erythritol) is a sugar alcohol.
3 harides, disaccharides, beta-glucosides, and sugar alcohol.
4 or the primary photoassimilates, sucrose and sugar alcohols.
5 lycerol, methylglyoxal, dihydroxyacetone and sugar alcohols.
6 lycerol, methylglyoxal, dihydroxyacetone and sugar alcohols.
7 urces, including a number of rare sugars and sugar alcohols.
8 PAD also detects carbohydrates, glycols, and sugar alcohols.
9 a containing ABA and a variety of sugars and sugar alcohols.
10 h accumulation of multiple disaccharides and sugar alcohols.
11 of total prebiotic carbohydrates, including sugar alcohols (0.4-6.6 mg), simple sugars (6-1507 mg),
12 /related compounds, 48 bile acids, 72 amines/sugars/alcohols, 21 metals, 8 catecholamines, 11 vitamin
14 arbon sources for many microorganisms, while sugar alcohols (alditols), glycols (glycerol), and alcoh
17 e differs from the other two species in that sugar alcohol and sucrose (Suc) are present in much high
18 ts are used to characterize the hydration of sugar alcohols and are related to sweet taste chemorecep
19 protected amino acids, primary and secondary sugar alcohols and partially protected thioglycosides.
20 oxylated compounds (polyols) such as sugars, sugar alcohols and sugar acids are vital to all known li
22 Water status and analyses of free sugars, sugar-alcohols and fructo-oligosaccharides (FOS) were ca
24 ction of amino acids, organic acids, sugars, sugar alcohols, and fatty acids, we characterised six co
27 he cecum, such as nonstarch polysaccharides, sugar alcohols, and resistant starch, in being substrate
30 om saturated fat, monounsaturated fat, added sugars, alcohol, and intakes of cholesterol and sodium.
32 several CR compounds such as amino acids and sugar alcohols are fully represented in stones with no o
33 als of whole leaves suggest that sucrose and sugar alcohols are more concentrated in the cytosol than
35 e.g., blackberries, raspberries) are high in sugar alcohol began, or when it started circulating in t
36 xoses, pentoses, tetroses, a sugar acid, and sugar alcohols but not disaccharides induced inward curr
38 that this review will clarify Rosaceae fruit sugar alcohol concentrations and individual sugar compos
39 ic generation of cultivars with an increased sugar alcohol content can result in increased boron upta
40 ead to the development of maltitol and other sugar alcohol derivatives as MRI contrast agents for a v
43 upgrading of saccharides (e.g., glucose) and sugar alcohols (e.g., glycerol) on metal and metal-oxide
44 iminate between sugars (e.g., lactulose) and sugar alcohols (e.g., mannitol), establishing a differen
49 analyses were metabolites from the sugar and sugar alcohol groups, with significantly higher concentr
51 ups have reported zero detectable amounts of sugar alcohol in fully ripe Rubus fruit, with the except
52 mM D-glucose resulted in the accumulation of sugar alcohol in pericytes that was markedly reduced by
53 lity, density and viscosity of sorbitol as a sugar alcohol in the ([mmim](MeO)(2)PO(2)) ionic liquid
54 at the concentration of the boron-complexing sugar alcohol in the plant tissue has a significant effe
55 lution of saccharides, their derivatives and sugar alcohols in (0.01, 0.05, 0.09 and 0.13) mol kg(-1)
56 oxy and deoxy derivatives, disaccharides and sugar alcohols in (0.05, 0.15, 0.25 and 0.35)molkg(-1) t
57 te to HPLC to analyze mixtures of sugars and sugar alcohols in biomedical applications and sheds ligh
60 at permitted characterization of the role of sugar alcohols in polyol-activated myo-inositol efflux.
61 es can retranslocate boron as complexes with sugar alcohols in the phloem suggests a possible mechani
64 This work focuses on the role of sorbitol, a sugar alcohol, in flower development and pollen tube gro
65 Thermal investigations of all synthesized sugar alcohols, including examples with exclusive 1,3-an
66 ase, whereas those of primary bile acids and sugar alcohols increase, reflecting the modified metabol
67 ns to monosaccharides and analysis of the 3H-sugar alcohols indicate that heparanase activities in CH
68 ic conversion of monosaccharides and related sugar alcohols into valuable products, which is a target
69 ibition by intracellular galactitol when the sugar alcohol is present in sufficiently high concentrat
73 t method for the detection of cancer using a sugar alcohol, maltitol, a common low caloric sugar subs
76 . sucrose and starch), little is known about sugar alcohol metabolism, its regulation, and the manner
78 secreted various biochemicals, predominantly sugar alcohols, mirroring the metabolite exchange observ
81 riched in primary metabolites represented by sugar alcohols (notably mannitol and erythritol), and am
82 im of discerning between different sugar and sugar alcohols of biomedical relevance, such as gut perm
83 strategy for the synthesis of higher-carbon sugar alcohols of the galacto-family featuring all hydro
84 , we screened the toxicity of four different sugar alcohols on several mosquito species, a biting mid
85 hloride (ChCl) in various mixing ratios with sugars, alcohols, organic acids, and urea, as well as a
86 r the first time found that novel glycylated sugar alcohols, particularly glycylglycerins, are tightl
88 rides (RFOs), fructooligosaccharides (FOSs), sugar alcohols (SAs), and resistant starch (RS), which c
90 lectrocatalytic oxidation of saccharides and sugar alcohols, seeking trends in the effect of reaction
91 gars such as glucose, fructose, sucrose, and sugar alcohols, small molecule artificial sweeteners suc
92 he reduction of GalA to the oxidation of the sugar alcohol sorbitol that has a higher reduction state
94 We investigated the relationship between sugar alcohol (sorbitol) content, boron uptake and distr
95 ids, amines, alcohols, sugars, amino-sugars, sugar alcohols, sugar acids, organic phosphates, hydroxy
99 utes to biosynthesis of a family of acylated sugar alcohols, the fumicicolins, which are related to b
101 rm a carbohydrate consisting of fructose and sugar alcohol, very similar to environmentally benign su
103 oliar compatible solutes, such as sugars and sugar alcohols, whereas nitrogen compounds accumulated i
104 moiety could be introduced by reaction of a sugar alcohol with acetic acid (1S)-phenyl-2-(phenylsulf