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IDNUMBER | ST029401 |
CAS | 57531-37-0 |
MDL NUMBER | MFCD03419295 |
Molecular formula | C3H2ClN3O2 |
Molecular weight | 147.52 |
Purity | 97% |
Selling terms | Not for personal use, R&D use only. |
IUPAC | 2-chloro-4-nitroimidazole |
Smiles | c1(c[nH]c(n1)Cl)[N+]([O-])=O |
THERAPEUTIC CATEGORY | anti amoebic |
ACCEPTORS | 2 |
DONORS | 1 |
ROTATION BONDS | 0 |
N+O | 5 |
Chiral Centers | 0 |
LogP | 0.49 |
LogS | -2.48 |
LIPINSKI | 4 |
Synonyms | TIMTEC-BB SBB000100;1H-IMIDAZOLE, 2-CHLORO-4-NITRO-;2-CHLORO-5-NITRO-1H-IMIDAZOLE;2-CHLORO-4-NITROIMIDAZOLE;2-Chloro-4-nitro-1H-imidazole;1H-Imidazole,2-chloro-4-nitro-(9CI);2-CHLORO-4-NITRO-1H-IMIDAZOLE, 98+%;2-Chloro-5-nitroimidazole |
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2-Chloro-4-nitro Imidazole is available from stock in g/mg amounts.
Purchase 2-Chloro-4-nitro Imidazole
Please contact us for manufacturing large (kg) amounts.
Product Categories:NITRO;Halides;Imidazoles & Benzimidazoles;API intermediates;Imidazoles & Benzimidazoles 2-Chloro-4-nitroimidazole
Xi Risk Statements 36/37/38 Safety Statements 26-36 HazardClass IRRITANT 2-Chloro-4-nitroimidazole
References
Watras, J., Widel M., Suwinski J., Salwinska E. 2-Chloro-4-nitroimidazole radiosensitizers of hypoxic tumor cells in vivo. Journal Neoplasma. 1987;34(3):253-9.
Abstract
The transplantable rhabdomyosarcoma in WAG/Rij rats was used to test the in vivo effectiveness of 1-methyl-2-chloro-4-nitroimidazole (P13) and its analog 1-(2-hydroxy-3-methoxy-propyl)-2-chloro-4-nitroimidazole (P40) as tumor-cell radiosensitizers after their i.p. administration at low doses. The results indicate that both compounds administered repeatedly at nontoxic concentrations (70-150 mg/kg body wt.) in combination with moderate fractional doses of irradiation (3.7 Gy) enhance the radiation effect on tumors. The local control of tumors on the 210th day in all experimental groups has been higher than in the control ones. In the case of P40 administered in the maximal dose, the increment in local control is statistically significant (p less than 0.05). The regrowth delay has also been longer after treatment with radiosensitizers. In the course of treatment we did not observe any symptoms of neurotoxicity of the compounds. The mean body weight of rats during the administration of compounds remained on the level of control rats whose tumors were irradiated only.
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