Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C6H9N3O4 |
| Molecular Weight | 187.1534 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OCC(O)CN1C=CN=C1[N+]([O-])=O
InChI
InChIKey=NUGLIYXAARVRPQ-UHFFFAOYSA-N
InChI=1S/C6H9N3O4/c10-4-5(11)3-8-2-1-7-6(8)9(12)13/h1-2,5,10-11H,3-4H2
| Molecular Formula | C6H9N3O4 |
| Molecular Weight | 187.1534 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Structure-function dependence and allopurinol inhibition of radiosensitizer/nitroreductase interaction: approaches to improving therapeutic ratios. | 1980 Spring |
|
| Activation of misonidazole by rat liver microsomes and purified NADPH-cytochrome c reductase. | 1982 Feb 15 |
|
| Oncogenic transformation systems involving mammalian cells in vitro to determine the relative risks of different treatment modalities. | 1984 Dec |
|
| The neurotoxicity of radiosensitizing drugs: a biochemical assessment of desmethylmisonidazole (DMM) in the rat. | 1985 Jan |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:01:47 GMT 2023
by
admin
on
Fri Dec 15 15:01:47 GMT 2023
|
| Record UNII |
H3N358OVQW
|
| Record Status |
Validated (UNII)
|
| Record Version |
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-
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C798
Created by
admin on Fri Dec 15 15:01:47 GMT 2023 , Edited by admin on Fri Dec 15 15:01:47 GMT 2023
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| Code System | Code | Type | Description | ||
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C1065
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C009997
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26106
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261036
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DTXSID50875669
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H3N358OVQW
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13551-92-3
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236-932-1
Created by
admin on Fri Dec 15 15:01:47 GMT 2023 , Edited by admin on Fri Dec 15 15:01:47 GMT 2023
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PRIMARY |