NCBI Taxonomy: 378682

Arctotis aspera (ncbi_taxid: 378682)

found 64 associated metabolites at species taxonomy rank level.

Ancestor: Arctotis

Child Taxonomies: Arctotis aspera var. scabra

(3S,6E)-Nerolidol

(S-(e))-3,7,11-Trimethyldodeca-1,6,10-trien-3-ol

C15H26O (222.1983546)


(3S,6E)-Nerolidol, also known as nerolidol or peruviol, belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Thus, (3S,6E)-nerolidol is considered to be an isoprenoid lipid molecule. (3S,6E)-Nerolidol is an isomer of nerolidol, a naturally occurring sesquiterpene found in the essential oils of many types of plants and flowers. An isomer of nerolidol, a naturally occurring sesquiterpene found in the essential oils of many types of plants and flowers [Wikipedia] Nerolidol is a natural membrane-active sesquiterpene, with antitumor, antibacterial, antifungal and antiparasitic activity[1]. Nerolidol is a natural membrane-active sesquiterpene, with antitumor, antibacterial, antifungal and antiparasitic activity[1].

   

Spathulenol

1H-Cycloprop(e)azulen-7-ol, decahydro-1,1,7-trimethyl-4-methylene-, (1aR-(1aalpha,4aalpha,7beta,7abeta,7balpha))-

C15H24O (220.18270539999997)


Spathulenol is a tricyclic sesquiterpenoid that is 4-methylidenedecahydro-1H-cyclopropa[e]azulene carrying three methyl substituents at positions 1, 1 and 7 as well as a hydroxy substituent at position 7. It has a role as a volatile oil component, a plant metabolite, an anaesthetic and a vasodilator agent. It is a sesquiterpenoid, a carbotricyclic compound, a tertiary alcohol and an olefinic compound. Spathulenol is a natural product found in Xylopia aromatica, Xylopia emarginata, and other organisms with data available. See also: Chamomile (part of). A tricyclic sesquiterpenoid that is 4-methylidenedecahydro-1H-cyclopropa[e]azulene carrying three methyl substituents at positions 1, 1 and 7 as well as a hydroxy substituent at position 7. Spathulenol is found in alcoholic beverages. Spathulenol is a constituent of Salvia sclarea (clary sage).

   

Nerolidol

[S-(E)]-3,7,11-trimethyldodeca-1,6,10-trien-3-ol

C15H26O (222.1983546)


A component of many essential oils. The (S)-enantiomer is the commoner and occurs mostly as the (S)-(E)-isomer. Flavouring agent. Nerolidol is found in many foods, some of which are coriander, sweet basil, roman camomile, and sweet orange. Nerolidol is found in bitter gourd. Nerolidol is a component of many essential oils. The (S)-enantiomer is the commoner and occurs mostly as the (S)-(E)-isomer. Nerolidol is a flavouring agent Nerolidol is a natural membrane-active sesquiterpene, with antitumor, antibacterial, antifungal and antiparasitic activity[1]. Nerolidol is a natural membrane-active sesquiterpene, with antitumor, antibacterial, antifungal and antiparasitic activity[1].

   

Nerolidol

(E)-3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol, trans-3,7,11-Trimethyl-1,6,10-dodecatrien-3-ol

C15H26O (222.1983546)


Nerolidol is a farnesane sesquiterpenoid that is dodeca-1,6,10-triene which carries methyl groups at positions 3, 7 and 11 and a hydroxy group at position 3. It is a natural product that is present in various flowers and plants with a floral odor. Chemically, it exists in two geometric isomers, trans and cis forms. It is widely used in cosmetics (e.g. shampoos and perfumes), in non-cosmetic products (e.g. detergents and cleansers) and also as a food flavoring agent. It has a role as a flavouring agent, a cosmetic, a pheromone, a neuroprotective agent, an antifungal agent, an anti-inflammatory agent, an antihypertensive agent, an antioxidant, a volatile oil component, an insect attractant and a herbicide. It is a farnesane sesquiterpenoid, a tertiary allylic alcohol and a volatile organic compound. Nerolidol is a natural product found in Xylopia sericea, Rhododendron calostrotum, and other organisms with data available. Nerolidol is found in bitter gourd. Nerolidol is a component of many essential oils. The (S)-enantiomer is the commoner and occurs mostly as the (S)-(E)-isomer. Nerolidol is a flavouring agent. Nerolidol has been shown to exhibit anti-fungal function (A7933).Nerolidol belongs to the family of Sesquiterpenes. These are terpenes with three consecutive isoprene units. A nerolidol in which the double bond at position 6 adopts a trans-configuration. Nerolidol is a natural membrane-active sesquiterpene, with antitumor, antibacterial, antifungal and antiparasitic activity[1]. Nerolidol is a natural membrane-active sesquiterpene, with antitumor, antibacterial, antifungal and antiparasitic activity[1]. trans-Nerolidol is a sesquiterpene alcohol. It can be isolated from f aerial parts of Warionia saharae ex Benth. trans-Nerolidol improves the anti-proliferative effect of Doxorubicin (HY-15142A) against intestinal cancer cells in vitro. trans-Nerolidol also has anti-fungal activity[1][2]. trans-Nerolidol is a sesquiterpene alcohol. It can be isolated from f aerial parts of Warionia saharae ex Benth. trans-Nerolidol improves the anti-proliferative effect of Doxorubicin (HY-15142A) against intestinal cancer cells in vitro. trans-Nerolidol also has anti-fungal activity[1][2].

   

10-HYDROXY-2,6,10-TRIMETHYLDODECA-2,6,11-TRIENAL

10-HYDROXY-2,6,10-TRIMETHYLDODECA-2,6,11-TRIENAL

C15H24O2 (236.1776204)


   

nerolidol

(±)-trans-Nerolidol

C15H26O (222.1983546)


A farnesane sesquiterpenoid that is dodeca-1,6,10-triene which carries methyl groups at positions 3, 7 and 11 and a hydroxy group at position 3. It is a natural product that is present in various flowers and plants with a floral odor. Chemically, it exists in two geometric isomers, trans and cis forms. It is widely used in cosmetics (e.g. shampoos and perfumes), in non-cosmetic products (e.g. detergents and cleansers) and also as a food flavoring agent. Nerolidol is a natural membrane-active sesquiterpene, with antitumor, antibacterial, antifungal and antiparasitic activity[1]. Nerolidol is a natural membrane-active sesquiterpene, with antitumor, antibacterial, antifungal and antiparasitic activity[1]. trans-Nerolidol is a sesquiterpene alcohol. It can be isolated from f aerial parts of Warionia saharae ex Benth. trans-Nerolidol improves the anti-proliferative effect of Doxorubicin (HY-15142A) against intestinal cancer cells in vitro. trans-Nerolidol also has anti-fungal activity[1][2]. trans-Nerolidol is a sesquiterpene alcohol. It can be isolated from f aerial parts of Warionia saharae ex Benth. trans-Nerolidol improves the anti-proliferative effect of Doxorubicin (HY-15142A) against intestinal cancer cells in vitro. trans-Nerolidol also has anti-fungal activity[1][2].

   

(3S,6E)-Nerolidol

[S-(E)]-3,7,11-trimethyldodeca-1,6,10-trien-3-ol

C15H26O (222.1983546)


A (6E)-nerolidol in which the hydroxy group at positon 3 adopts an S-configuration. Nerolidol is a natural membrane-active sesquiterpene, with antitumor, antibacterial, antifungal and antiparasitic activity[1]. Nerolidol is a natural membrane-active sesquiterpene, with antitumor, antibacterial, antifungal and antiparasitic activity[1].

   

6-hydroxy-3,5,8-trimethylidene-octahydroazuleno[6,5-b]furan-2-one

6-hydroxy-3,5,8-trimethylidene-octahydroazuleno[6,5-b]furan-2-one

C15H18O3 (246.1255878)


   

(3ar,4ar,7ar,9as)-3,5,8-trimethylidene-hexahydro-3ah-azuleno[6,5-b]furan-2,6-dione

(3ar,4ar,7ar,9as)-3,5,8-trimethylidene-hexahydro-3ah-azuleno[6,5-b]furan-2,6-dione

C15H16O3 (244.1099386)


   

(2e,6e,10s)-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trienal

(2e,6e,10s)-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trienal

C15H24O2 (236.1776204)


   

(7ar)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol

(7ar)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol

C15H24O (220.18270539999997)


   

3,5,8-trimethylidene-hexahydro-3ah-azuleno[6,5-b]furan-2,6-dione

3,5,8-trimethylidene-hexahydro-3ah-azuleno[6,5-b]furan-2,6-dione

C15H16O3 (244.1099386)


   

(3ar,8r,11as)-8-hydroxy-6-(hydroxymethyl)-10-methyl-3-methylidene-3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-2-one

(3ar,8r,11as)-8-hydroxy-6-(hydroxymethyl)-10-methyl-3-methylidene-3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-2-one

C15H20O4 (264.13615200000004)


   

[(3ar,11as)-10-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-6-yl]methyl acetate

[(3ar,11as)-10-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-6-yl]methyl acetate

C17H22O4 (290.1518012)


   

{10-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-6-yl}methyl acetate

{10-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-6-yl}methyl acetate

C17H22O4 (290.1518012)


   

{8-hydroxy-10-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-6-yl}methyl acetate

{8-hydroxy-10-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-6-yl}methyl acetate

C17H22O5 (306.1467162)


   

6-(hydroxymethyl)-3,10-dimethyl-3h,3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-2-one

6-(hydroxymethyl)-3,10-dimethyl-3h,3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-2-one

C15H22O3 (250.1568862)


   

[(3ar,8r,11as)-8-hydroxy-10-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-6-yl]methyl acetate

[(3ar,8r,11as)-8-hydroxy-10-methyl-3-methylidene-2-oxo-3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-6-yl]methyl acetate

C17H22O5 (306.1467162)


   

(3ar,4ar,6s,7ar,9as)-3,5,8-trimethylidene-2-oxo-octahydroazuleno[6,5-b]furan-6-yl acetate

(3ar,4ar,6s,7ar,9as)-3,5,8-trimethylidene-2-oxo-octahydroazuleno[6,5-b]furan-6-yl acetate

C17H20O4 (288.13615200000004)


   

8-hydroxy-6-(hydroxymethyl)-10-methyl-3-methylidene-3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-2-one

8-hydroxy-6-(hydroxymethyl)-10-methyl-3-methylidene-3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-2-one

C15H20O4 (264.13615200000004)


   

2-(4a-methyl-8-methylidene-7-oxo-2,3,4,8a-tetrahydro-1h-naphthalen-2-yl)prop-2-enoic acid

2-(4a-methyl-8-methylidene-7-oxo-2,3,4,8a-tetrahydro-1h-naphthalen-2-yl)prop-2-enoic acid

C15H18O3 (246.1255878)


   

3,5,8-trimethylidene-2-oxo-octahydroazuleno[6,5-b]furan-6-yl acetate

3,5,8-trimethylidene-2-oxo-octahydroazuleno[6,5-b]furan-6-yl acetate

C17H20O4 (288.13615200000004)


   

(3ar,11as)-6-(hydroxymethyl)-10-methyl-3-methylidene-3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-2-one

(3ar,11as)-6-(hydroxymethyl)-10-methyl-3-methylidene-3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-2-one

C15H20O3 (248.14123700000002)


   

(3s,3ar,11as)-6-(hydroxymethyl)-3,10-dimethyl-3h,3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-2-one

(3s,3ar,11as)-6-(hydroxymethyl)-3,10-dimethyl-3h,3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-2-one

C15H22O3 (250.1568862)


   

(1as,4as,7s,7ar,7bs)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol

(1as,4as,7s,7ar,7bs)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol

C15H24O (220.18270539999997)


   

2-[(2r,4as,8as)-4a-methyl-8-methylidene-7-oxo-2,3,4,8a-tetrahydro-1h-naphthalen-2-yl]prop-2-enoic acid

2-[(2r,4as,8as)-4a-methyl-8-methylidene-7-oxo-2,3,4,8a-tetrahydro-1h-naphthalen-2-yl]prop-2-enoic acid

C15H18O3 (246.1255878)


   

6-(hydroxymethyl)-10-methyl-3-methylidene-3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-2-one

6-(hydroxymethyl)-10-methyl-3-methylidene-3ah,4h,7h,8h,11h,11ah-cyclodeca[b]furan-2-one

C15H20O3 (248.14123700000002)


   

(3ar,4ar,6s,7ar,9as)-6-hydroxy-3,5,8-trimethylidene-octahydroazuleno[6,5-b]furan-2-one

(3ar,4ar,6s,7ar,9as)-6-hydroxy-3,5,8-trimethylidene-octahydroazuleno[6,5-b]furan-2-one

C15H18O3 (246.1255878)