O=C(Nc1cncc2ccccc12)C1CCN(Cc2ccccc2)c2ccc(Cl)cc21
RAL-THA-8416115c-2
Duplicate of:
MIC-UNK-91acba05-6
CN1CCC(C(=O)Nc2cncc3ccccc23)c2cc(Cl)ccc21
CCN1CCC(C(=O)Nc2cncc3ccccc23)c2cc(Cl)ccc21
CCCN1CCC(C(=O)Nc2cncc3ccccc23)c2cc(Cl)ccc21
O=C(Nc1cncc2ccccc12)C1CCN(Cc2ncc[nH]2)c2ccc(Cl)cc21
O=C(Nc1cncc2ccccc12)C1CCN(Cc2ccn[nH]2)c2ccc(Cl)cc21
O=C(O)CN1CCC(C(=O)Nc2cncc3ccccc23)c2cc(Cl)ccc21
NC(=O)CN1CCC(C(=O)Nc2cncc3ccccc23)c2cc(Cl)ccc21
CN(C)C(=O)CN1CCC(C(=O)Nc2cncc3ccccc23)c2cc(Cl)ccc21
CNC(=O)CN1CCC(C(=O)Nc2cncc3ccccc23)c2cc(Cl)ccc21
RAL-THA-8416115c-11
Duplicate of:
ALP-UNI-b33a865d-1
O=C(Nc1cncc2ccccc12)C1CCN(Cc2cnc[nH]2)c2ccc(Cl)cc21
O=C(Nc1cncc2ccccc12)C1CCN(Cc2nnn[nH]2)c2ccc(Cl)cc21
O=C(Nc1cncc2ccccc12)C1CCN(Cc2ncn[nH]2)c2ccc(Cl)cc21
O=C(Nc1cncc2ccccc12)C1CCN(Cc2cnn[nH]2)c2ccc(Cl)cc21
Follow up of ALP-POS-477dc5b7-2: Opportunistic SAR based on (likely) ease of synthesis from a common intermediate PLUS additional ideas to form hydrogen bond interaction(s) with Gln189.