Compound_ID;SMILES;EC50 on PPARg trans-AzoMDG548;S=C1NC(/C(C(N1)=O)=C/C2=CC=C(/N=N/C3=CC=CC=C3)C=C2)=O;inactive cis-AzoMDG548;S=C1NC(/C(C(N1)=O)=C/C2=CC=C(/N=N\C3=CC=CC=C3)C=C2)=O;not tested trans-AzoGW1929;O=C(C1=C(N[C@H](C(O)=O)CC2=CC=C(/N=N/C3=CC=CC=C3)C=C2)C=CC=C1)C4=CC=CC=C4;1.0±0.1 µM cis-AzoGW1929;O=C(C1=C(N[C@H](C(O)=O)CC2=CC=C(/N=N\C3=CC=CC=C3)C=C2)C=CC=C1)C4=CC=CC=C4;1.30±0.01 µM trans-AzoGW1929-2;O=C(C1=C(N[C@H](C(O)=O)CC2=CC=C(/N=N/C3=CC=C(Cl)C=C3)C=C2)C=CC=C1)C4=CC=CC=C4;1.6±0.1 µM cis-AzoGW1929-2;O=C(C1=C(N[C@H](C(O)=O)CC2=CC=C(/N=N\C(C=C3)=CC=C3Cl)C=C2)C=CC=C1)C4=CC=CC=C4;5.0±0.4 µM trans-AzoRosi;O=C(C(S1)CC2=CC=C(/N=N/C3=CC=CC=C3)C=C2)NC1=O;2.2±0.2 µM cis-AzoRosi;O=C(C(S1)CC2=CC=C(/N=N\C3=CC=CC=C3)C=C2)NC1=O;6.3±1.4 µM trans-AzoRosi-2;O=C(C(S1)CC2=CC=C(/N=N/C3=CC=C(Cl)C=C3)C=C2)NC1=O;2.9±0.2 µM cis-AzoRosi-2;O=C(C(S1)CC2=CC=C(/N=N\C3=CC=C(Cl)C=C3)C=C2)NC1=O;7.0±1.0 µM trans-AzoRosi-3;O=C(C(S1)CC2=CC=C(/N=N/C3=CC=C(C(F)(F)F)C=C3)C=C2)NC1=O;2.2±0.7 µM cis-AzoRosi-3;O=C(C(S1)CC2=CC=C(/N=N\C3=CC=C(C(F)(F)F)C=C3)C=C2)NC1=O;6.5±1.5 µM trans-AzoRosi-4;O=C(C(S1)CC2=CC=C(/N=N/C3=CC=C(C4=C(C)C=CC=C4)C=C3)C=C2)NC1=O;2.8±1.3 µM cis-AzoRosi-4;O=C(C(S1)CC2=CC=C(/N=N\C3=CC=C(C4=C(C)C=CC=C4)C=C3)C=C2)NC1=O;6.4±0.4 µM