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1,4-benzoquinones

Any member of the class of benzoquinones that is 1,4-benzoquinone or its C-substituted derivatives.

ChEBI ID: 132124

Members (19)

MemberDefinitionRole
17-(dimethylaminoethylamino)-17-demethoxygeldanamycinA 19-membered macrocyle that is geldanamycin in which the methoxy group attached to the benzoquinone moiety has been replaced by a 2-(N,N-dimethylamino)ethylamino group.alvespimycin
2,3-dimethoxy-5-methyl-6-decyl-1,4-benzoquinoneA member of the class of 1,4-benzoquinones that is 2,3-dimethoxybenzoquinone which has been substituted at positions 5 and 6 by decyl and methyl groups.6-decylubiquinone
2,5-bis(1-aziridinyl)-3,6-bis(2-methoxyethoxy)-4-benzoquinoneAziridyl benzoquinone
2,6-dichlorobenzoquinoneA member of the class of 1,4-benzoquinones that is p-benzoquinone in which the hydrogens at positions 2 and 6 have been replaced by chlorines. A highly toxic and carcinogenic disinfection by-product found in drinking water.2,6-dichlorobenzoquinone
aa 861A member of the class of benzoquinones that is p-benzoquinone in which the hydrogens are substituted by three methyl groups and a 12-hydroxydodeca-5,10-diyn-1-yl group.docebenone
chloranilA member of the class of 1,4-benzoquiones that is 1,4-benzoquinone in which all four hydrogens are substituted by chlorines.tetrachloro-1,4-benzoquinone
diaziquoneA 1,4-benzoquinone that is substituted at positions 2 and 5 have been replaced by aziridin-1-yl groups and at positions 3 and 6 by (ethoxycarbonyl)amino groups.diaziquone
dibromothymoquinonedibromothymoquinone
duroquinoneA member of the class of 1,4-benzoquinones that is 1,4-benzoquinone in which all four hydrogens are substituted by methyl groups.duroquinone
ethylenimine quinoneA member of the class of 1,4-benzoquinones that is p-benzoquinone in which the hydrogens at positions 2 and 5 are replaced by aziridin-1-yl groups.2,5-bis(aziridin-1-yl)-1,4-benzoquinone
geldanamycinAn ansamycin consisting of a 19-membered macrocyle incorporating a benzoquinone ring and a lactam functionality. It shows antimicrobial activity against many Gram-positive and some Gram-negative bacteria.geldanamycin
herbimycinA 19-membered macrocyle incorporating a benzoquinone ring and a lactam functionality. It is an ansamycin antibiotic that induces apoptosis and displays antitumour effects.herbimycin
idebenoneA member of the class of 1,4-benzoquinones which is substituted by methoxy groups at positions 2 and 3, by a methyl group at positions 5, and by a 10-hydroxydecyl group at positions 6. Initially developed for the treatment of Alzheimer's disease, benefits were modest; it was subsequently found to be of benefit for the symptomatic treatment of Friedreich's ataxia.idebenone
nsc 224070A member of the class of 1,4-benzoquinones that is 1,4-benzoquinone in which the hydrogens at positions 2 and 5 have been replaced by aziridin-1-yl groups while the hydrogens at positions 3 and 6 have been replaced by (2-hydroxyethyl)amino groups.2,5-bis(2-hydroxyethylamino)-3,6-diaziridinylbenzoquinone
priminA 1,4-benzoquinone having a methoxy substituent at the 2-position and a pentyl substituent at the 6-position.primin
quinoneThe simplest member of the class of 1,4-benzoquinones, obtained by the formal oxidation of hydroquinone to the corresponding diketone. It is a metabolite of benzene.1,4-benzoquinone
tanespimycinA 19-membered macrocyle that is geldanamycin in which the methoxy substituent attached to the benzoquinone moiety has been replaced by an allylamino group. It is a potent inhibitor of heat shock protein 90 (Hsp90). A less toxic analogue than geldanamycin, it induces apoptosis and displays antitumour effects.tanespimycin
thymoquinoneA member of the class of 1,4-benzoquinones that is 1,4-bezoquinone in which the hydrogens at positions 2 and 5 are replaced by methyl and isopropyl groups, respectively. It is a natural compound isolated from Nigella sativa which has demonstrated promising chemotherapeutic activity.thymoquinone
triaziquoneA member of the class of 1,4-benzoquinones that is 1,4-benzoquinone in which three of the ring hydrogens are replaced by aziridin-1-yl groups.triaziquone

Research

Studies (7,019)

TimeframeStudies, Drugs in This Class (%)All Drugs %
pre-19901,211 (17.25)18.7374
1990's1,221 (17.40)18.2507
2000's1,648 (23.48)29.6817
2010's2,215 (31.56)24.3611
2020's724 (10.31)2.80

Study Types

Publication TypeStudies, Drugs in This Class (%)All Drugs (%)
Trials131 (1.75%)5.53%
Reviews369 (4.93%)6.00%
Case Studies59 (0.79%)4.05%
Observational3 (0.04%)0.25%
Other6,927 (92.50%)84.16%