N6-substituted N-alkyladenosine-5'-uronamides: bifunctional ligands having recognition groups for A1 and A2 adenosine receptors.

DOI: 10.1021/jm00159a020

Source and publish data:

Journal of medicinal chemistry p. 1683 - 1689 (1986)

Update date:2022-07-29

Topics:

Authors:

Olsson Olsson

Kusachi Kusachi

Thompson

Ukena Ukena

Padgett Padgett

Daly Daly

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Article abstract of DOI:10.1021/jm00159a020

The coronary vasoactivity of N-ethyl-1'-deoxy-1'-(6-amino-9H-purin-9-yl)-beta-D-ribofuranuronamide (NECA, 1) is over 2 orders of magnitude greater than that of adenosine, and the vasoactivity of certain N6-substituted adenosines is as much as 1 order of m

Full text of DOI:10.1021/jm00159a020

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Product name:(2S,3S,4R,5R)-3,4-Dihydroxy-5-[6-(4-methoxy-phenylamino)-purin-9-yl]-tetrahydro-furan-2-carboxylic acid ethylamide

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