| Weight | 207.616 g/mol |
|---|---|
| Formula | C10H6ClNO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2797-51-5 (2797-51-5)
2-chloro-3-amino-1,4-naphthoquinone · CANQ
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- Antithrombotic and antiplatelet activities of 2-chloro-3-[4-(ethylcarboxy)-phenyl]-amino-1,4-naphthoquinone (NQ12), a newly synthesized 1,4-naphthoquinone derivative. (Biochemical Pharmacology, 2000)
- Antiplatelet Activity of J78 (2-Chloro-3-[2-bromo, 4-fluoro-phenyl]-amino-8-hydroxy-1,4-naphthoquinone), an Antithrombotic Agent, Is Mediated by Thromboxane (TX) A2 Receptor Blockade with TXA2 Synthase Inhibition and Suppression of Cytosolic Ca2+ Mobilization (Journal of Pharmacology and Experimental Therapeutics, 2004)
- Synthetic schistosomicides. XIV. 1,4-Naphthoquinone mono(O-acyloximes), 4-amino-1,2-naphthoquinones, 2-amino-3-chloro-1,4-naphthoquinones, and other naphthoquinones (Journal of Medicinal Chemistry, 1970)
- Antiplatelet effect of 2-chloro-3-(4-acetophenyl)-amino-1,4-naphthoquinone (NQ301): a possible mechanism through inhibition of intracellular Ca2+ mobilization. (Biological & Pharmaceutical Bulletin, 2001)
- Antiplatelet and Antithrombotic Activities of NQ301, 2-Chloro-3-(4-acetophenyl)-amino-1, 4-naphthoquinone (Biological & Pharmaceutical Bulletin, 1999)
- Potent inhibition of serum-stimulated responses in vascular smooth muscle cell proliferation by 2 -chloro -3 -(4 -hexylphenyl ) -amino -1,4-naphthoquinone, a newly synthesized 1,4-naphthoquinone derivative (Biological & Pharmaceutical Bulletin, 2007)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2-chloro-3-amino-1,4-naphthoquinone
- CANQ
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SMILESC1=CC=C2C(=C1)C(=O)C(=C(C2=O)Cl)N
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InChIKeyOBLNWSCLAYSJJR-UHFFFAOYSA-N
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