T2754
D-(+)-Turanose
≥98%
别名:
3-O-α-D-Glucopyranosyl-D-fructose
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关于此项目
经验公式（希尔记法）:
C12H22O11
化学文摘社编号:
分子量:
342.30
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
208-918-5
Beilstein/REAXYS Number:
93771
MDL number:
InChI key
SEWFWJUQVJHATO-PUVWEJBASA-N
InChI
1S/C12H22O11/c13-1-5-7(17)8(18)9(19)11(22-5)23-10-6(16)4(15)2-21-12(10,20)3-14/h4-11,13-20H,1-3H2/t4-,5-,6-,7-,8+,9-,10+,11-,12?/m1/s1
SMILES string
OC[C@H]1O[C@H](O[C@@H]2[C@@H](O)[C@@H](O)COC2(O)CO)[C@H](O)[C@@H](O)[C@@H]1O
biological source
synthetic
assay
≥98%
form
powder
optical activity
[α]20/D 74.8 to 76.8°, c = 4% (w/v) in water
technique(s)
gas chromatography (GC): suitable
color
white
solubility
water: 50 mg/mL, clear, colorless to faintly yellow
storage temp.
room temp
Quality Level
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Biochem/physiol Actions
Turanose is an analog of sucrose that is not metabolized by higher plants but is used as a carbon source by many bacteria, fungi, and other organisms. It is taken up into plant cells by sucrose transporters and is involved in intracellular sugar signaling.
Other Notes
To gain a comprehensive understanding of our extensive range of Disaccharides for your research, we encourage you to visit our Carbohydrates Category page.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
涉药品监管产品
此项目有
J Defaye et al.
Carbohydrate research, 237, 223-247 (1992-12-31)
Selective activation of the ketose unit in the isomeric glycosylfructoses, palatinose, leucrose, maltulose, turanose and lactulose, with pyridinium poly(hydrogen fluoride) resulted in the almost quantitative formation of glycosylated difructose dianhydrides. The reaction preferentially involves a reactive fructofuranosyl oxocarbenium ion and
J Matsuyama et al.
Caries research, 37(6), 410-415 (2003-10-23)
Sucrose has five structural isomers: palatinose, trehalulose, turanose, maltulose and leucrose. Although these isomers have been reported to be noncariogenic disaccharides, which cannot be utilized by mutans streptococci, there is no information about their fermentability by other bacteria in dental
A Mahdad-Benzerdjeb et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 68(2), 284-299 (2007-03-14)
A thorough study of the vibrational spectra of two disaccharides, melibiose and turanose, is presented in this work. The infrared and Raman spectra of these two compounds have been first recorded in the mid infrared range then in the far
Study on alpha-glucosidases in four human colon malignant tumors developed into nude mice.
C Castilla et al.
The International journal of biochemistry, 13(3), 381-387 (1981-01-01)
Janet Hsu et al.
Nanomedicine : nanotechnology, biology, and medicine, 8(5), 731-739 (2011-09-13)
Enzyme replacement therapies for lysosomal storage disorders are often hindered by suboptimal biodistribution of recombinant enzymes after systemic injection. This is the case for Pompe disease caused by acid α-glucosidase (GAA) deficiency, leading to excess glycogen storage throughout the body
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