Skip to main content
. Author manuscript; available in PMC: 2012 Aug 17.
Published in final edited form as: ACS Chem Neurosci. 2011 Aug 17;2(8):471–482. doi: 10.1021/cn100099n

Table 2.

SAR of 5,6 fused ring heterocycles

Compound Structurea mGlu5 IC50 (nM)b % Glu Maxc Synthetic Conditions
14 graphic file with name nihms-279132-t0013.jpg >30,000 i
15 graphic file with name nihms-279132-t0014.jpg 2460 ± 226 26.3 ± 14.4 iii
16 graphic file with name nihms-279132-t0015.jpg >10,000d 46.5 ± 7.8 i
17 graphic file with name nihms-279132-t0016.jpg >30,000 i
18 graphic file with name nihms-279132-t0017.jpg 61 ± 7 0.63 ± 0.12 i
19 graphic file with name nihms-279132-t0018.jpg >30,000 iii
20 graphic file with name nihms-279132-t0019.jpg >30,000 iii
21 graphic file with name nihms-279132-t0020.jpg >10,000d 60.4 ± 2.5 iii
22 graphic file with name nihms-279132-t0021.jpg >30,000 from 21e
23 graphic file with name nihms-279132-t0022.jpg 1520 ± 296 4.8 ± 2.3 from 21e
a

R = 3-cyano-5-fluorophenyl

b

Calcium mobilization mGlu5 assay; values are average of n ≥ 3

c

Amplitude of response in the presence of 30 μM test compound as a percentage of maximal response (100 μM glutamate); values are average of n ≥ 3

d

CRC does not plateau

e

Reaction of 21 with K2CO3 and MeI in DMF afforded a separable mixture of 22 and 23