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Quinones

The quinones are a class of organic compounds that are formally derived from aromatic compounds by conversion of an even number of –CH= groups into –C(=O)– groups with any necessary rearrangement of double bonds, resulting in a fully conjugated cyclic dione structure. Quinones exhibit numerous biological activities such as neurological, antibacterial, antiplasmodial, antioxidantal, trypanocidal, antitumor, and anti-HIV, and these activities have been proven to be related to the redox properties of their carbonyl functions.

2-Bromocyclohexa-2,5-diene-1,4-dione

2,5-di-tert-butylcyclohexa-2,5-diene-1,4-dione

sodium 4,5-dihydroxy-3,6-dioxocyclohexa-1,4-diene-1,2-bis(olate)

2,6-Diisopropylcyclohexa-2,5-diene-1,4-dione

2-(12-hydroxydodeca-5,10-diyn-1-yl)-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione

2,3,5-Trimethylcyclohexa-2,5-diene-1,4-dione

3,3',5,5'-Tetra-tert-butyl-[1,1'-bi(cyclohexylidene)]-2,2',5,5'-tetraene-4,4'-dione

2,5-Dihydroxy-3-undecylcyclohexa-2,5-diene-1,4-dione

2,5-Dichlorocyclohexa-2,5-diene-1,4-dione

2,6-Dimethylcyclohexa-2,5-diene-1,4-dione

2,5-Dimethylcyclohexa-2,5-diene-1,4-dione

2-(hydroxymethyl)-6-methoxycyclohexa-2,5-diene-1,4-dione

2,3,5,6-Tetrahydroxycyclohexa-2,5-diene-1,4-dione

3,3',5-Tri-tert-butyl-5'-chloro-[1,1'-bi(cyclohexyl-idene)]-2,2',5,5'-tetraene-4,4'-dione

2-Methoxycyclohexa-2,5-diene-1,4-dione

2,5-dimethoxycyclohexa-2,5-diene-1,4-dione

2,5-diethoxycyclohexa-2,5-diene-1,4-dione

2,3-Dimethylcyclohexa-2,5-diene-1,4-dione

barium 2,5-dichloro-3,6-dioxocyclohexa-1,4-diene-1,4-bis(olate)

2-bromo-5-methylcyclohexa-2,5-diene-1,4-dione

Ethyl 2-(3-chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-3-oxobutanoate

2-(1,4-Dioxo-1,4-dihydronaphthalen-2-yl)-2-methylpropanal

(R)-1-(5,8-Dihydroxy-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-4-methylpent-3-en-1-yl 2-methylbutanoate

N-Butyl-N-(3-chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)acetamide