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SCH 58261

CAS160098-96-4

C18H15N7O MW 345.36

Purity: 99 %

Ordering Information:

Cat. No. Axon 1253

Qty1: 5 mg / €90  $117

Qty2: 25 mg / €340  $442

Qty3: on request

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Biological Activity:   Highly selective and potent A2A adenosine receptor antagonist   References: online 1, 2, 3   P Popoli MD et al. Effects of SCH 58261, an Adenosine A2A Receptor Antagonist, on Quinpirole-Induced Turning in 6-Hydroxydopamine-Lesioned Rats: Lack of Tolerance after Chronic Caffeine Intake. Neuropsychopharmacol. 2000, 22, 522-529.   C Zocchi et al. The non-xanthine heterocyclic compound SCH 58261 is a new potent and selective A2a adenosine receptor antagonist. J. Pharmacol. Exp. Ther. 1996, 276(2), 398-404.     Chemical Name: 2-(2-Furanyl)-7-(2-phenylethyl)-7H-pyrazolo[4,3-e][1,2, 4]triazolo[1,5-c]pyrimidin-5-amine

SCH 58261 | A2A antagonist | Axon Medchem | Axon 1253 | SCH58261

Axon Ligands TM - Research chemicals for biological study. Some high-profile samples could be provided under terms of contract research synthesis.

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Axon Adenosine Receptor (AR) Ligands: e.g.

KW 6002 | A2A antagonist

SCH 442416 | A2A antagonist

SCH 58261 | A2A antagonist

CGS 21680 | A2A agonist

UK 432097 | A2A agonist

ADAC | A1 agonist

2-Chloroadenosine | A1/2A ago.

GR 79236 | A1 agonist

SDZ WAG 994 | A1 agonist

Rolofylline | A1 antagonist