O=C(/C=C/c1cnc2ccccc2n1)c1ccccc1
O=C(/C=C/c1cnc2ccccc2n1)c1ccc(F)cc1
O=C(/C=C/c1cnc2ccccc2n1)c1ccc(Cl)cc1
O=C(/C=C/c1cnc2ccccc2n1)c1ccc(Br)cc1
O=C(/C=C/c1cnc2ccccc2n1)c1ccc(I)cc1
Cc1ccc(C(=O)/C=C/c2cnc3ccccc3n2)cc1
COc1ccc(C(=O)/C=C/c2cnc3ccccc3n2)cc1
O=C(/C=C/c1cnc2ccccc2n1)c1ccc([N+](=O)[O-])cc1
O=C(/C=C/c1cnc2ccccc2n1)c1cccc([N+](=O)[O-])c1
O=C(/C=C/c1cnc2ccccc2n1)c1cccc(Br)c1
O=C(/C=C/c1cnc2ccccc2n1)c1ccc(O)cc1
O=C(/C=C/c1cnc2ccccc2n1)c1cccc(O)c1
Nc1ccc(C(=O)/C=C/c2cnc3ccccc3n2)cc1
Nc1cccc(C(=O)/C=C/c2cnc3ccccc3n2)c1
O=C(/C=C/c1cnc2ccccc2n1)c1ccncc1
O=C(/C=C/c1cnc2ccccc2n1)c1cccnc1
O=C(/C=C/c1cnc2ccccc2n1)c1ccccn1
O=C(/C=C/c1cnc2ccccc2n1)c1ccc2ccccc2c1
O=C(/C=C/c1cnc2ccccc2n1)c1cccc2ccccc12
Nc1ccccc1C(=O)/C=C/c1cnc2ccccc2n1
Structural features seen of similar compounds exhibiting activity (By eye)
I am working in the field of medicinal chemistry in search of potential drug targets for infectious diseases such as tuberculosis, cancer, microbial infections etc. First time trying to work try compounds for target to treat viral disease.