Home>>Natural Products>>6-(γ,γ-Dimethylallylamino)purine (N6-(2-lsopentenyl)adenine)

6-(γ,γ-Dimethylallylamino)purine (N6-(2-lsopentenyl)adenine) (Synonyms: Isopentenyladenine, N6-Isopentenyladenine, N6-(2-Isopentenyl)adenine, NSC 106958)

Catalog No.GC33611

6-(γ,γ-Dimethylallylamino)purine (N6-(2-lsopentenyl)adenine) is a plant growth substance.

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6-(γ,γ-Dimethylallylamino)purine (N6-(2-lsopentenyl)adenine) Chemical Structure

Cas No.: 2365-40-4

Size Price Stock Qty
10mM (in 1mL DMSO)
$50.00
In stock
100mg
$46.00
In stock
500mg
$91.00
In stock

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

6-(γ,γ-Dimethylallylamino)purine is a plant growth substance.

Derivative UV spectroscopic data show that the plant growth substances 6-(γ,γ-Dimethylallylamino)purine (N6-(delta 2-isopentenyl) adenine, i6Ade)and indolylacetic acid (IAA) can bind to the yeast alcohol dehydrogenase (ADH) and affect coenzyme-enzyme binding. At fixed ethanol concentrations (27.8 and 111.1 mM) and varying NAD+ concentrations (0.033-2 mM), as well as at fixed levels of coenzyme (0.67 and 2 mM), and at varying concentrations of ethanol (1.4-111.1 mM), the rate of ethanol oxidation is significantly inhibited by i6Ade and IAA. The kinetics of the ADH reaction is affected by two inhibition constants (Ki and Ki') which correspond to the dissociation constants of complexes EI and ESI, respectively. For i6Ade the Ki=0.52±0.06 mM and Ki'=0.74±0.07 mM, and for IAA the Ki=0.88±0.03 mM and Ki'=0.99±0.02 mM[1].

[1]. Zikmanis P, et al. Indolylacetic acid and N6-(delta 2-isopentenyl) adenine affect NADH binding to yeast alcohol dehydrogenase and inhibit in vitro the enzymatic oxidation of ethanol. Biofactors. 1990 Oct;2(4):237-40.

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