| Weight | 179.172 g/mol |
|---|---|
| Formula | C6H13NO5 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 5 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
D-Isoglucosamine (4429-04-3)
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- Sequence-specific alkali-labile lesions in DNA caused by d-isoglucosamine (Biochimica et Biophysica Acta, 1986)
- DNA strand breakage by Maillard intermediate D-isoglucosamine. (Bulletin of the Agricultural Chemical Society of Japan, 1987)
- Induction of single strand scission in .PHI.X174RFI DNA by D-isoglucosamine. (Agricultural and biological chemistry, 1985)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC1C(C(C(C(O1)(CN)O)O)O)O
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InChIKeyIXZISFNWUWKBOM-UHFFFAOYSA-N
- Pubchem - D-Isoglucosamine
- Wikipedia - Fructosamine
Fructosamines are compounds that result from glycation reactions between a sugar (such as fructose or glucose) and a primary amine, followed by isomerization via the Amadori rearrangement. Biologically, fructosamines are recognized by fructosamine-3-kinase, which may trigger the degradation of advanced glycation end-products (though the true clinical significance of this pathway is unclear). Fructosamine can also refer to the specific compound 1-amino-1-deoxy-D-fructose (isoglucosamine), first synthesized by Nobel laureate Hermann Emil Fischer in 1886.
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