Details
Stereochemistry | ACHIRAL |
Molecular Formula | C14H14O4P.H4N |
Molecular Weight | 295.2708 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[NH4+].[O-]P(=O)(OCC1=CC=CC=C1)OCC2=CC=CC=C2
InChI
InChIKey=PNTCBYMYXZCKMK-UHFFFAOYSA-N
InChI=1S/C14H15O4P.H3N/c15-19(16,17-11-13-7-3-1-4-8-13)18-12-14-9-5-2-6-10-14;/h1-10H,11-12H2,(H,15,16);1H3
Molecular Formula | C14H15O4P |
Molecular Weight | 278.2403 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | H3N |
Molecular Weight | 17.0305 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Synthesis of GDP-5-thiosugars and their use as glycosyl donor substrates for glycosyltransferases. | 2003 Aug 8 |
|
A chemical synthesis of UDP-LacNAc and its regioisomer for finding 'oligosaccharide transferases'. | 2006 Nov |
|
Synthesis of phosphate derivatives related to the glycosidase inhibitor salacinol. | 2007 Sep 3 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 05:45:23 GMT 2023
by
admin
on
Sat Dec 16 05:45:23 GMT 2023
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Record UNII |
P9AWN55JN7
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Record Status |
Validated (UNII)
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Record Version |
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Created by
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P9AWN55JN7
Created by
admin on Sat Dec 16 05:45:23 GMT 2023 , Edited by admin on Sat Dec 16 05:45:23 GMT 2023
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18763575
Created by
admin on Sat Dec 16 05:45:23 GMT 2023 , Edited by admin on Sat Dec 16 05:45:23 GMT 2023
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Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |