Details
Stereochemistry | ACHIRAL |
Molecular Formula | C4H7N5O.H2O4S |
Molecular Weight | 239.21 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OS(O)(=O)=O.NC1=NC(=O)C(N)=C(N)N1
InChI
InChIKey=RSKNEEODWFLVFF-UHFFFAOYSA-N
InChI=1S/C4H7N5O.H2O4S/c5-1-2(6)8-4(7)9-3(1)10;1-5(2,3)4/h5H2,(H5,6,7,8,9,10);(H2,1,2,3,4)
Molecular Formula | C4H7N5O |
Molecular Weight | 141.1313 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | H2O4S |
Molecular Weight | 98.078 |
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 |
---|---|---|
Tetrahydrofolate and 5-methyltetrahydrofolate are folates with high antioxidant activity. Identification of the antioxidant pharmacophore. | 2003 Dec 18 |
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Glyoxal formation by Fenton-induced degradation of carbohydrates and related compounds. | 2006 Aug 14 |
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Methylglyoxal in food and living organisms. | 2006 Dec |
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Inhibition of methylglyoxal-mediated protein modification in glyoxalase I overexpressing mouse lenses. | 2010 |
|
Novel riboswitch ligand analogs as selective inhibitors of guanine-related metabolic pathways. | 2010 Apr 22 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 00:39:52 GMT 2023
by
admin
on
Sat Dec 16 00:39:52 GMT 2023
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Record UNII |
9SZ7ZX1H0L
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Record Status |
Validated (UNII)
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Record Version |
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254-393-0
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135443549
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