NCBI Taxonomy: 634960

Santolina oblongifolia (ncbi_taxid: 634960)

found 54 associated metabolites at species taxonomy rank level.

Ancestor: Santolina

Child Taxonomies: none taxonomy data.

Scopoletin

7-hydroxy-6-methoxy-2H-chromen-2-one

C10H8O4 (192.0423)


Scopoletin is a hydroxycoumarin that is umbelliferone bearing a methoxy substituent at position 6. It has a role as a plant growth regulator and a plant metabolite. It is functionally related to an umbelliferone. Scopoletin is a natural product found in Ficus auriculata, Haplophyllum cappadocicum, and other organisms with data available. Scopoletin is a coumarin compound found in several plants including those in the genus Scopolia and the genus Brunfelsia, as well as chicory (Cichorium), redstem wormwood (Artemisia scoparia), stinging nettle (Urtica dioica), passion flower (Passiflora), noni (Morinda citrifolia fruit) and European black nightshade (Solanum nigrum) that is comprised of umbelliferone with a methoxy group substituent at position 6. Scopoletin is used to standardize and establish pharmacokinetic properties for products derived from the plants that produce it, such as noni extract. Although the mechanism(s) of action have not yet been established, this agent has potential antineoplastic, antidopaminergic, antioxidant, anti-inflammatory and anticholinesterase effects. Plant growth factor derived from the root of Scopolia carniolica or Scopolia japonica. See also: Arnica montana Flower (part of); Lycium barbarum fruit (part of); Viburnum opulus root (part of). Isolated from Angelica acutiloba (Dong Dang Gui). Scopoletin is found in many foods, some of which are lambsquarters, lemon, sunflower, and sherry. Scopoletin is found in anise. Scopoletin is isolated from Angelica acutiloba (Dong Dang Gui A hydroxycoumarin that is umbelliferone bearing a methoxy substituent at position 6. Acquisition and generation of the data is financially supported in part by CREST/JST. [Raw Data] CBA72_Scopoletin_pos_20eV.txt [Raw Data] CBA72_Scopoletin_pos_40eV.txt [Raw Data] CBA72_Scopoletin_neg_30eV.txt [Raw Data] CBA72_Scopoletin_neg_50eV.txt [Raw Data] CBA72_Scopoletin_pos_50eV.txt [Raw Data] CBA72_Scopoletin_pos_10eV.txt [Raw Data] CBA72_Scopoletin_neg_40eV.txt [Raw Data] CBA72_Scopoletin_neg_10eV.txt [Raw Data] CBA72_Scopoletin_pos_30eV.txt [Raw Data] CBA72_Scopoletin_neg_20eV.txt Scopoletin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=92-61-5 (retrieved 2024-07-12) (CAS RN: 92-61-5). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Scopoletin is an inhibitor of acetylcholinesterase (AChE). Scopoletin is an inhibitor of acetylcholinesterase (AChE).

   

Aesculetin

6,7-dihydroxychromen-2-one

C9H6O4 (178.0266)


Aesculetin, also known as cichorigenin or cichoriin aglucon, belongs to the class of organic compounds known as 6,7-dihydroxycoumarins. These are coumarins bearing two hydroxyl groups at positions 6 and 7 of the coumarin skeleton, respectively. Aesculetin is found, on average, in the highest concentration within sherries. Aesculetin has also been detected, but not quantified, in several different foods, such as horseradish, carrots, dandelions, grape wines, and highbush blueberries. This could make aesculetin a potential biomarker for the consumption of these foods. Esculetin is a hydroxycoumarin that is umbelliferone in which the hydrogen at position 6 is substituted by a hydroxy group. It is used in filters for absorption of ultraviolet light. It has a role as an antioxidant, an ultraviolet filter and a plant metabolite. Esculetin is a natural product found in Artemisia eriopoda, Euphorbia decipiens, and other organisms with data available. A hydroxycoumarin that is umbelliferone in which the hydrogen at position 6 is substituted by a hydroxy group. It is used in filters for absorption of ultraviolet light. Metabolite of infected sweet potato. Aesculetin is found in many foods, some of which are root vegetables, wild carrot, sweet basil, and carrot. D020011 - Protective Agents > D000975 - Antioxidants Acquisition and generation of the data is financially supported in part by CREST/JST. [Raw Data] CB031_Aesculetin_pos_20eV_CB000017.txt [Raw Data] CB031_Aesculetin_pos_10eV_CB000017.txt [Raw Data] CB031_Aesculetin_pos_40eV_CB000017.txt [Raw Data] CB031_Aesculetin_pos_50eV_CB000017.txt [Raw Data] CB031_Aesculetin_pos_30eV_CB000017.txt [Raw Data] CB031_Aesculetin_neg_10eV_000010.txt [Raw Data] CB031_Aesculetin_neg_20eV_000010.txt [Raw Data] CB031_Aesculetin_neg_30eV_000010.txt CONFIDENCE standard compound; ML_ID 39 Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1]. Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1]. Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1].

   

Herniarin

7-Methoxycoumarin, suitable for fluorescence, >=98.0\\% (TLC)

C10H8O3 (176.0473)


Herniarin, also known as 7-methoxycoumarin or ayapanin, belongs to the class of organic compounds known as coumarins and derivatives. These are polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one). Herniarin is a sweet, balsamic, and tonka tasting compound. Herniarin has been detected, but not quantified, in several different foods, such as barley, tarragons, roman camomiles, fruits, and wild celeries. This could make herniarin a potential biomarker for the consumption of these foods. Herniarin is a member of the class of coumarins that is coumarin substituted by a methoxy group at position 7. It has a role as a fluorochrome. 7-Methoxycoumarin is a natural product found in Haplopappus multifolius, Herniaria hirsuta, and other organisms with data available. See also: Chamomile (part of); Glycyrrhiza Glabra (part of). Present in Prunus mahaleb (mahaleb cherry). Herniarin is found in many foods, some of which are caraway, wild celery, barley, and fruits. A member of the class of coumarins that is coumarin substituted by a methoxy group at position 7. Herniarin is a natural coumarin occurs in some flowering plants, with antitumor effect. Herniarin is a natural coumarin occurs in some flowering plants, with antitumor effect.

   

Scopolin

6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one

C16H18O9 (354.0951)


Scopolin is a member of the class of coumarins that is scopoletin attached to a beta-D-glucopyranosyl residue at position 7 via a glycosidic linkage. It has a role as a plant metabolite. It is a monosaccharide derivative, a member of coumarins and a beta-D-glucoside. It is functionally related to a scopoletin. Scopolin is a natural product found in Artemisia ordosica, Astragalus onobrychis, and other organisms with data available. See also: Chamaemelum nobile flower (part of). A member of the class of coumarins that is scopoletin attached to a beta-D-glucopyranosyl residue at position 7 via a glycosidic linkage. Scopolin is a coumarin isolated from Arabidopsis thaliana (Arabidopsis) roots[1]. Scopolin attenuated hepatic steatosis through activation of SIRT1-mediated signaling cascades[2]. Scopolin is a coumarin isolated from Arabidopsis thaliana (Arabidopsis) roots[1]. Scopolin attenuated hepatic steatosis through activation of SIRT1-mediated signaling cascades[2]. Scopolin is a coumarin isolated from Arabidopsis thaliana (Arabidopsis) roots[1]. Scopolin attenuated hepatic steatosis through activation of SIRT1-mediated signaling cascades[2].

   

friedelanol

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

C30H52O (428.4018)


Epi-Friedelanol is a triterpenoid. Epifriedelanol is a natural product found in Plenckia populnea, Quercus glauca, and other organisms with data available.

   

Dammaradienol

2,6,6,10,11-pentamethyl-14-(6-methylhepta-1,5-dien-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-ol

C30H50O (426.3861)


Dammaradienol is found in herbs and spices. Dammaradienol is a constituent of Inula helenium (elecampane)

   

Epi-Friedelanol

4,4a,6b,8a,11,11,12b,14a-octamethyl-hexadecahydropicen-3-ol

C30H52O (428.4018)


   

Scopolin

6-methoxy-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H-chromen-2-one

C16H18O9 (354.0951)


Scopolin is a member of the class of compounds known as coumarin glycosides. Coumarin glycosides are aromatic compounds containing a carbohydrate moiety glycosidically bound to a coumarin moiety. Scopolin is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Scopolin can be found in a number of food items such as sweet potato, oat, wild celery, and potato, which makes scopolin a potential biomarker for the consumption of these food products. Scopolin is a glucoside of scopoletin formed by the action of the enzyme scopoletin glucosyltransferase . Scopolin is a coumarin isolated from Arabidopsis thaliana (Arabidopsis) roots[1]. Scopolin attenuated hepatic steatosis through activation of SIRT1-mediated signaling cascades[2]. Scopolin is a coumarin isolated from Arabidopsis thaliana (Arabidopsis) roots[1]. Scopolin attenuated hepatic steatosis through activation of SIRT1-mediated signaling cascades[2]. Scopolin is a coumarin isolated from Arabidopsis thaliana (Arabidopsis) roots[1]. Scopolin attenuated hepatic steatosis through activation of SIRT1-mediated signaling cascades[2].

   

Scopoletin

Scopoletin

C10H8O4 (192.0423)


relative retention time with respect to 9-anthracene Carboxylic Acid is 0.636 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.637 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.629 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.631 IPB_RECORD: 1582; CONFIDENCE confident structure Scopoletin is an inhibitor of acetylcholinesterase (AChE). Scopoletin is an inhibitor of acetylcholinesterase (AChE).

   

Esculetin

InChI=1\C9H6O4\c10-6-3-5-1-2-9(12)13-8(5)4-7(6)11\h1-4,10-11

C9H6O4 (178.0266)


D020011 - Protective Agents > D000975 - Antioxidants relative retention time with respect to 9-anthracene Carboxylic Acid is 0.434 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.428 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.430 Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1]. Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1]. Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1].

   

Dammaradienol

Dammaradienol

C30H50O (426.3861)


   

Scopoletol

2H-1-Benzopyran-2-one, 7-hydroxy-6-methoxy- (9CI)

C10H8O4 (192.0423)


Scopoletin is an inhibitor of acetylcholinesterase (AChE). Scopoletin is an inhibitor of acetylcholinesterase (AChE).

   

Ayapanin

5-18-01-00387 (Beilstein Handbook Reference)

C10H8O3 (176.0473)


Herniarin is a natural coumarin occurs in some flowering plants, with antitumor effect. Herniarin is a natural coumarin occurs in some flowering plants, with antitumor effect.

   

(3r,5s,6e,9s)-3,7,11-trimethyldodeca-1,6,10-triene-3,5,9-triol

(3r,5s,6e,9s)-3,7,11-trimethyldodeca-1,6,10-triene-3,5,9-triol

C15H26O3 (254.1882)


   

7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-dien-4-yl acetate

7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-dien-4-yl acetate

C15H12O4 (256.0736)


   

(4s,6e,10r)-10-hydroxy-2,6,10-trimethyl-8-oxododeca-2,6,11-trien-4-yl acetate

(4s,6e,10r)-10-hydroxy-2,6,10-trimethyl-8-oxododeca-2,6,11-trien-4-yl acetate

C17H26O4 (294.1831)


   

1-hydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-1,6-dien-2-yl)-dodecahydrocyclopenta[a]phenanthren-7-yl acetate

1-hydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-1,6-dien-2-yl)-dodecahydrocyclopenta[a]phenanthren-7-yl acetate

C32H52O3 (484.3916)


   

3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-1,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-ol

3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-1,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-ol

C30H50O (426.3861)


   

[(1r,2r,6s,7r,10s)-6-(hydroxymethyl)-6,9-dimethyltricyclo[5.4.0.0²,¹⁰]undec-8-en-2-yl]methanol

[(1r,2r,6s,7r,10s)-6-(hydroxymethyl)-6,9-dimethyltricyclo[5.4.0.0²,¹⁰]undec-8-en-2-yl]methanol

C15H24O2 (236.1776)


   

2-methyl-1-[(2s,6s)-4-methyl-6-(2-methylprop-1-en-1-yl)-5,6-dihydro-2h-pyran-2-yl]but-3-en-2-ol

2-methyl-1-[(2s,6s)-4-methyl-6-(2-methylprop-1-en-1-yl)-5,6-dihydro-2h-pyran-2-yl]but-3-en-2-ol

C15H24O2 (236.1776)


   

2-[(1z)-4-(thiophen-2-yl)but-1-en-3-yn-1-yl]furan

2-[(1z)-4-(thiophen-2-yl)but-1-en-3-yn-1-yl]furan

C12H8OS (200.0296)


   

(2s)-2-methyl-1-[(2r,6s)-4-methyl-6-(2-methylprop-1-en-1-yl)-5,6-dihydro-2h-pyran-2-yl]but-3-en-2-ol

(2s)-2-methyl-1-[(2r,6s)-4-methyl-6-(2-methylprop-1-en-1-yl)-5,6-dihydro-2h-pyran-2-yl]but-3-en-2-ol

C15H24O2 (236.1776)


   

[6-(hydroxymethyl)-6,9-dimethyltricyclo[5.4.0.0²,¹⁰]undec-8-en-2-yl]methanol

[6-(hydroxymethyl)-6,9-dimethyltricyclo[5.4.0.0²,¹⁰]undec-8-en-2-yl]methanol

C15H24O2 (236.1776)


   

(1r,3ar,3br,5ar,7s,9ar,9br,11as)-1-hydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-1,6-dien-2-yl)-dodecahydrocyclopenta[a]phenanthren-7-yl acetate

(1r,3ar,3br,5ar,7s,9ar,9br,11as)-1-hydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-1,6-dien-2-yl)-dodecahydrocyclopenta[a]phenanthren-7-yl acetate

C32H52O3 (484.3916)


   
   

2,6,10-trimethyldodeca-3,6,11-triene-2,8,10-triol

2,6,10-trimethyldodeca-3,6,11-triene-2,8,10-triol

C15H26O3 (254.1882)


   

8-(acetyloxy)-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl acetate

8-(acetyloxy)-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl acetate

C19H30O5 (338.2093)


   

(4s,5r,7e)-7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-dien-4-yl 3-methylbutanoate

(4s,5r,7e)-7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-dien-4-yl 3-methylbutanoate

C18H18O4 (298.1205)


   

(4s,5r,7z)-7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-dien-4-yl acetate

(4s,5r,7z)-7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-dien-4-yl acetate

C15H12O4 (256.0736)


   

3,11-dihydroxy-3,7,11-trimethyldodeca-1,6,9-trien-5-yl acetate

3,11-dihydroxy-3,7,11-trimethyldodeca-1,6,9-trien-5-yl acetate

C17H28O4 (296.1987)


   

(1s,3ar,3br,5ar,7s,9ar,9br,11ar)-1-[(4e)-6-hydroxy-6-methylhepta-1,4-dien-2-yl]-3a,3b,6,6,9a-pentamethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-ol

(1s,3ar,3br,5ar,7s,9ar,9br,11ar)-1-[(4e)-6-hydroxy-6-methylhepta-1,4-dien-2-yl]-3a,3b,6,6,9a-pentamethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-ol

C30H50O2 (442.3811)


   

10-hydroxy-2,6,10-trimethyl-8-oxododeca-2,6,11-trien-4-yl acetate

10-hydroxy-2,6,10-trimethyl-8-oxododeca-2,6,11-trien-4-yl acetate

C17H26O4 (294.1831)


   

7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-diene

7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-diene

C13H10O2 (198.0681)


   

2-methyl-1-[4-methyl-6-(2-methylprop-1-en-1-yl)-5,6-dihydro-2h-pyran-2-yl]but-3-en-2-ol

2-methyl-1-[4-methyl-6-(2-methylprop-1-en-1-yl)-5,6-dihydro-2h-pyran-2-yl]but-3-en-2-ol

C15H24O2 (236.1776)


   

(4s,6e,8s,10r)-8,10-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl acetate

(4s,6e,8s,10r)-8,10-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl acetate

C17H28O4 (296.1987)


   

7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-dien-4-yl 3-methylbutanoate

7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-dien-4-yl 3-methylbutanoate

C18H18O4 (298.1205)


   

1-[(1s,3ar,7s,7ar)-7-isopropyl-4-methyl-2,3,3a,6,7,7a-hexahydro-1h-inden-1-yl]ethanone

1-[(1s,3ar,7s,7ar)-7-isopropyl-4-methyl-2,3,3a,6,7,7a-hexahydro-1h-inden-1-yl]ethanone

C15H24O (220.1827)


   

8,10-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl acetate

8,10-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl acetate

C17H28O4 (296.1987)


   

2-[4-(thiophen-2-yl)but-1-en-3-yn-1-yl]furan

2-[4-(thiophen-2-yl)but-1-en-3-yn-1-yl]furan

C12H8OS (200.0296)


   

(3e,6e,8s,10r)-2,6,10-trimethyldodeca-3,6,11-triene-2,8,10-triol

(3e,6e,8s,10r)-2,6,10-trimethyldodeca-3,6,11-triene-2,8,10-triol

C15H26O3 (254.1882)


   

(3r,5s,6e,9e)-3,11-dihydroxy-3,7,11-trimethyldodeca-1,6,9-trien-5-yl acetate

(3r,5s,6e,9e)-3,11-dihydroxy-3,7,11-trimethyldodeca-1,6,9-trien-5-yl acetate

C17H28O4 (296.1987)


   

(5r,7e)-7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-diene

(5r,7e)-7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-diene

C13H10O2 (198.0681)


   

(4s,5r,7e)-7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-dien-4-yl acetate

(4s,5r,7e)-7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-dien-4-yl acetate

C15H12O4 (256.0736)


   

(2r)-2-methyl-1-[(2r,6r)-4-methyl-6-(2-methylprop-1-en-1-yl)-5,6-dihydro-2h-pyran-2-yl]but-3-en-2-ol

(2r)-2-methyl-1-[(2r,6r)-4-methyl-6-(2-methylprop-1-en-1-yl)-5,6-dihydro-2h-pyran-2-yl]but-3-en-2-ol

C15H24O2 (236.1776)


   

1-(6-hydroxy-6-methylhept-4-en-2-yl)-3a,3b,6,6,9a-pentamethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-ol

1-(6-hydroxy-6-methylhept-4-en-2-yl)-3a,3b,6,6,9a-pentamethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-ol

C30H52O2 (444.3967)


   

(4r,5r,7e)-7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-dien-4-ol

(4r,5r,7e)-7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-dien-4-ol

C13H10O3 (214.063)


   

3,7,11-trimethyldodeca-1,6,10-triene-3,5,9-triol

3,7,11-trimethyldodeca-1,6,10-triene-3,5,9-triol

C15H26O3 (254.1882)


   

(1r,3ar,3br,5ar,7s,9ar,9br,11ar)-1-[(2s,4e)-6-hydroxy-6-methylhept-4-en-2-yl]-3a,3b,6,6,9a-pentamethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-ol

(1r,3ar,3br,5ar,7s,9ar,9br,11ar)-1-[(2s,4e)-6-hydroxy-6-methylhept-4-en-2-yl]-3a,3b,6,6,9a-pentamethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-ol

C30H52O2 (444.3967)


   

(1s,3ar,3br,5ar,7s,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-1,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl acetate

(1s,3ar,3br,5ar,7s,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-1,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl acetate

C32H52O2 (468.3967)


   

(3r,5s,6e,9s)-9-(acetyloxy)-3-hydroxy-3,7,11-trimethyldodeca-1,6,10-trien-5-yl acetate

(3r,5s,6e,9s)-9-(acetyloxy)-3-hydroxy-3,7,11-trimethyldodeca-1,6,10-trien-5-yl acetate

C19H30O5 (338.2093)


   

1-(6-hydroxy-6-methylhepta-1,4-dien-2-yl)-3a,3b,6,6,9a-pentamethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-ol

1-(6-hydroxy-6-methylhepta-1,4-dien-2-yl)-3a,3b,6,6,9a-pentamethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-ol

C30H50O2 (442.3811)


   

3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-1,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl acetate

3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-1,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl acetate

C32H52O2 (468.3967)


   

7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-dien-4-ol

7-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]nona-2,8-dien-4-ol

C13H10O3 (214.063)


   

(2r)-2-methyl-1-[(2r,6s)-4-methyl-6-(2-methylprop-1-en-1-yl)-5,6-dihydro-2h-pyran-2-yl]but-3-en-2-ol

(2r)-2-methyl-1-[(2r,6s)-4-methyl-6-(2-methylprop-1-en-1-yl)-5,6-dihydro-2h-pyran-2-yl]but-3-en-2-ol

C15H24O2 (236.1776)