Inhibidores

(±)5-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid.

Microcystin-LY, from Microcystis aeruginosa, is a heptapeptide toxin that triggers oxidative stress by activating the Nrf2 pathway, most effective at 3μM.

Questiomycin A derivatives 12 is a Questiomycin A derivative.

1) Non-toxicity: belong to flower-stem dye, easy to biodegrade, no carcinogenic toxicity.

α-conotoxin GI, a conopeptide isolated from the venom of the cone snail Conus geographus, is a competitive antagonist of the muscle-type nicotinic acetylcholine

Azido-PEG12-t-butyl ester, a soluble PEG with azide/reactive t-butyl, forms triazoles via Click Chemistry; deprotectable in acid.

2', 3'-cGAMP-C2-SH is a ADC cytotoxin.

mTORC1-IN-1 (T1), a rapamycin homologue (rapalog) and selective inhibitor of mTORC1, controls cell growth and metabolism, with implications in various diseases

Antitubercular agent-10 shows potent antitubercular activity with a MIC value of 30 nM.

Funobactam is a potent β-lactamase inhibitor.

ERK1/2 inhibitor 5 targets MAPK pathway, potentially aiding cancer and inflammation research.