| Weight | 151.234 g/mol |
|---|---|
| Formula | C8H9NS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
3,4-Dihydro-2H-1,4-benzothiazine (3080-99-7)
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- Irreversible Inhibition of Mitochondrial Complex I by 7(2Aminoethyl)3,4Dihydro5Hydroxy2H1,4Benzothiazine3Carboxylic Acid (DHBT1): A Putative Nigral Endotoxin of Relevance to Parkinson's Disease (Journal of Neurochemistry, 2002)
- Brain Mitochondria Catalyze the Oxidation of 7(2Aminoethyl)3,4Dihydro5Hydroxy2H1,4Benzothiazine3Carboxylic Acid (DHBT1) to Intermediates that Irreversibly Inhibit Complex I and Scavenge Glutathione: Potential Relevance to the Pathogenesis of Parkinson's Disease (Journal of Neurochemistry, 2002)
- 4-(3-(Dimethylamino)propyl)-3,4-dihydro-2-(1-hydroxyethyl)-3-phenyl-2H-1,4-benzothiazine and related compounds. A new class of antiinflammatory agents. (Journal of Medicinal Chemistry, 1973)
- Antiinflammatory 3,4-dihydro-2-alkyl-3-oxo-2H-1,2-benzothiazine-4-carboxamide 1,1-dioxides. (Journal of Medicinal Chemistry, 1971)
- Novel and Potent Aldose Reductase Inhibitors : 4-Benzyl- and 4-(Benzothiazol-2-ylmethyl)-3, 4-dihydro-3-oxo-2H-1, 4-benzothiazine-2-acetic Acid Derivatives (Chemical & Pharmaceutical Bulletin, 1994)
- Potential antihypertensive agents. 3. 3,4-Dihydro-2H-1,4-benzothiazine derivatives. (Journal of Medicinal Chemistry, 1969)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CSC2=CC=CC=C2N1
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InChIKeyYBBLSBDJIKMXNQ-UHFFFAOYSA-N
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3,4-Dihydro-2H-1,4-benzothiazine
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