Representative LC/UV chromatogram under typical analytical conditions (C18 column; mobile phase: 5–100% ACN / H2O (0.05% H3PO4), linear gradient 20 min; flow rate: 0.2 mL/min; detection: 210 nm).
NMR Spectral Data
Representative 1H NMR (500 MHz) spectrum confirming the structure of Macrosphelide A. Representative 13C NMR (125 MHz) spectrum supporting structural assignment of Macrosphelide A.
Source Organism
Paraconiothyrium sporulosum.
Summary
Macrosphelide A is a 16-membered macrolide natural product that inhibits cell adhesion and cancer metabolism.
Details
Macrosphelide A is a 16-membered macrolide natural product originally identified as an inhibitor of cell-cell adhesion between HL-60 leukemia cells and LPS-activated endothelial cells (IC50 = 3.5 µM). It lacks significant cytocidal or broad antimicrobial activity at high concentrations, indicating a selective biological mode of action. More recent mechanistic studies revealed that macrosphelide A exerts anticancer effects by simultaneously targeting key metabolic enzymes involved in the Warburg effect, including enolase 1 (ENO1), aldolase A (ALDOA), and fumarate hydratase (FH). Direct inhibition of ENO1 enzymatic activity was experimentally confirmed. In cancer cells, treatment reduces glucose consumption, lactate production, and proliferation, and induces apoptosis. Thus, macrosphelide A functions both as a cell-adhesion modulator and a multitarget metabolic inhibitor with antitumor potential.