Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C5H10O5 |
| Molecular Weight | 150.1301 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC[C@@H](O)[C@H](O)[C@H](O)C=O
InChI
InChIKey=PYMYPHUHKUWMLA-UOWFLXDJSA-N
InChI=1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h1,3-5,7-10H,2H2/t3-,4-,5-/m1/s1
| Molecular Formula | C5H10O5 |
| Molecular Weight | 150.1301 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/16232684
Sources: https://www.ncbi.nlm.nih.gov/pubmed/16232684
There is no information in scientific papers related to the biological or pharmacological activities of D-lyxose. It is known, that this sugar occurs only rarely in nature and is epimer of the Xylose, and can be obtained from D-xylulose enzymatically using L-ribose isomerase from toluene-treated cells of Acinetobacter sp. strain DL-28.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:03:06 GMT 2025
by
admin
on
Mon Mar 31 19:03:06 GMT 2025
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| Record UNII |
M795K6HJOL
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| Record Status |
FAILED
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| Record Version |
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