Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C5H13O8P |
| Molecular Weight | 232.1257 |
| 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)COP(O)(O)=O
InChI
InChIKey=VJDOAZKNBQCAGE-LMVFSUKVSA-N
InChI=1S/C5H13O8P/c6-1-3(7)5(9)4(8)2-13-14(10,11)12/h3-9H,1-2H2,(H2,10,11,12)/t3-,4+,5-/m0/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Reduction precedes cytidylyl transfer without substrate channeling in distinct active sites of the bifunctional CDP-ribitol synthase from Haemophilus influenzae. | 2001 Apr 24 |
|
| Substrate specificity and kinetic mechanism of Escherichia coli ribulokinase. | 2001 Dec 15 |
|
| Structure of a highly phosphorylated O-polysaccharide of Proteus mirabilis O41. | 2004 May 17 |
|
| Genomic characterization of ribitol teichoic acid synthesis in Staphylococcus aureus: genes, genomic organization and gene duplication. | 2006 Apr 5 |
|
| Structural and genetic relationships between the O-antigens of Escherichia coli O118 and O151. | 2010 Dec |
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35320-17-3
Created by
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26554
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0BA496N6TQ
Created by
admin on Sat Dec 16 11:26:27 GMT 2023 , Edited by admin on Sat Dec 16 11:26:27 GMT 2023
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151104
Created by
admin on Sat Dec 16 11:26:27 GMT 2023 , Edited by admin on Sat Dec 16 11:26:27 GMT 2023
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SUBSTANCE RECORD
