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tetrol

A polyol that contains 4 hydroxy groups.

ChEBI ID: 33573

Members (20)

MemberDefinitionRole
1,23,25-trihydroxyvitamin d3A hydroxycalciol that consists of vitamin D3 (calciol) bearing additional hydroxy substituents at positions 1, 23 and 25 (with 1alpha,23S-configuration). An intermediate in the degradation pathway of 1alpha,25-(OH)2D3.1alpha,23(S),25-trihydroxyvitamin D3
23-hydroxytormentic acidA pentacyclic triterpenoid that is asiatic acid substituted by a hydroxy group at position 19. It has been isolated from the leaves of Rosa laevigata.19alpha-hydroxyasiatic acid
3,4-dihydroxyphenylglycolA tetrol composed of ethyleneglycol having a 3,4-dihydroxyphenyl group at the 1-position.3,4-dihydroxyphenylethyleneglycol
32,33,34,35-bacteriohopanetetrolA hopanoid that is bacteriohopane carrying four hydroxy substituents at positions 32, 33, 34 and 35.bacteriohopane-32,33,34,35-tetrol
8-amino-8-demethylriboflavinA benzopteridine that is riboflavin in which the methyl group at position 8 has been replaced by an amino group.8-amino-8-demethylriboflavin
bacterioruberinA C50 carotenoid that is a red-coloured pigment found in several Halobacterium and Haloarcula species.bacterioruberin
benzoylaconineA diterpene alkaloid with formula C32H45NO10 that is isolated from several Aconitum species.benzoylaconine
benzoylmesaconineA diterpene alkaloid with formula C31H43NO10 that is isolated from several Aconitum species.benzoylmesaconine
conduritol bA tetrol that is cyclohexene in which a hydrogen attached to each of the carbons at positions 3, 4, 5, and 6 is replaced by a hydroxy group. The group consists of six possible diastereoisomers, known as conduritols A to F, some of which can exist as two distinct enantiomers.conduritol
conduritol epoxideAn epoxide resulting from the epoxidation of the double bond of a conduritol.conduritol epoxide
demethylbellidifolinA member of the class of xanthones that is xanthone which is substituted by hydroxy groups at positions 1, 3, 5, and 8. A natural product found particularly in Iris nigricans and Gentiana campestris.bellidin
dipyridamoleA pyrimidopyrimidine that is 2,2',2'',2'''-(pyrimido[5,4-d]pyrimidine-2,6-diyldinitrilo)tetraethanol substituted by piperidin-1-yl groups at positions 4 and 8 respectively. A vasodilator agent, it inhibits the formation of blood clots.dipyridamole
glaucarubinoneA quassinoid with formula C25H34O10. It is a natural product isolated from several plant species and exhibits anti-cancer and anti-malarial properties.glaucarubinone
hetacillinA lignan that consists of tetrahydrofuran substituted by a 3,4-dihydroxyphenyl group at position 2, a hydroxymethyl group at position 3 and a 4-hydroxy-3-methoxybenzyl group at position 4. It has been isolated from Taxus yunnanensis.taxiresinol
madecassic acidA pentacyclic triterpenoid that is ursane substituted by a carboxy group at position 28 and hydroxy groups at positions 2, 3, 6 and 23 (the 2alpha,3beta,6beta stereoisomer).madecassic acid
masoprocolA tetrol that is butane which is substituted at positions 2 and 3 by 3,4-dihydroxybenzyl groups. Masoprocol, the meso-form found in the leaves of the creosote bush (Larrea divaricata), is a potent lipoxygenase inhibitor.nordihydroguaiaretic acid
megestrol acetateA sesquiterpene lactone with formula C15H20O8. It is a neurotoxic natural product found in plants of the family Illiciaceae.anisatin
nbi 31772An isoquinoline substituted by 3,4-dihydroxybenzoyl, carboxy, hydroxy, and hydroxy groups at positions 1, 3, 6, and 7, respectively. It is a potent inhibitor of insulin-like growth factor-1 binding protein (IGFBP).NBI-31772
niga-ichigoside f1A triterpenoid saponin that is 19alpha-hydroxyasiatic acid attached to a beta-D-glucopyranosyl residue at position 28 via a glycosidic linkage. It has been isolated from the leaves of Rosa laevigata.19alpha-hydroxyasiatic acid-28-O-beta-D-glucopyrannoside
pentaerythritolA tetrol that is neopentane in which one of the methyl hydrogens of all four methyl groups are replaced by hydroxy groups. It is a chemical intermediate used in the production of explosives, plastics, paints, appliances, and cosmetics.pentaerythritol

Research

Studies (8,740)

TimeframeStudies, Drugs in This Class (%)All Drugs %
pre-19903,595 (41.13)18.7374
1990's2,308 (26.41)18.2507
2000's1,629 (18.64)29.6817
2010's1,016 (11.62)24.3611
2020's192 (2.20)2.80

Study Types

Publication TypeStudies, Drugs in This Class (%)All Drugs (%)
Trials939 (10.06%)5.53%
Reviews771 (8.26%)6.00%
Case Studies458 (4.91%)4.05%
Observational10 (0.11%)0.25%
Other7,159 (76.67%)84.16%