NCBI Taxonomy: 1458965

Chiliadenus montanus (ncbi_taxid: 1458965)

found 98 associated metabolites at species taxonomy rank level.

Ancestor: Chiliadenus

Child Taxonomies: none taxonomy data.

Chrysosplenetin

4H-1-Benzopyran-4-one, 5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6,7-trimethoxy-

C19H18O8 (374.1002)


Chrysosplenetin, also known as quercetagetin 3,6,7,3-tetramethyl ether or 3,6,7,3-tetra-methylquercetagetin, is a member of the class of compounds known as 7-o-methylated flavonoids. 7-o-methylated flavonoids are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone. Thus, chrysosplenetin is considered to be a flavonoid lipid molecule. Chrysosplenetin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Chrysosplenetin can be found in german camomile, which makes chrysosplenetin a potential biomarker for the consumption of this food product. Chrysosplenetin is an O-methylated flavonol. It can be found in the root of Berneuxia thibetica and in Chamomilla recutita . Chrysosplenetin is a tetramethoxyflavone that is the 3,6,7,3-tetramethyl ether derivative of quercetagetin. It has a role as an antiviral agent and a plant metabolite. It is a tetramethoxyflavone and a dihydroxyflavone. It is functionally related to a quercetagetin. Chrysosplenetin is a natural product found in Haplophyllum myrtifolium, Cleome amblyocarpa, and other organisms with data available. Chrysosplenetin is one of the polymethoxylated flavonoids in Artemisia annua L. (Compositae) and other several Chinese herbs. Chrysosplenetin inhibits P-gp activity and reverses the up-regulated P-gp and MDR1 levels induced by artemisinin (ART). Chrysosplenetin significantly augments the rat plasma level and anti-malarial efficacy of ART, partially due to the uncompetitive inhibition effect of Chrysosplenetin on rat CYP3A[1]. Chrysosplenetin is one of the polymethoxylated flavonoids in Artemisia annua L. (Compositae) and other several Chinese herbs. Chrysosplenetin inhibits P-gp activity and reverses the up-regulated P-gp and MDR1 levels induced by artemisinin (ART). Chrysosplenetin significantly augments the rat plasma level and anti-malarial efficacy of ART, partially due to the uncompetitive inhibition effect of Chrysosplenetin on rat CYP3A[1].

   

chrysoplenol D

4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5-hydroxy-3,6,7-trimethoxy-

C18H16O8 (360.0845)


3,4,5-trihydroxy-3,6,7-trimethoxyflavone is a trimethoxyflavone that is the 3,6,7-trimethyl ether derivative of quercetagetin. It has a role as an antineoplastic agent and a metabolite. It is a trihydroxyflavone and a trimethoxyflavone. It is functionally related to a quercetagetin. Chrysosplenol D is a natural product found in Psiadia viscosa, Chrysosplenium oppositifolium, and other organisms with data available. See also: Vitex negundo fruit (part of). Chrysosplenol D is a methoxy flavonoid that induces ERK1/2-mediated apoptosis in triple negative human breast cancer cells. Chrysosplenol D also exhibits anti-inflammatory and moderate antitrypanosomal activities[1][2][3][4]. Chrysosplenol D is a methoxy flavonoid that induces ERK1/2-mediated apoptosis in triple negative human breast cancer cells. Chrysosplenol D also exhibits anti-inflammatory and moderate antitrypanosomal activities[1][2][3][4].

   

Pachypodol

4H-1-Benzopyran-4-one, 5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,7-dimethoxy-

C18H16O7 (344.0896)


Pachypodol is a trimethoxyflavone that is quercetin in which the hydroxy groups at position 3, 7 and 3 are replaced by methoxy groups. It has been isolated from Combretum quadrangulare and Euodia elleryana. It has a role as a plant metabolite and an antiemetic. It is a dihydroxyflavone and a trimethoxyflavone. It is functionally related to a quercetin. Pachypodol is a natural product found in Larrea cuneifolia, Macaranga triloba, and other organisms with data available. A trimethoxyflavone that is quercetin in which the hydroxy groups at position 3, 7 and 3 are replaced by methoxy groups. It has been isolated from Combretum quadrangulare and Euodia elleryana. Pachypodol exerts antioxidant and cytoprotective effects in HepG2 cells[1].Pachypodol inhibits the growth of CaCo 2 colon cancer cell line in vitro(IC50 = 185.6 mM)[2]. Pachypodol exerts antioxidant and cytoprotective effects in HepG2 cells[1].Pachypodol inhibits the growth of CaCo 2 colon cancer cell line in vitro(IC50 = 185.6 mM)[2].

   

Patuletin

2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-6-methoxy-4H-1-benzopyran-4-one, 9ci

C16H12O8 (332.0532)


Pigment from flowers of French marigold Tagetes patula. Patuletin is found in german camomile, herbs and spices, and spinach. Patuletin is found in german camomile. Patuletin is a pigment from flowers of French marigold Tagetes patul D004791 - Enzyme Inhibitors

   

Methylprednisolone

6a_Methylprednisolone

C22H30O5 (374.2093)


H - Systemic hormonal preparations, excl. sex hormones and insulins > H02 - Corticosteroids for systemic use > H02A - Corticosteroids for systemic use, plain > H02AB - Glucocorticoids D - Dermatologicals > D10 - Anti-acne preparations > D10A - Anti-acne preparations for topical use > D10AA - Corticosteroids, combinations for treatment of acne D - Dermatologicals > D07 - Corticosteroids, dermatological preparations > D07A - Corticosteroids, plain > D07AA - Corticosteroids, weak (group i) D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D005938 - Glucocorticoids C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone C308 - Immunotherapeutic Agent > C574 - Immunosuppressant > C211 - Therapeutic Corticosteroid COVID info from DrugBank, clinicaltrial, clinicaltrials, clinical trial, clinical trials D002491 - Central Nervous System Agents > D018696 - Neuroprotective Agents D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents D005765 - Gastrointestinal Agents > D000932 - Antiemetics D000893 - Anti-Inflammatory Agents D020011 - Protective Agents Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS CONFIDENCE standard compound; INTERNAL_ID 904; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8731; ORIGINAL_PRECURSOR_SCAN_NO 8728 CONFIDENCE standard compound; INTERNAL_ID 904; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8721; ORIGINAL_PRECURSOR_SCAN_NO 8719 CONFIDENCE standard compound; INTERNAL_ID 904; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8747; ORIGINAL_PRECURSOR_SCAN_NO 8745 CONFIDENCE standard compound; INTERNAL_ID 904; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8759; ORIGINAL_PRECURSOR_SCAN_NO 8757 CONFIDENCE standard compound; INTERNAL_ID 904; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8784; ORIGINAL_PRECURSOR_SCAN_NO 8783 CONFIDENCE standard compound; INTERNAL_ID 904; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8757; ORIGINAL_PRECURSOR_SCAN_NO 8755 CONFIDENCE standard compound; INTERNAL_ID 2810 CONFIDENCE standard compound; INTERNAL_ID 1076 CONFIDENCE standard compound; EAWAG_UCHEM_ID 2621

   

Artemetin

4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-5-hydroxy-3,6,7-trimethoxy-

C20H20O8 (388.1158)


Artemetin is found in common verbena. Artemetin is a constituent of Artemisia species, Kuhnia eupatorioides (preferred genus name Brickellia), Achillea species, Brickellia species and others in the Compositae [CCD] Constituent of Artemisia subspecies, Kuhnia eupatorioides (preferred genus name Brickellia), Achillea subspecies, Brickellia subspecies and others in the Compositae [CCD]. Artemetin is found in common verbena. Artemetin is a member of flavonoids and an ether. Artemetin is a natural product found in Achillea santolina, Psiadia viscosa, and other organisms with data available. Artemitin is a flavonol found in Laggera pterodonta (DC.) Benth., with antioxidative, anti-inflammatory, and antiviral activity[1]. Artemitin is a flavonol found in Laggera pterodonta (DC.) Benth., with antioxidative, anti-inflammatory, and antiviral activity[1].

   

Casticin

5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-3,6,7-trimethoxy-4H-benzopyran-4-one, 9CI

C19H18O8 (374.1002)


Casticin is a tetramethoxyflavone that consists of quercetagetin in which the hydroxy groups at positions 3, 6, 7 and 4 have been replaced by methoxy groups. It has been isolated from Eremophila mitchellii. It has a role as an apoptosis inducer and a plant metabolite. It is a tetramethoxyflavone and a dihydroxyflavone. It is functionally related to a quercetagetin. Casticin is a natural product found in Psiadia viscosa, Psiadia dentata, and other organisms with data available. See also: Chaste tree fruit (part of). A tetramethoxyflavone that consists of quercetagetin in which the hydroxy groups at positions 3, 6, 7 and 4 have been replaced by methoxy groups. It has been isolated from Eremophila mitchellii. Casticin is found in fruits. Casticin is a constituent of Vitex agnus-castus (agnus castus) seeds Casticin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=479-91-4 (retrieved 2024-07-01) (CAS RN: 479-91-4). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Casticin is a methyoxylated flavonol isolated from Vitex rotundifolia, with antimitotic and anti-inflammatory effect. Casticin inhibits the activation of STAT3. Casticin is a methyoxylated flavonol isolated from Vitex rotundifolia, with antimitotic and anti-inflammatory effect. Casticin inhibits the activation of STAT3.

   

Hexamethylquercetagetin

4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-3,5,6,7-tetramethoxy-

C21H22O8 (402.1315)


3-methoxysinensetin, also known as 356734-hexamethoxyflavone, is a member of the class of compounds known as 7-o-methylated flavonoids. 7-o-methylated flavonoids are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone. Thus, 3-methoxysinensetin is considered to be a flavonoid lipid molecule. 3-methoxysinensetin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). 3-methoxysinensetin can be found in grapefruit and sweet orange, which makes 3-methoxysinensetin a potential biomarker for the consumption of these food products. 2-(3,4-dimethoxyphenyl)-3,5,6,7-tetramethoxy-1-benzopyran-4-one is a member of flavonoids and an ether. Hexamethylquercetagetin is a natural product found in Pulicaria arabica, Chiliadenus montanus, and other organisms with data available. See also: Tangerine peel (part of); Citrus aurantium fruit rind (part of). Hexamethylquercetagetin is found in citrus. Hexamethylquercetagetin is isolated from peel of Citrus specie D004791 - Enzyme Inhibitors

   

Jaceidin

5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-4H-1-benzopyran-4-one, 9CI

C18H16O8 (360.0845)


Jaceidin is an ether and a member of flavonoids. Jaceidin is a natural product found in Centaurea bracteata, Pentanema britannicum, and other organisms with data available. Jaceidin is found in fruits. Jaceidin is found in buds of Prunus avium (wild cherry). Found in buds of Prunus avium (wild cherry)

   

Centaureidin

4H-1-Benzopyran-4-one,5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3,6-dimethoxy-

C18H16O8 (360.0845)


   

Velutin

4H-1-Benzopyran-4-one, 5-hydroxy-2-(4-hydroxy-3-methyoxyphenyl)-7-methoxy-

C17H14O6 (314.079)


Velutin is a dimethoxyflavone that is luteolin in which the hydroxy groups at positions 7 and 3 are replaced by methoxy groups. It has a role as an anti-inflammatory agent, a plant metabolite, a melanin synthesis inhibitor, an antibacterial agent, an antioxidant and an anti-allergic agent. It is a dimethoxyflavone and a dihydroxyflavone. It is functionally related to a 4,5,7-trihydroxy-3-methoxyflavone. Velutin is a natural product found in Avicennia officinalis, Lantana montevidensis, and other organisms with data available. See also: Acai (part of). A dimethoxyflavone that is luteolin in which the hydroxy groups at positions 7 and 3 are replaced by methoxy groups. [Raw Data] CB095_Velutin_neg_50eV_000026.txt [Raw Data] CB095_Velutin_neg_40eV_000026.txt [Raw Data] CB095_Velutin_neg_30eV_000026.txt [Raw Data] CB095_Velutin_neg_20eV_000026.txt [Raw Data] CB095_Velutin_neg_10eV_000026.txt [Raw Data] CB095_Velutin_pos_50eV_CB000040.txt [Raw Data] CB095_Velutin_pos_40eV_CB000040.txt [Raw Data] CB095_Velutin_pos_30eV_CB000040.txt [Raw Data] CB095_Velutin_pos_20eV_CB000040.txt [Raw Data] CB095_Velutin_pos_10eV_CB000040.txt Velutin is an aglycone extracted from Flammulina velutipes, with inhibitory activity against melanin biosynthesis. Velutin reduces osteoclast differentiation and down-regulates HIF-1α through the NF-κB pathway[1][2]. Velutin is an aglycone extracted from Flammulina velutipes, with inhibitory activity against melanin biosynthesis. Velutin reduces osteoclast differentiation and down-regulates HIF-1α through the NF-κB pathway[1][2]. Velutin is an aglycone extracted from Flammulina velutipes, with inhibitory activity against melanin biosynthesis. Velutin reduces osteoclast differentiation and down-regulates HIF-1α through the NF-κB pathway[1][2].

   

1,4,7-Eudesmanetriol

(-)-1beta,4beta,7alpha-Trihydroxyeudesmane

C15H28O3 (256.2038)


   

Penduletin

5-Hydroxy-2- (4-hydroxyphenyl) -3,6,7-trimethoxy-4H-1-benzopyran-4-one

C18H16O7 (344.0896)


   

Chrysosplenol D

2-(3,4-Dihydroxyphenyl)-5-hydroxy-3,6,7-trimethoxy-4H-1-benzopyran-4-one

C18H16O8 (360.0845)


Chrysosplenol D is a methoxy flavonoid that induces ERK1/2-mediated apoptosis in triple negative human breast cancer cells. Chrysosplenol D also exhibits anti-inflammatory and moderate antitrypanosomal activities[1][2][3][4]. Chrysosplenol D is a methoxy flavonoid that induces ERK1/2-mediated apoptosis in triple negative human breast cancer cells. Chrysosplenol D also exhibits anti-inflammatory and moderate antitrypanosomal activities[1][2][3][4].

   

Centaureidin

5,7-Dihydroxy-2- (3-hydroxy-4-methoxyphenyl) -3,6-dimethoxy-4H-1-benzopyran-4-one

C18H16O8 (360.0845)


A trihydroxyflavone that consists of quercetagetin in which the hydroxy groups at positions 3, 6 and 4 have been replaced by methoxy groups. It has been isolated from Eremophila mitchellii and Athroisma proteiforme.

   

6-O-Acetylastragalin

2- (4-Hydroxyphenyl) -3- [ (6-O-acetyl-beta-D-glucopyranosyl) oxy ] -5-hydroxy-7-hydroxy-4H-1-benzopyran-4-one

C23H22O12 (490.1111)


   

Hexamethylquercetagetin

2- (3,4-Dimethoxyphenyl) -3,5,6,7-tetramethoxy-4H-1-benzopyran-4-one

C21H22O8 (402.1315)


   

Casticin

4H-1-Benzopyran-4-one, 5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-3,6,7-trimethoxy-

C19H18O8 (374.1002)


[Raw Data] CB178_Casticin_pos_50eV_CB000067.txt [Raw Data] CB178_Casticin_pos_40eV_CB000067.txt [Raw Data] CB178_Casticin_pos_30eV_CB000067.txt [Raw Data] CB178_Casticin_pos_20eV_CB000067.txt [Raw Data] CB178_Casticin_pos_10eV_CB000067.txt Casticin is a methyoxylated flavonol isolated from Vitex rotundifolia, with antimitotic and anti-inflammatory effect. Casticin inhibits the activation of STAT3. Casticin is a methyoxylated flavonol isolated from Vitex rotundifolia, with antimitotic and anti-inflammatory effect. Casticin inhibits the activation of STAT3.

   

Patuletin

2- (3,4-Dihydroxyphenyl) -3,5,7-trihydroxy-6-methoxy-4H-1-benzopyran-4-one

C16H12O8 (332.0532)


A trimethoxyflavone that is quercetagetin methylated at position 6. D004791 - Enzyme Inhibitors

   

Artemetin

4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-5-hydroxy-3,6,7-trimethoxy-

C20H20O8 (388.1158)


Artemitin is a flavonol found in Laggera pterodonta (DC.) Benth., with antioxidative, anti-inflammatory, and antiviral activity[1]. Artemitin is a flavonol found in Laggera pterodonta (DC.) Benth., with antioxidative, anti-inflammatory, and antiviral activity[1].

   

3,7-Dimethylocta-2,7-diene-1,6-diol

3,7-Dimethylocta-2,7-diene-1,6-diol

C10H18O2 (170.1307)


   

Jaceidin

5,7,4-Trihydroxy-3,6,3-trimethoxyflavone

C18H16O8 (360.0845)


   

Costic acid

2-(4a-methyl-8-methylidene-decahydronaphthalen-2-yl)prop-2-enoic acid

C15H22O2 (234.162)


   

Isointermedeol

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

C15H26O (222.1984)


   

2-[(2R,4aR,8R,8aR)-8-hydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid

2-[(2R,4aR,8R,8aR)-8-hydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid

C15H24O3 (252.1725)


   

603-56-5

4H-1-Benzopyran-4-one, 5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6,7-trimethoxy-

C19H18O8 (374.1002)


Chrysosplenetin is one of the polymethoxylated flavonoids in Artemisia annua L. (Compositae) and other several Chinese herbs. Chrysosplenetin inhibits P-gp activity and reverses the up-regulated P-gp and MDR1 levels induced by artemisinin (ART). Chrysosplenetin significantly augments the rat plasma level and anti-malarial efficacy of ART, partially due to the uncompetitive inhibition effect of Chrysosplenetin on rat CYP3A[1]. Chrysosplenetin is one of the polymethoxylated flavonoids in Artemisia annua L. (Compositae) and other several Chinese herbs. Chrysosplenetin inhibits P-gp activity and reverses the up-regulated P-gp and MDR1 levels induced by artemisinin (ART). Chrysosplenetin significantly augments the rat plasma level and anti-malarial efficacy of ART, partially due to the uncompetitive inhibition effect of Chrysosplenetin on rat CYP3A[1].

   

Chrysosplenetin

4H-1-Benzopyran-4-one, 5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6,7-trimethoxy-

C19H18O8 (374.1002)


Chrysosplenetin is a tetramethoxyflavone that is the 3,6,7,3-tetramethyl ether derivative of quercetagetin. It has a role as an antiviral agent and a plant metabolite. It is a tetramethoxyflavone and a dihydroxyflavone. It is functionally related to a quercetagetin. Chrysosplenetin is a natural product found in Haplophyllum myrtifolium, Cleome amblyocarpa, and other organisms with data available. A tetramethoxyflavone that is the 3,6,7,3-tetramethyl ether derivative of quercetagetin. Chrysosplenetin is one of the polymethoxylated flavonoids in Artemisia annua L. (Compositae) and other several Chinese herbs. Chrysosplenetin inhibits P-gp activity and reverses the up-regulated P-gp and MDR1 levels induced by artemisinin (ART). Chrysosplenetin significantly augments the rat plasma level and anti-malarial efficacy of ART, partially due to the uncompetitive inhibition effect of Chrysosplenetin on rat CYP3A[1]. Chrysosplenetin is one of the polymethoxylated flavonoids in Artemisia annua L. (Compositae) and other several Chinese herbs. Chrysosplenetin inhibits P-gp activity and reverses the up-regulated P-gp and MDR1 levels induced by artemisinin (ART). Chrysosplenetin significantly augments the rat plasma level and anti-malarial efficacy of ART, partially due to the uncompetitive inhibition effect of Chrysosplenetin on rat CYP3A[1].

   

chrysoplenol D

4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5-hydroxy-3,6,7-trimethoxy-

C18H16O8 (360.0845)


3,4,5-trihydroxy-3,6,7-trimethoxyflavone is a trimethoxyflavone that is the 3,6,7-trimethyl ether derivative of quercetagetin. It has a role as an antineoplastic agent and a metabolite. It is a trihydroxyflavone and a trimethoxyflavone. It is functionally related to a quercetagetin. Chrysosplenol D is a natural product found in Psiadia viscosa, Chrysosplenium oppositifolium, and other organisms with data available. See also: Vitex negundo fruit (part of). A trimethoxyflavone that is the 3,6,7-trimethyl ether derivative of quercetagetin. Chrysosplenol D is a methoxy flavonoid that induces ERK1/2-mediated apoptosis in triple negative human breast cancer cells. Chrysosplenol D also exhibits anti-inflammatory and moderate antitrypanosomal activities[1][2][3][4]. Chrysosplenol D is a methoxy flavonoid that induces ERK1/2-mediated apoptosis in triple negative human breast cancer cells. Chrysosplenol D also exhibits anti-inflammatory and moderate antitrypanosomal activities[1][2][3][4].

   

2-(8-hydroxy-4a,8-dimethyl-octahydronaphthalen-2-yl)prop-2-enoic acid

2-(8-hydroxy-4a,8-dimethyl-octahydronaphthalen-2-yl)prop-2-enoic acid

C15H24O3 (252.1725)


   

2-(4-hydroxy-3-methoxyphenyl)-3,5,6,7-tetramethoxychromen-4-one

2-(4-hydroxy-3-methoxyphenyl)-3,5,6,7-tetramethoxychromen-4-one

C20H20O8 (388.1158)


   

(2e,6r)-3,7-dimethylocta-2,7-diene-1,6-diol

(2e,6r)-3,7-dimethylocta-2,7-diene-1,6-diol

C10H18O2 (170.1307)


   

3a-(hydroxymethyl)-6-(2-hydroxypropan-2-yl)-8a-methyl-hexahydro-1h-azulen-4-one

3a-(hydroxymethyl)-6-(2-hydroxypropan-2-yl)-8a-methyl-hexahydro-1h-azulen-4-one

C15H26O3 (254.1882)


   

(6r,9e)-11-methoxy-3,7,11-trimethyldodeca-1,9-diene-3,6,7-triol

(6r,9e)-11-methoxy-3,7,11-trimethyldodeca-1,9-diene-3,6,7-triol

C16H30O4 (286.2144)


   

methyl 2-(4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl)prop-2-enoate

methyl 2-(4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl)prop-2-enoate

C16H22O3 (262.1569)


   

(2e)-3,7-dimethylocta-2,7-diene-1,6-diol

(2e)-3,7-dimethylocta-2,7-diene-1,6-diol

C10H18O2 (170.1307)


   

(2e,5r)-5-hydroxy-3,6-dimethylhepta-2,6-dien-1-yl acetate

(2e,5r)-5-hydroxy-3,6-dimethylhepta-2,6-dien-1-yl acetate

C11H18O3 (198.1256)


   

2-[(3s,3ar,5r,7as)-3a-acetyl-3-hydroxy-7a-methyl-hexahydro-1h-inden-5-yl]prop-2-enoic acid

2-[(3s,3ar,5r,7as)-3a-acetyl-3-hydroxy-7a-methyl-hexahydro-1h-inden-5-yl]prop-2-enoic acid

C15H22O4 (266.1518)


   

(3e,6e)-2,6-dimethylocta-3,6-diene-1,2,8-triol

(3e,6e)-2,6-dimethylocta-3,6-diene-1,2,8-triol

C10H18O3 (186.1256)


   

5-(2-hydroxypropan-2-yl)-2-methyl-2-(4-oxopentyl)cyclohexan-1-one

5-(2-hydroxypropan-2-yl)-2-methyl-2-(4-oxopentyl)cyclohexan-1-one

C15H26O3 (254.1882)


   

7-hydroxy-3,7-dimethylocta-2,5-dien-1-yl acetate

7-hydroxy-3,7-dimethylocta-2,5-dien-1-yl acetate

C12H20O3 (212.1412)


   

8-hydroxy-4a,8-dimethyl-4,5,6,7-tetrahydro-3h-naphthalen-2-one

8-hydroxy-4a,8-dimethyl-4,5,6,7-tetrahydro-3h-naphthalen-2-one

C12H18O2 (194.1307)


   

2-[(2r,4ar,8ar)-4a-methyl-8-methylidene-octahydronaphthalen-2-yl]prop-2-enoic acid

2-[(2r,4ar,8ar)-4a-methyl-8-methylidene-octahydronaphthalen-2-yl]prop-2-enoic acid

C15H22O2 (234.162)


   

(1r,4s,4ar,6s,8ar)-6-isopropyl-4,8a-dimethyl-hexahydro-1h-naphthalene-1,4,6-triol

(1r,4s,4ar,6s,8ar)-6-isopropyl-4,8a-dimethyl-hexahydro-1h-naphthalene-1,4,6-triol

C15H28O3 (256.2038)


   

3,3'-di-o-methylquercetin

3,3'-di-o-methylquercetin

C17H14O7 (330.0739)


   

2-[(2r,4ar,8as)-8a-hydroxy-4a-methyl-8-methylidene-hexahydro-1h-naphthalen-2-yl]prop-2-enoic acid

2-[(2r,4ar,8as)-8a-hydroxy-4a-methyl-8-methylidene-hexahydro-1h-naphthalen-2-yl]prop-2-enoic acid

C15H22O3 (250.1569)


   

6-methyl-2,10-dimethylidene-12-oxatricyclo[7.3.1.0¹,⁶]tridecan-11-one

6-methyl-2,10-dimethylidene-12-oxatricyclo[7.3.1.0¹,⁶]tridecan-11-one

C15H20O2 (232.1463)


   

methyl 1-hydroxy-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalene-2-carboxylate

methyl 1-hydroxy-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalene-2-carboxylate

C14H20O4 (252.1362)


   

2-(7,8a-dihydroxy-4a-methyl-8-methylidene-hexahydro-1h-naphthalen-2-yl)prop-2-enoic acid

2-(7,8a-dihydroxy-4a-methyl-8-methylidene-hexahydro-1h-naphthalen-2-yl)prop-2-enoic acid

C15H22O4 (266.1518)


   

3-methyl-5-[(3s,6s)-4-methylidene-6-(2-methylprop-1-en-1-yl)-1,2-dioxan-3-yl]pent-1-en-3-ol

3-methyl-5-[(3s,6s)-4-methylidene-6-(2-methylprop-1-en-1-yl)-1,2-dioxan-3-yl]pent-1-en-3-ol

C15H24O3 (252.1725)


   

1-hydroxy-4,8a-dimethyl-octahydroazulen-6-one

1-hydroxy-4,8a-dimethyl-octahydroazulen-6-one

C12H20O2 (196.1463)


   

(2s,3e,6e)-2,6-dimethylocta-3,6-diene-1,2,8-triol

(2s,3e,6e)-2,6-dimethylocta-3,6-diene-1,2,8-triol

C10H18O3 (186.1256)


   

2-[(8ar)-2,4a-dimethyl-8-methylidene-hexahydro-1h-naphthalen-2-yl]prop-2-enoic acid

2-[(8ar)-2,4a-dimethyl-8-methylidene-hexahydro-1h-naphthalen-2-yl]prop-2-enoic acid

C16H24O2 (248.1776)


   

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

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

C12H18O2 (194.1307)


   

1-[3-hydroxy-5-(2-hydroxypropan-2-yl)-7a-methyl-hexahydro-1h-inden-3a-yl]ethanone

1-[3-hydroxy-5-(2-hydroxypropan-2-yl)-7a-methyl-hexahydro-1h-inden-3a-yl]ethanone

C15H26O3 (254.1882)


   

2-[(4ar,8r,8ar)-8-hydroxy-4a,8-dimethyl-octahydronaphthalen-2-yl]prop-2-enoic acid

2-[(4ar,8r,8ar)-8-hydroxy-4a,8-dimethyl-octahydronaphthalen-2-yl]prop-2-enoic acid

C15H24O3 (252.1725)


   

2-[(2r,4as,7r)-7-methoxy-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl]prop-2-enoic acid

2-[(2r,4as,7r)-7-methoxy-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl]prop-2-enoic acid

C16H24O3 (264.1725)


   

2-(3a-acetyl-3-hydroxy-7a-methyl-hexahydro-1h-inden-5-yl)prop-2-enoic acid

2-(3a-acetyl-3-hydroxy-7a-methyl-hexahydro-1h-inden-5-yl)prop-2-enoic acid

C15H22O4 (266.1518)


   

2-[(2r,4ar,8s,8ar)-8a-hydroxy-4a,8-dimethyl-octahydronaphthalen-2-yl]prop-2-enoic acid

2-[(2r,4ar,8s,8ar)-8a-hydroxy-4a,8-dimethyl-octahydronaphthalen-2-yl]prop-2-enoic acid

C15H24O3 (252.1725)


   

3-methyl-5-[(3r,6s)-4-methylidene-6-(2-methylprop-1-en-1-yl)-1,2-dioxan-3-yl]pent-1-en-3-ol

3-methyl-5-[(3r,6s)-4-methylidene-6-(2-methylprop-1-en-1-yl)-1,2-dioxan-3-yl]pent-1-en-3-ol

C15H24O3 (252.1725)


   

(6e)-10-hydroxy-2,6,10-trimethyldodeca-6,11-dien-4-one

(6e)-10-hydroxy-2,6,10-trimethyldodeca-6,11-dien-4-one

C15H26O2 (238.1933)


   

(2e,5e)-7-hydroxy-3,7-dimethylocta-2,5-dien-1-yl acetate

(2e,5e)-7-hydroxy-3,7-dimethylocta-2,5-dien-1-yl acetate

C12H20O3 (212.1412)


   

methyl (1r,2r,4as)-1-hydroxy-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalene-2-carboxylate

methyl (1r,2r,4as)-1-hydroxy-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalene-2-carboxylate

C14H20O4 (252.1362)


   

(2r)-2-{2-[(2r)-butan-2-yloxy]-4-methylphenyl}-2-{[(2s)-butan-2-yloxy]methyl}oxirane

(2r)-2-{2-[(2r)-butan-2-yloxy]-4-methylphenyl}-2-{[(2s)-butan-2-yloxy]methyl}oxirane

C18H28O3 (292.2038)


   

(9ar)-7-(2-hydroxypropan-2-yl)-9a-methyl-1h,2h,4h,6h,7h,8h,9h-cyclopenta[8]annulen-5-one

(9ar)-7-(2-hydroxypropan-2-yl)-9a-methyl-1h,2h,4h,6h,7h,8h,9h-cyclopenta[8]annulen-5-one

C15H24O2 (236.1776)


   

(1s,3as,4r,8as)-1-hydroxy-4,8a-dimethyl-octahydroazulen-6-one

(1s,3as,4r,8as)-1-hydroxy-4,8a-dimethyl-octahydroazulen-6-one

C12H20O2 (196.1463)


   

2-(8a-hydroxy-4a-methyl-8-methylidene-hexahydro-1h-naphthalen-2-yl)prop-2-enoic acid

2-(8a-hydroxy-4a-methyl-8-methylidene-hexahydro-1h-naphthalen-2-yl)prop-2-enoic acid

C15H22O3 (250.1569)


   

2-(8a-hydroxy-4a,8-dimethyl-1,2,3,4,5,6-hexahydronaphthalen-2-yl)prop-2-enoic acid

2-(8a-hydroxy-4a,8-dimethyl-1,2,3,4,5,6-hexahydronaphthalen-2-yl)prop-2-enoic acid

C15H22O3 (250.1569)


   

(1r,4s,4ar,6s,8ar)-4,8a-dimethyl-6-(prop-1-en-2-yl)-hexahydro-1h-naphthalene-1,4,6-triol

(1r,4s,4ar,6s,8ar)-4,8a-dimethyl-6-(prop-1-en-2-yl)-hexahydro-1h-naphthalene-1,4,6-triol

C15H26O3 (254.1882)


   

2,6-dimethylocta-3,6-diene-1,2,8-triol

2,6-dimethylocta-3,6-diene-1,2,8-triol

C10H18O3 (186.1256)


   

2-[(2r,4ar,8ar)-8a-hydroxy-4a-methyl-8-methylidene-hexahydro-1h-naphthalen-2-yl]prop-2-enoic acid

2-[(2r,4ar,8ar)-8a-hydroxy-4a-methyl-8-methylidene-hexahydro-1h-naphthalen-2-yl]prop-2-enoic acid

C15H22O3 (250.1569)


   

quercetin 3,4'-dimethyl ether

quercetin 3,4'-dimethyl ether

C17H14O7 (330.0739)


   

2-[(2r,4as)-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl]prop-2-enoic acid

2-[(2r,4as)-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl]prop-2-enoic acid

C15H20O3 (248.1412)


   

(2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(2-isopropyl-5-methylphenoxy)oxane-3,4,5-triol

(2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(2-isopropyl-5-methylphenoxy)oxane-3,4,5-triol

C16H24O6 (312.1573)


   

(2r,3e,6e)-2,6-dimethylocta-3,6-diene-1,2,8-triol

(2r,3e,6e)-2,6-dimethylocta-3,6-diene-1,2,8-triol

C10H18O3 (186.1256)


   

(3r,4as,8ar)-3-(2-hydroxypropan-2-yl)-8a-methyl-5-methylidene-hexahydro-1h-naphthalen-4a-ol

(3r,4as,8ar)-3-(2-hydroxypropan-2-yl)-8a-methyl-5-methylidene-hexahydro-1h-naphthalen-4a-ol

C15H26O2 (238.1933)


   

2-(hydroxymethyl)-6-(2-isopropyl-5-methylphenoxy)oxane-3,4,5-triol

2-(hydroxymethyl)-6-(2-isopropyl-5-methylphenoxy)oxane-3,4,5-triol

C16H24O6 (312.1573)


   

1-[(3s,3ar,5r,7as)-3-hydroxy-5-(2-hydroxypropan-2-yl)-7a-methyl-hexahydro-1h-inden-3a-yl]ethanone

1-[(3s,3ar,5r,7as)-3-hydroxy-5-(2-hydroxypropan-2-yl)-7a-methyl-hexahydro-1h-inden-3a-yl]ethanone

C15H26O3 (254.1882)


   

2-[(2r,4as,7s)-7-methoxy-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl]prop-2-enoic acid

2-[(2r,4as,7s)-7-methoxy-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl]prop-2-enoic acid

C16H24O3 (264.1725)


   

5-hydroxy-3,6-dimethylhepta-2,6-dien-1-yl acetate

5-hydroxy-3,6-dimethylhepta-2,6-dien-1-yl acetate

C11H18O3 (198.1256)


   

(2e)-5-hydroxy-3,6-dimethylhepta-2,6-dien-1-yl acetate

(2e)-5-hydroxy-3,6-dimethylhepta-2,6-dien-1-yl acetate

C11H18O3 (198.1256)


   

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

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

C15H26O (222.1984)


   

(2r,5r)-5-(2-hydroxypropan-2-yl)-2-methyl-2-(4-oxopentyl)cyclohexan-1-one

(2r,5r)-5-(2-hydroxypropan-2-yl)-2-methyl-2-(4-oxopentyl)cyclohexan-1-one

C15H26O3 (254.1882)


   

(7r,9ar)-7-(2-hydroxypropan-2-yl)-9a-methyl-1h,2h,4h,6h,7h,8h,9h-cyclopenta[8]annulen-5-one

(7r,9ar)-7-(2-hydroxypropan-2-yl)-9a-methyl-1h,2h,4h,6h,7h,8h,9h-cyclopenta[8]annulen-5-one

C15H24O2 (236.1776)


   

(1s,6r)-6-methyl-2,10-dimethylidene-12-oxatricyclo[7.3.1.0¹,⁶]tridecan-11-one

(1s,6r)-6-methyl-2,10-dimethylidene-12-oxatricyclo[7.3.1.0¹,⁶]tridecan-11-one

C15H20O2 (232.1463)


   

2-[(2r,4as,7r,8as)-7,8a-dihydroxy-4a-methyl-8-methylidene-hexahydro-1h-naphthalen-2-yl]prop-2-enoic acid

2-[(2r,4as,7r,8as)-7,8a-dihydroxy-4a-methyl-8-methylidene-hexahydro-1h-naphthalen-2-yl]prop-2-enoic acid

C15H22O4 (266.1518)


   

2-[(2r,4ar,8as)-8a-hydroxy-4a,8-dimethyl-1,2,3,4,5,6-hexahydronaphthalen-2-yl]prop-2-enoic acid

2-[(2r,4ar,8as)-8a-hydroxy-4a,8-dimethyl-1,2,3,4,5,6-hexahydronaphthalen-2-yl]prop-2-enoic acid

C15H22O3 (250.1569)


   

2-[(2r,4ar,8r,8ar)-8-hydroxy-4a,8-dimethyl-octahydronaphthalen-2-yl]prop-2-enoic acid

2-[(2r,4ar,8r,8ar)-8-hydroxy-4a,8-dimethyl-octahydronaphthalen-2-yl]prop-2-enoic acid

C15H24O3 (252.1725)


   

methyl 2-[(2r,4as)-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl]prop-2-enoate

methyl 2-[(2r,4as)-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl]prop-2-enoate

C16H22O3 (262.1569)


   

methyl (1s,2s,4ar)-1-hydroxy-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalene-2-carboxylate

methyl (1s,2s,4ar)-1-hydroxy-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalene-2-carboxylate

C14H20O4 (252.1362)


   

2-(4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl)prop-2-enoic acid

2-(4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl)prop-2-enoic acid

C15H20O3 (248.1412)


   

2-[(2r,4as,7r)-7-(acetyloxy)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl]prop-2-enoic acid

2-[(2r,4as,7r)-7-(acetyloxy)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl]prop-2-enoic acid

C17H24O4 (292.1675)


   

7-(2-hydroxypropan-2-yl)-9a-methyl-1h,2h,4h,6h,7h,8h,9h-cyclopenta[8]annulen-5-one

7-(2-hydroxypropan-2-yl)-9a-methyl-1h,2h,4h,6h,7h,8h,9h-cyclopenta[8]annulen-5-one

C15H24O2 (236.1776)


   

3-(2-hydroxypropan-2-yl)-8a-methyl-5-methylidene-hexahydro-1h-naphthalen-4a-ol

3-(2-hydroxypropan-2-yl)-8a-methyl-5-methylidene-hexahydro-1h-naphthalen-4a-ol

C15H26O2 (238.1933)


   

[(2r,3s,4s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl 2-[(2r,4as)-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl]prop-2-enoate

[(2r,3s,4s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl 2-[(2r,4as)-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl]prop-2-enoate

C21H30O8 (410.1941)


   

(1s,6r,9r)-6-methyl-2,10-dimethylidene-12-oxatricyclo[7.3.1.0¹,⁶]tridecan-11-one

(1s,6r,9r)-6-methyl-2,10-dimethylidene-12-oxatricyclo[7.3.1.0¹,⁶]tridecan-11-one

C15H20O2 (232.1463)


   

2-(butoxymethyl)-2-(2,4-dimethylphenyl)oxirane

2-(butoxymethyl)-2-(2,4-dimethylphenyl)oxirane

C15H22O2 (234.162)


   

(3r,4ar,8ar)-3-(2-hydroxypropan-2-yl)-8a-methyl-5-methylidene-hexahydro-1h-naphthalen-4a-ol

(3r,4ar,8ar)-3-(2-hydroxypropan-2-yl)-8a-methyl-5-methylidene-hexahydro-1h-naphthalen-4a-ol

C15H26O2 (238.1933)


   

2-[4-methyl-2-(sec-butoxy)phenyl]-2-(sec-butoxymethyl)oxirane

2-[4-methyl-2-(sec-butoxy)phenyl]-2-(sec-butoxymethyl)oxirane

C18H28O3 (292.2038)