NCBI Taxonomy: 186954

Ligularia fischeri (ncbi_taxid: 186954)

found 113 associated metabolites at species taxonomy rank level.

Ancestor: Ligularia

Child Taxonomies: Ligularia fischeri var. spiciformis

alpha-Farnesene

3,7,11-Trimethyl-1,3,6,10-dodecatetraene, (trans,trans)-

C15H24 (204.1878)


alpha-Farnesene belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. (3E,6E)-alpha-Farnesene, also known as trans-alpha-Farnesene, is a sweet, bergamot, and citrus tasting flavouring ingredient. (3E,6E)-alpha-Farnesene is a constituent of the natural coating of apples and pears and other fruit. It has been identified in gingers, cottonseeds, common oregano, sweet oranges, spearmints, guava, pomes, and pears. This could make (3E,6E)-alpha-farnesene a potential biomarker for the consumption of these foods. Alpha-farnesene is a farnesene that is 1,3,6,10-tetraene substituted by methyl groups at positions 3, 7 and 11 respectively. alpha-Farnesene is a natural product found in Eupatorium cannabinum, Lonicera japonica, and other organisms with data available. See also: Chamomile (part of); Cannabis sativa subsp. indica top (part of). Constituent of the natural coating of apples and pears and other fruit. Flavouring ingredient. (3E,6E)-alpha-Farnesene is found in many foods, some of which are cottonseed, spearmint, ginger, and fruits.

   

Squalene

InChI=1/C30H50/c1-25(2)15-11-19-29(7)23-13-21-27(5)17-9-10-18-28(6)22-14-24-30(8)20-12-16-26(3)4/h15-18,23-24H,9-14,19-22H2,1-8H3/b27-17+,28-18+,29-23+,30-24

C30H50 (410.3912)


Squalene is an unsaturated aliphatic hydrocarbon (carotenoid) with six unconjugated double bonds found in human sebum (5\\\\%), fish liver oils, yeast lipids, and many vegetable oils (e.g. palm oil, cottonseed oil, rapeseed oil). Squalene is a volatile component of the scent material from Saguinus oedipus (cotton-top tamarin monkey) and Saguinus fuscicollis (saddle-back tamarin monkey) (Hawleys Condensed Chemical Reference). Squalene is a component of adult human sebum that is principally responsible for fixing fingerprints (ChemNetBase). It is a natural organic compound originally obtained for commercial purposes primarily from shark liver oil, though there are botanical sources as well, including rice bran, wheat germ, and olives. All higher organisms produce squalene, including humans. It is a hydrocarbon and a triterpene. Squalene is a biochemical precursor to the whole family of steroids. Oxidation of one of the terminal double bonds of squalene yields 2,3-squalene oxide which undergoes enzyme-catalyzed cyclization to afford lanosterol, which is then elaborated into cholesterol and other steroids. Squalene is a low-density compound often stored in the bodies of cartilaginous fishes such as sharks, which lack a swim bladder and must therefore reduce their body density with fats and oils. Squalene, which is stored mainly in the sharks liver, is lighter than water with a specific gravity of 0.855 (Wikipedia) Squalene is used as a bactericide. It is also an intermediate in the manufacture of pharmaceuticals, rubber chemicals, and colouring materials (Physical Constants of Chemical Substances). Trans-squalene is a clear, slightly yellow liquid with a faint odor. Density 0.858 g / cm3. Squalene is a triterpene consisting of 2,6,10,15,19,23-hexamethyltetracosane having six double bonds at the 2-, 6-, 10-, 14-, 18- and 22-positions with (all-E)-configuration. It has a role as a human metabolite, a plant metabolite, a Saccharomyces cerevisiae metabolite and a mouse metabolite. Squalene is originally obtained from shark liver oil. It is a natural 30-carbon isoprenoid compound and intermediate metabolite in the synthesis of cholesterol. It is not susceptible to lipid peroxidation and provides skin protection. It is ubiquitously distributed in human tissues where it is transported in serum generally in association with very low density lipoproteins. Squalene is investigated as an adjunctive cancer therapy. Squalene is a natural product found in Ficus septica, Garcinia multiflora, and other organisms with data available. squalene is a metabolite found in or produced by Saccharomyces cerevisiae. A natural 30-carbon triterpene. See also: Olive Oil (part of); Shark Liver Oil (part of). A triterpene consisting of 2,6,10,15,19,23-hexamethyltetracosane having six double bonds at the 2-, 6-, 10-, 14-, 18- and 22-positions with (all-E)-configuration. COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Squalene is an intermediate product in the synthesis of cholesterol, and shows several pharmacological properties such as hypolipidemic, hepatoprotective, cardioprotective, antioxidant, and antitoxicant activity. Squalene also has anti-fungal activity and can be used for the research of Trichophyton mentagrophytes research[2]. Squalene is an intermediate product in the synthesis of cholesterol, and shows several pharmacological properties such as hypolipidemic, hepatoprotective, cardioprotective, antioxidant, and antitoxicant activity. Squalene also has anti-fungal activity and can be used for the research of Trichophyton mentagrophytes research[2].

   

Amyrin

(3S,4aR,5R,6aR,6bR,8S,8aR,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-eicosahydro-picen-3-ol

C30H50O (426.3861)


Beta-amyrin is a pentacyclic triterpenoid that is oleanane substituted at the 3beta-position by a hydroxy group and containing a double bond between positions 12 and 13. It is one of the most commonly occurring triterpenoids in higher plants. It has a role as a plant metabolite and an Aspergillus metabolite. It is a pentacyclic triterpenoid and a secondary alcohol. It derives from a hydride of an oleanane. beta-Amyrin is a natural product found in Ficus pertusa, Ficus septica, and other organisms with data available. See also: Calendula Officinalis Flower (part of); Viburnum opulus bark (part of); Centaurium erythraea whole (part of). A pentacyclic triterpenoid that is oleanane substituted at the 3beta-position by a hydroxy group and containing a double bond between positions 12 and 13. It is one of the most commonly occurring triterpenoids in higher plants. β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1]. β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1].

   

Epi-alpha-amyrin

(3S,4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-Octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-eicosahydro-picen-3-ol

C30H50O (426.3861)


Alpha-amyrin is a pentacyclic triterpenoid that is ursane which contains a double bond between positions 12 and 13 and in which the hydrogen at the 3beta position is substituted by a hydroxy group. It is a pentacyclic triterpenoid and a secondary alcohol. It derives from a hydride of an ursane. alpha-Amyrin is a natural product found in Ficus septica, Ficus virens, and other organisms with data available. See also: Calendula Officinalis Flower (part of); Viburnum opulus bark (part of); Eupatorium perfoliatum whole (part of) ... View More ... Carissol is found in beverages. Carissol is a constituent of Carissa carandas (karanda). Constituent of Carissa carandas (karanda). Carissol is found in beverages and fruits.

   

Spartioidine

Seneciphylline

C18H23NO5 (333.1576)


A pyrrolizine alkaloid that is 13,19-didehydrosenecionane carrying a hydroxy substituent at position 12 and two oxo substituents at positions 11 and 16. CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 2297 [Raw Data] CB082b_Seneciphylline_pos_40eV_CB000034.txt [Raw Data] CB082b_Seneciphylline_pos_30eV_CB000034.txt [Raw Data] CB082b_Seneciphylline_pos_20eV_CB000034.txt [Raw Data] CB082b_Seneciphylline_pos_10eV_CB000034.txt [Raw Data] CB082b_Seneciphylline_pos_50eV_CB000034.txt Seneciphylline is a toxic pyrrolizidine alkaloid in Gynura japonica[1]. Seneciphylline significantly increases the activities of epoxide hydrase and glutathione-S-transferase but causes reduction of cytochrome P-450 and related monooxygenase activities[2].

   

Sarracine

7-Angelyl-9-sarracinylplatynecine

C18H27NO5 (337.1889)


   

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.

   

(6beta,8alpha)-6-Hydroxy-7(11)-eremophilen-12,8-olide

4-hydroxy-3,4a,5-trimethyl-2H,4H,4aH,5H,6H,7H,8H,8aH,9H,9aH-naphtho[2,3-b]furan-2-one

C15H22O3 (250.1569)


(6beta,8alpha)-6-Hydroxy-7(11)-eremophilen-12,8-olide is found in giant butterbur. (6beta,8alpha)-6-Hydroxy-7(11)-eremophilen-12,8-olide is a constituent of Petasites japonicus (sweet coltsfoot) Constituent of Petasites japonicus (sweet coltsfoot). 6b-Hydroxy-7(11)-eremophilen-12,8a-olide is found in giant butterbur and green vegetables.

   

(6beta,8betaOH)-6,8-Dihydroxy-7(11)-eremophilen-12,8-olide

4,9a-dihydroxy-3,4a,5-trimethyl-2H,4H,4aH,5H,6H,7H,8H,8aH,9H,9aH-naphtho[2,3-b]furan-2-one

C15H22O4 (266.1518)


(6beta,8aOH)-6,8-Dihydroxy-7(11)-eremophilen-12,8-olide is found in green vegetables. (6beta,8aOH)-6,8-Dihydroxy-7(11)-eremophilen-12,8-olide is a constituent of Petasites japonicus (sweet coltsfoot). Constituent of Petasites japonicus (sweet coltsfoot). 6b,8a-Dihydroxy-7(11)-eremophilen-12,8-olide is found in green vegetables.

   

6b-Hydroxy-8a-methoxy-7(11)-eremophilen-12,8-olide

4-hydroxy-9a-methoxy-3,4a,5-trimethyl-2H,4H,4aH,5H,6H,7H,8H,8aH,9H,9aH-naphtho[2,3-b]furan-2-one

C16H24O4 (280.1675)


6b-Hydroxy-8a-methoxy-7(11)-eremophilen-12,8-olide is found in green vegetables. 6b-Hydroxy-8a-methoxy-7(11)-eremophilen-12,8-olide is a constituent of Petasites japonicus (sweet coltsfoot). Constituent of Petasites japonicus (sweet coltsfoot). 6b-Hydroxy-8a-methoxy-7(11)-eremophilen-12,8-olide is found in green vegetables.

   

Squalen

2,6,10,15,19,23-Hexamethyltetracosa-2,6,10,14,18,22-hexaene

C30H50 (410.3912)


   

Seneciphylline

4-ethylidene-7-hydroxy-7-methyl-6-methylidene-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11-ene-3,8-dione

C18H23NO5 (333.1576)


   

Methyl ferulate

Methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid

C11H12O4 (208.0736)


Methyl ferulate, also known as methyl ferulic acid, belongs to coumaric acids and derivatives class of compounds. Those are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring. Methyl ferulate is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Methyl ferulate can be found in garden onion, which makes methyl ferulate a potential biomarker for the consumption of this food product. Ferulic acid methyl ester (Methyl ferulate) is a derivative of ferulic acid, isolated from Stemona tuberosa, with anti-inflammatory and antioxidant properties[1][2]. Ferulic acid methyl ester is a cell membrane and brain permeable compound, shows free radical scavenging ability, used in the research of neurodegenerative disorders[1]. Ferulic acid methyl ester inhibits COX-2 expression, blocks p-p38 and p-JNK in primary bone marrow derived-macrophages[2]. Ferulic acid methyl ester (Methyl ferulate) is a derivative of ferulic acid, isolated from Stemona tuberosa, with anti-inflammatory and antioxidant properties[1][2]. Ferulic acid methyl ester is a cell membrane and brain permeable compound, shows free radical scavenging ability, used in the research of neurodegenerative disorders[1]. Ferulic acid methyl ester inhibits COX-2 expression, blocks p-p38 and p-JNK in primary bone marrow derived-macrophages[2].

   

1ST14177

(1,6)Dioxacyclododecino(2,3,4-gh)pyrrolizine-2,7-dione, 3-ethylidene-3,4,5,6,9,11,13,14,14a,14b-decahydro-6-hydroxy-6-methyl-5-methylene-, (3Z,6R,14aR,14bR)-

C18H23NO5 (333.1576)


Seneciphylline is a white powder. (NTP, 1992) LSM-2853 is a citraconoyl group. Seneciphylline is a natural product found in Senecio bollei, Tussilago farfara, and other organisms with data available. Seneciphylline is a toxic pyrrolizidine alkaloid in Gynura japonica[1]. Seneciphylline significantly increases the activities of epoxide hydrase and glutathione-S-transferase but causes reduction of cytochrome P-450 and related monooxygenase activities[2].

   

Platyphyllide

(8R-cis)-6,7,8,8a-Tetrahydro-8-(1-methylethenyl)-2H-naphtho[1,8-bc]furan-2-one

C14H14O2 (214.0994)


   

β-Amyrin

beta-amyrin-H2O

C30H50O (426.3861)


Beta-amyrin, also known as amyrin or (3beta)-olean-12-en-3-ol, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Thus, beta-amyrin is considered to be an isoprenoid lipid molecule. Beta-amyrin is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Beta-amyrin can be synthesized from oleanane. Beta-amyrin is also a parent compound for other transformation products, including but not limited to, erythrodiol, glycyrrhetaldehyde, and 24-hydroxy-beta-amyrin. Beta-amyrin can be found in a number of food items such as thistle, pepper (c. baccatum), wakame, and endive, which makes beta-amyrin a potential biomarker for the consumption of these food products. The amyrins are three closely related natural chemical compounds of the triterpene class. They are designated α-amyrin (ursane skeleton), β-amyrin (oleanane skeleton) and δ-amyrin. Each is a pentacyclic triterpenol with the chemical formula C30H50O. They are widely distributed in nature and have been isolated from a variety of plant sources such as epicuticular wax. In plant biosynthesis, α-amyrin is the precursor of ursolic acid and β-amyrin is the precursor of oleanolic acid. All three amyrins occur in the surface wax of tomato fruit. α-Amyrin is found in dandelion coffee . β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1]. β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1].

   

Methyl ferulate

(E)-Methyl-4-hydroxy-3-methoxycinnamate

C11H12O4 (208.0736)


Ferulic acid methyl ester (Methyl ferulate) is a derivative of ferulic acid, isolated from Stemona tuberosa, with anti-inflammatory and antioxidant properties[1][2]. Ferulic acid methyl ester is a cell membrane and brain permeable compound, shows free radical scavenging ability, used in the research of neurodegenerative disorders[1]. Ferulic acid methyl ester inhibits COX-2 expression, blocks p-p38 and p-JNK in primary bone marrow derived-macrophages[2]. Ferulic acid methyl ester (Methyl ferulate) is a derivative of ferulic acid, isolated from Stemona tuberosa, with anti-inflammatory and antioxidant properties[1][2]. Ferulic acid methyl ester is a cell membrane and brain permeable compound, shows free radical scavenging ability, used in the research of neurodegenerative disorders[1]. Ferulic acid methyl ester inhibits COX-2 expression, blocks p-p38 and p-JNK in primary bone marrow derived-macrophages[2].

   

Euparin

1-[6-hydroxy-2-(prop-1-en-2-yl)-1-benzofuran-5-yl]ethan-1-one

C13H12O3 (216.0786)


Euparin is a member of benzofurans. It has a role as a metabolite. Euparin is a natural product found in Eupatorium cannabinum, Liatris acidota, and other organisms with data available. A natural product found in Eupatorium cannabinum subspecies asiaticum.

   

methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C11H12O4 (208.0736)


   

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).

   

Squalene

InChI=1\C30H50\c1-25(2)15-11-19-29(7)23-13-21-27(5)17-9-10-18-28(6)22-14-24-30(8)20-12-16-26(3)4\h15-18,23-24H,9-14,19-22H2,1-8H3\b27-17+,28-18+,29-23+,30-24

C30H50 (410.3912)


Squalene, also known as (e,e,e,e)-squalene or all-trans-squalene, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Squalene can be found in a number of food items such as apricot, savoy cabbage, peach (variety), and bitter gourd, which makes squalene a potential biomarker for the consumption of these food products. Squalene can be found primarily in blood, feces, and sweat, as well as throughout most human tissues. In humans, squalene is involved in several metabolic pathways, some of which include risedronate action pathway, steroid biosynthesis, alendronate action pathway, and fluvastatin action pathway. Squalene is also involved in several metabolic disorders, some of which include cholesteryl ester storage disease, CHILD syndrome, hyper-igd syndrome, and wolman disease. Squalene is a natural 30-carbon organic compound originally obtained for commercial purposes primarily from shark liver oil (hence its name, as Squalus is a genus of sharks), although plant sources (primarily vegetable oils) are now used as well, including amaranth seed, rice bran, wheat germ, and olives. Yeast cells have been genetically engineered to produce commercially useful quantities of "synthetic" squalene . COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Window width to select the precursor ion was 3 Da.; CONE_VOLTAGE was 20 V.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 19HP8024 to the Mass Spectrometry Society of Japan. Squalene is an intermediate product in the synthesis of cholesterol, and shows several pharmacological properties such as hypolipidemic, hepatoprotective, cardioprotective, antioxidant, and antitoxicant activity. Squalene also has anti-fungal activity and can be used for the research of Trichophyton mentagrophytes research[2]. Squalene is an intermediate product in the synthesis of cholesterol, and shows several pharmacological properties such as hypolipidemic, hepatoprotective, cardioprotective, antioxidant, and antitoxicant activity. Squalene also has anti-fungal activity and can be used for the research of Trichophyton mentagrophytes research[2].

   

5-Acetyl-7-methoxybenzofuran

5-Acetyl-7-methoxybenzofuran

C11H10O3 (190.063)


   

Seneciphylline

Senenciphylline

C18H23NO5 (333.1576)


relative retention time with respect to 9-anthracene Carboxylic Acid is 0.402 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.399 Seneciphylline is a toxic pyrrolizidine alkaloid in Gynura japonica[1]. Seneciphylline significantly increases the activities of epoxide hydrase and glutathione-S-transferase but causes reduction of cytochrome P-450 and related monooxygenase activities[2].

   

6beta-Hydroxyeremphilenolide

4-hydroxy-3,4a,5-trimethyl-2H,4H,4aH,5H,6H,7H,8H,8aH,9H,9aH-naphtho[2,3-b]furan-2-one

C15H22O3 (250.1569)


   

6beta,8beta-Dihydroxyeremophilenolide

4,9a-dihydroxy-3,4a,5-trimethyl-2H,4H,4aH,5H,6H,7H,8H,8aH,9H,9aH-naphtho[2,3-b]furan-2-one

C15H22O4 (266.1518)


   

Isointermedeol

1,4a-dimethyl-7-(prop-1-en-2-yl)-decahydronaphthalen-1-ol

C15H26O (222.1984)


   

6-Hydroxy-8-methoxy-7(11)-eremophilen-12,8-olide

4-hydroxy-9a-methoxy-3,4a,5-trimethyl-2H,4H,4aH,5H,6H,7H,8H,8aH,9H,9aH-naphtho[2,3-b]furan-2-one

C16H24O4 (280.1675)


   

(1aR,4S,4aS,5S,9aS)-4,4a,6-Trimethyl-9-oxo-2,3,4,4a,5,9-hexahydro-1aH-oxireno[8,8a]naphtho[2,3-b]furan-5-yl 2-methylpropanoate

(1aR,4S,4aS,5S,9aS)-4,4a,6-Trimethyl-9-oxo-2,3,4,4a,5,9-hexahydro-1aH-oxireno[8,8a]naphtho[2,3-b]furan-5-yl 2-methylpropanoate

C19H24O5 (332.1624)


A natural product found in Pittocaulon velatum.

   

Farnesene

1,6,10-Dodecatriene, 7,11-dimethyl-3-methylene-, (6E)-

C15H24 (204.1878)


Isol. (without stereochemical distinction) from oil of Cymbopogon nardus (citronella), Cananga odorata (ylang ylang) and others (E)-β-Farnesene (trans-β-Farnesene) is a volatile sesquiterpene hydrocarbon which can be found in Phlomis aurea Decne essential oil. (E)-β-Farnesene can be used as a feeding stimulant for the sand fly Lutzomyia longipalpis[1][2]. (E)-β-Farnesene (trans-β-Farnesene) is a volatile sesquiterpene hydrocarbon which can be found in Phlomis aurea Decne essential oil. (E)-β-Farnesene can be used as a feeding stimulant for the sand fly Lutzomyia longipalpis[1][2].

   

viminalol

(3S,4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-Octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-eicosahydro-picen-3-ol

C30H50O (426.3861)


Alpha-amyrin is a pentacyclic triterpenoid that is ursane which contains a double bond between positions 12 and 13 and in which the hydrogen at the 3beta position is substituted by a hydroxy group. It is a pentacyclic triterpenoid and a secondary alcohol. It derives from a hydride of an ursane. alpha-Amyrin is a natural product found in Ficus septica, Ficus virens, and other organisms with data available. See also: Calendula Officinalis Flower (part of); Viburnum opulus bark (part of); Eupatorium perfoliatum whole (part of) ... View More ...

   

5-acetyl-6-hydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-3-yl 2-methylbut-2-enoate

5-acetyl-6-hydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-3-yl 2-methylbut-2-enoate

C18H20O5 (316.1311)


   

(1s,3s,4s,10s,11r)-4-[(4as,5r,9ar)-3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-9a-yl]-7,10,11-trimethyl-2,5-dioxatetracyclo[8.4.0.0¹,³.0⁴,⁸]tetradec-7-en-6-one

(1s,3s,4s,10s,11r)-4-[(4as,5r,9ar)-3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-9a-yl]-7,10,11-trimethyl-2,5-dioxatetracyclo[8.4.0.0¹,³.0⁴,⁸]tetradec-7-en-6-one

C30H38O5 (478.2719)


   

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

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

C30H38O4 (462.277)


   

1-[3,6-dihydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethanone

1-[3,6-dihydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethanone

C13H14O4 (234.0892)


   

4-{3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-9a-yl}-7,10,11-trimethyl-2,5-dioxatetracyclo[8.4.0.0¹,³.0⁴,⁸]tetradec-7-en-6-one

4-{3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-9a-yl}-7,10,11-trimethyl-2,5-dioxatetracyclo[8.4.0.0¹,³.0⁴,⁸]tetradec-7-en-6-one

C30H38O5 (478.2719)


   

(4r,4ar,5s,8r)-8-hydroxy-3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h-indeno[1,2-b]furan-4-yl 2-methylpropanoate

(4r,4ar,5s,8r)-8-hydroxy-3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h-indeno[1,2-b]furan-4-yl 2-methylpropanoate

C18H24O5 (320.1624)


   

(1r,11r)-7-hydroxy-11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-trien-3-one

(1r,11r)-7-hydroxy-11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-trien-3-one

C14H14O3 (230.0943)


   

9a-methoxy-3,4a,5-trimethyl-4h,5h,8ah,9h-naphtho[2,3-b]furan-2,6-dione

9a-methoxy-3,4a,5-trimethyl-4h,5h,8ah,9h-naphtho[2,3-b]furan-2,6-dione

C16H20O4 (276.1362)


   

(4ar,5s,8ar,9as)-9a-hydroxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2-one

(4ar,5s,8ar,9as)-9a-hydroxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2-one

C15H22O3 (250.1569)


   

3,3,5-trimethyl-4-[(3e,7e,11e)-3,8,12,16-tetramethylheptadeca-3,7,11,15-tetraen-1-yl]cyclohex-1-ene

3,3,5-trimethyl-4-[(3e,7e,11e)-3,8,12,16-tetramethylheptadeca-3,7,11,15-tetraen-1-yl]cyclohex-1-ene

C30H50 (410.3912)


   

7-(hydroxymethyl)-hexahydro-1h-pyrrolizin-1-yl 2-methylbut-2-enoate

7-(hydroxymethyl)-hexahydro-1h-pyrrolizin-1-yl 2-methylbut-2-enoate

C13H21NO3 (239.1521)


   

(2r,3s)-5-acetyl-6-hydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-3-yl (2z)-2-methylbut-2-enoate

(2r,3s)-5-acetyl-6-hydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-3-yl (2z)-2-methylbut-2-enoate

C18H20O5 (316.1311)


   

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

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

C19H25ClO5 (368.139)


   

(1s,8s,9s,10s,13r)-6,9,10-trimethyl-4,14-dioxatetracyclo[7.5.0.0¹,¹³.0³,⁷]tetradeca-3(7),5-dien-8-ol

(1s,8s,9s,10s,13r)-6,9,10-trimethyl-4,14-dioxatetracyclo[7.5.0.0¹,¹³.0³,⁷]tetradeca-3(7),5-dien-8-ol

C15H20O3 (248.1412)


   

1-[6-hydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethanone

1-[6-hydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethanone

C13H14O3 (218.0943)


   

(1s,4as,7r,8as)-1,4a-dimethyl-7-(prop-1-en-2-yl)-octahydronaphthalen-1-ol

(1s,4as,7r,8as)-1,4a-dimethyl-7-(prop-1-en-2-yl)-octahydronaphthalen-1-ol

C15H26O (222.1984)


   

9a-hydroxy-4-methoxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2-one

9a-hydroxy-4-methoxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2-one

C16H24O4 (280.1675)


   

(1r,7s,7ar)-7-(hydroxymethyl)-hexahydro-1h-pyrrolizin-1-yl (2z)-2-methylbut-2-enoate

(1r,7s,7ar)-7-(hydroxymethyl)-hexahydro-1h-pyrrolizin-1-yl (2z)-2-methylbut-2-enoate

C13H21NO3 (239.1521)


   

3,4a,5-trimethyl-4h,5h,8ah,9h,9ah-naphtho[2,3-b]furan-2,6-dione

3,4a,5-trimethyl-4h,5h,8ah,9h,9ah-naphtho[2,3-b]furan-2,6-dione

C15H18O3 (246.1256)


   

(4s,4ar,5s,8ar,9as)-9a-hydroxy-4-methoxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2-one

(4s,4ar,5s,8ar,9as)-9a-hydroxy-4-methoxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2-one

C16H24O4 (280.1675)


   

3,4a,5-trimethyl-4h,5h,8ah,9h-naphtho[2,3-b]furan-6-one

3,4a,5-trimethyl-4h,5h,8ah,9h-naphtho[2,3-b]furan-6-one

C15H18O2 (230.1307)


   

1-[(2r,3s)-3,6-dihydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethanone

1-[(2r,3s)-3,6-dihydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethanone

C13H14O4 (234.0892)


   

(4r,4as,5r,8as,9ar)-4-hydroxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h,9ah-naphtho[2,3-b]furan-2-one

(4r,4as,5r,8as,9ar)-4-hydroxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h,9ah-naphtho[2,3-b]furan-2-one

C15H22O3 (250.1569)


   

(4s,4as,5s,8s,8ar)-8-chloro-8a-hydroxy-3,4a,5-trimethyl-9-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-4-yl 2-methylpropanoate

(4s,4as,5s,8s,8ar)-8-chloro-8a-hydroxy-3,4a,5-trimethyl-9-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-4-yl 2-methylpropanoate

C19H25ClO5 (368.139)


   

(4s,4ar,5s,8ar,9ar)-4-hydroxy-9a-methoxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2-one

(4s,4ar,5s,8ar,9ar)-4-hydroxy-9a-methoxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2-one

C16H24O4 (280.1675)


   

(4s,4ar,5s,8ar,9as)-4-hydroxy-9a-methoxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2-one

(4s,4ar,5s,8ar,9as)-4-hydroxy-9a-methoxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2-one

C16H24O4 (280.1675)


   

(11z)-7-hydroxy-3',6,7,14-tetramethyl-2,9-dioxa-14-azaspiro[bicyclo[9.5.1]heptadecane-5,2'-oxiran]-11-ene-3,8,17-trione 7'-hydroxy-3,6',7',14'-tetramethyl-3',8'-dioxo-2',9'-dioxa-14'-azaspiro[oxirane-2,5'-tricyclo[9.5.1.0¹⁴,¹⁷]heptadecan]-11'-en-14'-ium-17'-olate

(11z)-7-hydroxy-3',6,7,14-tetramethyl-2,9-dioxa-14-azaspiro[bicyclo[9.5.1]heptadecane-5,2'-oxiran]-11-ene-3,8,17-trione 7'-hydroxy-3,6',7',14'-tetramethyl-3',8'-dioxo-2',9'-dioxa-14'-azaspiro[oxirane-2,5'-tricyclo[9.5.1.0¹⁴,¹⁷]heptadecan]-11'-en-14'-ium-17'-olate

C38H54N2O14 (762.3575)


   

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

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

C20H25ClO5 (380.139)


   

[(1s,7r,7ar)-7-{[(2z)-2-methylbut-2-enoyl]oxy}-hexahydro-1h-pyrrolizin-1-yl]methyl (2z)-2-{[(3-hydroxy-3-methylbutanoyl)oxy]methyl}but-2-enoate

[(1s,7r,7ar)-7-{[(2z)-2-methylbut-2-enoyl]oxy}-hexahydro-1h-pyrrolizin-1-yl]methyl (2z)-2-{[(3-hydroxy-3-methylbutanoyl)oxy]methyl}but-2-enoate

C23H35NO7 (437.2413)


   

(1r,11r)-11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-triene-3,9-dione

(1r,11r)-11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-triene-3,9-dione

C14H12O3 (228.0786)


   

7,8,11-trimethyl-13,14-dioxatetracyclo[7.4.1.0¹,¹⁰.0³,⁸]tetradec-10-en-12-one

7,8,11-trimethyl-13,14-dioxatetracyclo[7.4.1.0¹,¹⁰.0³,⁸]tetradec-10-en-12-one

C15H20O3 (248.1412)


   

[(1s,7s,7as)-7-hydroxy-hexahydro-1h-pyrrolizin-1-yl]methyl 3-methyl-2-(propanoyloxy)but-2-enoate

[(1s,7s,7as)-7-hydroxy-hexahydro-1h-pyrrolizin-1-yl]methyl 3-methyl-2-(propanoyloxy)but-2-enoate

C16H25NO5 (311.1733)


   

(4ar,5r)-2-[(1r,2e)-1-(2,5-dihydroxy-3-methylphenyl)-3,7-dimethylocta-2,6-dien-1-yl]-3,4a,5-trimethyl-4h,5h-naphtho[2,3-b]furan-6-one

(4ar,5r)-2-[(1r,2e)-1-(2,5-dihydroxy-3-methylphenyl)-3,7-dimethylocta-2,6-dien-1-yl]-3,4a,5-trimethyl-4h,5h-naphtho[2,3-b]furan-6-one

C32H38O4 (486.277)


   

(1r,11r)-6-hydroxy-11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-trien-3-one

(1r,11r)-6-hydroxy-11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-trien-3-one

C14H14O3 (230.0943)


   

6,9,10-trimethyl-2-oxo-4,14-dioxatetracyclo[7.5.0.0¹,¹³.0³,⁷]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate

6,9,10-trimethyl-2-oxo-4,14-dioxatetracyclo[7.5.0.0¹,¹³.0³,⁷]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate

C19H24O5 (332.1624)


   

(4as,5r,8ar)-3,4a,5-trimethyl-4h,5h,8ah,9h-naphtho[2,3-b]furan-6-one

(4as,5r,8ar)-3,4a,5-trimethyl-4h,5h,8ah,9h-naphtho[2,3-b]furan-6-one

C15H18O2 (230.1307)


   

(1s,8s,9s,10s,13r)-6,9,10-trimethyl-2-oxo-4,14-dioxatetracyclo[7.5.0.0¹,¹³.0³,⁷]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate

(1s,8s,9s,10s,13r)-6,9,10-trimethyl-2-oxo-4,14-dioxatetracyclo[7.5.0.0¹,¹³.0³,⁷]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate

C19H24O5 (332.1624)


   

(4ar,5r)-2-[(1r)-1-(2,5-dihydroxy-3-methylphenyl)-3,7-dimethylocta-2,6-dien-1-yl]-3,4a,5-trimethyl-4h,5h-naphtho[2,3-b]furan-6-one

(4ar,5r)-2-[(1r)-1-(2,5-dihydroxy-3-methylphenyl)-3,7-dimethylocta-2,6-dien-1-yl]-3,4a,5-trimethyl-4h,5h-naphtho[2,3-b]furan-6-one

C32H38O4 (486.277)


   

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

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

C15H22O3 (250.1569)


   

(4s,4ar,5s,8ar,9as)-4,9a-dihydroxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2-one

(4s,4ar,5s,8ar,9as)-4,9a-dihydroxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2-one

C15H22O4 (266.1518)


   

6,9,10-trimethyl-4,14-dioxatetracyclo[7.5.0.0¹,¹³.0³,⁷]tetradeca-3(7),5-dien-8-yl 2-(hydroxymethyl)prop-2-enoate

6,9,10-trimethyl-4,14-dioxatetracyclo[7.5.0.0¹,¹³.0³,⁷]tetradeca-3(7),5-dien-8-yl 2-(hydroxymethyl)prop-2-enoate

C19H24O5 (332.1624)


   

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

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

C20H25ClO5 (380.139)


   

(7-hydroxy-hexahydro-1h-pyrrolizin-1-yl)methyl 2-methylbut-2-enoate

(7-hydroxy-hexahydro-1h-pyrrolizin-1-yl)methyl 2-methylbut-2-enoate

C13H21NO3 (239.1521)


   

(4s,4ar,5s,8ar,9ar)-4-hydroxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h,9ah-naphtho[2,3-b]furan-2-one

(4s,4ar,5s,8ar,9ar)-4-hydroxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h,9ah-naphtho[2,3-b]furan-2-one

C15H22O3 (250.1569)


   

1-[(2s)-6-hydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethanone

1-[(2s)-6-hydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethanone

C13H14O3 (218.0943)


   

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

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

C30H38O4 (462.277)


   

1-ethyl 3-(7-hydroxy-hexahydro-1h-pyrrolizin-1-yl)methyl 2-(propan-2-ylidene)propanedioate

1-ethyl 3-(7-hydroxy-hexahydro-1h-pyrrolizin-1-yl)methyl 2-(propan-2-ylidene)propanedioate

C16H25NO5 (311.1733)


   

(1r,11r)-11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-trien-3-one

(1r,11r)-11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-trien-3-one

C14H14O2 (214.0994)


   

(7-hydroxy-hexahydro-1h-pyrrolizin-1-yl)methyl 3-methyl-2-(propanoyloxy)but-2-enoate

(7-hydroxy-hexahydro-1h-pyrrolizin-1-yl)methyl 3-methyl-2-(propanoyloxy)but-2-enoate

C16H25NO5 (311.1733)


   

(1s,8s,9s,10s,13r)-6,9,10-trimethyl-4,14-dioxatetracyclo[7.5.0.0¹,¹³.0³,⁷]tetradeca-3(7),5-dien-8-yl 2-(hydroxymethyl)prop-2-enoate

(1s,8s,9s,10s,13r)-6,9,10-trimethyl-4,14-dioxatetracyclo[7.5.0.0¹,¹³.0³,⁷]tetradeca-3(7),5-dien-8-yl 2-(hydroxymethyl)prop-2-enoate

C19H24O5 (332.1624)


   

6,9,10-trimethyl-4,14-dioxatetracyclo[7.5.0.0¹,¹³.0³,⁷]tetradeca-3(7),5-dien-8-ol

6,9,10-trimethyl-4,14-dioxatetracyclo[7.5.0.0¹,¹³.0³,⁷]tetradeca-3(7),5-dien-8-ol

C15H20O3 (248.1412)


   

9a-hydroxy-3,4a,5-trimethyl-4h,5h,8ah,9h-naphtho[2,3-b]furan-2,6-dione

9a-hydroxy-3,4a,5-trimethyl-4h,5h,8ah,9h-naphtho[2,3-b]furan-2,6-dione

C15H18O4 (262.1205)


   

[(1s,7s,7as)-7-hydroxy-hexahydro-1h-pyrrolizin-1-yl]methyl (2z)-2-methylbut-2-enoate

[(1s,7s,7as)-7-hydroxy-hexahydro-1h-pyrrolizin-1-yl]methyl (2z)-2-methylbut-2-enoate

C13H21NO3 (239.1521)


   

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

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

C15H20O4 (264.1362)


   

7-hydroxy-11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-trien-3-one

7-hydroxy-11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-trien-3-one

C14H14O3 (230.0943)


   

stigmast-5-en-3-ol, (3β)-

stigmast-5-en-3-ol, (3β)-

C29H50O (414.3861)


   

4a,5-dimethyl-3-(prop-1-en-2-yl)-1,3,4,5,6,7-hexahydronaphthalen-2-one

4a,5-dimethyl-3-(prop-1-en-2-yl)-1,3,4,5,6,7-hexahydronaphthalen-2-one

C15H22O (218.1671)


   

3-hydroxy-7-(prop-1-en-2-yl)-5,6,7,8-tetrahydronaphthalene-1-carbaldehyde

3-hydroxy-7-(prop-1-en-2-yl)-5,6,7,8-tetrahydronaphthalene-1-carbaldehyde

C14H16O2 (216.115)


   

5-{2,5-dihydroxy-7-oxabicyclo[4.1.0]heptan-2-yl}-1,4-dihydroxy-3-(2-methyl-1,2,4a,5,6,7,8,8a-octahydronaphthalene-1-carbonyl)pyridin-2-one

5-{2,5-dihydroxy-7-oxabicyclo[4.1.0]heptan-2-yl}-1,4-dihydroxy-3-(2-methyl-1,2,4a,5,6,7,8,8a-octahydronaphthalene-1-carbonyl)pyridin-2-one

C23H29NO7 (431.1944)


   

(1r,3r,4r,10r,11s)-4-[(4ar,5s,9as)-3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-9a-yl]-7,10,11-trimethyl-2,5-dioxatetracyclo[8.4.0.0¹,³.0⁴,⁸]tetradec-7-en-6-one

(1r,3r,4r,10r,11s)-4-[(4ar,5s,9as)-3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-9a-yl]-7,10,11-trimethyl-2,5-dioxatetracyclo[8.4.0.0¹,³.0⁴,⁸]tetradec-7-en-6-one

C30H38O5 (478.2719)


   

5,6-dimethoxy-2-(prop-1-en-2-yl)-1-benzofuran

5,6-dimethoxy-2-(prop-1-en-2-yl)-1-benzofuran

C13H14O3 (218.0943)


   

(4s,4ar,5s,8ar,9as)-4-hydroxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h,9ah-naphtho[2,3-b]furan-2-one

(4s,4ar,5s,8ar,9as)-4-hydroxy-3,4a,5-trimethyl-4h,5h,6h,7h,8h,8ah,9h,9ah-naphtho[2,3-b]furan-2-one

C15H22O3 (250.1569)


   

9a-methoxy-3,4a,5-trimethyl-5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2,4-dione

9a-methoxy-3,4a,5-trimethyl-5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2,4-dione

C16H22O4 (278.1518)


   

(1s,11s)-6-hydroxy-11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-trien-3-one

(1s,11s)-6-hydroxy-11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-trien-3-one

C14H14O3 (230.0943)


   

9a-{3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-9a-yl}-3,4a,5-trimethyl-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-2-one

9a-{3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-9a-yl}-3,4a,5-trimethyl-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-2-one

C30H38O4 (462.277)


   

(4as,5r,8ar,9ar)-9a-hydroxy-3,4a,5-trimethyl-4h,5h,8ah,9h-naphtho[2,3-b]furan-2,6-dione

(4as,5r,8ar,9ar)-9a-hydroxy-3,4a,5-trimethyl-4h,5h,8ah,9h-naphtho[2,3-b]furan-2,6-dione

C15H18O4 (262.1205)


   

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

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

C15H24 (204.1878)


   

(4as,5r,8ar,9ar)-9a-methoxy-3,4a,5-trimethyl-4h,5h,8ah,9h-naphtho[2,3-b]furan-2,6-dione

(4as,5r,8ar,9ar)-9a-methoxy-3,4a,5-trimethyl-4h,5h,8ah,9h-naphtho[2,3-b]furan-2,6-dione

C16H20O4 (276.1362)


   

(1r,3r,7s,8r,9r)-7,8,11-trimethyl-13,14-dioxatetracyclo[7.4.1.0¹,¹⁰.0³,⁸]tetradec-10-en-12-one

(1r,3r,7s,8r,9r)-7,8,11-trimethyl-13,14-dioxatetracyclo[7.4.1.0¹,¹⁰.0³,⁸]tetradec-10-en-12-one

C15H20O3 (248.1412)


   

1-(7-methoxy-1-benzofuran-5-yl)ethanone

1-(7-methoxy-1-benzofuran-5-yl)ethanone

C11H10O3 (190.063)


   

{7-[(2-methylbut-2-enoyl)oxy]-hexahydro-1h-pyrrolizin-1-yl}methyl 2-{[(3-hydroxy-3-methylbutanoyl)oxy]methyl}but-2-enoate

{7-[(2-methylbut-2-enoyl)oxy]-hexahydro-1h-pyrrolizin-1-yl}methyl 2-{[(3-hydroxy-3-methylbutanoyl)oxy]methyl}but-2-enoate

C23H35NO7 (437.2413)


   

2-[(2r,8s,8ar)-8,8a-dimethyl-2,3,4,6,7,8-hexahydro-1h-naphthalen-2-yl]propan-2-ol

2-[(2r,8s,8ar)-8,8a-dimethyl-2,3,4,6,7,8-hexahydro-1h-naphthalen-2-yl]propan-2-ol

C15H26O (222.1984)


   

11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-trien-3-one

11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-trien-3-one

C14H14O2 (214.0994)


   

(7r)-3-hydroxy-7-(prop-1-en-2-yl)-5,6,7,8-tetrahydronaphthalene-1-carbaldehyde

(7r)-3-hydroxy-7-(prop-1-en-2-yl)-5,6,7,8-tetrahydronaphthalene-1-carbaldehyde

C14H16O2 (216.115)


   

6-hydroxy-11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-trien-3-one

6-hydroxy-11-(prop-1-en-2-yl)-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-4(12),5,7-trien-3-one

C14H14O3 (230.0943)


   

(4ar,5s,8ar,9as)-9a-hydroxy-3,4a,5-trimethyl-5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2,4-dione

(4ar,5s,8ar,9as)-9a-hydroxy-3,4a,5-trimethyl-5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2,4-dione

C15H20O4 (264.1362)


   

(4as,5r,8ar,9ar)-3,4a,5-trimethyl-4h,5h,8ah,9h,9ah-naphtho[2,3-b]furan-2,6-dione

(4as,5r,8ar,9ar)-3,4a,5-trimethyl-4h,5h,8ah,9h,9ah-naphtho[2,3-b]furan-2,6-dione

C15H18O3 (246.1256)


   

(4as,5s)-3-hydroxy-4a,5-dimethyl-5,6,7,8-tetrahydronaphthalen-2-one

(4as,5s)-3-hydroxy-4a,5-dimethyl-5,6,7,8-tetrahydronaphthalen-2-one

C12H16O2 (192.115)


   

5,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carbaldehyde

5,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carbaldehyde

C30H48O3 (456.3603)


   

(3r,4ar,5s)-4a,5-dimethyl-3-(prop-1-en-2-yl)-1,3,4,5,6,7-hexahydronaphthalen-2-one

(3r,4ar,5s)-4a,5-dimethyl-3-(prop-1-en-2-yl)-1,3,4,5,6,7-hexahydronaphthalen-2-one

C15H22O (218.1671)


   

(4ar,5s,8ar,9ar)-9a-methoxy-3,4a,5-trimethyl-5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2,4-dione

(4ar,5s,8ar,9ar)-9a-methoxy-3,4a,5-trimethyl-5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-2,4-dione

C16H22O4 (278.1518)


   

(4r,4ar,5s,8r)-8-(acetyloxy)-3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h-indeno[1,2-b]furan-4-yl 2-methylpropanoate

(4r,4ar,5s,8r)-8-(acetyloxy)-3,4a,5-trimethyl-2-oxo-4h,5h,6h,7h,8h-indeno[1,2-b]furan-4-yl 2-methylpropanoate

C20H26O6 (362.1729)


   

(4ar,5s,6as,6br,8ar,10s,12ar,12br,14bs)-5,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carbaldehyde

(4ar,5s,6as,6br,8ar,10s,12ar,12br,14bs)-5,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carbaldehyde

C30H48O3 (456.3603)