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. 2017 Apr;69(2):93–139. doi: 10.1124/pr.116.013078

TABLE 7.

Interaction of prototypical membrane-permeable P-site inhibitors with mACs, sAC, sGC, and adenosine receptors

AC activity was determined in the presence of Mg2+ and in the presence of stimulators (GαS-GTPγS and/or FSK) to ensure maximum catalytic activity and, hence, highest inhibitor potency possible. For ACs, pIC50 values are listed. For adenosine receptors, pKi values are listed. Structures of P-site inhibitors are shown in Fig. 13. 2′,5′-Dideoxy-3′-ATP (Table 8 and Fig. 15) is mechanistically related to the P-site inhibitors shown here.

AC SQ22,536 NKY80 Vidarabine
AC1 4.27a, 3.95b, 3.92c 4.04a, 3.48b 4.31a, 3.86b
AC2 3.71a, 3.41b, 3.17c, 3.54d 3.11a, >3.00b, >3.00e, >3.00d 3.61a, 3.26b, 3.15e
AC3 3.96a, 4.00d 4.03a, 3.64e, 3.89d 4.07a
AC4 3.55a 3.95a 4.03a
AC5 5.46a, 5.02b, 5.66d 5.15a, 4.09b, 4.82e, 5.08d 5.67a, 4.70b, 5.00e
AC6 5.25a 4.80a 5.34a
AC7 3.38a 3.09a 3.64a
AC8 >3.00a, 3.92c >3.00a >3.00a
AC9 > 3.00a >3.00a >3.00a
5C1:2C2 N.D. N.D. N.D.
sAC >>3.00f >>3.00f >>3.00f
sGC N.D. N.D. N.D.
Mouse heart AC, wild type 5.20b 4.37b 4.98b
Mouse heart AC, AC5 knockout 5.30b 4.41b 5.00b
Rat heart AC, left ventricle N.D. 4.48g 4.73g
Rat heart, right ventricle N.D. 4.62g 5.12g
Adenosine A1 receptor 4.86h 4.62h >4.00h
Adenosine A2A receptor 4.76h 5.52h >4.00h
Adenosine A3 receptor >4.22h >4.00h >4.00h