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Cytosamine

O25H29N 5010S glucopyranosyl)-/ -erythro-hexopyranosyl]cytosine triacetate (cytosamine triacetate) 2, 3, 5 -Tri-0-acetyl-6-0-(mesitylenesulfonyl)guanosine AMSGOS 38 525... [Pg.420]

Antibiotic substances related in structure to amicetin have been isolated from other Streptomyces cultures. Sensi and coworkers166 have isolated amicetin B, which only differs from amicetin by the absence of the dexfro-a-methylserine moiety in its structure. This antibiotic substance is identical with Plicacetin, an antibiotic substance isolated by Haskell and coworkers167 176 from Streptomyces plicatus. The structural relationship of Plicacetin (amicetin B) to amicetin was also established by partial synthesis.167 Acylation of cytosamine (XXXVII) with p-nitrobenzoyl chloride, followed by reduction of the nitro group of the mono-acylated derivative, yielded Plicacetin. [Pg.326]

O24H36N4O9 l-N-[2,3,6-Trideoxy-4-0-(4,6-dideoxy-4-dimethylamino-a-D-glucopyranosyl)-j -eryt/iro-hexopyranosyl]cytosine triacetate (cytosamine triacetate) CYTSAC 32 379... [Pg.420]

C18H30N4O6 398.458 Alkaline degrad. prod, of the antibiotic Amicetin. Aminoacyl cytosamine derivs. are used as bactericides. [Pg.274]

C24H3SCI6N8O4S2U, Bis(protonated thiamine chloride) tetrachlorodi-oxouranate(VI), 40B, 428 C28H36N4O9, Cytosamine triacetate, 40B, 401... [Pg.232]

See other pages where Cytosamine is mentioned: [Pg.322]    [Pg.324]    [Pg.325]    [Pg.325]    [Pg.326]    [Pg.379]    [Pg.293]    [Pg.294]    [Pg.204]    [Pg.205]    [Pg.206]    [Pg.206]    [Pg.274]    [Pg.1024]    [Pg.1278]   
See also in sourсe #XX -- [ Pg.324 ]

See also in sourсe #XX -- [ Pg.293 ]



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Cytosamine triacetate

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