New 2,6,9-trisubstituted adenines as adenosine receptor antagonists: a preliminary SAR profile

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The Length and Flexibility of the 2-Substituent of 9-Ethyladenine Derivatives Modulate Affinity and Selectivity for the Human A2A Adenosine Receptor.

P2860

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New 2,6,9-trisubstituted adenines as adenosine receptor antagonists: a preliminary SAR profile

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2007 nî lūn-bûn

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2007年の論文

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New 2,6,9-trisubstituted adeni ...... sts: a preliminary SAR profile

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New 2,6,9-trisubstituted adeni ...... ts: a preliminary SAR profile.

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New 2,6,9-trisubstituted adeni ...... sts: a preliminary SAR profile

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New 2,6,9-trisubstituted adeni ...... ts: a preliminary SAR profile.

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New 2,6,9-trisubstituted adeni ...... sts: a preliminary SAR profile

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New 2,6,9-trisubstituted adeni ...... ts: a preliminary SAR profile.

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P1476

New 2,6,9-trisubstituted adeni ...... sts: a preliminary SAR profile

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Catia Lambertucci

http://www.w3.org/2001/XMLSchema#string

Chiara Bolcato

http://www.w3.org/2001/XMLSchema#string

Dhuldeo D Kachare

http://www.w3.org/2001/XMLSchema#string

Diego Dal Ben

http://www.w3.org/2001/XMLSchema#string

Giampiero Spalluto

http://www.w3.org/2001/XMLSchema#string

Gloria Cristalli

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Karl-Norbert Klotz

http://www.w3.org/2001/XMLSchema#string

Rosaria Volpini

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P2860

Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction

Medicinal chemistry of adenosine A2A receptor agonists

Medicinal chemistry and pharmacology of A2B adenosine receptors

International Union of Pharmacology. XXV. Nomenclature and classification of adenosine receptors

N(6)-alkyl-2-alkynyl derivatives of adenosine as potent and selective agonists at the human adenosine A(3) receptor and a starting point for searching A(2B) ligands

Structure-affinity relationships of adenosine A2B receptor ligands

Highlights on the development of A(2A) adenosine receptor agonists and antagonists

Anilide derivatives of an 8-phenylxanthine carboxylic congener are highly potent and selective antagonists at human A(2B) adenosine receptors

Cloning of two adenosine receptor subtypes from mouse bone marrow-derived mast cells

Method for the synthesis of uric acid derivatives.

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s11302-007-9068-9

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339-346

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scholarly article

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10.1007/S11302-007-9068-9

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5449164

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18404447

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2072915

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New 2,6,9-trisubstituted adenines as adenosine receptor antagonists: a preliminary SAR profile

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New 2,6,9-trisubstituted adenines as adenosine receptor antagonists: a preliminary SAR profile

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P1433

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