NCBI Taxonomy: 81509

Pegolettia (ncbi_taxid: 81509)

found 76 associated metabolites at genus taxonomy rank level.

Ancestor: Plucheinae

Child Taxonomies: Pegolettia plumosa, Pegolettia gariepina, Pegolettia oxyodonta, Pegolettia lanceolata, Pegolettia retrofracta, Pegolettia senegalensis, Pegolettia pinnatilobata, Pegolettia baccharidifolia

Globulol

(1aR,4R,4aS,7R,7aS,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol

C15H26O (222.1984)


Ledol is a sesquiterpenoid. Ledol is a natural product found in Waitzia acuminata, Aloysia gratissima, and other organisms with data available. Ledol is found in allspice. Ledol is a constituent of Valeriana officinalis (valerian), Piper species and others. Constituent of Eucalyptus globulus (Tasmanian blue gum). Globulol is found in allspice and pepper (spice). Ledol ((+)-Ledol) is an antifungal agent that can be isolated from the essential oil fractions of Rhododendron tomentosum. Ledol is also the expectorant and antitussive agent, which is simultaneously responsible for adverse reactions such as dizziness, nausea and vomiting[1]. Ledol ((+)-Ledol) is an antifungal agent that can be isolated from the essential oil fractions of Rhododendron tomentosum. Ledol is also the expectorant and antitussive agent, which is simultaneously responsible for adverse reactions such as dizziness, nausea and vomiting[1].

   

Lupeyl acetate

[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-1-isopropenyl-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate

C32H52O2 (468.3967)


Lupeol acetate is an organic molecular entity. It has a role as a metabolite. Lupeol acetate is a natural product found in Euphorbia dracunculoides, Euphorbia larica, and other organisms with data available. Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1]. Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1].

   

Thymol

Thymol, Pharmaceutical Secondary Standard; Certified Reference Material

C10H14O (150.1045)


Thymol is a phenol that is a natural monoterpene derivative of cymene. It has a role as a volatile oil component. It is a member of phenols and a monoterpenoid. It derives from a hydride of a p-cymene. A phenol obtained from thyme oil or other volatile oils. It is used as a stabilizer in pharmaceutic preparations. It has been used for its antiseptic, antibacterial, and antifungal actions, and was formerly used as a vermifuge. (Dorland, 28th ed) Thymol is a natural product found in Xylopia aromatica, Xylopia sericea, and other organisms with data available. A phenol obtained from thyme oil or other volatile oils used as a stabilizer in pharmaceutical preparations, and as an antiseptic (antibacterial or antifungal) agent. See also: Paeonia lactiflora root (part of); Elymus repens root (part of); Eucalyptol; thymol (component of) ... View More ... Thymol is a phenol obtained from thyme oil or other volatile oils. It is used as a stabilizer in pharmaceutic preparations. It has been used for its antiseptic, antibacterial, and antifungal actions, and was formerly used as a vermifuge. Thymol is a monoterpene phenol derivative of cymene, C10H13OH, isomeric with carvacrol, found in oil of thyme, and extracted as a white crystalline substance of a pleasant aromatic odor and strong antiseptic properties. It is also called "hydroxy cymene". In a 1994 report released by five top cigarette companies, thymol is one of the 599 additives to cigarettes. Its use or purpose, however, is unknown, like most cigarette additives. Found in many essential oils. Especies found in the Labiatae. Rich sources are thyme oil, seed oil of Ptychotis ajowan and oils of horsemint (Monarda punctata) and Ocimum subspecies Flavouring ingredient C254 - Anti-Infective Agent > C28394 - Topical Anti-Infective Agent D000890 - Anti-Infective Agents > D000935 - Antifungal Agents A phenol that is a natural monoterpene derivative of cymene. Thymol is the main monoterpene phenol occurring in essential oils isolated from plants belonging to the Lamiaceae family, and other plants such as those belonging to the Verbenaceae, Scrophulariaceae, Ranunculaceae and Apiaceae families. Thymol has antioxidant, anti-inflammatory, antibacterial and antifungal effects[1]. Thymol is the main monoterpene phenol occurring in essential oils isolated from plants belonging to the Lamiaceae family, and other plants such as those belonging to the Verbenaceae, Scrophulariaceae, Ranunculaceae and Apiaceae families. Thymol has antioxidant, anti-inflammatory, antibacterial and antifungal effects[1].

   

Tomentosin

(3aR,7S,8aR)-7-methyl-3-methylidene-6-(3-oxobutyl)-4,7,8,8a-tetrahydro-3aH-cyclohepta[b]furan-2-one

C15H20O3 (248.1412)


Tomentosin is a sesquiterpene lactone. Tomentosin is a natural product found in Apalochlamys spectabilis, Leucophyta brownii, and other organisms with data available.

   

gamma-Humulene

(1E,6Z)-1,8,8-trimethyl-5-methylidenecycloundeca-1,6-diene (1E,6Z)-humula-1(11),4(13),5-triene

C15H24 (204.1878)


   

Taraxasterol

(3S,4aR,6aR,6aR,6bR,8aR,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol

C30H50O (426.3861)


Constituent of dandelion roots (Taraxacum officinale), Roman chamomile flowers (Anthemis nobilis) and many other plants. Taraxasterol is found in many foods, some of which are soy bean, chicory, evening primrose, and common grape. Taraxasterol is found in alcoholic beverages. Taraxasterol is a constituent of dandelion roots (Taraxacum officinale), Roman chamomile flowers (Anthemis nobilis) and many other plants Taraxasterol is a pentacyclic triterpenoid isolated from Taraxacum mongolicum. Taraxasterol has a role as a metabolite and an anti-inflammatory agent[1]. Taraxasterol is a pentacyclic triterpenoid isolated from Taraxacum mongolicum. Taraxasterol has a role as a metabolite and an anti-inflammatory agent[1].

   

alpha-eudesmol

2-(4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl)propan-2-ol

C15H26O (222.1984)


A eudesmane sesquiterpenoid in which the eudesmane skeleton carries a hydroxy substituent at C-11 and has a double bond between C-3 and C-4.

   

Germacrene D

(1E,6E,8S)-1-methyl-8-(1-methylethyl)-5-methylidenecyclodeca-1,6-diene

C15H24 (204.1878)


Germacrene d, also known as germacrene d, (s-(e,e))-isomer, is a member of the class of compounds known as germacrane sesquiterpenoids. Germacrane sesquiterpenoids are sesquiterpenoids having the germacrane skeleton, with a structure characterized by a cyclodecane ring substituted with an isopropyl and two methyl groups. Germacrene d can be found in a number of food items such as peppermint, roman camomile, hyssop, and common walnut, which makes germacrene d a potential biomarker for the consumption of these food products.

   

Geranyl 3-methylbutanoate

Butanoic acid, 3-methyl-, (2E)-3,7-dimethyl-2,6-octadienyl ester

C15H26O2 (238.1933)


Constituent of various plant subspecies including kumquat peel oil and lovage leaf and root. Flavouring ingredient. Geranyl 3-methylbutanoate is found in citrus, herbs and spices, and fruits. Neryl isovalerate is a constituent of numerous plant species Neryl isovalerate is a flavouring agent

   

Thymol

[5-methyl-2-(propan-2-yl)phenyl]oxidanesulfonic acid

C10H14O (150.1045)


Thymol Sulfate is also known as Thymol sulfuric acid. Thymol Sulfate is considered to be practically insoluble (in water) and acidic. Thymol (also known as 2-isopropyl-5-methylphenol, IPMP), C10H14O, is a natural monoterpenoid phenol derivative of p-Cymene, isomeric with carvacrol, found in oil of thyme, and extracted from Thymus vulgaris (common thyme), ajwain,[4] and various other plants as a white crystalline substance of a pleasant aromatic odor and strong antiseptic properties. Thymol also provides the distinctive, strong flavor of the culinary herb thyme, also produced from T. vulgaris. Thymol is only slightly soluble in water at neutral pH, but it is extremely soluble in alcohols and other organic solvents. It is also soluble in strongly alkaline aqueous solutions due to deprotonation of the phenol. Its dissociation constant (pKa) is 10.59±0.10.[5] Thymol absorbs maximum UV radiation at 274 nm.[6] Ancient Egyptians used thyme for embalming.[9] The ancient Greeks used it in their baths and burned it as incense in their temples, believing it was a source of courage. The spread of thyme throughout Europe was thought to be due to the Romans, as they used it to purify their rooms and to "give an aromatic flavour to cheese and liqueurs".[10] In the European Middle Ages, the herb was placed beneath pillows to aid sleep and ward off nightmares.[11] In this period, women also often gave knights and warriors gifts that included thyme leaves, because it was believed to bring courage to the bearer. Thyme was also used as incense and placed on coffins during funerals, because it was supposed to ensure passage into the next life.[12] The bee balms Monarda fistulosa and Monarda didyma, North American wildflowers, are natural sources of thymol. The Blackfoot Native Americans recognized these plants' strong antiseptic action and used poultices of the plants for skin infections and minor wounds. A tisane made from them was also used to treat mouth and throat infections caused by dental caries and gingivitis.[13] Thymol was first isolated by German chemist Caspar Neumann in 1719.[14] In 1853, French chemist Alexandre Lallemand[15] (1816-1886) named thymol and determined its empirical formula.[16] Thymol was first synthesized by Swedish chemist Oskar Widman[17] (1852-1930) in 1882.[18]

   

Lupeol acetate

1,2,5,14,18,18-hexamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-yl acetate

C32H52O2 (468.3967)


   

Taraxasterol acetate

4,4,6a,6b,8a,12,14b-Heptamethyl-11-methylidene-docosahydropicen-3-yl acetic acid

C32H52O2 (468.3967)


Taraxasterol acetate, also known as urs-20(30)-en-3-ol acetate, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Taraxasterol acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Taraxasterol acetate can be found in burdock, which makes taraxasterol acetate a potential biomarker for the consumption of this food product.

   

Taraxasterol

(3S,4aR,6aR,6aR,6bR,8aR,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol

C30H50O (426.3861)


Taraxasterol is a pentacyclic triterpenoid that is taraxastane with a beta-hydroxy group at position 3. It has a role as a metabolite and an anti-inflammatory agent. It is a pentacyclic triterpenoid and a secondary alcohol. It derives from a hydride of a taraxastane. Taraxasterol is a natural product found in Eupatorium altissimum, Eupatorium perfoliatum, and other organisms with data available. See also: Calendula Officinalis Flower (part of). A pentacyclic triterpenoid that is taraxastane with a beta-hydroxy group at position 3. Taraxasterol is a pentacyclic triterpenoid isolated from Taraxacum mongolicum. Taraxasterol has a role as a metabolite and an anti-inflammatory agent[1]. Taraxasterol is a pentacyclic triterpenoid isolated from Taraxacum mongolicum. Taraxasterol has a role as a metabolite and an anti-inflammatory agent[1].

   

Lupeol acetate

Acetic acid (1R,3aR,4S,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-1-isopropenyl-3a,5a,5b,8,8,11a-hexamethyl-eicosahydro-cyclopenta[a]chrysen-9-yl ester

C32H52O2 (468.3967)


Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1]. Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1].

   

Germacrene D

1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)-, [s-(E,E)]-

C15H24 (204.1878)


(-)-germacrene D is a germacrene D. It is an enantiomer of a (+)-germacrene D. (-)-Germacrene D is a natural product found in Teucrium montanum, Stachys obliqua, and other organisms with data available. See also: Clary Sage Oil (part of).

   

Ledol

(1aR,4R,4aS,7R,7aS,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol

C15H26O (222.1984)


Ledol is a sesquiterpenoid. Ledol is a natural product found in Waitzia acuminata, Aloysia gratissima, and other organisms with data available. Constituent of Valeriana officinalis (valerian), Piper subspecies and others. Ledol is found in many foods, some of which are fats and oils, common sage, tea, and allspice. Ledol ((+)-Ledol) is an antifungal agent that can be isolated from the essential oil fractions of Rhododendron tomentosum. Ledol is also the expectorant and antitussive agent, which is simultaneously responsible for adverse reactions such as dizziness, nausea and vomiting[1]. Ledol ((+)-Ledol) is an antifungal agent that can be isolated from the essential oil fractions of Rhododendron tomentosum. Ledol is also the expectorant and antitussive agent, which is simultaneously responsible for adverse reactions such as dizziness, nausea and vomiting[1].

   

neryl isovalerate

neryl isovalerate

C15H26O2 (238.1933)


   

octadecane-1,3-diol

octadecane-1,3-diol

C18H38O2 (286.2872)


   

Thymol

InChI=1\C10H14O\c1-7(2)9-5-4-8(3)6-10(9)11\h4-7,11H,1-3H

C10H14O (150.1045)


Thymol, also known as 1-hydroxy-5-methyl-2-isopropylbenzene or 2-isopropyl-5-methylphenol, is a member of the class of compounds known as aromatic monoterpenoids. Aromatic monoterpenoids are monoterpenoids containing at least one aromatic ring. Thus, thymol is considered to be an isoprenoid lipid molecule. Thymol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Thymol can be synthesized from p-cymene. Thymol can also be synthesized into thymol sulfate and thymol sulfate(1-). Thymol is a camphor, herbal, and medicinal tasting compound and can be found in a number of food items such as anise, common oregano, caraway, and highbush blueberry, which makes thymol a potential biomarker for the consumption of these food products. Thymol can be found primarily in saliva and urine, as well as in human liver and skeletal muscle tissues. Thymol exists in all eukaryotes, ranging from yeast to humans. C254 - Anti-Infective Agent > C28394 - Topical Anti-Infective Agent D000890 - Anti-Infective Agents > D000935 - Antifungal Agents Thymol is the main monoterpene phenol occurring in essential oils isolated from plants belonging to the Lamiaceae family, and other plants such as those belonging to the Verbenaceae, Scrophulariaceae, Ranunculaceae and Apiaceae families. Thymol has antioxidant, anti-inflammatory, antibacterial and antifungal effects[1]. Thymol is the main monoterpene phenol occurring in essential oils isolated from plants belonging to the Lamiaceae family, and other plants such as those belonging to the Verbenaceae, Scrophulariaceae, Ranunculaceae and Apiaceae families. Thymol has antioxidant, anti-inflammatory, antibacterial and antifungal effects[1].

   

geranyl isovalerate

(2Z)-3,7-dimethylocta-2,6-dien-1-yl 3-methylbutanoate

C15H26O2 (238.1933)


   

(1Z,6E)-gamma-humulene

(1Z,6E)-1,8,8-trimethyl-5-methylidenecycloundeca-1,6-diene (1Z,6E)-humula-1(11),4(13),5-triene

C15H24 (204.1878)


   

473-16-5

2-Naphthalenemethanol, 1,2,3,4,4a,5,6,8a-octahydro-alpha,alpha,4a,8-tetramethyl-, (2R,4aR,8aR)-

C15H26O (222.1984)


   

Lupeol acetate

1,2,5,14,18,18-hexamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-yl acetate

C32H52O2 (468.3967)


Lupeyl acetate, also known as lupeyl acetic acid, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Lupeyl acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Lupeyl acetate can be found in burdock, date, and fig, which makes lupeyl acetate a potential biomarker for the consumption of these food products. Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1]. Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1].

   

3-(3,4-dihydroxyphenyl)propyl (3s)-3-hydroxydocosanoate

3-(3,4-dihydroxyphenyl)propyl (3s)-3-hydroxydocosanoate

C31H54O5 (506.3971)


   

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

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

C15H20O3 (248.1412)


   

(3ar,4r,5as,6s,9ar,9bs)-4,6-dihydroxy-5a,9-dimethyl-3-methylidene-3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-2-one

(3ar,4r,5as,6s,9ar,9bs)-4,6-dihydroxy-5a,9-dimethyl-3-methylidene-3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-2-one

C15H20O4 (264.1362)


   

(3as,11as)-6,10-dimethyl-3-methylidene-3ah,5h,8h,9h,11ah-cyclodeca[b]furan-2,4-dione

(3as,11as)-6,10-dimethyl-3-methylidene-3ah,5h,8h,9h,11ah-cyclodeca[b]furan-2,4-dione

C15H18O3 (246.1256)


   

(1ar,4r,7r,7bs)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-ol

(1ar,4r,7r,7bs)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-ol

C15H26O (222.1984)


   

6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl furan-3-carboxylate

6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl furan-3-carboxylate

C20H22O5 (342.1467)


   

(3ar,11as)-6,10-dimethyl-3-methylidene-3ah,5h,8h,9h,11ah-cyclodeca[b]furan-2,4-dione

(3ar,11as)-6,10-dimethyl-3-methylidene-3ah,5h,8h,9h,11ah-cyclodeca[b]furan-2,4-dione

C15H18O3 (246.1256)


   

4,6-dihydroxy-5a,9-dimethyl-3-methylidene-3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-2-one

4,6-dihydroxy-5a,9-dimethyl-3-methylidene-3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-2-one

C15H20O4 (264.1362)


   

5a,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-4-yl 4-hydroxy-2-methylbut-2-enoate

5a,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-4-yl 4-hydroxy-2-methylbut-2-enoate

C20H26O5 (346.178)


   

(4r,4as,7s,7as)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-ol

(4r,4as,7s,7as)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-ol

C15H26O (222.1984)


   

6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl 2-(hydroxymethyl)but-2-enoate

6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl 2-(hydroxymethyl)but-2-enoate

C20H26O5 (346.178)


   

(2z,6e,10z)-6,10-dimethyl-2-(4-methylpent-3-en-1-yl)dodeca-2,6,10-triene-1,12-diol

(2z,6e,10z)-6,10-dimethyl-2-(4-methylpent-3-en-1-yl)dodeca-2,6,10-triene-1,12-diol

C20H34O2 (306.2559)


   

6,10-dimethyl-3-methylidene-3ah,5h,8h,9h,11ah-cyclodeca[b]furan-2,4-dione

6,10-dimethyl-3-methylidene-3ah,5h,8h,9h,11ah-cyclodeca[b]furan-2,4-dione

C15H18O3 (246.1256)


   

6,10-dimethyl-2-(4-methylpent-3-en-1-yl)dodeca-2,6,10-triene-1,12-diol

6,10-dimethyl-2-(4-methylpent-3-en-1-yl)dodeca-2,6,10-triene-1,12-diol

C20H34O2 (306.2559)


   

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

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

C15H20O3 (248.1412)


   

3,7-dimethylocta-2,6-dien-1-yl 3-methylbutanoate

3,7-dimethylocta-2,6-dien-1-yl 3-methylbutanoate

C15H26O2 (238.1933)


   

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

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

C15H20O3 (248.1412)


   

2-[(1r,3e,7e,10r)-4,8-dimethyl-10-[(3-methylbutanoyl)oxy]cyclodeca-3,7-dien-1-yl]prop-2-enoic acid

2-[(1r,3e,7e,10r)-4,8-dimethyl-10-[(3-methylbutanoyl)oxy]cyclodeca-3,7-dien-1-yl]prop-2-enoic acid

C20H30O4 (334.2144)


   

(3ar,4r,11as)-6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl (2e)-4-hydroxy-2-methylbut-2-enoate

(3ar,4r,11as)-6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl (2e)-4-hydroxy-2-methylbut-2-enoate

C20H26O5 (346.178)


   

(6s,7e)-1-hydroxy-3,8-dimethyl-5-oxatricyclo[10.1.1.0²,⁶]tetradeca-2,7,11-trien-4-one

(6s,7e)-1-hydroxy-3,8-dimethyl-5-oxatricyclo[10.1.1.0²,⁶]tetradeca-2,7,11-trien-4-one

C15H18O3 (246.1256)


   

6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl 4-hydroxy-2-methylbut-2-enoate

6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl 4-hydroxy-2-methylbut-2-enoate

C20H26O5 (346.178)


   

6-ethenyl-6-methyl-3-methylidene-2-oxo-7-(prop-1-en-2-yl)-tetrahydro-3ah-1-benzofuran-4-yl 4-hydroxy-2-methylbut-2-enoate

6-ethenyl-6-methyl-3-methylidene-2-oxo-7-(prop-1-en-2-yl)-tetrahydro-3ah-1-benzofuran-4-yl 4-hydroxy-2-methylbut-2-enoate

C20H26O5 (346.178)


   

3-(3,4-dihydroxyphenyl)propyl 3-hydroxyoctadecanoate

3-(3,4-dihydroxyphenyl)propyl 3-hydroxyoctadecanoate

C27H46O5 (450.3345)


   

(3ar,4r,11as)-6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl (5r)-5-hydroxy-2,5-dihydrofuran-3-carboxylate

(3ar,4r,11as)-6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl (5r)-5-hydroxy-2,5-dihydrofuran-3-carboxylate

C20H24O6 (360.1573)


   

2-[(1r,3e,7e,10r)-4,8-dimethyl-10-{[(2r)-2-methylbutanoyl]oxy}cyclodeca-3,7-dien-1-yl]prop-2-enoic acid

2-[(1r,3e,7e,10r)-4,8-dimethyl-10-{[(2r)-2-methylbutanoyl]oxy}cyclodeca-3,7-dien-1-yl]prop-2-enoic acid

C20H30O4 (334.2144)


   

(3ar,4r,5as,9as,9bs)-5a,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-4-yl furan-3-carboxylate

(3ar,4r,5as,9as,9bs)-5a,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-4-yl furan-3-carboxylate

C20H22O5 (342.1467)


   

(3ar,4r,5as,9as,9bs)-5a,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-4-yl (2e)-4-hydroxy-2-methylbut-2-enoate

(3ar,4r,5as,9as,9bs)-5a,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-4-yl (2e)-4-hydroxy-2-methylbut-2-enoate

C20H26O5 (346.178)


   

3-(3,4-dihydroxyphenyl)propyl 3-hydroxyicosanoate

3-(3,4-dihydroxyphenyl)propyl 3-hydroxyicosanoate

C29H50O5 (478.3658)


   

6-ethenyl-6-methyl-3-methylidene-2-oxo-7-(prop-1-en-2-yl)-tetrahydro-3ah-1-benzofuran-4-yl 4-hydroxy-2-(hydroxymethyl)but-2-enoate

6-ethenyl-6-methyl-3-methylidene-2-oxo-7-(prop-1-en-2-yl)-tetrahydro-3ah-1-benzofuran-4-yl 4-hydroxy-2-(hydroxymethyl)but-2-enoate

C20H26O6 (362.1729)


   

(4ar,6ar,6br,8ar,12as,12bs,14as,14br)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-hexadecahydropicen-3-yl acetate

(4ar,6ar,6br,8ar,12as,12bs,14as,14br)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-hexadecahydropicen-3-yl acetate

C32H52O2 (468.3967)


   

2-[(1r,3e,7e,10r)-4,8-dimethyl-10-{[(2e)-2-methylbut-2-enoyl]oxy}cyclodeca-3,7-dien-1-yl]prop-2-enoic acid

2-[(1r,3e,7e,10r)-4,8-dimethyl-10-{[(2e)-2-methylbut-2-enoyl]oxy}cyclodeca-3,7-dien-1-yl]prop-2-enoic acid

C20H28O4 (332.1987)


   

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

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

C15H20O3 (248.1412)


   

5a-methyl-3,9-dimethylidene-2-oxo-octahydronaphtho[1,2-b]furan-4-yl furan-3-carboxylate

5a-methyl-3,9-dimethylidene-2-oxo-octahydronaphtho[1,2-b]furan-4-yl furan-3-carboxylate

C20H22O5 (342.1467)


   

1-hydroxy-3,8-dimethyl-5-oxatricyclo[10.1.1.0²,⁶]tetradeca-2,7,11-trien-4-one

1-hydroxy-3,8-dimethyl-5-oxatricyclo[10.1.1.0²,⁶]tetradeca-2,7,11-trien-4-one

C15H18O3 (246.1256)


   

3-(3,4-dihydroxyphenyl)propyl (3s)-3-hydroxyoctadecanoate

3-(3,4-dihydroxyphenyl)propyl (3s)-3-hydroxyoctadecanoate

C27H46O5 (450.3345)


   

5a,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-4-yl furan-3-carboxylate

5a,9-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,6h,7h,9ah,9bh-naphtho[1,2-b]furan-4-yl furan-3-carboxylate

C20H22O5 (342.1467)


   

3-(3,4-dihydroxyphenyl)propyl 3-hydroxydocosanoate

3-(3,4-dihydroxyphenyl)propyl 3-hydroxydocosanoate

C31H54O5 (506.3971)


   

6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl 5-hydroxy-2,5-dihydrofuran-3-carboxylate

6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl 5-hydroxy-2,5-dihydrofuran-3-carboxylate

C20H24O6 (360.1573)


   

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

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

C15H20O3 (248.1412)


   

(3ar,4r,11as)-6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl furan-3-carboxylate

(3ar,4r,11as)-6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl furan-3-carboxylate

C20H22O5 (342.1467)


   

(3ar,4r,11as)-4-hydroxy-6,10-dimethyl-3-methylidene-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-one

(3ar,4r,11as)-4-hydroxy-6,10-dimethyl-3-methylidene-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-2-one

C15H20O3 (248.1412)


   

6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl 4-hydroxy-2-(hydroxymethyl)but-2-enoate

6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl 4-hydroxy-2-(hydroxymethyl)but-2-enoate

C20H26O6 (362.1729)


   

2-{4,8-dimethyl-10-[(2-methylbut-2-enoyl)oxy]cyclodeca-3,7-dien-1-yl}prop-2-enoic acid

2-{4,8-dimethyl-10-[(2-methylbut-2-enoyl)oxy]cyclodeca-3,7-dien-1-yl}prop-2-enoic acid

C20H28O4 (332.1987)


   

(3s)-octadecane-1,3-diol

(3s)-octadecane-1,3-diol

C18H38O2 (286.2872)


   

8-isopropyl-1-methyl-5-methylidenecyclodeca-1,6-diene

8-isopropyl-1-methyl-5-methylidenecyclodeca-1,6-diene

C15H24 (204.1878)


   

(3as,4r,6r,7r,7as)-6-ethenyl-6-methyl-3-methylidene-2-oxo-7-(prop-1-en-2-yl)-tetrahydro-3ah-1-benzofuran-4-yl (2e)-4-hydroxy-2-methylbut-2-enoate

(3as,4r,6r,7r,7as)-6-ethenyl-6-methyl-3-methylidene-2-oxo-7-(prop-1-en-2-yl)-tetrahydro-3ah-1-benzofuran-4-yl (2e)-4-hydroxy-2-methylbut-2-enoate

C20H26O5 (346.178)


   

2-{4,8-dimethyl-10-[(2-methylbutanoyl)oxy]cyclodeca-3,7-dien-1-yl}prop-2-enoic acid

2-{4,8-dimethyl-10-[(2-methylbutanoyl)oxy]cyclodeca-3,7-dien-1-yl}prop-2-enoic acid

C20H30O4 (334.2144)


   

(3as,4r,6r,7r,7as)-6-ethenyl-6-methyl-3-methylidene-2-oxo-7-(prop-1-en-2-yl)-tetrahydro-3ah-1-benzofuran-4-yl (2e)-4-hydroxy-2-(hydroxymethyl)but-2-enoate

(3as,4r,6r,7r,7as)-6-ethenyl-6-methyl-3-methylidene-2-oxo-7-(prop-1-en-2-yl)-tetrahydro-3ah-1-benzofuran-4-yl (2e)-4-hydroxy-2-(hydroxymethyl)but-2-enoate

C20H26O6 (362.1729)


   

2-{4,8-dimethyl-10-[(3-methylbutanoyl)oxy]cyclodeca-3,7-dien-1-yl}prop-2-enoic acid

2-{4,8-dimethyl-10-[(3-methylbutanoyl)oxy]cyclodeca-3,7-dien-1-yl}prop-2-enoic acid

C20H30O4 (334.2144)


   

3-(3,4-dihydroxyphenyl)propyl (3s)-3-hydroxyicosanoate

3-(3,4-dihydroxyphenyl)propyl (3s)-3-hydroxyicosanoate

C29H50O5 (478.3658)


   

(3ar,4r,11as)-6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl (2e)-2-(hydroxymethyl)but-2-enoate

(3ar,4r,11as)-6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl (2e)-2-(hydroxymethyl)but-2-enoate

C20H26O5 (346.178)


   

(3ar,4r,5as,9ar,9bs)-5a-methyl-3,9-dimethylidene-2-oxo-octahydronaphtho[1,2-b]furan-4-yl furan-3-carboxylate

(3ar,4r,5as,9ar,9bs)-5a-methyl-3,9-dimethylidene-2-oxo-octahydronaphtho[1,2-b]furan-4-yl furan-3-carboxylate

C20H22O5 (342.1467)


   

(3ar,4r,11as)-6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl (2e)-4-hydroxy-2-(hydroxymethyl)but-2-enoate

(3ar,4r,11as)-6,10-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,11ah-cyclodeca[b]furan-4-yl (2e)-4-hydroxy-2-(hydroxymethyl)but-2-enoate

C20H26O6 (362.1729)