Structural Formula Vector Image
Title: Nucleocidin
CAS Registry Number: 24751-69-7
CAS Name: 4¢-C-Fluoroadenosine 5¢-sulfamate
Additional Names: 9-(4-fluoro-5-O-sulfamoylpentofuranosyl)adenine; 4¢-fluoro-5¢-O-sulfamoyladenosine
Molecular Formula: C10H13FN6O6S
Molecular Weight: 364.31
Percent Composition: C 32.97%, H 3.60%, F 5.21%, N 23.07%, O 26.35%, S 8.80%
Literature References: Antitrypanosomal antibiotic produced by Streptomyces calvus. The first naturally occurring derivative of a fluoro sugar. Isoln and activity studies: Thomas et al., Antibiot. Annu. 1956-1957, 716; Hewitt et al., ibid. 722. Partial structure: Waller et al., J. Am. Chem. Soc. 79, 1011 (1957). Revised formula and structure: Morton et al., ibid. 91, 1535 (1969). Synthesis: Jenkins et al., ibid. 93, 4323 (1971).
Properties: As the monohydrate, crystalline, weakly alkaline substance. mp >190° (dec). uv max (methanol): 259 nm (e 15000). LD50 i.p. in mice: ~0.2 mg/kg (Thomas).
Melting point: mp >190° (dec)
Absorption maximum: uv max (methanol): 259 nm (e 15000)
Toxicity data: LD50 i.p. in mice: ~0.2 mg/kg (Thomas)

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