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. Author manuscript; available in PMC: 2014 Jun 1.
Published in final edited form as: Trends Endocrinol Metab. 2013 Mar 14;24(6):290–300. doi: 10.1016/j.tem.2013.02.001

TABLE 1.

P1 or Adenosine receptors:

Receptor Agonist Antagonist Transduction mechanism REF
A1 Adenosine
N6-Cyclopentyladenosine
(CPA)CCPA
2′-MeCCPA
GR79236
S-ENVA
CVT510
Caffeine
Theophylline
8-Cyclopentyl-1,3 dimethylxanthine (CPX)
8-Cyclopentyl-1,3-dipropylxanthine (DPCPX)
8-Phenyl-1,3-dipropylxanthine
PSB36
N-0840
MRS1754
WRC-0571
Gi/odiminish cAMP [3-8]
A2A Adenosine
ATL146e
CGS21680
Regadenoson
HE-NECA
CVT3146
Caffeine
Theophylline
Istradefylline
SCH58261
SCH442416
ZM241385
KF17837
KW6002
GS increase cAMP [3-8]
A2B Adenosine
5′-N-ethylcarboxamidoadenosine
BAY606583
LUF5835
LUF5845
NECA (non selective)
Caffeine
Theophylline
CVT6883
MRS1706
MRS17541
PSB603
PSB0788
PSB1115
Enprofylline
MRE2029
GS increase cAMP [3-8]
A3 Adenosine
2-(1-Hexynyl)-N-methyladenosine
CF101 (IB-MECA)
2-Cl-IB-MECA
CP532903
MRS3558
DBXRM
VT160
Caffeine
Theophylline
MRS1191
MRS1220
MRS1334
MRS1523
MRS3777
MRE3008F20
PSB10
PSB11
VUF5574
L268605
Gi/o Gq/11 decrease cAMP and increase IP3 [3-8]