中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
—— | [(3aS,6R,6aS)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-6-yl] formate | 139348-79-1 | C8H12O5 | 188.18 |
D-吡喃葡萄糖 | D-Galactose | 10257-28-0 | C6H12O6 | 180.158 |
中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
—— | 1,2-O-isopropylidene-α-L-erythrofuranose | 76821-48-2 | C7H12O4 | 160.17 |
—— | 1,2-O-isopropylidene-3-O-methyl-β-D-threofuranose | 76768-63-3 | C8H14O4 | 174.197 |
—— | 3-O-Benzyl-1,2-O-isopropylidene-β-D-threofuranose | 76768-64-4 | C14H18O4 | 250.295 |
—— | 1,2-O-isopropylidene-α-L-glycero-tetrofuranos-3-ulose | 22528-94-5 | C7H10O4 | 158.154 |
—— | 3-amino-3-deoxy-1,2-O-isopropylidene-α-L-erythrofuranose | 22893-98-7 | C7H13NO3 | 159.185 |
—— | 3-amino-3-deoxy-1,2-O-isopropylidene-β-D-threofuranose | 78039-16-4 | C7H13NO3 | 159.185 |
—— | 3-O-Benzoyl-1,2-O-isopropylidene-β-D-threofuranose | 76778-02-4 | C14H16O5 | 264.278 |
—— | 3-azido-3-deoxy-1,2-O-isopropylidene-α-L-erythrofuranose | 77994-69-5 | C7H11N3O3 | 185.183 |
—— | 3-azido-3-deoxy-1,2-O-isopropylidene-β-D-threofuranose | 78039-18-6 | C7H11N3O3 | 185.183 |
Although words describing depression may not exist across all cultures, the symptoms of depression do. In a study of the Arab community in Dubai, we conducted four focus groups, two each with males and females, to identify the terms and descriptions people use for depression, what symptoms they associate with it, their views on its causes, and their strategies for coping with it. All individuals knew someone who met the description of depression. The key symptoms of depression identified included: social withdrawal, feeling afraid, irritability, loss of sleep, loss of appetite, sadness, crying, excessive thinking, feeling bored and loss of interest in sex. Causes of depression identified included: stresses in the family and in the society, relationships, lack of support, marital conflicts, and problems with children. The most effective coping strategy identified was that of going to religious places and talking to religious professionals.
Fluorinated carbohydrates are valuable tools for enzymological studies due to their increased metabolic stability compared to their non‐fluorinated analogues. Replacing different hydroxyl groups within the same monosaccharide by fluorine allows to influence a wide range of sugar–receptor interactions and enzymatic transformations. In the past, this principle was frequently used to study the metabolism of highly abundant carbohydrates, while the metabolic fate of rare sugars is still poorly studied. Rare sugars, however, are key intermediates of many metabolic routes, such as the pentose phosphate pathway (PPP). Here we present the design and purely chemical synthesis of a set of three deoxyfluorinated analogues of the rare sugars