NCBI Taxonomy: 280796

Anthelia (ncbi_taxid: 280796)

found 13 associated metabolites at genus taxonomy rank level.

Ancestor: Antheliaceae

Child Taxonomies: Anthelia julacea, Anthelia juratzkana

Campesterol

(1S,2R,5S,10S,11S,14R,15R)-14-[(2R,5R)-5,6-dimethylheptan-2-yl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-ol

C28H48O (400.37049579999996)


Campesterol is a phytosterol, meaning it is a steroid derived from plants. As a food additive, phytosterols have cholesterol-lowering properties (reducing cholesterol absorption in intestines), and may act in cancer prevention. Phytosterols naturally occur in small amount in vegetable oils, especially soybean oil. One such phytosterol complex, isolated from vegetable oil, is cholestatin, composed of campesterol, stigmasterol, and brassicasterol, and is marketed as a dietary supplement. Sterols can reduce cholesterol in human subjects by up to 15\\\\\%. The mechanism behind phytosterols and the lowering of cholesterol occurs as follows : the incorporation of cholesterol into micelles in the gastrointestinal tract is inhibited, decreasing the overall amount of cholesterol absorbed. This may in turn help to control body total cholesterol levels, as well as modify HDL, LDL and TAG levels. Many margarines, butters, breakfast cereals and spreads are now enriched with phytosterols and marketed towards people with high cholesterol and a wish to lower it. -- Wikipedia. Campesterol is a member of phytosterols, a 3beta-sterol, a 3beta-hydroxy-Delta(5)-steroid and a C28-steroid. It has a role as a mouse metabolite. It derives from a hydride of a campestane. Campesterol is a natural product found in Haplophyllum bucharicum, Bugula neritina, and other organisms with data available. Campesterol is a steroid derivative that is the simplest sterol, characterized by the hydroxyl group in position C-3 of the steroid skeleton, and saturated bonds throughout the sterol structure, with the exception of the 5-6 double bond in the B ring. Campesterol. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=474-62-4 (retrieved 2024-07-01) (CAS RN: 474-62-4). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects. Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects.

   

2-Methyl-5-(1,2,2-trimethylcyclopentyl)phenol

2-Methyl-5-(1,2,2-trimethylcyclopentyl)phenol

C15H22O (218.1670562)


   

Campesterol

Campesterol

C28H48O (400.37049579999996)


Disclaimer: While authors make an effort to ensure that the content of this record is accurate, the authors make no representations or warranties in relation to the accuracy or completeness of the record. This record do not reflect any viewpoints of the affiliation and organization to which the authors belong. Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects. Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects.

   

(1r,3as,3bs,4r,5r,5ar,7s,9ar,9bs,11ar)-1-[(2r,5s)-5,6-dimethylheptan-2-yl]-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-4,5,5a,7-tetrol

(1r,3as,3bs,4r,5r,5ar,7s,9ar,9bs,11ar)-1-[(2r,5s)-5,6-dimethylheptan-2-yl]-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-4,5,5a,7-tetrol

C28H50O4 (450.37089000000003)


   

(1s,2s)-1-[(1r,4as,9r,11ar)-1-(acetyloxy)-9-hydroxy-7-methyl-11-methylidene-1h,4ah,5h,6h,9h,10h,11ah-cyclonona[c]pyran-4-yl]-1-(acetyloxy)-4-methylpent-3-en-2-yl acetate

(1s,2s)-1-[(1r,4as,9r,11ar)-1-(acetyloxy)-9-hydroxy-7-methyl-11-methylidene-1h,4ah,5h,6h,9h,10h,11ah-cyclonona[c]pyran-4-yl]-1-(acetyloxy)-4-methylpent-3-en-2-yl acetate

C26H36O8 (476.2410056)


   

(1r,2s,5e,10r,11r,18s,21r)-5,15,17,17-tetramethyl-9-methylidene-12,16-dioxapentacyclo[12.6.1.0¹,¹¹.0²,¹⁰.0¹⁸,²¹]henicosa-5,14-dien-13-one

(1r,2s,5e,10r,11r,18s,21r)-5,15,17,17-tetramethyl-9-methylidene-12,16-dioxapentacyclo[12.6.1.0¹,¹¹.0²,¹⁰.0¹⁸,²¹]henicosa-5,14-dien-13-one

C24H32O3 (368.23513219999995)


   

(1r,4as,9r,11ar)-1-(acetyloxy)-4-[(1s,2s)-1,2-bis(acetyloxy)-4-methylpent-3-en-1-yl]-7-methyl-11-methylidene-1h,4ah,5h,6h,9h,10h,11ah-cyclonona[c]pyran-9-yl 3-oxobutanoate

(1r,4as,9r,11ar)-1-(acetyloxy)-4-[(1s,2s)-1,2-bis(acetyloxy)-4-methylpent-3-en-1-yl]-7-methyl-11-methylidene-1h,4ah,5h,6h,9h,10h,11ah-cyclonona[c]pyran-9-yl 3-oxobutanoate

C30H40O10 (560.2621340000001)


   

(1s,2r)-1-[(1r,4as,9s,10s,11as)-1,9-bis(acetyloxy)-10-hydroxy-7-methyl-11-methylidene-1h,4ah,5h,6h,9h,10h,11ah-cyclonona[c]pyran-4-yl]-2-(benzoyloxy)-4-methylpent-3-en-1-yl acetate

(1s,2r)-1-[(1r,4as,9s,10s,11as)-1,9-bis(acetyloxy)-10-hydroxy-7-methyl-11-methylidene-1h,4ah,5h,6h,9h,10h,11ah-cyclonona[c]pyran-4-yl]-2-(benzoyloxy)-4-methylpent-3-en-1-yl acetate

C33H40O10 (596.2621340000001)


   

1-(acetyloxy)-1-[1-(acetyloxy)-9-hydroxy-7-methyl-11-methylidene-1h,4ah,5h,6h,9h,10h,11ah-cyclonona[c]pyran-4-yl]-4-methylpent-3-en-2-yl acetate

1-(acetyloxy)-1-[1-(acetyloxy)-9-hydroxy-7-methyl-11-methylidene-1h,4ah,5h,6h,9h,10h,11ah-cyclonona[c]pyran-4-yl]-4-methylpent-3-en-2-yl acetate

C26H36O8 (476.2410056)


   

1-(5,6-dimethylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-4,5,5a,7-tetrol

1-(5,6-dimethylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-4,5,5a,7-tetrol

C28H50O4 (450.37089000000003)


   

1-(acetyloxy)-4-[1,2-bis(acetyloxy)-4-methylpent-3-en-1-yl]-7-methyl-11-methylidene-1h,4ah,5h,6h,9h,10h,11ah-cyclonona[c]pyran-9-yl 3-oxobutanoate

1-(acetyloxy)-4-[1,2-bis(acetyloxy)-4-methylpent-3-en-1-yl]-7-methyl-11-methylidene-1h,4ah,5h,6h,9h,10h,11ah-cyclonona[c]pyran-9-yl 3-oxobutanoate

C30H40O10 (560.2621340000001)