Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C5H6N2O4 |
| Molecular Weight | 158.1121 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)[C@@H]1CC(=O)NC(=O)N1
InChI
InChIKey=UFIVEPVSAGBUSI-REOHCLBHSA-N
InChI=1S/C5H6N2O4/c8-3-1-2(4(9)10)6-5(11)7-3/h2H,1H2,(H,9,10)(H2,6,7,8,11)/t2-/m0/s1
| Molecular Formula | C5H6N2O4 |
| Molecular Weight | 158.1121 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Thorpe-Ingold effects in cyclizations to five-membered and six-membered rings containing planar segments. The rearrangement of N(1)-alkyl-substituted dihydroorotic acids to hydantoinacetic acids in base. | 2004 Apr 7 |
|
| Rate of promoter class turn-over in yeast evolution. | 2006 Feb 10 |
|
| Mutations of RNA polymerase II activate key genes of the nucleoside triphosphate biosynthetic pathways. | 2008 Sep 17 |
|
| Development and analysis of an in vivo-compatible metabolic network of Mycobacterium tuberculosis. | 2010 Nov 23 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:30:41 GMT 2023
by
admin
on
Sat Dec 16 08:30:41 GMT 2023
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| Record UNII |
4LPL64ZNA5
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| Record Status |
Validated (UNII)
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| Record Version |
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78694-7
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79661-5
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79653-2
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79654-0
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m6111
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17025
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439216
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4LPL64ZNA5
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DTXSID30331399
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5988-19-2
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