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pyranose
pyranose Chem. (ˈpaɪər-, ˈpɪrənəʊz) [f. pyran + -ose2.] A structure containing a saturated pyran ring, frequently assumed by sugars; a sugar having this structure. Freq. attrib.1927 Goodyear & Haworth in Jrnl. Chem. Soc. 3141 On the basis of the conclusions now reached, the formula (A) must be accep...
Oxford English Dictionary
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Pyranose
There are also conformational and stereochemical effects specific to the pyranose ring. Nomenclature
To name conformations of pyranose, first the conformer is determined.
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Pyranose oxidase
The systematic name of this enzyme class is pyranose:oxygen 2-oxidoreductase. Use in biosensors
Recently, pyranose oxidase has been gaining on popularity within biosensors.
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furanose
furanose Chem. (ˈfjʊərənəʊz, -s) [f. furan + -ose2.] A structure containing a furan ring thought to be sometimes assumed by monosaccharide sugars that contain four or more carbon atoms; also, a sugar having this structure. Freq. attrib., as furanose form, furanose ring, etc.1927 Goodyear & Haworth i...
Oxford English Dictionary
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Pyranose dehydrogenase (acceptor)
Pyranose dehydrogenase (acceptor) (, pyranose dehydrogenase, pyranose-quinone oxidoreductase, quinone-dependent pyranose dehydrogenase, PDH) is an enzyme with systematic name pyranose:acceptor oxidoreductase.
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septanose
septanose Chem. (ˈsɛptənəʊz, -s) [a. G. septanose (Micheel & Suckfüll 1933, in Ann. d. Chem. DII. 89), f. L. sept-em seven + -anose after furanose, pyranose.] A structure containing a seven-membered ring, adopted by some sugars; a sugar having this structure. Freq. attrib. Hence ˈseptanoside, a glyc...
Oxford English Dictionary
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pyranoside
pyranoside Chem. (paɪər-, pɪˈrænəsaɪd) [f. prec. + -ide.] Any glycoside in the pyranose form.1932 Jrnl. Chem. Soc. 2254 Usually the product is also contaminated with small amounts of the corresponding pyranosides. 1934, 1966 [see furanoside]. 1970 R. W. McGilvery Biochem. xxviii. 715 Furanosides and...
Oxford English Dictionary
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Casuarinin
After conversion of casuarictin to pedunculagin, the pyranose ring of the glucose opens and the family of compounds including casuariin, casuarinin, castalagin
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D-Ribose pyranase
For most cells, ribose is transported into the cell in the pyranose form. With this said, D-Ribose Pyranase needs to be present to convert the pyranose form into the furanose form.
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How is protein cavity centre related to binding? I am confused and I have the following questions: 1\. What are (in the context of article below) protein cavity centres? 2\. How are they related to binding? ...
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And a little later:
> The binding-site center is computed as the hexose pyranose ring centroid for the positive examples, and as the ligand or empty The hexose pyranose-ring atoms are located up to 2.9 ̊ A away from the ring’s centroid.
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Casuarictin
Casuarictin is transformed into pedunculagin via loss of a gallate group, and further into castalagin via glucose pyranose ring opening.
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Isomaltose
Both of the sugars are dimers of glucose, which is a pyranose sugar. Isomaltose is a reducing sugar.
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Glycal
Conformation
Glycals can be formed as pyranose (six-membered) or furanose (five-membered) rings, depending on the monosaccharide used as a starting material The glycal conformation that has been studied in most depth is that of the pyranose endo-glycal.
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PDH
Angiotensin-converting enzyme, an enzyme
Plesiochronous digital hierarchy, in telecommunications networks
Pound–Drever–Hall technique for stabilizing a laser's output
Pyranose
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