Submission Details

Molecule(s):
CNC(=O)OC1CCN(C(=O)N2CCCCC2)CC1

GIA-UNK-595fac82-1

CNC(=O)OC1CCN(C(=O)N2CCCCC2)CC1

CNC(=O)OC1CCN(C(=O)c2ccccc2)CC1

GIA-UNK-595fac82-2

CNC(=O)OC1CCN(C(=O)c2ccccc2)CC1

CNC(=O)OC1CCN(C(=O)c2ccncc2)CC1

GIA-UNK-595fac82-3

CNC(=O)OC1CCN(C(=O)c2ccncc2)CC1

CNC(=O)OC1CCN(S(=O)(=O)c2ccccc2)CC1

GIA-UNK-595fac82-4

CNC(=O)OC1CCN(S(=O)(=O)c2ccccc2)CC1

CNC(=O)OC1CCN(Cc2ccccc2)CC1

GIA-UNK-595fac82-5

CNC(=O)OC1CCN(Cc2ccccc2)CC1


Design Rationale:

By eye. Replacement of the inspired fragment, bearing primary chloride, with other possibility of a semi/covalent inhibition of the enzyme. Substitution with a carbamate (like e.g. physostigmine and Acetylcholinesterase inhibitors).

Other Notes:

Simple and easy chemical synthesis, most of building blocks are commercially available

Inspired By:
Discussion: