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Cat. No. Product Name Information
PC-63435

Neladenoson dalanate hydrochloride

A1AR agonist

Neladenoson dalanate (BAY 10-67197) is a potent, selective, orally acitve partial adenosine A1 receptor (A1AR) agonist (EC50=0.1 nM) for the treatment of chronic heart failure.
PC-63434

Neladenoson dalanate

A1AR agonist

Neladenoson dalanate (BAY 10-67197) is a potent, selective, orally acitve partial adenosine A1 receptor (A1AR) agonist (EC50=0.1 nM) for the treatment of chronic heart failure.
PC-43415

LUF6000

A3AR modulator

LUF6000 is a potent, selective, positive allosteric modulator (enhancer) of human A3 adenosine receptor, enhance Emax but without affecting agonist potency.
PC-43386

CGS 21680 hydrochloride

A2AR agonist

CGS 21680 hydrochloride is a specific adenosine A2A subtype receptor agonist with Ki of 27 nM.
PC-43385

CGS 21680

A2AR agonist

CGS 21680 is a specific adenosine A2A subtype receptor agonist with Ki of 27 nM.
PC-43007

2-Cl-IB-MECA

A3AR agonist

2-Cl-IB-MECA (Chloro-IB-MECA, CF-102, Namodenoson) is a potent, selective A3 adenosine receptor (A3AR) agonist with Ki of 0.33 nM, 2500- and 1400-fold selectivity over A1 and A2a receptors.
PC-63144

AZD4635

A2AR inhibitor

AZD4635 (Imaradenant, HTL 1071) is a potent, selective and orally available adenosine 2A receptor (A2AR) inhibitor with Ki of 1.7 nM, > 30-fold selectivity over other adenosine receptors.
PC-63020

SCH 412348

A2AR antagonist

SCH 412348 is a potent and highly selective A2A receptor competitive antagonist with Ki of 0.6 nM.
PC-61367

Ciforadenant

A2AR antagonist

Ciforadenant (CPI-444, V 81444) is a potent, orally active, adenosine A2A receptor antagonist that is being investigated in solid tumors as a single agent and in combination with the anti-PD-L1 antibody atezolizumab.
PC-61328

KW3902

Adenosine A1 receptor inhibitor

Rolofylline (KW3902) is a potent, selective and orally active adenosine A1 receptor antagonist with Ki of 1.3 nM.
PC-60741

Tonapofylline

A1AR antagonist

Tonapofylline (BG9928) is a potent, selective and orally bioavailable adenosine A1 (A1A) receptor antagonist with Ki of 7 nM.
PC-70073

ST-4206

A2AR antagonist

ST-4206 is a metabolite of ST1535, which is potent, selective A2A adenosine receptor antagonist with Ki of 6.6 nM.

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