Submission Details

Molecule(s):
O=C(CCl)c1ccc(Br)c2[nH]c(=O)n(-c3cccnc3)c12

NIM-UNI-0ea3b7bf-1

O=C(CCl)c1ccc(Br)c2[nH]c(=O)n(-c3cccnc3)c12

O=C(CCl)c1ccc(Cc2ccc(Br)cc2)c2[nH]c(=O)n(-c3cccnc3)c12

NIM-UNI-0ea3b7bf-2

O=C(CCl)c1ccc(Cc2ccc(Br)cc2)c2[nH]c(=O)n(-c3cccnc3)c12

N#Cc1ccc(C(=O)CCl)c2c1[nH]c(=O)n2-c1cccnc1

NIM-UNI-0ea3b7bf-3

N#Cc1ccc(C(=O)CCl)c2c1[nH]c(=O)n2-c1cccnc1

O=C(CCl)c1cccc2c1n(-c1cccnc1)c(=O)n2-c1ccccc1

NIM-UNI-0ea3b7bf-4

O=C(CCl)c1cccc2c1n(-c1cccnc1)c(=O)n2-c1ccccc1


Design Rationale:

New scaffold based on overlaying inhibitors. Also considered ease of synthesis, and handles for elaborating using cross-coupling.

Other Notes:

Resubmitting compounds with alpha chloro so they are covalent inhibitors.

Inspired By:
Discussion: