Submission Details

Molecule(s):
O=C(CC(=O)N1CCOCC1)NC1CCCCC1

GIA-UNK-3f36037a-1

O=C(CC(=O)N1CCOCC1)NC1CCCCC1

O=C(CC(=O)N1CCOCC1)Nc1ccccc1

GIA-UNK-3f36037a-2

O=C(CC(=O)N1CCOCC1)Nc1ccccc1

O=C(CCl)CNC(=O)CC(=O)NC1CCCCC1

GIA-UNK-3f36037a-3

O=C(CCl)CNC(=O)CC(=O)NC1CCCCC1

O=C(CCl)CNC(=O)CC(=O)Nc1ccccc1

GIA-UNK-3f36037a-4

O=C(CCl)CNC(=O)CC(=O)Nc1ccccc1

O=C(CCl)CNC(=O)CC(=O)NCc1ccccc1

GIA-UNK-3f36037a-5

O=C(CCl)CNC(=O)CC(=O)NCc1ccccc1

O=C(CC(=O)N1CCOCC1)NCc1ccccc1

GIA-UNK-3f36037a-6

O=C(CC(=O)N1CCOCC1)NCc1ccccc1

O=C(CC(=O)Nc1ccncc1)Nc1ccccc1

GIA-UNK-3f36037a-7

O=C(CC(=O)Nc1ccncc1)Nc1ccccc1


Design Rationale:

Malonamides could be used as potential scaffold, due to ther ability to act as a valid peptidomimetic, as it can simulate secondary structure of the natural substrate. Both chloromethyl fragment (covalent interaction) and morpholine fragment (non covalent interaction) are presented as alternative.

Other Notes:

Easy synthesis, for example starting from the opening of Meldrum's acid.

Inspired By:
Discussion: