1960
DOI: 10.1021/jm50010a005
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Potential Anticancer Agents--XXXL. The Relationship of Analogues of 1-Methyl-3-nitro-1-nitrosoguanidine (NSC-9369)

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Cited by 45 publications
(12 citation statements)
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“…For related structures, see: Hakkinen et al (1988); Lightfoot et al (1993). For the use of the title compound as a potential cancer chemotherapeutic, see: Garcia-Rio et al (2011); Skinner et al (1960). For its use as an antimicrobial, see: Uri & Scola (1992) and as a precursor in methylene production and production of heterocyclic rings, see: Hudlicky (1980).…”
Section: Related Literaturementioning
confidence: 99%
See 1 more Smart Citation
“…For related structures, see: Hakkinen et al (1988); Lightfoot et al (1993). For the use of the title compound as a potential cancer chemotherapeutic, see: Garcia-Rio et al (2011); Skinner et al (1960). For its use as an antimicrobial, see: Uri & Scola (1992) and as a precursor in methylene production and production of heterocyclic rings, see: Hudlicky (1980).…”
Section: Related Literaturementioning
confidence: 99%
“…(Hudlicky, 1980) Recently, these N-nitroso compounds have gained attention due to their potential cancer chemotherapeutic abilities. (Skinner et al, 1960); (Garcia-Rio et al, 2011) Additionally, the title compound was also found to behave as an antimicrobial agent against yeasts, fungi, Gram-negative, and Gram-positive bacteria. (Uri & Scola, 1992) The title compound was also shown to behave as a nitrosylating reagent in the formation of a new diruthenium complex.…”
Section: S1 Commentmentioning
confidence: 99%
“…Of the seven denitrosated nitrosamidines and nitrosamides tested (Table 2), N-methyl-N-nitroguanidine, 2-nitramino-2-imidazoline, N-methylurea, N-ethylurea, 2-imidazolidone, N-methylurethane, and N-ethylurethane were incapable of prophage induction, although all of their parent N-nitroso derivatives were effective inducers, demonstrating the necessity of the nitroso group for the biological response. Denitrosated derivatives, generally, appear to be biologically inert (11,27,40).…”
Section: Resltsmentioning
confidence: 99%
“…The N-nitroso compounds are of great interest from a biological point of view, because a wide variety of structurally related compounds possessing the N-nitroso-N-alkyl functionality have demonstrated cancer chemotherapeutic potential [10,11]. Besides, the discovery of the bioregulatory roles of nitric oxide [12][13][14][15][16], and its anti-carcinogen properties [17,18], has greatly increased the interest in nitrosation reactions because nitroso compounds are able to delivery nitric oxide in a controlled manner [19].…”
Section: Introductionmentioning
confidence: 99%