Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D03MJM
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| Former ID |
DNC009771
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| Drug Name |
Trans-(R(S))-2-Hydroxy-1-phenylethyl nitrate
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| Synonyms |
CHEMBL563619; trans-(R(S))-2-Hydroxy-1-phenylethyl nitrate; BDBM50293660
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
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Download2D MOL |
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| Formula |
C8H9NO4
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| Canonical SMILES |
C1=CC=C(C=C1)C(CO)O[N+](=O)[O-]
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| InChI |
1S/C8H9NO4/c10-6-8(13-9(11)12)7-4-2-1-3-5-7/h1-5,8,10H,6H2/t8-/m0/s1
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| InChIKey |
HJZAIMHRCPGGNJ-QMMMGPOBSA-N
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Glutathione reductase (GR) | Target Info | Inhibitor | [1] |
| BioCyc | Glutathione redox reactions II | |||
| Glutathione redox reactions I | ||||
| KEGG Pathway | Glutathione metabolism | |||
| Thyroid hormone synthesis | ||||
| Pathwhiz Pathway | Glutamate Metabolism | |||
| Glutathione Metabolism | ||||
| WikiPathways | Metapathway biotransformation | |||
| Sulfation Biotransformation Reaction | ||||
| Oxidative Stress | ||||
| NRF2 pathway | ||||
| Nuclear Receptors Meta-Pathway | ||||
| Selenium Micronutrient Network | ||||
| Glutathione metabolism | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | In vitro inhibition of human erythrocyte glutathione reductase by some new organic nitrates. Bioorg Med Chem Lett. 2009 Jul 1;19(13):3661-3. | |||
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