C-1027

It is already primed to undergo the cycloaromatization reaction without external activation to produce the toxic 1,4-benzenoid diradical species.

[10] C-1027 shows promise as an anticancer drug and is currently undergoing phase II clinical trials in China,[11] with a 30% success rate.

[8] The structure of C-1027 is composed of a nine-membered enediyne complex, a deoxygenated aminosugar, a β-amino acid, and a benzoxazolinate moiety.

Starting with acetyl-CoA, PKSE iteratively combines 7 units of malonyl-CoA creating an intermediate heptaene, which is then catalyzed by accessory enzymes into a 9 membered enediyne.

Chorismate is sequentially acted upon by a 2-amino-2-deoxyisochorismate synthase, and an iron–sulfur FMN-dependent ADIC dehydrogenase to synthesize 3-enolpyruvoylanthranilate (OPA).

C-1027 Mechanism
Enediyne Biosynthesis
Deoxy Aminosugar Biosynthesis
B-Amino Acid Biosynthesis
Benzoxazolinate Biosynthesis
C-1027 Biosynthesis