O=C(Cc1cccc(Cl)c1)Nc1cncc2cccc(F)c12
O=C(Cc1cccc(Cl)c1)Nc1cncc2cccc(Cl)c12
Cc1cccc2cncc(NC(=O)Cc3cccc(Cl)c3)c12
COc1cccc2cncc(NC(=O)Cc3cccc(Cl)c3)c12
O=C1C(c2cccc(Cl)c2)CCN1c1cncc2cccc(F)c12
O=C1C(c2cccc(Cl)c2)CCN1c1cncc2cccc(Cl)c12
Cc1cccc2cncc(N3CCC(c4cccc(Cl)c4)C3=O)c12
COc1cccc2cncc(N3CCC(c4cccc(Cl)c4)C3=O)c12
O=C1C(c2cccc(Cl)c2)CCCN1c1cncc2cccc(F)c12
O=C1C(c2cccc(Cl)c2)CCCN1c1cncc2cccc(Cl)c12
Cc1cccc2cncc(N3CCCC(c4cccc(Cl)c4)C3=O)c12
COc1cccc2cncc(N3CCCC(c4cccc(Cl)c4)C3=O)c12
Similiar reasoning to one in EDJ-MED-6af13d92 - bending amide out of plane with peri- substituent. It would work much better with N-substituent that does not catastrophically compromise activity, but synthesis of such compound will be much harder.