NCBI Taxonomy: 54829

Ferula communis (ncbi_taxid: 54829)

found 179 associated metabolites at species taxonomy rank level.

Ancestor: Ferula

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).

   

Scoparone

6,7-dimethoxychromen-2-one

C11H10O4 (206.0579)


Scoparone is a member of the class of coumarins that is esculetin in which the two hydroxy groups at positions 6 and 7 are replaced by methoxy groups. It is a major constituent of the Chinese herbal medicine Yin Chen Hao, and exhibits a variety of pharmacological activities such as anti-inflammatory, anti-allergic, and anti-tumor activities. It has a role as a plant metabolite, an anti-inflammatory agent, an antilipemic drug, an immunosuppressive agent, an antihypertensive agent and an anti-allergic agent. It is a member of coumarins and an aromatic ether. It is functionally related to an esculetin. Scoparone is a natural product found in Haplophyllum ramosissimum, Haplophyllum thesioides, and other organisms with data available. A member of the class of coumarins that is esculetin in which the two hydroxy groups at positions 6 and 7 are replaced by methoxy groups. It is a major constituent of the Chinese herbal medicine Yin Chen Hao, and exhibits a variety of pharmacological activities such as anti-inflammatory, anti-allergic, and anti-tumor activities. D005765 - Gastrointestinal Agents > D002756 - Cholagogues and Choleretics Scoparone is found in anise. Scoparone is found in several citrus oil D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents D002317 - Cardiovascular Agents > D000889 - Anti-Arrhythmia Agents D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents Found in several citrus oils Scoparone is isolated from Artemisia capillaris Thunb., has anticoagulant, vasorelaxant antioxidant, anti-inflammatory activities[1]. Scoparone is isolated from Artemisia capillaris Thunb., has anticoagulant, vasorelaxant antioxidant, anti-inflammatory activities[1].

   

Imperatorin

InChI=1/C16H14O4/c1-10(2)5-7-19-16-14-12(6-8-18-14)9-11-3-4-13(17)20-15(11)16/h3-6,8-9H,7H2,1-2H

C16H14O4 (270.0892)


Imperatorin is a member of the class of psoralens that is psoralen substituted by a prenyloxy group at position 8. Isolated from Angelica dahurica and Angelica koreana, it acts as a acetylcholinesterase inhibitor. It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor and a metabolite. Imperatorin is a natural product found in Allium wallichii, Ammi visnaga, and other organisms with data available. Imperatorin is found in anise. Imperatorin is present in Aegle marmelos (bael fruit) and seeds of Pastinaca sativa (parsnip).Imperatorin is a furocoumarin and a phytochemical that has been isolated from Urena lobata L. (Malvaceae). It is biosynthesized from umbelliferone, a coumarin derivative.Imperatorin has been shown to exhibit anti-hypertrophic and anti-convulsant functions (A7784, A7785).Imperatorin belongs to the family of Furanocoumarins. These are polycyclic aromatic compounds containing a furan ring fused to a coumarin moeity. See also: Angelica Dahurica Root (part of); Aegle marmelos fruit (part of); Ammi majus seed (part of) ... View More ... Imperatorin is found in anise. Imperatorin is present in Aegle marmelos (bael fruit) and seeds of Pastinaca sativa (parsnip).Imperatorin is a furocoumarin and a phytochemical that has been isolated from Urena lobata L. (Malvaceae). It is biosynthesized from umbelliferone, a coumarin derivative A member of the class of psoralens that is psoralen substituted by a prenyloxy group at position 8. Isolated from Angelica dahurica and Angelica koreana, it acts as a acetylcholinesterase inhibitor. D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins Present in Aegle marmelos (bael fruit) and seeds of Pastinaca sativa (parsnip) INTERNAL_ID 2244; CONFIDENCE Reference Standard (Level 1) CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 2244 Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM. Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM.

   

Isoscopoletin

2H-1-Benzopyran-2-one, 6-hydroxy-7-methoxy-

C10H8O4 (192.0423)


Isoscopoletin is a hydroxycoumarin that is esculetin in which the hydroxy group at position 7 is replaced by a methoxy group. It is the major primary metabolite of scoparone. It has a role as a plant metabolite. It is a hydroxycoumarin and an aromatic ether. It is functionally related to an esculetin. Isoscopoletin is a natural product found in Clausena dunniana, Olea capensis, and other organisms with data available. Isoscopoletin (6-Hydroxy-7-methoxycoumarin) is an active constituent in Artemisia argyi leaves. Isoscopoletin shows substantial inhibition against cell proliferation, with IC50s of 4.0 μM and 1.6 μM for human CCRF-CEM leukaemia cells and multidrug resistant subline CEM/ADR5000, respectively[1]. Isoscopoletin (6-Hydroxy-7-methoxycoumarin) possesses inhibitory activity against HBV replication[2]. Isoscopoletin (6-Hydroxy-7-methoxycoumarin) is an active constituent in Artemisia argyi leaves. Isoscopoletin shows substantial inhibition against cell proliferation, with IC50s of 4.0 μM and 1.6 μM for human CCRF-CEM leukaemia cells and multidrug resistant subline CEM/ADR5000, respectively[1]. Isoscopoletin (6-Hydroxy-7-methoxycoumarin) possesses inhibitory activity against HBV replication[2].

   

Falcarindiol

(Z)-(3S,8S)-Heptadeca-1,9-diene-4,6-diyne-3,8-diol

C17H24O2 (260.1776)


Constituent of roots of several plants including the common carrot (Daucus carota) and Angelica acutiloba (Dong Dang Gui). Falcarindiol is found in many foods, some of which are wild carrot, carrot, garden tomato (variety), and caraway. Falcarindiol is found in caraway. Falcarindiol is a constituent of roots of several plants including the common carrot (Daucus carota) and Angelica acutiloba (Dong Dang Gui). Falcarindiol is a natural product found in Anthriscus nitida, Chaerophyllum aureum, and other organisms with data available. (+)-(3R,8S)-Falcarindiol is a polyacetylene found in carrots, has antimycobacterial activity, with an IC50 of 6 μM and MIC of 24 μM against Mycobacterium tuberculosis H37Ra[1][2]. Antineoplastic and anti-inflammatory activity[2]. (+)-(3R,8S)-Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. (+)-(3R,8S)-Falcarindiol is a polyacetylene found in carrots, has antimycobacterial activity, with an IC50 of 6 μM and MIC of 24 μM against Mycobacterium tuberculosis H37Ra[1][2]. Antineoplastic and anti-inflammatory activity[2]. (+)-(3R,8S)-Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. (+)-(3R,8S)-Falcarindiol is a polyacetylene found in carrots, has antimycobacterial activity, with an IC50 of 6 μM and MIC of 24 μM against Mycobacterium tuberculosis H37Ra[1][2]. Antineoplastic and anti-inflammatory activity[2]. (+)-(3R,8S)-Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. (+)-(3R,8S)-Falcarindiol is a polyacetylene found in carrots, has antimycobacterial activity, with an IC50 of 6 μM and MIC of 24 μM against Mycobacterium tuberculosis H37Ra[1][2]. Antineoplastic and anti-inflammatory activity[2]. (+)-(3R,8S)-Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

   

alpha-Tocopherol

2H-1-Benzopyran-6-ol, 3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-, (2R*(4R*,8R*))-(+-)-

C29H50O2 (430.3811)


Alpha-tocopherol is a pale yellow, viscous liquid. (NTP, 1992) (R,R,R)-alpha-tocopherol is an alpha-tocopherol that has R,R,R configuration. The naturally occurring stereoisomer of alpha-tocopherol, it is found particularly in sunflower and olive oils. It has a role as an antioxidant, a nutraceutical, an antiatherogenic agent, an EC 2.7.11.13 (protein kinase C) inhibitor, an anticoagulant, an immunomodulator, an antiviral agent, a micronutrient, an algal metabolite and a plant metabolite. It is an enantiomer of a (S,S,S)-alpha-tocopherol. In 1922, vitamin E was demonstrated to be an essential nutrient. Vitamin E is a term used to describe 8 different fat soluble tocopherols and tocotrienols, alpha-tocopherol being the most biologically active. Vitamin E acts as an antioxidant, protecting cell membranes from oxidative damage. The antioxidant effects are currently being researched for use in the treatment of diseases causing bone loss, cardiovascular diseases, diabetes mellitus and associated comorbidities, eye diseases, inflammatory diseases (including skin conditions), lipid disorders, neurological diseases, and radiation damage. Though this research is so far inconclusive, vitamin E remains a popular supplement and is generally considered safe by the FDA. Vitamin E is a natural product found in Monteverdia ilicifolia, Calea jamaicensis, and other organisms with data available. Alpha-Tocopherol is the orally bioavailable alpha form of the naturally-occurring fat-soluble vitamin E, with potent antioxidant and cytoprotective activities. Upon administration, alpha-tocopherol neutralizes free radicals, thereby protecting tissues and organs from oxidative damage. Alpha-tocopherol gets incorporated into biological membranes, prevents protein oxidation and inhibits lipid peroxidation, thereby maintaining cell membrane integrity and protecting the cell against damage. In addition, alpha-tocopherol inhibits the activity of protein kinase C (PKC) and PKC-mediated pathways. Alpha-tocopherol also modulates the expression of various genes, plays a key role in neurological function, inhibits platelet aggregation and enhances vasodilation. Compared with other forms of tocopherol, alpha-tocopherol is the most biologically active form and is the form that is preferentially absorbed and retained in the body. A generic descriptor for all tocopherols and tocotrienols that exhibit alpha-tocopherol activity. By virtue of the phenolic hydrogen on the 2H-1-benzopyran-6-ol nucleus, these compounds exhibit varying degree of antioxidant activity, depending on the site and number of methyl groups and the type of isoprenoids. See also: Alpha-Tocopherol Acetate (is active moiety of); Tocopherol (related); Vitamin E (related) ... View More ... alpha-Tocopherol is traditionally recognized as the most active form of vitamin E in humans and is a powerful biological antioxidant. The measurement of "vitamin E" activity in international units (IU) was based on fertility enhancement by the prevention of spontaneous abortions in pregnant rats relative to alpha-Tocopherol. Natural vitamin E exists in eight different forms or isomers: four tocopherols and four tocotrienols. In foods, the most abundant sources of vitamin E are vegetable oils such as palm oil, sunflower, corn, soybean, and olive oil. Nuts, sunflower seeds, and wheat germ are also good sources. Constituent of many vegetable oils such as soya and sunflower oils. Dietary supplement and nutrient. Nutriceutical with anticancer and antioxidant props. Added to fats and oils to prevent rancidity. The naturally-occurring tocopherol is a single stereoisomer; synthetic forms are a mixture of all eight possible isomers An alpha-tocopherol that has R,R,R configuration. The naturally occurring stereoisomer of alpha-tocopherol, it is found particularly in sunflower and olive oils. α-Tocopherol (alpha-tocopherol) is a type of vitamin E. Its E number is "E307". Vitamin E exists in eight different forms, four tocopherols and four tocotrienols. All feature a chromane ring, with a hydroxyl group that can donate a hydrogen atom to reduce free radicals and a hydrophobic side chain which allows for penetration into biological membranes. Compared to the others, α-tocopherol is preferentially absorbed and accumulated in humans. Vitamin E is found in a variety of tissues, being lipid-soluble, and taken up by the body in a wide variety of ways. The most prevalent form, α-tocopherol, is involved in molecular, cellular, biochemical processes closely related to overall lipoprotein and lipid homeostasis. Ongoing research is believed to be "critical for manipulation of vitamin E homeostasis in a variety of oxidative stress-related disease conditions in humans."[2] One of these disease conditions is the α-tocopherol role in the use by malaria parasites to protect themselves from the highly oxidative environment in erythrocytes.[3] DL-α-Tocopherol. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=16826-11-2 (retrieved 2024-06-29) (CAS RN: 10191-41-0). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). DL-alpha-Tocopherol is a synthetic vitamin E, with antioxidation effect. DL-alpha-Tocopherol protects human skin fibroblasts against the cytotoxic effect of UVB[1]. DL-alpha-Tocopherol is a synthetic vitamin E, with antioxidation effect. DL-alpha-Tocopherol protects human skin fibroblasts against the cytotoxic effect of UVB[1]. rel-α-Vitamin E (rel-D-α-Tocopherol) is a vitamin with antioxidant properties and also a mixture[1]. α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant[1][2]. α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant[1][2].

   

Elemicin

4-(2-Ethyl-benzoimidazol-1-yl)-4-oxo-butyricacid

C12H16O3 (208.1099)


Elemicin is an olefinic compound. Elemicin is a natural product found in Anemopsis californica, Asarum celsum, and other organisms with data available. Constituent of Elemi oil and Myristica fragrans (nutmeg). Elemicin is found in many foods, some of which are nutmeg, carrot, parsley, and tarragon. Elemicin is found in carrot. Elemicin is a constituent of Elemi oil and Myristica fragrans (nutmeg). Elemicin is an orally active alkenylbenzene widely distributed in many herbs and spices. Elemicin inhibits Stearoyl-CoA Desaturase 1 (SCD1) by metabolic activation. Elemicin has anti-influenza activities, antimicrobial, antioxidant, and antiviral activities. Elemicin and its reactive metabolite of 1′-Hydroxyelemicin can induce hepatotoxicity[1][2][3][4]. Elemicin is a alkenylbenzene widely distributed in many herbs and spices. Elemicin inhibits Stearoyl-CoA Desaturase 1 (SCD1) by metabolic activation. Elemicin is one of the main components in aromatic food and has antimicrobial, antioxidant, and antiviral activities. Elemicin possesses genotoxicity and carcinogenicity[1]. Elemicin is a alkenylbenzene widely distributed in many herbs and spices. Elemicin inhibits Stearoyl-CoA Desaturase 1 (SCD1) by metabolic activation. Elemicin is one of the main components in aromatic food and has antimicrobial, antioxidant, and antiviral activities. Elemicin possesses genotoxicity and carcinogenicity[1].

   

Umbelliprenin

7-{[(2E,6Z)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy}-2H-chromen-2-one

C24H30O3 (366.2195)


Isolated from Angelica archangelica (angelica). Umbelliprenin is found in many foods, some of which are coriander, fats and oils, herbs and spices, and green vegetables. Umbelliprenin is found in coriander. Umbelliprenin is isolated from Angelica archangelica (angelica

   

Nevskin

7-[(2,6-dihydroxy-2,5,5,8a-tetramethyl-decahydronaphthalen-1-yl)methoxy]-2H-chromen-2-one

C24H32O5 (400.225)


Constituent of Ferula assa-foetida (asafoetida). Nevskin is found in herbs and spices and green vegetables. Nevskin is found in green vegetables. Nevskin is a constituent of Ferula assa-foetida (asafoetida)

   

Falcarindiol

1,9-Heptadecadiene-4,6-diyne-3,8-diol, [S-[R*,R*-(Z)]]-

C17H24O2 (260.1776)


Falcarindiol is an organic molecular entity. It has a role as a metabolite. 1,9-Heptadecadiene-4,6-diyne-3,8-diol is a natural product found in Peucedanum oreoselinum, Oplopanax horridus, and other organisms with data available. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

   

Ethyl 2-(2-hydroxyphenyl)-2-oxoacetate

Ethyl 2-(2-hydroxyphenyl)-2-oxoacetate

C10H10O4 (194.0579)


   

Imperatorin

Imperatorin

C16H14O4 (270.0892)


Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM. Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM.

   

Nevskin

7-[(2,6-dihydroxy-2,5,5,8a-tetramethyl-decahydronaphthalen-1-yl)methoxy]-2H-chromen-2-one

C24H32O5 (400.225)


   

samarcandin

7-[[(1S,2R,4aR,6R,8aS)-2,6-dihydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one

C24H32O5 (400.225)


Origin: Plant, Coumarins

   

Scopoletin

7-hydroxy-6-methoxychromen-2-one

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).

   

Scoparone

6,7-dimethoxycoumarin

C11H10O4 (206.0579)


Annotation level-1 D005765 - Gastrointestinal Agents > D002756 - Cholagogues and Choleretics D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents D002317 - Cardiovascular Agents > D000889 - Anti-Arrhythmia Agents D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents Scoparone is isolated from Artemisia capillaris Thunb., has anticoagulant, vasorelaxant antioxidant, anti-inflammatory activities[1]. Scoparone is isolated from Artemisia capillaris Thunb., has anticoagulant, vasorelaxant antioxidant, anti-inflammatory activities[1].

   

Umbelliprenin

7-{[(2E,6Z)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy}-2H-chromen-2-one

C24H30O3 (366.2195)


   

VITAMIN E

DL-alpha-Tocopherol

C29H50O2 (430.3811)


Window width to select the precursor ion was 3 Da.; CONE_VOLTAGE was 40 V.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 19HP8024 to the Mass Spectrometry Society of Japan. COVID info from COVID-19 Disease Map, clinicaltrial, clinicaltrials, clinical trial, clinical trials D020011 - Protective Agents > D000975 - Antioxidants D018977 - Micronutrients > D014815 - Vitamins 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 15 V.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 19HP8024 to the Mass Spectrometry Society of Japan. 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. DL-alpha-Tocopherol is a synthetic vitamin E, with antioxidation effect. DL-alpha-Tocopherol protects human skin fibroblasts against the cytotoxic effect of UVB[1]. DL-alpha-Tocopherol is a synthetic vitamin E, with antioxidation effect. DL-alpha-Tocopherol protects human skin fibroblasts against the cytotoxic effect of UVB[1]. rel-α-Vitamin E (rel-D-α-Tocopherol) is a vitamin with antioxidant properties and also a mixture[1]. α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant[1][2]. α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant[1][2].

   

falcarindiol

1,9-Heptadecadiene-4,6-diyne-3,8-diol, (3R,8S,9Z)-

C17H24O2 (260.1776)


(+)-(3R,8S)-Falcarindiol is a polyacetylene found in carrots, has antimycobacterial activity, with an IC50 of 6 μM and MIC of 24 μM against Mycobacterium tuberculosis H37Ra[1][2]. Antineoplastic and anti-inflammatory activity[2]. (+)-(3R,8S)-Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. (+)-(3R,8S)-Falcarindiol is a polyacetylene found in carrots, has antimycobacterial activity, with an IC50 of 6 μM and MIC of 24 μM against Mycobacterium tuberculosis H37Ra[1][2]. Antineoplastic and anti-inflammatory activity[2]. (+)-(3R,8S)-Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. (+)-(3R,8S)-Falcarindiol is a polyacetylene found in carrots, has antimycobacterial activity, with an IC50 of 6 μM and MIC of 24 μM against Mycobacterium tuberculosis H37Ra[1][2]. Antineoplastic and anti-inflammatory activity[2]. (+)-(3R,8S)-Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. (+)-(3R,8S)-Falcarindiol is a polyacetylene found in carrots, has antimycobacterial activity, with an IC50 of 6 μM and MIC of 24 μM against Mycobacterium tuberculosis H37Ra[1][2]. Antineoplastic and anti-inflammatory activity[2]. (+)-(3R,8S)-Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Falcarindiol, an orally active polyacetylenic oxylipin, activates PPARγ and increases the expression of the cholesterol transporter ABCA1 in cells. Falcarindiol induces apoptosis and autophagy. Falcarindiol has anti-inflammatory, antifungal, anticancer and antidiabetic properties[1][2]. Falcarindiol is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

   

Elemicin

Benzene, 1,2,3-trimethoxy-5-(2-propenyl)- (9CI)

C12H16O3 (208.1099)


Elemicin is an orally active alkenylbenzene widely distributed in many herbs and spices. Elemicin inhibits Stearoyl-CoA Desaturase 1 (SCD1) by metabolic activation. Elemicin has anti-influenza activities, antimicrobial, antioxidant, and antiviral activities. Elemicin and its reactive metabolite of 1′-Hydroxyelemicin can induce hepatotoxicity[1][2][3][4]. Elemicin is a alkenylbenzene widely distributed in many herbs and spices. Elemicin inhibits Stearoyl-CoA Desaturase 1 (SCD1) by metabolic activation. Elemicin is one of the main components in aromatic food and has antimicrobial, antioxidant, and antiviral activities. Elemicin possesses genotoxicity and carcinogenicity[1]. Elemicin is a alkenylbenzene widely distributed in many herbs and spices. Elemicin inhibits Stearoyl-CoA Desaturase 1 (SCD1) by metabolic activation. Elemicin is one of the main components in aromatic food and has antimicrobial, antioxidant, and antiviral activities. Elemicin possesses genotoxicity and carcinogenicity[1].

   

Isoscopoletin

2H-1-Benzopyran-2-one, 6-hydroxy-7-methoxy-

C10H8O4 (192.0423)


Isoscopoletin is a hydroxycoumarin that is esculetin in which the hydroxy group at position 7 is replaced by a methoxy group. It is the major primary metabolite of scoparone. It has a role as a plant metabolite. It is a hydroxycoumarin and an aromatic ether. It is functionally related to an esculetin. Isoscopoletin is a natural product found in Clausena dunniana, Olea capensis, and other organisms with data available. A hydroxycoumarin that is esculetin in which the hydroxy group at position 7 is replaced by a methoxy group. It is the major primary metabolite of scoparone. Isoscopoletin, also known as 6-hydroxy-7-methoxycoumarin or 7-methoxyesculetin, is a member of the class of compounds known as hydroxycoumarins. Hydroxycoumarins are coumarins that contain one or more hydroxyl groups attached to the coumarin skeleton. Isoscopoletin is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Isoscopoletin can be found in coriander and eggplant, which makes isoscopoletin a potential biomarker for the consumption of these food products. Isoscopoletin (6-Hydroxy-7-methoxycoumarin) is an active constituent in Artemisia argyi leaves. Isoscopoletin shows substantial inhibition against cell proliferation, with IC50s of 4.0 μM and 1.6 μM for human CCRF-CEM leukaemia cells and multidrug resistant subline CEM/ADR5000, respectively[1]. Isoscopoletin (6-Hydroxy-7-methoxycoumarin) possesses inhibitory activity against HBV replication[2]. Isoscopoletin (6-Hydroxy-7-methoxycoumarin) is an active constituent in Artemisia argyi leaves. Isoscopoletin shows substantial inhibition against cell proliferation, with IC50s of 4.0 μM and 1.6 μM for human CCRF-CEM leukaemia cells and multidrug resistant subline CEM/ADR5000, respectively[1]. Isoscopoletin (6-Hydroxy-7-methoxycoumarin) possesses inhibitory activity against HBV replication[2].

   

Ammidin

InChI=1\C16H14O4\c1-10(2)5-7-19-16-14-12(6-8-18-14)9-11-3-4-13(17)20-15(11)16\h3-6,8-9H,7H2,1-2H

C16H14O4 (270.0892)


D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM. Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM.

   

Ephanyl

2H-1-Benzopyran-6-ol, 3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-, (2R*(4R*,8R*))-(+-)- (9CI)

C29H50O2 (430.3811)


COVID info from COVID-19 Disease Map, clinicaltrial, clinicaltrials, clinical trial, clinical trials D020011 - Protective Agents > D000975 - Antioxidants D018977 - Micronutrients > D014815 - Vitamins Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS rel-α-Vitamin E (rel-D-α-Tocopherol) is a vitamin with antioxidant properties and also a mixture[1]. α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant[1][2]. α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant[1][2].

   

(2r)-2-[(2s,4e)-2-hydroxy-6-oxohept-4-en-2-yl]-2h,3h-furo[3,2-c]chromen-4-one

(2r)-2-[(2s,4e)-2-hydroxy-6-oxohept-4-en-2-yl]-2h,3h-furo[3,2-c]chromen-4-one

C18H18O5 (314.1154)


   

(1r,3ar,4r,8as)-8a-hydroxy-1-isopropyl-3a,6-dimethyl-3-oxo-2,4,7,8-tetrahydro-1h-azulen-4-yl 4-methoxybenzoate

(1r,3ar,4r,8as)-8a-hydroxy-1-isopropyl-3a,6-dimethyl-3-oxo-2,4,7,8-tetrahydro-1h-azulen-4-yl 4-methoxybenzoate

C23H30O5 (386.2093)


   

3-hydroxy-3-isopropyl-6,8a-dimethyl-8-[(2-methylbut-2-enoyl)oxy]-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

3-hydroxy-3-isopropyl-6,8a-dimethyl-8-[(2-methylbut-2-enoyl)oxy]-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

C28H38O6 (470.2668)


   

4-hydroxy-3-[(2e,6e)-5-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]chromen-2-one

4-hydroxy-3-[(2e,6e)-5-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]chromen-2-one

C24H30O4 (382.2144)


   

(3r,3ar,4s,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-oxo-2,3a,4,5-tetrahydro-1h-azulen-4-yl 4-methoxybenzoate

(3r,3ar,4s,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-oxo-2,3a,4,5-tetrahydro-1h-azulen-4-yl 4-methoxybenzoate

C23H30O5 (386.2093)


   

5-hydroxy-5-isopropyl-2a,7a-dimethyl-hexahydro-1ah-azuleno[5,6-b]oxiren-6-yl 4-hydroxybenzoate

5-hydroxy-5-isopropyl-2a,7a-dimethyl-hexahydro-1ah-azuleno[5,6-b]oxiren-6-yl 4-hydroxybenzoate

C22H30O5 (374.2093)


   

(3r,3as,5r,8ar)-3a-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3,4,5,8-hexahydroazulen-5-yl 3,4-dimethoxybenzoate

(3r,3as,5r,8ar)-3a-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3,4,5,8-hexahydroazulen-5-yl 3,4-dimethoxybenzoate

C24H34O5 (402.2406)


   

1,8-bis(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

1,8-bis(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

C27H36O8 (488.241)


   

3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl benzoate

3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl benzoate

C22H30O3 (342.2195)


   

4-hydroxy-3-[(2e,6e,10e)-12-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]chromen-2-one

4-hydroxy-3-[(2e,6e,10e)-12-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]chromen-2-one

C24H30O4 (382.2144)


   

3-hydroxy-3-isopropyl-6,8a-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-1,2,3a,4,5,8-hexahydroazulen-1-yl 2-methylbut-2-enoate

3-hydroxy-3-isopropyl-6,8a-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-1,2,3a,4,5,8-hexahydroazulen-1-yl 2-methylbut-2-enoate

C25H38O5 (418.2719)


   

7-{[(3e)-3,7-dimethyl-5-oxoocta-3,6-dien-1-yl]oxy}chromen-2-one

7-{[(3e)-3,7-dimethyl-5-oxoocta-3,6-dien-1-yl]oxy}chromen-2-one

C19H20O4 (312.1362)


   

2-(4,8-dimethylcyclodeca-2,7-dien-1-yl)propan-2-ol

2-(4,8-dimethylcyclodeca-2,7-dien-1-yl)propan-2-ol

C15H26O (222.1984)


   

7-{[(3s,4e)-3-hydroxy-3,7-dimethylocta-4,6-dien-1-yl]oxy}chromen-2-one

7-{[(3s,4e)-3-hydroxy-3,7-dimethylocta-4,6-dien-1-yl]oxy}chromen-2-one

C19H22O4 (314.1518)


   

3-hydroxy-3-isopropyl-6,8a-dimethyl-8-[(2-methylbut-2-enoyl)oxy]-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxybenzoate

3-hydroxy-3-isopropyl-6,8a-dimethyl-8-[(2-methylbut-2-enoyl)oxy]-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxybenzoate

C27H36O6 (456.2512)


   

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl benzoate

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl benzoate

C22H30O3 (342.2195)


   

(1s,3r,3as,4s,8s,8as)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

(1s,3r,3as,4s,8s,8as)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

C25H34O7 (446.2304)


   

2-[6-(5-ethenyl-5-methyloxolan-2-yl)-6-methyl-1,2-dioxan-3-yl]propan-2-ol

2-[6-(5-ethenyl-5-methyloxolan-2-yl)-6-methyl-1,2-dioxan-3-yl]propan-2-ol

C15H26O4 (270.1831)


   

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

C24H32O4 (384.23)


   

1-(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxybenzoate

1-(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxybenzoate

C24H32O6 (416.2199)


   

2,6-dimethyl-9-{2-methyl-5-oxopyrano[3,2-c]chromen-2-yl}nona-2,6-dienal

2,6-dimethyl-9-{2-methyl-5-oxopyrano[3,2-c]chromen-2-yl}nona-2,6-dienal

C24H26O4 (378.1831)


   

(1r,3as,4r,8s,8as)-1-hydroxy-1-isopropyl-3a,6-dimethyl-8-{[(2e)-2-methylbut-2-enoyl]oxy}-2,3,4,7,8,8a-hexahydroazulen-4-yl 4-methoxybenzoate

(1r,3as,4r,8s,8as)-1-hydroxy-1-isopropyl-3a,6-dimethyl-8-{[(2e)-2-methylbut-2-enoyl]oxy}-2,3,4,7,8,8a-hexahydroazulen-4-yl 4-methoxybenzoate

C28H38O6 (470.2668)


   

(1s,3as,8r,8ar)-1-isopropyl-3a,6-dimethyl-2,3,4,7,8,8a-hexahydroazulene-1,8-diol

(1s,3as,8r,8ar)-1-isopropyl-3a,6-dimethyl-2,3,4,7,8,8a-hexahydroazulene-1,8-diol

C15H26O2 (238.1933)


   

(3s,3ar,5as,10as)-3,5a,8-trimethyl-2,5-dioxo-3h,3ah,4h,6h,9h,10h-azuleno[3a,3-b]furan-6-yl 4-methoxybenzoate

(3s,3ar,5as,10as)-3,5a,8-trimethyl-2,5-dioxo-3h,3ah,4h,6h,9h,10h-azuleno[3a,3-b]furan-6-yl 4-methoxybenzoate

C23H26O6 (398.1729)


   

(2r)-2-[(3e)-4,8-dimethylnona-3,7-dien-1-yl]-2-methylpyrano[3,2-c]chromen-5-one

(2r)-2-[(3e)-4,8-dimethylnona-3,7-dien-1-yl]-2-methylpyrano[3,2-c]chromen-5-one

C24H28O3 (364.2038)


   

(2e,6e)-2,6-dimethyl-9-[(2r)-2-methyl-5-oxopyrano[3,2-c]chromen-2-yl]nona-2,6-dienal

(2e,6e)-2,6-dimethyl-9-[(2r)-2-methyl-5-oxopyrano[3,2-c]chromen-2-yl]nona-2,6-dienal

C24H26O4 (378.1831)


   

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 3,4-dimethoxybenzoate

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 3,4-dimethoxybenzoate

C24H34O5 (402.2406)


   

2-hydroxy-3-[(6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]chromen-4-one

2-hydroxy-3-[(6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]chromen-4-one

C24H30O3 (366.2195)


   

7-{[(3z,5e)-7-hydroxy-3,7-dimethylocta-3,5-dien-1-yl]oxy}chromen-2-one

7-{[(3z,5e)-7-hydroxy-3,7-dimethylocta-3,5-dien-1-yl]oxy}chromen-2-one

C19H22O4 (314.1518)


   

4-hydroxy-3-[(2e,5s,6e)-5-{[(2z,6e,10e)-12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl]oxy}-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]chromen-2-one

4-hydroxy-3-[(2e,5s,6e)-5-{[(2z,6e,10e)-12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl]oxy}-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]chromen-2-one

C48H58O7 (746.4182)


   

7-{[(3r,4e)-3-hydroxy-3,7-dimethylocta-4,6-dien-1-yl]oxy}chromen-2-one

7-{[(3r,4e)-3-hydroxy-3,7-dimethylocta-4,6-dien-1-yl]oxy}chromen-2-one

C19H22O4 (314.1518)


   

(3r,3as,4s,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-oxo-2,3a,4,5-tetrahydro-1h-azulen-4-yl (2e)-2-methylbut-2-enoate

(3r,3as,4s,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-oxo-2,3a,4,5-tetrahydro-1h-azulen-4-yl (2e)-2-methylbut-2-enoate

C20H30O4 (334.2144)


   

3-hydroxy-3-isopropyl-6,8a-dimethyl-8-[(2-methylbut-2-enoyl)oxy]-1,2,3a,4,5,8-hexahydroazulen-4-yl benzoate

3-hydroxy-3-isopropyl-6,8a-dimethyl-8-[(2-methylbut-2-enoyl)oxy]-1,2,3a,4,5,8-hexahydroazulen-4-yl benzoate

C27H36O5 (440.2563)


   

(3s,3ar,4s,9ar,9bs)-3-(acetyloxy)-3,6,9-trimethyl-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl benzoate

(3s,3ar,4s,9ar,9bs)-3-(acetyloxy)-3,6,9-trimethyl-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl benzoate

C24H24O7 (424.1522)


   

2-(acetyloxy)-5-hydroxy-5-isopropyl-2a,7a-dimethyl-hexahydro-1ah-azuleno[5,6-b]oxiren-6-yl 2-methylbut-2-enoate

2-(acetyloxy)-5-hydroxy-5-isopropyl-2a,7a-dimethyl-hexahydro-1ah-azuleno[5,6-b]oxiren-6-yl 2-methylbut-2-enoate

C22H34O6 (394.2355)


   

2-[(3e)-4,8-dimethylnona-3,7-dien-1-yl]-2-methylpyrano[3,2-c]chromen-5-one

2-[(3e)-4,8-dimethylnona-3,7-dien-1-yl]-2-methylpyrano[3,2-c]chromen-5-one

C24H28O3 (364.2038)


   

methyl 2-(2-hydroxyphenyl)-2-oxoacetate

methyl 2-(2-hydroxyphenyl)-2-oxoacetate

C9H8O4 (180.0423)


   

(1s,3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}-1,2,3a,4,5,8-hexahydroazulen-1-yl (2z)-2-methylbut-2-enoate

(1s,3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}-1,2,3a,4,5,8-hexahydroazulen-1-yl (2z)-2-methylbut-2-enoate

C25H38O5 (418.2719)


   

1,8-bis(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 3,4-dimethoxybenzoate

1,8-bis(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 3,4-dimethoxybenzoate

C28H38O9 (518.2516)


   

1-isopropyl-3a,6-dimethyl-2,5-dioxo-3,4,7,8-tetrahydroazulen-6-yl 2-methylbut-2-enoate

1-isopropyl-3a,6-dimethyl-2,5-dioxo-3,4,7,8-tetrahydroazulen-6-yl 2-methylbut-2-enoate

C20H28O4 (332.1987)


   

(1s,3as,5s,6s,8ar)-6,8a-dihydroxy-1-isopropyl-3a,6-dimethyl-hexahydro-1h-azulen-5-yl (2z)-2-methylbut-2-enoate

(1s,3as,5s,6s,8ar)-6,8a-dihydroxy-1-isopropyl-3a,6-dimethyl-hexahydro-1h-azulen-5-yl (2z)-2-methylbut-2-enoate

C20H34O4 (338.2457)


   

7-{[(3e)-3,7-dimethyl-5-oxoocta-3,7-dien-1-yl]oxy}chromen-2-one

7-{[(3e)-3,7-dimethyl-5-oxoocta-3,7-dien-1-yl]oxy}chromen-2-one

C19H20O4 (312.1362)


   

2-(9-hydroxy-4,8-dimethylnona-3,7-dien-1-yl)-2-methylpyrano[3,2-c]chromen-5-one

2-(9-hydroxy-4,8-dimethylnona-3,7-dien-1-yl)-2-methylpyrano[3,2-c]chromen-5-one

C24H28O4 (380.1987)


   

7-{[(4e)-3-hydroxy-3,7-dimethylocta-4,6-dien-1-yl]oxy}chromen-2-one

7-{[(4e)-3-hydroxy-3,7-dimethylocta-4,6-dien-1-yl]oxy}chromen-2-one

C19H22O4 (314.1518)


   

(1r,3as,4r,8s,8as)-1-hydroxy-1-isopropyl-3a,6-dimethyl-8-{[(2z)-2-methylbut-2-enoyl]oxy}-2,3,4,7,8,8a-hexahydroazulen-4-yl 4-methoxybenzoate

(1r,3as,4r,8s,8as)-1-hydroxy-1-isopropyl-3a,6-dimethyl-8-{[(2z)-2-methylbut-2-enoyl]oxy}-2,3,4,7,8,8a-hexahydroazulen-4-yl 4-methoxybenzoate

C28H38O6 (470.2668)


   

7-{[(2e)-3,7-dimethylocta-2,6-dien-1-yl]oxy}-6-methoxychromen-2-one

7-{[(2e)-3,7-dimethylocta-2,6-dien-1-yl]oxy}-6-methoxychromen-2-one

C20H24O4 (328.1675)


   

4-hydroxy-3-[(2e,5r,6e)-5-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]chromen-2-one

4-hydroxy-3-[(2e,5r,6e)-5-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]chromen-2-one

C24H30O4 (382.2144)


   

(3r,3as,5r,8ar)-3a-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3,4,5,8-hexahydroazulen-5-yl acetate

(3r,3as,5r,8ar)-3a-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3,4,5,8-hexahydroazulen-5-yl acetate

C17H28O3 (280.2038)


   

4-hydroxy-3-nonylchromen-2-one

4-hydroxy-3-nonylchromen-2-one

C18H24O3 (288.1725)


   

4-hydroxy-3-[(2e,6e,10z)-12-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]chromen-2-one

4-hydroxy-3-[(2e,6e,10z)-12-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]chromen-2-one

C24H30O4 (382.2144)


   

2-[(5e)-2,9-dihydroxy-6,10-dimethylundeca-5,10-dien-2-yl]-2h,3h-furo[3,2-c]chromen-4-one

2-[(5e)-2,9-dihydroxy-6,10-dimethylundeca-5,10-dien-2-yl]-2h,3h-furo[3,2-c]chromen-4-one

C24H30O5 (398.2093)


   

6,8a-dihydroxy-1-isopropyl-3a,6-dimethyl-hexahydro-1h-azulen-5-yl 2-methylbut-2-enoate

6,8a-dihydroxy-1-isopropyl-3a,6-dimethyl-hexahydro-1h-azulen-5-yl 2-methylbut-2-enoate

C20H34O4 (338.2457)


   

(1s,3r,3as,4s,8ar)-1-(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

(1s,3r,3as,4s,8ar)-1-(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

C25H34O6 (430.2355)


   

2-(2-hydroxy-6-oxohept-4-en-2-yl)-2h,3h-furo[3,2-c]chromen-4-one

2-(2-hydroxy-6-oxohept-4-en-2-yl)-2h,3h-furo[3,2-c]chromen-4-one

C18H18O5 (314.1154)


   

(2r)-2-[(2s,5e,9r)-2,9-dihydroxy-6,10-dimethylundeca-5,10-dien-2-yl]-2h,3h-furo[3,2-c]chromen-4-one

(2r)-2-[(2s,5e,9r)-2,9-dihydroxy-6,10-dimethylundeca-5,10-dien-2-yl]-2h,3h-furo[3,2-c]chromen-4-one

C24H30O5 (398.2093)


   

(2e,6e,10e)-12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trienal

(2e,6e,10e)-12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trienal

C24H28O4 (380.1987)


   

7-{[(1s,4ar,6s,8as)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-hexahydro-1h-naphthalen-1-yl]methoxy}chromen-2-one

7-{[(1s,4ar,6s,8as)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-hexahydro-1h-naphthalen-1-yl]methoxy}chromen-2-one

C24H30O4 (382.2144)


   

(2e,6e,10e)-12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl benzoate

(2e,6e,10e)-12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl benzoate

C31H34O5 (486.2406)


   

(2z,6e,10e)-12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl acetate

(2z,6e,10e)-12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl acetate

C26H32O5 (424.225)


   

14-hydroxy-1-(2-hydroxyphenyl)-5,9,13-trimethyltetradeca-4,8,12-trien-1-one

14-hydroxy-1-(2-hydroxyphenyl)-5,9,13-trimethyltetradeca-4,8,12-trien-1-one

C23H32O3 (356.2351)


   

(1s,3r,3as,4s,8r,8ar)-1,8-bis(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

(1s,3r,3as,4s,8r,8ar)-1,8-bis(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

C27H36O8 (488.241)


   

4-hydroxy-3-(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)chromen-2-one

4-hydroxy-3-(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)chromen-2-one

C24H30O3 (366.2195)


   

(2s,3s)-3-hydroxy-2-[(3e)-7-hydroxy-4,8-dimethylnona-3,8-dien-1-yl]-2-methyl-3h,4h-pyrano[2,3-b]chromen-5-one

(2s,3s)-3-hydroxy-2-[(3e)-7-hydroxy-4,8-dimethylnona-3,8-dien-1-yl]-2-methyl-3h,4h-pyrano[2,3-b]chromen-5-one

C24H30O5 (398.2093)


   

8-(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

8-(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

C25H34O6 (430.2355)


   

(3r,3ar,4s,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-oxo-2,3a,4,5-tetrahydro-1h-azulen-4-yl (2z)-2-methylbut-2-enoate

(3r,3ar,4s,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-oxo-2,3a,4,5-tetrahydro-1h-azulen-4-yl (2z)-2-methylbut-2-enoate

C20H30O4 (334.2144)


   

7-{[(2e)-3,7-dimethyl-5-oxoocta-2,6-dien-1-yl]oxy}chromen-2-one

7-{[(2e)-3,7-dimethyl-5-oxoocta-2,6-dien-1-yl]oxy}chromen-2-one

C19H20O4 (312.1362)


   

4-(2-hydroxypropan-2-yl)-1,6-dimethyl-octahydro-2h-naphthalene-1,5-diol

4-(2-hydroxypropan-2-yl)-1,6-dimethyl-octahydro-2h-naphthalene-1,5-diol

C15H28O3 (256.2038)


   

(3s,3ar,5ar,6r,10as)-3,5a,8-trimethyl-2,5-dioxo-3h,3ah,4h,6h,9h,10h-azuleno[3a,3-b]furan-6-yl 4-methoxybenzoate

(3s,3ar,5ar,6r,10as)-3,5a,8-trimethyl-2,5-dioxo-3h,3ah,4h,6h,9h,10h-azuleno[3a,3-b]furan-6-yl 4-methoxybenzoate

C23H26O6 (398.1729)


   

(2z,6e)-2,6-dimethyl-9-[(2r)-2-methyl-5-oxopyrano[3,2-c]chromen-2-yl]nona-2,6-dien-1-yl acetate

(2z,6e)-2,6-dimethyl-9-[(2r)-2-methyl-5-oxopyrano[3,2-c]chromen-2-yl]nona-2,6-dien-1-yl acetate

C26H30O5 (422.2093)


   

2-(2,9-dihydroxy-6,10-dimethylundeca-5,10-dien-2-yl)-2h,3h-furo[3,2-c]chromen-4-one

2-(2,9-dihydroxy-6,10-dimethylundeca-5,10-dien-2-yl)-2h,3h-furo[3,2-c]chromen-4-one

C24H30O5 (398.2093)


   

3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 2-methylbut-2-enoate

3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 2-methylbut-2-enoate

C20H32O3 (320.2351)


   

3-hydroxy-3-isopropyl-6,8a-dimethyl-8-oxo-2,3a,4,5-tetrahydro-1h-azulen-4-yl 3-methylbutanoate

3-hydroxy-3-isopropyl-6,8a-dimethyl-8-oxo-2,3a,4,5-tetrahydro-1h-azulen-4-yl 3-methylbutanoate

C20H32O4 (336.23)


   

(2r)-2-[(3e,7e)-9-hydroxy-4,8-dimethylnona-3,7-dien-1-yl]-2-methylpyrano[3,2-c]chromen-5-one

(2r)-2-[(3e,7e)-9-hydroxy-4,8-dimethylnona-3,7-dien-1-yl]-2-methylpyrano[3,2-c]chromen-5-one

C24H28O4 (380.1987)


   

3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxy-3-methoxybenzoate

3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxy-3-methoxybenzoate

C23H32O5 (388.225)


   

2-[(2-hydroxy-2-methyl-3-{[(2e)-2-methylbut-2-enoyl]oxy}butanoyl)oxy]-1-(7-methoxy-2h-1,3-benzodioxol-5-yl)propyl (2e)-2-methylbut-2-enoate

2-[(2-hydroxy-2-methyl-3-{[(2e)-2-methylbut-2-enoyl]oxy}butanoyl)oxy]-1-(7-methoxy-2h-1,3-benzodioxol-5-yl)propyl (2e)-2-methylbut-2-enoate

C26H34O10 (506.2152)


   

1-(2-hydroxyphenyl)-5,9,13-trimethyltetradeca-4,8,12-trien-1-one

1-(2-hydroxyphenyl)-5,9,13-trimethyltetradeca-4,8,12-trien-1-one

C23H32O2 (340.2402)


   

3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

C23H32O5 (388.225)


   

(3r,3as,4s,8r,8as)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

(3r,3as,4s,8r,8as)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

C23H32O5 (388.225)


   

(1s,3r,3as,4s,8s,8ar)-1,8-bis(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

(1s,3r,3as,4s,8s,8ar)-1,8-bis(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

C27H36O8 (488.241)


   

3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

C23H32O4 (372.23)


   

(2e,6e)-2,6-dimethyl-9-[(2r)-2-methyl-5-oxopyrano[3,2-c]chromen-2-yl]nona-2,6-dien-1-yl acetate

(2e,6e)-2,6-dimethyl-9-[(2r)-2-methyl-5-oxopyrano[3,2-c]chromen-2-yl]nona-2,6-dien-1-yl acetate

C26H30O5 (422.2093)


   

4-hydroxy-3-(12-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)chromen-2-one

4-hydroxy-3-(12-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)chromen-2-one

C24H30O4 (382.2144)


   

12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trienal

12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trienal

C24H28O4 (380.1987)


   

7-{[(2s,4as,6s)-2,6-dihydroxy-2,5,5,8a-tetramethyl-hexahydro-1h-naphthalen-1-yl]methoxy}chromen-2-one

7-{[(2s,4as,6s)-2,6-dihydroxy-2,5,5,8a-tetramethyl-hexahydro-1h-naphthalen-1-yl]methoxy}chromen-2-one

C24H32O5 (400.225)


   

(1s,3r,3as,4s,8r,8ar)-1,8-bis(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 3,4-dimethoxybenzoate

(1s,3r,3as,4s,8r,8ar)-1,8-bis(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 3,4-dimethoxybenzoate

C28H38O9 (518.2516)


   

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

C23H32O4 (372.23)


   

1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

C25H34O7 (446.2304)


   

(2r)-2-[(3e,7z)-9-hydroxy-4,8-dimethylnona-3,7-dien-1-yl]-2-methylpyrano[3,2-c]chromen-5-one

(2r)-2-[(3e,7z)-9-hydroxy-4,8-dimethylnona-3,7-dien-1-yl]-2-methylpyrano[3,2-c]chromen-5-one

C24H28O4 (380.1987)


   

2-hydroxy-3-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]chromen-4-one

2-hydroxy-3-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]chromen-4-one

C24H30O3 (366.2195)


   

7-{[(4as)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-hexahydro-1h-naphthalen-1-yl]methoxy}chromen-2-one

7-{[(4as)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-hexahydro-1h-naphthalen-1-yl]methoxy}chromen-2-one

C24H30O4 (382.2144)


   

(3r,3as,4s,8r,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-{[(2z)-2-methylbut-2-enoyl]oxy}-1,2,3a,4,5,8-hexahydroazulen-4-yl benzoate

(3r,3as,4s,8r,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-{[(2z)-2-methylbut-2-enoyl]oxy}-1,2,3a,4,5,8-hexahydroazulen-4-yl benzoate

C27H36O5 (440.2563)


   

3-hydroxy-3-isopropyl-6,8a-dimethyl-8-[(2-methylbut-2-enoyl)oxy]-1,2,3a,4,5,8-hexahydroazulen-4-yl 3,4-dimethoxybenzoate

3-hydroxy-3-isopropyl-6,8a-dimethyl-8-[(2-methylbut-2-enoyl)oxy]-1,2,3a,4,5,8-hexahydroazulen-4-yl 3,4-dimethoxybenzoate

C29H40O7 (500.2774)


   

(4e,8e,12z)-14-hydroxy-1-(2-hydroxyphenyl)-5,9,13-trimethyltetradeca-4,8,12-trien-1-one

(4e,8e,12z)-14-hydroxy-1-(2-hydroxyphenyl)-5,9,13-trimethyltetradeca-4,8,12-trien-1-one

C23H32O3 (356.2351)


   

(1as,2s,2as,5r,5as,6s,7ar)-2-(acetyloxy)-5-hydroxy-5-isopropyl-2a,7a-dimethyl-hexahydro-1ah-azuleno[5,6-b]oxiren-6-yl (2e)-2-methylbut-2-enoate

(1as,2s,2as,5r,5as,6s,7ar)-2-(acetyloxy)-5-hydroxy-5-isopropyl-2a,7a-dimethyl-hexahydro-1ah-azuleno[5,6-b]oxiren-6-yl (2e)-2-methylbut-2-enoate

C22H34O6 (394.2355)


   

(3s,3ar,4s,9ar,9bs)-3-(acetyloxy)-3,6,9-trimethyl-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 3,4-dimethoxybenzoate

(3s,3ar,4s,9ar,9bs)-3-(acetyloxy)-3,6,9-trimethyl-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 3,4-dimethoxybenzoate

C26H28O9 (484.1733)


   

3-hydroxy-2-(7-hydroxy-4,8-dimethylnona-3,8-dien-1-yl)-2-methyl-3h,4h-pyrano[2,3-b]chromen-5-one

3-hydroxy-2-(7-hydroxy-4,8-dimethylnona-3,8-dien-1-yl)-2-methyl-3h,4h-pyrano[2,3-b]chromen-5-one

C24H30O5 (398.2093)


   

1,8-dihydroxy-1-isopropyl-3a,6-dimethyl-3,7,8,8a-tetrahydro-2h-azulen-4-one

1,8-dihydroxy-1-isopropyl-3a,6-dimethyl-3,7,8,8a-tetrahydro-2h-azulen-4-one

C15H24O3 (252.1725)


   

(2r,3s)-3-hydroxy-4-{[(1s,2s)-1-(7-methoxy-2h-1,3-benzodioxol-5-yl)-1-{[(2z)-2-methylbut-2-enoyl]oxy}propan-2-yl]oxy}-3-methyl-4-oxobutan-2-yl (2z)-2-methylbut-2-enoate

(2r,3s)-3-hydroxy-4-{[(1s,2s)-1-(7-methoxy-2h-1,3-benzodioxol-5-yl)-1-{[(2z)-2-methylbut-2-enoyl]oxy}propan-2-yl]oxy}-3-methyl-4-oxobutan-2-yl (2z)-2-methylbut-2-enoate

C26H34O10 (506.2152)


   

(3r,3as,4s,8r,8as)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2z)-2-methylbut-2-enoate

(3r,3as,4s,8r,8as)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2z)-2-methylbut-2-enoate

C20H32O4 (336.23)


   

2-(4,8-dimethylnona-3,7-dien-1-yl)-2-methylpyrano[3,2-c]chromen-5-one

2-(4,8-dimethylnona-3,7-dien-1-yl)-2-methylpyrano[3,2-c]chromen-5-one

C24H28O3 (364.2038)


   

(1s)-1-(7-methoxy-2h-1,3-benzodioxol-5-yl)propan-1-ol

(1s)-1-(7-methoxy-2h-1,3-benzodioxol-5-yl)propan-1-ol

C11H14O4 (210.0892)


   

(3r,3as,4s,8r,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-{[(2z)-2-methylbut-2-enoyl]oxy}-1,2,3a,4,5,8-hexahydroazulen-4-yl 3,4-dimethoxybenzoate

(3r,3as,4s,8r,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-{[(2z)-2-methylbut-2-enoyl]oxy}-1,2,3a,4,5,8-hexahydroazulen-4-yl 3,4-dimethoxybenzoate

C29H40O7 (500.2774)


   

2-(4,8-dimethylnona-3,7-dien-1-yl)-3-hydroxy-2-methyl-3h,4h-pyrano[2,3-b]chromen-5-one

2-(4,8-dimethylnona-3,7-dien-1-yl)-3-hydroxy-2-methyl-3h,4h-pyrano[2,3-b]chromen-5-one

C24H30O4 (382.2144)


   

{1a-isopropyl-3a-methyl-2h,3h,4h,7h,8h-azuleno[1,8a-b]oxiren-6-yl}methyl 4-methoxybenzoate

{1a-isopropyl-3a-methyl-2h,3h,4h,7h,8h-azuleno[1,8a-b]oxiren-6-yl}methyl 4-methoxybenzoate

C23H30O4 (370.2144)


   

1-(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

1-(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

C25H34O6 (430.2355)


   

(3r,3as,4s,8s,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-{[(2e)-2-methylbut-2-enoyl]oxy}-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxybenzoate

(3r,3as,4s,8s,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-{[(2e)-2-methylbut-2-enoyl]oxy}-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxybenzoate

C27H36O6 (456.2512)


   

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxy-3-methoxybenzoate

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxy-3-methoxybenzoate

C23H32O5 (388.225)


   

(3r,3as,4s,8r,8as)-8-(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

(3r,3as,4s,8r,8as)-8-(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

C25H34O6 (430.2355)


   

(2s,3s)-2-[(3e)-4,8-dimethylnona-3,7-dien-1-yl]-3-hydroxy-2-methyl-3h,4h-pyrano[2,3-b]chromen-5-one

(2s,3s)-2-[(3e)-4,8-dimethylnona-3,7-dien-1-yl]-3-hydroxy-2-methyl-3h,4h-pyrano[2,3-b]chromen-5-one

C24H30O4 (382.2144)


   

3-hydroxy-3-isopropyl-6,8a-dimethyl-8-oxo-2,3a,4,5-tetrahydro-1h-azulen-4-yl 2-methylbut-2-enoate

3-hydroxy-3-isopropyl-6,8a-dimethyl-8-oxo-2,3a,4,5-tetrahydro-1h-azulen-4-yl 2-methylbut-2-enoate

C20H30O4 (334.2144)


   

(1s,3r,3as,4s,8ar)-1,3-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 3,4-dimethoxybenzoate

(1s,3r,3as,4s,8ar)-1,3-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 3,4-dimethoxybenzoate

C24H34O6 (418.2355)


   

4-hydroxy-3-(5-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)chromen-2-one

4-hydroxy-3-(5-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)chromen-2-one

C24H30O4 (382.2144)


   

(1e)-3-isopropyl-10-methyl-6-methylidenecyclodec-1-ene

(1e)-3-isopropyl-10-methyl-6-methylidenecyclodec-1-ene

C15H26 (206.2034)


   

(2e,10e)-12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl benzoate

(2e,10e)-12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl benzoate

C31H34O5 (486.2406)


   

(3r,3ar,4s,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-oxo-2,3a,4,5-tetrahydro-1h-azulen-4-yl 3-methylbutanoate

(3r,3ar,4s,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-oxo-2,3a,4,5-tetrahydro-1h-azulen-4-yl 3-methylbutanoate

C20H32O4 (336.23)


   

(4e,8e)-1-(2-hydroxyphenyl)-5,9,13-trimethyltetradeca-4,8,12-trien-1-one

(4e,8e)-1-(2-hydroxyphenyl)-5,9,13-trimethyltetradeca-4,8,12-trien-1-one

C23H32O2 (340.2402)


   

(2as,5r,7ar)-2-(acetyloxy)-5-hydroxy-5-isopropyl-2a,7a-dimethyl-hexahydro-1ah-azuleno[5,6-b]oxiren-6-yl (2z)-2-methylbut-2-enoate

(2as,5r,7ar)-2-(acetyloxy)-5-hydroxy-5-isopropyl-2a,7a-dimethyl-hexahydro-1ah-azuleno[5,6-b]oxiren-6-yl (2z)-2-methylbut-2-enoate

C22H34O6 (394.2355)


   

(3ar,6s)-1-isopropyl-3a,6-dimethyl-2,5-dioxo-3,4,7,8-tetrahydroazulen-6-yl (2z)-2-methylbut-2-enoate

(3ar,6s)-1-isopropyl-3a,6-dimethyl-2,5-dioxo-3,4,7,8-tetrahydroazulen-6-yl (2z)-2-methylbut-2-enoate

C20H28O4 (332.1987)


   

12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl acetate

12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl acetate

C26H32O5 (424.225)


   

2,6-dimethyl-9-{2-methyl-5-oxopyrano[3,2-c]chromen-2-yl}nona-2,6-dien-1-yl acetate

2,6-dimethyl-9-{2-methyl-5-oxopyrano[3,2-c]chromen-2-yl}nona-2,6-dien-1-yl acetate

C26H30O5 (422.2093)


   

(1s,4s,4ar,5r,6s,8as)-4-(2-hydroxypropan-2-yl)-1,6-dimethyl-octahydro-2h-naphthalene-1,5-diol

(1s,4s,4ar,5r,6s,8as)-4-(2-hydroxypropan-2-yl)-1,6-dimethyl-octahydro-2h-naphthalene-1,5-diol

C15H28O3 (256.2038)


   

4-hydroxy-3-(5-{[12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl]oxy}-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)chromen-2-one

4-hydroxy-3-(5-{[12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl]oxy}-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)chromen-2-one

C48H58O7 (746.4182)


   

(3r,3as,4s,8r,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-{[(2z)-2-methylbut-2-enoyl]oxy}-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

(3r,3as,4s,8r,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-{[(2z)-2-methylbut-2-enoyl]oxy}-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

C28H38O6 (470.2668)


   

7-{[(2z,6z)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy}chromen-2-one

7-{[(2z,6z)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy}chromen-2-one

C24H30O3 (366.2195)


   

4-hydroxy-3-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]chromen-2-one

4-hydroxy-3-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]chromen-2-one

C24H30O3 (366.2195)


   

(3s,3ar,4s,9ar,9bs)-3,6,9-trimethyl-3-[(3-methylbut-2-enoyl)oxy]-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 3,4-dimethoxybenzoate

(3s,3ar,4s,9ar,9bs)-3,6,9-trimethyl-3-[(3-methylbut-2-enoyl)oxy]-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 3,4-dimethoxybenzoate

C29H32O9 (524.2046)


   

(3r,3as,4s,8r,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-{[(2z)-2-methylbut-2-enoyl]oxy}-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxybenzoate

(3r,3as,4s,8r,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-{[(2z)-2-methylbut-2-enoyl]oxy}-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxybenzoate

C27H36O6 (456.2512)


   

(1r)-5-formyl-2,4,4-trimethylcyclohexa-2,5-dien-1-yl (2e)-2-[(acetyloxy)methyl]but-2-enoate

(1r)-5-formyl-2,4,4-trimethylcyclohexa-2,5-dien-1-yl (2e)-2-[(acetyloxy)methyl]but-2-enoate

C17H22O5 (306.1467)


   

12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl benzoate

12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl benzoate

C31H34O5 (486.2406)


   

(1r)-5-formyl-2,4,4-trimethylcyclohexa-2,5-dien-1-yl (2e)-2-methylbut-2-enoate

(1r)-5-formyl-2,4,4-trimethylcyclohexa-2,5-dien-1-yl (2e)-2-methylbut-2-enoate

C15H20O3 (248.1412)


   

(2e,10e)-12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl acetate

(2e,10e)-12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl acetate

C26H32O5 (424.225)


   

3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 3-(4-hydroxyphenyl)prop-2-enoate

3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 3-(4-hydroxyphenyl)prop-2-enoate

C24H32O4 (384.23)


   

(2e,6e,10e)-12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl acetate

(2e,6e,10e)-12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trien-1-yl acetate

C26H32O5 (424.225)


   

2-[(4e)-2-hydroxy-6-oxohept-4-en-2-yl]-2h,3h-furo[3,2-c]chromen-4-one

2-[(4e)-2-hydroxy-6-oxohept-4-en-2-yl]-2h,3h-furo[3,2-c]chromen-4-one

C18H18O5 (314.1154)


   

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2z)-2-methylbut-2-enoate

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2z)-2-methylbut-2-enoate

C20H32O3 (320.2351)


   

2-[(3r,6r)-6-[(2s,5s)-5-ethenyl-5-methyloxolan-2-yl]-6-methyl-1,2-dioxan-3-yl]propan-2-ol

2-[(3r,6r)-6-[(2s,5s)-5-ethenyl-5-methyloxolan-2-yl]-6-methyl-1,2-dioxan-3-yl]propan-2-ol

C15H26O4 (270.1831)


   

(2s,3s)-3-hydroxy-2-[(3e,7r)-7-hydroxy-4,8-dimethylnona-3,8-dien-1-yl]-2-methyl-3h,4h-pyrano[2,3-b]chromen-5-one

(2s,3s)-3-hydroxy-2-[(3e,7r)-7-hydroxy-4,8-dimethylnona-3,8-dien-1-yl]-2-methyl-3h,4h-pyrano[2,3-b]chromen-5-one

C24H30O5 (398.2093)


   

7-{[(2z)-3,7-dimethyl-5-oxoocta-2,6-dien-1-yl]oxy}chromen-2-one

7-{[(2z)-3,7-dimethyl-5-oxoocta-2,6-dien-1-yl]oxy}chromen-2-one

C19H20O4 (312.1362)


   

1-(7-methoxy-2h-1,3-benzodioxol-5-yl)propan-1-ol

1-(7-methoxy-2h-1,3-benzodioxol-5-yl)propan-1-ol

C11H14O4 (210.0892)


   

3-hydroxy-3-isopropyl-6,8a-dimethyl-8-oxo-2,3a,4,5-tetrahydro-1h-azulen-4-yl 4-methoxybenzoate

3-hydroxy-3-isopropyl-6,8a-dimethyl-8-oxo-2,3a,4,5-tetrahydro-1h-azulen-4-yl 4-methoxybenzoate

C23H30O5 (386.2093)


   

3-[(9e)-8-hydroxy-3-oxoheptadec-9-en-4,6-diyn-1-yl]-3-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]-1-benzopyran-2,4-dione

3-[(9e)-8-hydroxy-3-oxoheptadec-9-en-4,6-diyn-1-yl]-3-[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]-1-benzopyran-2,4-dione

C41H52O5 (624.3815)


   

polyanthin

polyanthin

C26H32O5 (424.225)


   

8a-hydroxy-1-isopropyl-3a,6-dimethyl-3-oxo-2,4,7,8-tetrahydro-1h-azulen-4-yl 4-methoxybenzoate

8a-hydroxy-1-isopropyl-3a,6-dimethyl-3-oxo-2,4,7,8-tetrahydro-1h-azulen-4-yl 4-methoxybenzoate

C23H30O5 (386.2093)


   

(3s,8r)-heptadeca-1,9-dien-4,6-diyne-3,8-diol

(3s,8r)-heptadeca-1,9-dien-4,6-diyne-3,8-diol

C17H24O2 (260.1776)


   

(2e,6e)-2,6-dimethyl-9-[(2s)-2-methyl-5-oxopyrano[3,2-c]chromen-2-yl]nona-2,6-dien-1-yl acetate

(2e,6e)-2,6-dimethyl-9-[(2s)-2-methyl-5-oxopyrano[3,2-c]chromen-2-yl]nona-2,6-dien-1-yl acetate

C26H30O5 (422.2093)


   

1-hydroxy-1-isopropyl-3a,6-dimethyl-8-[(2-methylbut-2-enoyl)oxy]-2,3,4,7,8,8a-hexahydroazulen-4-yl 4-methoxybenzoate

1-hydroxy-1-isopropyl-3a,6-dimethyl-8-[(2-methylbut-2-enoyl)oxy]-2,3,4,7,8,8a-hexahydroazulen-4-yl 4-methoxybenzoate

C28H38O6 (470.2668)


   

3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 2-methylbut-2-enoate

3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 2-methylbut-2-enoate

C20H32O4 (336.23)


   

(3r,3as,4s,8r,8as)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-2-methylbut-2-enoate

(3r,3as,4s,8r,8as)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl (2e)-2-methylbut-2-enoate

C20H32O4 (336.23)


   

(3r,3as,4s,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-oxo-2,3a,4,5-tetrahydro-1h-azulen-4-yl (2z)-2-methylbut-2-enoate

(3r,3as,4s,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-8-oxo-2,3a,4,5-tetrahydro-1h-azulen-4-yl (2z)-2-methylbut-2-enoate

C20H30O4 (334.2144)


   

[(1ar,3ar,8ar)-1a-isopropyl-3a-methyl-2h,3h,4h,7h,8h-azuleno[1,8a-b]oxiren-6-yl]methyl 4-methoxybenzoate

[(1ar,3ar,8ar)-1a-isopropyl-3a-methyl-2h,3h,4h,7h,8h-azuleno[1,8a-b]oxiren-6-yl]methyl 4-methoxybenzoate

C23H30O4 (370.2144)


   

(2r)-2,5,7,8-tetramethyl-2-[(4s,8s)-4,8,12-trimethyltridecyl]-3,4-dihydro-1-benzopyran-6-ol

(2r)-2,5,7,8-tetramethyl-2-[(4s,8s)-4,8,12-trimethyltridecyl]-3,4-dihydro-1-benzopyran-6-ol

C29H50O2 (430.3811)


   

(1s,3r,3as,4s,8ar)-1-(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxybenzoate

(1s,3r,3as,4s,8ar)-1-(acetyloxy)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxybenzoate

C24H32O6 (416.2199)


   

1-(7-methoxy-2h-1,3-benzodioxol-5-yl)-1-{[(2z)-2-methylbut-2-enoyl]oxy}propan-2-yl (2z)-2-methylbut-2-enoate

1-(7-methoxy-2h-1,3-benzodioxol-5-yl)-1-{[(2z)-2-methylbut-2-enoyl]oxy}propan-2-yl (2z)-2-methylbut-2-enoate

C21H26O7 (390.1678)


   

(1as,2ar,5r,5as,6s,7ar)-5-hydroxy-5-isopropyl-2a,7a-dimethyl-hexahydro-1ah-azuleno[5,6-b]oxiren-6-yl 4-hydroxybenzoate

(1as,2ar,5r,5as,6s,7ar)-5-hydroxy-5-isopropyl-2a,7a-dimethyl-hexahydro-1ah-azuleno[5,6-b]oxiren-6-yl 4-hydroxybenzoate

C22H30O5 (374.2093)


   

2-[(1r,2e,4r,7e)-4,8-dimethylcyclodeca-2,7-dien-1-yl]propan-2-ol

2-[(1r,2e,4r,7e)-4,8-dimethylcyclodeca-2,7-dien-1-yl]propan-2-ol

C15H26O (222.1984)


   

3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 3,4-dimethoxybenzoate

3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 3,4-dimethoxybenzoate

C24H34O5 (402.2406)