NCBI Taxonomy: 2126662

Parasenecio petasitoides (ncbi_taxid: 2126662)

found 88 associated metabolites at species taxonomy rank level.

Ancestor: Parasenecio

Child Taxonomies: none taxonomy data.

(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].

   

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].

   

Fukinone

(4aR,5S,8aR)-4a,5-dimethyl-3-propan-2-ylidene-4,5,6,7,8,8a-hexahydro-1H-naphthalen-2-one

C15H24O (220.18270539999997)


Constituent of Petasites japonicus (sweet coltsfoot). Fukinone is found in burdock, giant butterbur, and green vegetables. Fukinone is found in burdock. Fukinone is a constituent of Petasites japonicus (sweet coltsfoot)

   

Tussilagone

[1-(1-acetyloxyethyl)-4-methylidene-2-oxo-7-propan-2-yl-3,3a,5,6,7,7a-hexahydro-1H-inden-5-yl] (E)-3-methylpent-2-enoate

C23H34O5 (390.24061140000003)


Constituent of Tussilago farfara (coltsfoot). 9alpha-(3-Methyl-2E-pentenoyloxy)-4S-hydroxy-10(14)-oplopen-3-one 4-acetate is found in tea. Tussilagone is found in tea. Tussilagone is a constituent of Tussilago farfara (coltsfoot). Tussilagone, a major active component in Tussilago farfara, has anti-inflammatory effect. Tussilagone ameliorates inflammatory responses in dextran sulphate sodium-induced murine colitis. Tussilagone inhibits the inflammatory response and improves survival in cecal ligation and puncture (CLP)-induced septic mice[1][2]. Tussilagone, a major active component in Tussilago farfara, has anti-inflammatory effect. Tussilagone ameliorates inflammatory responses in dextran sulphate sodium-induced murine colitis. Tussilagone inhibits the inflammatory response and improves survival in cecal ligation and puncture (CLP)-induced septic mice[1][2].

   

Jacquinelin

(3S,3aS,9aS,9bS)-9-(hydroxymethyl)-3,6-dimethyl-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

C15H18O4 (262.1205028)


Jacquinelin, also known as 11,13-dihydro-8-deoxylactucin or jacquilenin, is a member of the class of compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom. Jacquinelin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Jacquinelin can be found in chicory and endive, which makes jacquinelin a potential biomarker for the consumption of these food products.

   

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].

   

Fukinone

(4aR,5S,8aR)-4a,5-dimethyl-3-propan-2-ylidene-4,5,6,7,8,8a-hexahydro-1H-naphthalen-2-one

C15H24O (220.18270539999997)


   

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].

   

3-hydroxy-9-(hydroxymethyl)-3,6-dimethyl-3ah,4h,5h,6h,6ah,9ah,9bh-azuleno[4,5-b]furan-2,7-dione

3-hydroxy-9-(hydroxymethyl)-3,6-dimethyl-3ah,4h,5h,6h,6ah,9ah,9bh-azuleno[4,5-b]furan-2,7-dione

C15H20O5 (280.13106700000003)


   

(3ar,4r,7s,7ar)-7,7a-dimethyl-2-oxo-hexahydro-1h-inden-4-yl (2z)-2-methylbut-2-enoate

(3ar,4r,7s,7ar)-7,7a-dimethyl-2-oxo-hexahydro-1h-inden-4-yl (2z)-2-methylbut-2-enoate

C16H24O3 (264.1725354)


   

(3r,3as,5s,8r,11as)-5,8-dihydroxy-3,6,10-trimethyl-3h,3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-one

(3r,3as,5s,8r,11as)-5,8-dihydroxy-3,6,10-trimethyl-3h,3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-one

C15H22O4 (266.1518012)


   

(1s,3r,4s,7r,8r,10r,13r)-3,4,13-trimethyl-12-oxo-11,14-dioxatetracyclo[8.3.1.0¹,¹⁰.0³,⁸]tetradecan-7-yl 2-methylbut-2-enoate

(1s,3r,4s,7r,8r,10r,13r)-3,4,13-trimethyl-12-oxo-11,14-dioxatetracyclo[8.3.1.0¹,¹⁰.0³,⁸]tetradecan-7-yl 2-methylbut-2-enoate

C20H28O5 (348.1936638)


   

(1s,3r,4s,7r,8r,10r,13r)-3,4,13-trimethyl-12-oxo-11,14-dioxatetracyclo[8.3.1.0¹,¹⁰.0³,⁸]tetradecan-7-yl (2z)-2-methylbut-2-enoate

(1s,3r,4s,7r,8r,10r,13r)-3,4,13-trimethyl-12-oxo-11,14-dioxatetracyclo[8.3.1.0¹,¹⁰.0³,⁸]tetradecan-7-yl (2z)-2-methylbut-2-enoate

C20H28O5 (348.1936638)


   

3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h,8ah,9h,9ah-naphtho[2,3-b]furan-8-yl 2-methylbut-2-enoate

3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h,8ah,9h,9ah-naphtho[2,3-b]furan-8-yl 2-methylbut-2-enoate

C20H28O4 (332.19874880000003)


   

(3s,4ar,5s,8r,8ar)-3,4a,5-trimethyl-2-oxo-3h,4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-8-yl 2-methylbut-2-enoate

(3s,4ar,5s,8r,8ar)-3,4a,5-trimethyl-2-oxo-3h,4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-8-yl 2-methylbut-2-enoate

C20H28O4 (332.19874880000003)


   

9a-hydroxy-3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-8-yl 2-methylbut-2-enoate

9a-hydroxy-3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-8-yl 2-methylbut-2-enoate

C20H28O5 (348.1936638)


   

5,9-dihydroxy-3,6,10-trimethyl-3h,3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-one

5,9-dihydroxy-3,6,10-trimethyl-3h,3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-one

C15H22O4 (266.1518012)


   

9-(hydroxymethyl)-3,6-dimethyl-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione

9-(hydroxymethyl)-3,6-dimethyl-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione

C15H18O4 (262.1205028)


   

9-(hydroxymethyl)-3,6-dimethyl-3h,3ah,4h,5h,6h,6ah,9ah,9bh-azuleno[4,5-b]furan-2,7-dione

9-(hydroxymethyl)-3,6-dimethyl-3h,3ah,4h,5h,6h,6ah,9ah,9bh-azuleno[4,5-b]furan-2,7-dione

C15H20O4 (264.13615200000004)


   

(3s,3as,6s,6as,9ar,9bs)-9-(hydroxymethyl)-3,6-dimethyl-3h,3ah,4h,5h,6h,6ah,9ah,9bh-azuleno[4,5-b]furan-2,7-dione

(3s,3as,6s,6as,9ar,9bs)-9-(hydroxymethyl)-3,6-dimethyl-3h,3ah,4h,5h,6h,6ah,9ah,9bh-azuleno[4,5-b]furan-2,7-dione

C15H20O4 (264.13615200000004)


   

(3ar,4r,7s,7ar)-7,7a-dimethyl-2-oxo-hexahydro-1h-inden-4-yl 2-methylbut-2-enoate

(3ar,4r,7s,7ar)-7,7a-dimethyl-2-oxo-hexahydro-1h-inden-4-yl 2-methylbut-2-enoate

C16H24O3 (264.1725354)


   

(3s,4ar,5s,8r,8ar)-3,4a,5-trimethyl-2-oxo-3h,4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-8-yl (2z)-2-methylbut-2-enoate

(3s,4ar,5s,8r,8ar)-3,4a,5-trimethyl-2-oxo-3h,4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-8-yl (2z)-2-methylbut-2-enoate

C20H28O4 (332.19874880000003)


   

(3s,3as,5s,11as)-5-hydroxy-3,6,10-trimethyl-3h,3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-one

(3s,3as,5s,11as)-5-hydroxy-3,6,10-trimethyl-3h,3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-one

C15H22O3 (250.1568862)


   

(4ar,5s,8r,8ar,9ar)-3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h,8ah,9h,9ah-naphtho[2,3-b]furan-8-yl (2z)-2-methylbut-2-enoate

(4ar,5s,8r,8ar,9ar)-3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h,8ah,9h,9ah-naphtho[2,3-b]furan-8-yl (2z)-2-methylbut-2-enoate

C20H28O4 (332.19874880000003)


   

(3r,4ar,5s,8r,8ar)-3,4a,5-trimethyl-2-oxo-3h,4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-8-yl 2-methylbut-2-enoate

(3r,4ar,5s,8r,8ar)-3,4a,5-trimethyl-2-oxo-3h,4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-8-yl 2-methylbut-2-enoate

C20H28O4 (332.19874880000003)


   

5-hydroxy-3,6,10-trimethyl-3h,3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-one

5-hydroxy-3,6,10-trimethyl-3h,3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-one

C15H22O3 (250.1568862)


   

(3s,3as,5s,9r,11as)-5,9-dihydroxy-3,6,10-trimethyl-3h,3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-one

(3s,3as,5s,9r,11as)-5,9-dihydroxy-3,6,10-trimethyl-3h,3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-one

C15H22O4 (266.1518012)


   

(3r,3as,6s,6as,9ar,9bs)-9-(hydroxymethyl)-3,6-dimethyl-3h,3ah,4h,5h,6h,6ah,9ah,9bh-azuleno[4,5-b]furan-2,7-dione

(3r,3as,6s,6as,9ar,9bs)-9-(hydroxymethyl)-3,6-dimethyl-3h,3ah,4h,5h,6h,6ah,9ah,9bh-azuleno[4,5-b]furan-2,7-dione

C15H20O4 (264.13615200000004)


   

5,8-dihydroxy-3,6,10-trimethyl-3h,3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-one

5,8-dihydroxy-3,6,10-trimethyl-3h,3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-one

C15H22O4 (266.1518012)


   

3-{4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-3-methoxyphenyl}prop-2-en-1-ol

3-{4-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-3-methoxyphenyl}prop-2-en-1-ol

C20H28O3 (316.2038338)


   

3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-8-yl 2-methylbut-2-enoate

3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-8-yl 2-methylbut-2-enoate

C20H28O3 (316.2038338)


   

(1s,3ar,5r,7s,7as)-1-[(1r)-1-(acetyloxy)ethyl]-7-isopropyl-4-methylidene-2-oxo-hexahydro-1h-inden-5-yl 3-methylpent-2-enoate

(1s,3ar,5r,7s,7as)-1-[(1r)-1-(acetyloxy)ethyl]-7-isopropyl-4-methylidene-2-oxo-hexahydro-1h-inden-5-yl 3-methylpent-2-enoate

C23H34O5 (390.24061140000003)


   

(3s,3as,5s,8r,11as)-5,8-dihydroxy-3,6,10-trimethyl-3h,3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-one

(3s,3as,5s,8r,11as)-5,8-dihydroxy-3,6,10-trimethyl-3h,3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-one

C15H22O4 (266.1518012)


   

(3r,4ar,5s,8ar)-4a,5-dimethyl-3-(prop-1-en-2-yl)-octahydronaphthalen-2-one

(3r,4ar,5s,8ar)-4a,5-dimethyl-3-(prop-1-en-2-yl)-octahydronaphthalen-2-one

C15H24O (220.18270539999997)


   

(3r,3ar,6s,6as,9ar,9br)-3-hydroxy-9-(hydroxymethyl)-3,6-dimethyl-3ah,4h,5h,6h,6ah,9ah,9bh-azuleno[4,5-b]furan-2,7-dione

(3r,3ar,6s,6as,9ar,9br)-3-hydroxy-9-(hydroxymethyl)-3,6-dimethyl-3ah,4h,5h,6h,6ah,9ah,9bh-azuleno[4,5-b]furan-2,7-dione

C15H20O5 (280.13106700000003)


   

(4ar,5s,8r,8ar,9as)-9a-hydroxy-3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-8-yl (2z)-2-methylbut-2-enoate

(4ar,5s,8r,8ar,9as)-9a-hydroxy-3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-8-yl (2z)-2-methylbut-2-enoate

C20H28O5 (348.1936638)


   

(3r,4ar,5s,8r,8ar)-3,4a,5-trimethyl-2-oxo-3h,4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-8-yl (2z)-2-methylbut-2-enoate

(3r,4ar,5s,8r,8ar)-3,4a,5-trimethyl-2-oxo-3h,4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-8-yl (2z)-2-methylbut-2-enoate

C20H28O4 (332.19874880000003)


   

(2e)-3-(4-{[(2e)-3,7-dimethylocta-2,6-dien-1-yl]oxy}-3-methoxyphenyl)prop-2-en-1-ol

(2e)-3-(4-{[(2e)-3,7-dimethylocta-2,6-dien-1-yl]oxy}-3-methoxyphenyl)prop-2-en-1-ol

C20H28O3 (316.2038338)


   

(4ar,5s,8r,8ar)-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-8-yl (2z)-2-methylbut-2-enoate

(4ar,5s,8r,8ar)-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-8-yl (2z)-2-methylbut-2-enoate

C20H28O3 (316.2038338)