Nimustine
Title: Nimustine
CAS Registry Number: 42471-28-3
CAS Name: N¢-[(4-Amino-2-methyl-5-pyrimidinyl)methyl]-N-(2-chloroethyl)-N-nitrosourea
Molecular Formula: C9H13ClN6O2
Molecular Weight: 272.69
Percent Composition: C 39.64%, H 4.81%, Cl 13.00%, N 30.82%, O 11.73%
Literature References: Chloroethylnitrosourea derivative with antitumor activity. Prepn: H. Nakao et al., DE 2257360; eidem, US 4003901 (1973, 1977 both to Sankyo); eidem, Yakugaku Zasshi 94, 1932 (1974), C.A. 82, 43263y (1975). Effects on macrophage cytostatic activity in rats: N. Saijo et al., Br. J. Cancer 42, 162 (1980). Distribution, excretion, metabolism in mice: M. Tanaka et al., Cancer Treat. Rep. 64, 575 (1980). Exptl and clinical effect: N. Saijo et al., Cancer Chemother. Pharmacol. 4, 165 (1980). Acute toxicity: H. Masuda et al., Sankyo Kenkyusho Nempo 29, 118 (1977), C.A. 88, 146298s (1978).
Properties: Pale yellow crystals from ethanol, dec 125°.
 
Derivative Type: Hydrochloride
CAS Registry Number: 55661-38-6
Manufacturers' Codes: NSC-245382
Trademarks: ACNU (Baxter); Nidran (Sankyo)
Molecular Formula: C9H13ClN6O2.HCl
Molecular Weight: 309.15
Percent Composition: C 34.97%, H 4.56%, Cl 22.94%, N 27.18%, O 10.35%
Properties: White to light yellow cryst powder. uv max (0.04N HCl): 245 nm (E1%1cm 480-510). Sol in methanol, slightly sol in abs ethanol, n-butanol. Practically insol in ethyl acetate, ether, chloroform, benzene, n-hexane. Gradually develops greenish yellow color in light; decomposes slowly in humid air. LD50 in mice, rats (mg/kg): 62, 46 i.v. (Masuda).
Absorption maximum: uv max (0.04N HCl): 245 nm (E1%1cm 480-510)
Toxicity data: LD50 in mice, rats (mg/kg): 62, 46 i.v. (Masuda)
 
Therap-Cat: Antineoplastic.
Keywords: Antineoplastic; Alkylating Agents; Nitrosoureas.

Others monographs:
PIPESAcrisorcinBINAPGlycidol
Thionaphthene-2-carboxylic Acid1,1-DiphenylhydrazineZinc PermanganateD-Amino Acid Oxidase
Cynarin(e)Calcium BorateButylateFenretinide
DifenamizoleBromodiphenhydramineBufotoxinAtrolactamide
©2016 DrugLead US FDA&EMEA