| Weight | 168.196 g/mol |
|---|---|
| Formula | C7H5FN2S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
2-amino-5-fluorobenzothiazole (20358-07-0)
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- DNA damage and cell cycle arrest induced by 2-(4-amino-3-methylphenyl)-5-fluorobenzothiazole (5F 203, NSC 703786) is attenuated in aryl hydrocarbon receptor deficient MCF-7 cells (British Journal of Cancer, 2003)
- Genotoxic profiling of MCF-7 breast Cancer cell line elucidates gene expression modifications underlying toxicity of the anticancer drug 2-(4-amino-3-methylphenyl)-5-fluorobenzothiazole (Molecular Pharmacology, 2003)
- Anti-tumor drug candidate 2-(4-amino-3-methylphenyl)-5-fluorobenzothiazole induces single-strand breaks and DNA-protein cross-links in sensitive MCF-7 breast cancer cells (Cancer Chemotherapy and Pharmacology, 2006)
- Synthesis and Antidiabetic Activity of 2-Amino [5(4-Sulfonylbenzylidine)-2,4-thiazolidinedione] -7-chloro-6-fluorobenzothiazole. (ChemInform, 2006)
- The antitumor drug candidate 2-(4-amino-3-methylphenyl)-5-fluorobenzothiazole induces NF-kappaB activity in drug-sensitive MCF-7 cells. (Anti-Cancer Drugs, 2005)
- 2-(4-Amino-3-methylphenyl)-5-fluorobenzothiazole is a ligand and shows species-specific partial agonism of the aryl hydrocarbon receptor (Toxicology and Applied Pharmacology, 2009)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C=C1F)N=C(S2)N
-
InChIKeyYHBIGBYIUMCLJS-UHFFFAOYSA-N
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