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2-amino-6-hydroxypurine

Levinson et al. (1991) reported that a nitrogenous waste, guanine (2-amino-6-hydroxypurine), functioned as an aggregation pheromone of the flour mite Ac. siro, together with ammonia as a kairomone. However, because guanine is nonvolatile, it should probably be classified as an arrestant rather than an aggregation pheromone. [Pg.95]

Amino-6-hydroxypurine, AEl6 6-Amino-2-hydroxypurine, AE17 2-Am i no-4-hydroxypyr i midi ne, AC67... [Pg.618]

Pnrlne Nucleic acid component adenine (6-aminopurine) guanine (2-amino-6-hydroxypurine)... [Pg.3]

CAS 73-40-5 EINECS/ELINCS 200-799-8 Synonyms 2-Amino-1,7-dihydro-6H-purin-6-one 2-Amino-6-hydroxypurine 2-Aminohypoxanthine 2-Amino-6-oxypurine Cl 75170... [Pg.1958]

Adenine (29, 6-aminopurine) and guanine (8, 2-amino-6-hydroxypurine) are obtained from the hydrolytic cleavage of nucleic acids (see below). Deamination with HNO2 converts adenine into hypoxanthine, and guanine into xanthine. [Pg.478]

See other pages where 2-amino-6-hydroxypurine is mentioned: [Pg.905]    [Pg.312]    [Pg.1139]    [Pg.1139]    [Pg.1124]    [Pg.1124]    [Pg.413]    [Pg.1182]    [Pg.247]    [Pg.227]    [Pg.431]    [Pg.1079]    [Pg.1079]    [Pg.1350]    [Pg.1350]    [Pg.417]    [Pg.1215]    [Pg.1296]    [Pg.1296]    [Pg.1346]    [Pg.1346]    [Pg.1124]    [Pg.1124]   


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2- Hydroxypurine

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