Chemical Formula: C23H24O6
Chemical Formula C23H24O6
Found 230 metabolite its formula value is C23H24O6
Gartanin
Gartanin is a member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3, 5 and 8 and prenyl groups at positions 2 and 4. It has a role as an antineoplastic agent and a plant metabolite. It is a member of xanthones and a polyphenol. Gartanin is a natural product found in Morus insignis, Pentadesma butyracea, and other organisms with data available. A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3, 5 and 8 and prenyl groups at positions 2 and 4. Constituent of the fruits of Garcinia mangostana (mangosteen). Gartanin is found in fruits and purple mangosteen. Gartanin is found in fruits. Gartanin is a constituent of the fruits of Garcinia mangostana (mangosteen) Gartanin is a natural xanthone of mangosteen, with antioxidant, anti-inflammatory, antifungal, neuroprotective and antineoplastic properties. Gartanin induces cell cycle arrest and autophagy and suppresses migration in human glioma cells[1][2]. Gartanin is a natural xanthone of mangosteen, with antioxidant, anti-inflammatory, antifungal, neuroprotective and antineoplastic properties. Gartanin induces cell cycle arrest and autophagy and suppresses migration in human glioma cells[1][2].
gamma-Mangostin
Gamma-mangostin is a member of the class of xanthones that is 9H-xanthene substituted by hydroxy group at positions 1, 3, 6 and 7, an oxo group at position 9 and prenyl groups at positions 2 and 8. Isolated from the stems of Cratoxylum cochinchinense, it exhibits antitumour activity. It has a role as an antineoplastic agent, a protein kinase inhibitor and a plant metabolite. It is a member of xanthones and a member of phenols. gamma-Mangostin is a natural product found in Hypericum androsaemum, Garcinia xipshuanbannaensis, and other organisms with data available. See also: Garcinia mangostana fruit rind (part of). A member of the class of xanthones that is 9H-xanthene substituted by hydroxy group at positions 1, 3, 6 and 7, an oxo group at position 9 and prenyl groups at positions 2 and 8. Isolated from the stems of Cratoxylum cochinchinense, it exhibits antitumour activity. Constituent of Garcinia mangostana (mangosteen). gamma-Mangostin is found in fruits and purple mangosteen. gamma-Mangostin is found in fruits. gamma-Mangostin is a constituent of Garcinia mangostana (mangosteen) Gamma-Mangostin is a novel competitive 5-hydroxytryptamine 2A (5-HT2A) receptors antagonist, purified from the fruit hull of the medicinal plant Garcinia mangostana. Gamma-Mangostin is a inhibitor of Transthyretin (TTR) fibrillization, it binds to the thyroxine (T4)-binding sites and stabilized the TTR tetramer[2]. Gamma-Mangostin inhibits [3H] spiperone binding to cultured rat aortic myocytes (IC50=3.5 nM) and reduces The perfusion pressure response of rat coronary artery to 5-HT2A (IC50=0.32 μM) [1]. Gamma-Mangostin is a novel competitive 5-hydroxytryptamine 2A (5-HT2A) receptor antagonist and potent epoxidase 2 (COX-2) inhibitor, as well as a transthyroxin protein (TTR) profibrosis inhibitor. Gamma-Mangostin binds to the thyroxine (T4)-binding sites and stabilized the TTR tetramer[2]. Gamma-Mangostin inhibits [3H] spiperone binding to cultured rat aortic myocytes (IC50=3.5 nM) and reduces The perfusion pressure response of rat coronary artery to 5-HT2A (IC50=0.32 μM). Gamma-Mangostin has anti-inflammatory, antibacterial, antioxidant and anticancer activities, and can be used in the study of metabolic disorders such as diabetes[1][2][3][4][5]. Gamma-Mangostin is a novel competitive 5-hydroxytryptamine 2A (5-HT2A) receptors antagonist, purified from the fruit hull of the medicinal plant Garcinia mangostana. Gamma-Mangostin is a inhibitor of Transthyretin (TTR) fibrillization, it binds to the thyroxine (T4)-binding sites and stabilized the TTR tetramer[2]. Gamma-Mangostin inhibits [3H] spiperone binding to cultured rat aortic myocytes (IC50=3.5 nM) and reduces The perfusion pressure response of rat coronary artery to 5-HT2A (IC50=0.32 μM) [1].
4-(1,1-Dimethyl-2-propenyl)-1,3,5,6-tetrahydroxy-7-prenylxanthone
4-(1,1-Dimethyl-2-propenyl)-1,3,5,6-tetrahydroxy-7-prenylxanthone is found in fruits. 4-(1,1-Dimethyl-2-propenyl)-1,3,5,6-tetrahydroxy-7-prenylxanthone is a constituent of the root bark of Rheedia brasiliensis (bakupari). Constituent of the root bark of Rheedia brasiliensis (bakupari). 4-(1,1-Dimethyl-2-propenyl)-1,3,5,6-tetrahydroxy-7-prenylxanthone is found in herbs and spices and fruits.
BR-Xanthone A
Constituent of the dry fruit hulls of Garcinia mangostana (mangosteen). BR-Xanthone A is found in fruits and purple mangosteen. BR-Xanthone A is found in fruits. BR-Xanthone A is a constituent of the dry fruit hulls of Garcinia mangostana (mangosteen).
Curcumin I
Curcumin I is found in herbs and spices. Curcumin I is isolated from the rhizomes of Curcuma longa (turmeric). Isolated from the rhizomes of Curcuma longa (turmeric). Curcumin I is found in herbs and spices.
Cudratricusxanthone A
Isonormangostin
Dimethylcurcumin
Dimethylcurcumin is a synthetic chemical compound that is loosely based on a compound found in curcumin. It is a novel anti-androgen that enhances androgen receptor degradation. Dimethylcurcumin (ASC-J9) is an androgen receptor degradation enhancer that effectively suppresses castration resistant prostate cancer cell proliferation and invasion. Dimethylcurcumin (ASC-J9) is an androgen receptor degradation enhancer that effectively suppresses castration resistant prostate cancer cell proliferation and invasion.
Dihydrorotenone
Dihydrorotenone, a natural pesticide, is a potent mitochondrial inhibitor. Dihydrorotenone probably induces Parkinsonian syndrome. Dihydrorotenone induces human plasma cell apoptosis by triggering endoplasmic reticulum stress and activating p38 signaling pathway[1]. Dihydrorotenone, a natural pesticide, is a potent mitochondrial inhibitor. Dihydrorotenone probably induces Parkinsonian syndrome. Dihydrorotenone induces human plasma cell apoptosis by triggering endoplasmic reticulum stress and activating p38 signaling pathway[1].
Rotenonic acid
cudraxanthone L
7a-O-Methyldeguelol
cudratricusxanthone A
A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 2, 3, 6 and 8, an isoprenyl group at position 1 and a 2-methylbut-3-en-2-yl group at position 5. It is isolated from the root barks of Cudrania tricuspidata and exhibits cytotoxicity towards human cancer cell lines.
Macluraxanthone B
A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3, 6 and 7, a dimethylallyl group at position 2 and a prenyl group at position 4. Isolated from Maclura tinctoria and Cudrania tricuspidata, it exhibits anti-HIV and antineoplastic activity.
Macluraxanthone C
A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3, 5 and 6, a dimethylallyl group at position 2 and a prenyl group at position 4. Isolated from Maclura tinctoria and Cudrania tricuspidata, it exhibits anti-HIV and antineoplastic activity.
Xanthone V1a
Xanthone V1a is a natural product found in Garcinia lancilimba, Maclura tricuspidata, and Vismia guineensis with data available.
Muxiangrin III
6,6-Dimethylpyrano[2,3:6,5]-2-hydroxy-3,4,4-trimethoxychalcone
Egonolbutanoate
A butanoate ester of egonol isolated from the fruits of Styrax agrestis.
1,7-dihydroxy-3-(6-hydroxy-3,7-dimethylocta-2,7-dienyloxy)-xanthen-9-one|cochinxanthone B
3beta-hydroxy-8beta-(p-hydroxyphenylacetyloxy)guaia-4(15),10(14),11(13)-trien-1alpha,5alpha,6beta,7alphaH-12,6-olide|8-O-p-hydroxyphenylacetylintegrifolin|ixerochinolide
7-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-1,3,5,6-tetrahydroxy-9H-xanthen-9-one
CRATOXYARBORENONE B
A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3, 5 and 7 and two isoprenyl groups at positions 2 and 8 respectively. It is isolated from Cratoxylum Sumatranum and exhibits cytotoxicity towards the KB (human oral epidermoid) cancer cell line.
10-Cinnamoyloxy-8,9-epoxy-6-hydroxythymol-isobutyrat
1,3-dihydroxy-7-(6-hydroxy-3,7-dimethylocta-2,7-dienyloxy)-xanthen-9-one|cochinxanthone A
1,3,7-trihydroxy-2-(2-hydroxy-3-methylbut-3-enyl)-4-(3-methylbut-2-enyl)-xanthone
1,3,5,8-tetrahydroxy-2-(3-methylbut-2-enyl)-4-(1,1-dimethylprop-2-enyl)xanthone|pedunxanthone B
(E)-1-(5-hydroxy-2,2-dimethyl-2H-chromen-6-yl)-3-(3,4,5-trimethoxy-phenyl)prop-2-en-1-one
1,3-dihydroxy-7-(7-hydroxy-3,7-dimethylocta-2,5-dienyloxy)-xanthen-9-one|cochinxanthone C
(E)-1-(5-hydroxy-2,2-dimethyl-2H-chromen-6-yl)-3-(2,4,5-trimethoxyphenyl)prop-2-en-1-one|Glabrachalcone
2-(3,4-dimethoxyphenyl)-5-methoxy-8,8-dimethyl-2,3-dihydro-8H-pyrano[2,3-f]chromen-4-one
3-(3,4-dimethoxyphenyl)-1-(5-hydroxy-7-methoxy-2,2-dimethyl-2H-chromen-6-yl)propenone|glychalcone B
2-hydroxy-3,4,4-trimethoxy-5,6-(2,2-dimethylpyrano)chalcone
1,9-bis(3,4-methylenedioxyphenyl)-1 ,3-nonanedione
SCHEMBL4513214
SCHEMBL1934352
1,3,6,7-tetrahydroxy-2,8-bis(3-methylbut-2-enyl)xanthen-9-one
Gartanin
Gartanin is a natural xanthone of mangosteen, with antioxidant, anti-inflammatory, antifungal, neuroprotective and antineoplastic properties. Gartanin induces cell cycle arrest and autophagy and suppresses migration in human glioma cells[1][2]. Gartanin is a natural xanthone of mangosteen, with antioxidant, anti-inflammatory, antifungal, neuroprotective and antineoplastic properties. Gartanin induces cell cycle arrest and autophagy and suppresses migration in human glioma cells[1][2].
Rotenone
Dihydrorotenone, a natural pesticide, is a potent mitochondrial inhibitor. Dihydrorotenone probably induces Parkinsonian syndrome. Dihydrorotenone induces human plasma cell apoptosis by triggering endoplasmic reticulum stress and activating p38 signaling pathway[1]. Dihydrorotenone, a natural pesticide, is a potent mitochondrial inhibitor. Dihydrorotenone probably induces Parkinsonian syndrome. Dihydrorotenone induces human plasma cell apoptosis by triggering endoplasmic reticulum stress and activating p38 signaling pathway[1].
BR-xanthone A
Normangostin
Gamma-Mangostin is a novel competitive 5-hydroxytryptamine 2A (5-HT2A) receptors antagonist, purified from the fruit hull of the medicinal plant Garcinia mangostana. Gamma-Mangostin is a inhibitor of Transthyretin (TTR) fibrillization, it binds to the thyroxine (T4)-binding sites and stabilized the TTR tetramer[2]. Gamma-Mangostin inhibits [3H] spiperone binding to cultured rat aortic myocytes (IC50=3.5 nM) and reduces The perfusion pressure response of rat coronary artery to 5-HT2A (IC50=0.32 μM) [1]. Gamma-Mangostin is a novel competitive 5-hydroxytryptamine 2A (5-HT2A) receptor antagonist and potent epoxidase 2 (COX-2) inhibitor, as well as a transthyroxin protein (TTR) profibrosis inhibitor. Gamma-Mangostin binds to the thyroxine (T4)-binding sites and stabilized the TTR tetramer[2]. Gamma-Mangostin inhibits [3H] spiperone binding to cultured rat aortic myocytes (IC50=3.5 nM) and reduces The perfusion pressure response of rat coronary artery to 5-HT2A (IC50=0.32 μM). Gamma-Mangostin has anti-inflammatory, antibacterial, antioxidant and anticancer activities, and can be used in the study of metabolic disorders such as diabetes[1][2][3][4][5]. Gamma-Mangostin is a novel competitive 5-hydroxytryptamine 2A (5-HT2A) receptors antagonist, purified from the fruit hull of the medicinal plant Garcinia mangostana. Gamma-Mangostin is a inhibitor of Transthyretin (TTR) fibrillization, it binds to the thyroxine (T4)-binding sites and stabilized the TTR tetramer[2]. Gamma-Mangostin inhibits [3H] spiperone binding to cultured rat aortic myocytes (IC50=3.5 nM) and reduces The perfusion pressure response of rat coronary artery to 5-HT2A (IC50=0.32 μM) [1].
4-(1,1-Dimethyl-2-propenyl)-1,3,5,6-tetrahydroxy-7-prenylxanthone
Egonol-2-Methylpropanoate
A fatty acid ester obtained by the formal condensation of egonol with isobutyric acid. It has been isolated from the fruits of Styrax agrestis.
(1R,6S,13R)-16,17-Dimethoxy-6-propan-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one
Cochinchinoxanthone
A polycyclic cage xanthone isolated from the stems of Cratoxylum cochinchinense and has been shown to exhibit cytotoxic activity against human colon cancer cell line.
Ixerochinolide
A sesquiterpene lactone isolated from Ixeris chinensis and has been shown to exhibit cytotoxic activity against human PC-3 tumor cells.
5-O-Demethylpaxanthonin
A member of the class of xanthones consisting of paxanthonin in which the methoxy group at position 5 is replaced by a hydroxy group. Isolated from the roots of Hypericum roeperianum and leaves of Hypericum styphelioides, it exhibits antioxidant and antifungal activities.
1,7-Bis(3,4-dimethoxyphenyl)hepta-1,6-diene-3,5-dione
2-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-1,3,6,7-tetrahydroxyxanthen-9-one
3,6,8-trihydroxy-1,1-bis(3-methylbut-2-en-1-yl)xanthene-2,9-dione
3-(2h-1,3-benzodioxol-5-yl)-1-[2,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-3-hydroxyprop-2-en-1-one
10,16-dihydroxy-6,6,19,19-tetramethyl-5,13,18-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁷,²²]docosa-1(22),3,9,11,14,16-hexaen-2-one
1,3,7-trihydroxy-2-[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]-4-(3-methylbut-2-en-1-yl)xanthen-9-one
4-(3,7-dimethylocta-2,6-dien-1-yl)-1,3,5,6-tetrahydroxyxanthen-9-one
3-[4,5-dimethoxy-2-(2-methylbut-3-en-2-yl)phenyl]-5-hydroxy-7-methoxychromen-4-one
(1r)-1-(5,8-dihydroxy-1,4-dioxonaphthalen-2-yl)-4-methylpent-3-en-1-yl 5-methylhexa-3,5-dienoate
1,3-dihydroxy-7-{[(2e,6r)-6-hydroxy-3,7-dimethylocta-2,7-dien-1-yl]oxy}xanthen-9-one
4,8,9-trihydroxy-2,3,3-trimethyl-11-(3-methylbut-2-en-1-yl)-2h-furo[3,2-b]xanthen-5-one
(2s)-4,7,8-trihydroxy-2,3,3-trimethyl-9-(3-methylbut-2-en-1-yl)-2h-furo[3,2-b]xanthen-5-one
(2s)-4,7-dihydroxy-2-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-en-1-yl)-2h,3h-furo[3,2-b]xanthen-5-one
1,9-bis(2h-1,3-benzodioxol-5-yl)-3-hydroxynon-2-en-1-one
1,3,5,6-tetrahydroxy-4-[(2s)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]xanthen-9-one
5,10-dihydroxy-7-(3-hydroxy-3-methylbutyl)-2,2-dimethyl-1,11-dioxatetracen-6-one
(2s)-4,7-dihydroxy-2-(2-hydroxypropan-2-yl)-11-(3-methylbut-2-en-1-yl)-2h,3h-furo[3,2-b]xanthen-5-one
1,3,6,7-tetrahydroxy-2,4-bis(3-methylbut-2-en-1-yl)xanthen-9-one
8,10-dihydroxy-2-(2-hydroxypropan-2-yl)-7-(3-methylbut-2-en-1-yl)-1h,2h-furo[3,2-a]xanthen-11-one
1,3,5,7-tetrahydroxy-2,4-bis(3-methylbut-2-en-1-yl)xanthen-9-one
3-(3,4-dimethoxyphenyl)-1-(5-hydroxy-7-methoxy-2,2-dimethylchromen-6-yl)prop-2-en-1-one
(2r)-5-[(4s)-6,7-dimethoxy-3,4-dihydro-2h-1-benzopyran-4-carbonyl]-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-4-ol
1,3-dihydroxy-7-{[(2e,5e)-7-hydroxy-3,7-dimethylocta-2,5-dien-1-yl]oxy}xanthen-9-one
anticancer flavonoid pmv70p691-106
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3-(3,4-dimethoxyphenyl)-6-hydroxy-7-methoxy-8-(3-methylbut-2-en-1-yl)chromen-4-one
7-(3,7-dimethylocta-2,6-dien-1-yl)-1,3,5,6-tetrahydroxyxanthen-9-one
5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-4-(3-methylbut-2-en-1-yl)-1h,2h-furo[2,3-c]xanthen-6-one
1,6,7-trihydroxy-4-(3-methylbut-2-en-1-yl)-3-[(3-methylbut-2-en-1-yl)oxy]xanthen-9-one
(2e)-3-(3,4-dimethoxyphenyl)-1-(7-hydroxy-5-methoxy-2,2-dimethylchromen-8-yl)prop-2-en-1-one
3-(3,4-dimethoxyphenyl)-1-(7-hydroxy-5-methoxy-2,2-dimethylchromen-8-yl)prop-2-en-1-one
(2r)-4,8,9-trihydroxy-2,3,3-trimethyl-7-(3-methylbut-2-en-1-yl)-2h-furo[3,2-b]xanthen-5-one
2-(2h-1,3-benzodioxol-5-yl)-5,7-dimethoxy-8-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one
1,3,5,6-tetrahydroxy-4-[5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]xanthen-9-one
4,7-dihydroxy-2-(2-hydroxypropan-2-yl)-11-(3-methylbut-2-en-1-yl)-2h,3h-furo[3,2-b]xanthen-5-one
(2-{5-hydroxy-4-methyl-2-[(2-methylpropanoyl)oxy]phenyl}oxiran-2-yl)methyl 3-phenylprop-2-enoate
6-[(4s)-6,7-dimethoxy-3,4-dihydro-2h-1-benzopyran-4-carbonyl]-2,2-dimethylchromen-5-ol
4,9-dihydroxy-2-(2-hydroxypropan-2-yl)-11-(3-methylbut-2-en-1-yl)-2h,3h-furo[3,2-b]xanthen-5-one
2-hydroxy-1-{5-hydroxy-2-phenyl-4h,8h,9h-furo[2,3-h]chromen-9-yl}-2-methylpropyl acetate
1,3,5,6-tetrahydroxy-7-(3-methylbut-2-en-1-yl)-2-(2-methylbut-3-en-2-yl)xanthen-9-one
1,3,6,7-tetrahydroxy-8-(3-methylbut-2-en-1-yl)-2-(2-methylbut-3-en-2-yl)xanthen-9-one
{2-[4-(hydroxymethyl)-2-[(2-methylpropanoyl)oxy]phenyl]oxiran-2-yl}methyl (2e)-3-phenylprop-2-enoate
(2s)-4,8,9-trihydroxy-2,3,3-trimethyl-11-(2-methylbut-3-en-2-yl)-2h-furo[3,2-b]xanthen-5-one
4,8,9-trihydroxy-2,3,3-trimethyl-11-(2-methylbut-3-en-2-yl)-2h-furo[3,2-b]xanthen-5-one
4,7-dihydroxy-2-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-en-1-yl)-2h,3h-furo[3,2-b]xanthen-5-one
(2s)-4,7,8-trihydroxy-2,3,3-trimethyl-11-(3-methylbut-2-en-1-yl)-2h-furo[3,2-b]xanthen-5-one
(2z)-1,9-bis(2h-1,3-benzodioxol-5-yl)-3-hydroxynon-2-en-1-one
2-(3,7-dimethylocta-2,6-dien-1-yl)-1,3,5,8-tetrahydroxyxanthen-9-one
2-(3,7-dimethylocta-2,6-dien-1-yl)-1,3,6,7-tetrahydroxyxanthen-9-one
1-(5-hydroxy-2,2-dimethylchromen-6-yl)-3-(2,4,5-trimethoxyphenyl)prop-2-en-1-one
(4s,9r)-15,16-dihydroxy-4,5,5,9,10,10-hexamethyl-3,8,13-trioxapentacyclo[10.8.0.0²,⁶.0⁷,¹¹.0¹⁴,¹⁹]icosa-1,6,11,14,16,18-hexaen-20-one
(1s,12r)-16,17-dimethoxy-15-(3-methylbut-2-en-1-yl)-5,7,11,19-tetraoxapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13,15,17-hexaene
1,3,5,6-tetrahydroxy-2,4-bis(3-methylbut-2-en-1-yl)xanthen-9-one
6,8-dihydroxy-17,17-dimethyl-15-(3-methylbut-2-en-1-yl)-3,16-dioxapentacyclo[11.4.1.0²,¹¹.0²,¹⁵.0⁴,⁹]octadeca-4,6,8,11-tetraene-10,14-dione
8-hydroxy-3,6,9-trimethylidene-2-oxo-octahydroazuleno[4,5-b]furan-4-yl 2-(4-hydroxyphenyl)acetate
1,3-dihydroxy-7-[(7-hydroxy-3,7-dimethylocta-2,5-dien-1-yl)oxy]xanthen-9-one
(2r)-4,8,9-trihydroxy-2,3,3-trimethyl-6-(3-methylbut-2-en-1-yl)-2h-furo[3,2-b]xanthen-5-one
3,4,5,8-tetrahydroxy-1,2-bis(3-methylbut-2-en-1-yl)xanthen-9-one
[(2s)-2-[4-(hydroxymethyl)-2-[(2-methylpropanoyl)oxy]phenyl]oxiran-2-yl]methyl (2e)-3-phenylprop-2-enoate
(1r)-1-(5,8-dihydroxy-1,4-dioxonaphthalen-2-yl)-4-methylpent-3-en-1-yl (3e)-5-methylhexa-3,5-dienoate
2,4',5,6-tetramethoxy-4-(4-methoxyphenyl)-[1,1'-biphenyl]-3-ol
(2s)-2-(2h-1,3-benzodioxol-5-yl)-5,7-dimethoxy-8-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one
5,8,9-trihydroxy-1,1,2-trimethyl-7-(3-methylbut-2-en-1-yl)-2h-furo[2,3-c]xanthen-6-one
12-hydroxy-5-methoxy-2,2,9-trimethyl-11-oxo-8,10-dihydro-1-oxatetraphen-9-yl acetate
1,3,5,6-tetrahydroxy-2-(3-methylbut-2-en-1-yl)-4-(2-methylbut-3-en-2-yl)xanthen-9-one
(2s)-5,9,10-trihydroxy-1,1,2-trimethyl-4-(3-methylbut-2-en-1-yl)-2h-furo[2,3-c]xanthen-6-one
4,7,8-trihydroxy-2,3,3-trimethyl-11-(3-methylbut-2-en-1-yl)-2h-furo[3,2-b]xanthen-5-one
(6as,12as)-9-hydroxy-2,3-dimethoxy-8-(3-methylbut-2-en-1-yl)-6a,12a-dihydro-6h-5,7-dioxatetraphen-12-one
3-(3,4-dimethoxyphenyl)-7-hydroxy-6-methoxy-8-(3-methylbut-2-en-1-yl)chromen-4-one
8,8-dimethyl-3-(2,4,5-trimethoxyphenyl)-2h,3h-pyrano[2,3-f]chromen-4-one
(2r)-4,9-dihydroxy-2-(2-hydroxypropan-2-yl)-11-(3-methylbut-2-en-1-yl)-2h,3h-furo[3,2-b]xanthen-5-one
7,10,12-trihydroxy-2,2-dimethyl-8-(2-methylbut-3-en-2-yl)-3,4-dihydro-1,11-dioxatetracen-6-one
(2s)-4,9-dihydroxy-2-(2-hydroxypropan-2-yl)-11-(3-methylbut-2-en-1-yl)-2h,3h-furo[3,2-b]xanthen-5-one
1,3,5,6-tetrahydroxy-2,7-bis(3-methylbut-2-en-1-yl)xanthen-9-one
2-[(1r,4r)-2,2-dimethyl-4-(prop-1-en-2-yl)cyclopentyl]-1,3,5,6-tetrahydroxyxanthen-9-one
1,3,5,6-tetrahydroxy-8-(3-methylbut-2-en-1-yl)-2-(2-methylbut-3-en-2-yl)xanthen-9-one
2-(3,4-dimethoxyphenyl)-5-methoxy-8,8-dimethyl-2h,3h-pyrano[2,3-f]chromen-4-one
(2r)-5,8,9-trihydroxy-1,1,2-trimethyl-7-(3-methylbut-2-en-1-yl)-2h-furo[2,3-c]xanthen-6-one
2,3,6,8-tetrahydroxy-1,5-bis(3-methylbut-2-en-1-yl)xanthen-9-one
(5r)-4-[(3-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methyl]-3-(4-hydroxyphenyl)-5-methoxy-5h-furan-2-one
(2s)-5,9,10-trihydroxy-1,1,2-trimethyl-4-(2-methylbut-3-en-2-yl)-2h-furo[2,3-c]xanthen-6-one
4,7,8-trihydroxy-2,3,3-trimethyl-9-(3-methylbut-2-en-1-yl)-2h-furo[3,2-b]xanthen-5-one
1,3,5-trihydroxy-6-[(3-methylbut-2-en-1-yl)oxy]-2-(2-methylbut-3-en-2-yl)xanthen-9-one
5,9,10-trihydroxy-1,1,2-trimethyl-4-(2-methylbut-3-en-2-yl)-2h-furo[2,3-c]xanthen-6-one
1,2,5,6-tetrahydroxy-7-(3-methylbut-2-en-1-yl)-4-(2-methylbut-3-en-2-yl)xanthen-9-one
5,9,10-trihydroxy-1,1,2-trimethyl-4-(3-methylbut-2-en-1-yl)-2h-furo[2,3-c]xanthen-6-one
(6r,7r,17s,18r)-3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]icosa-1(20),2,4,9,12,15-hexaen-14-one
[(2s)-2-{5-hydroxy-4-methyl-2-[(2-methylpropanoyl)oxy]phenyl}oxiran-2-yl]methyl (2e)-3-phenylprop-2-enoate
1,7-dihydroxy-3-[(6-hydroxy-3,7-dimethylocta-2,7-dien-1-yl)oxy]xanthen-9-one
(3ar,4s,6ar,9s,9ar,9br)-9-methyl-3,6-dimethylidene-2,8-dioxo-octahydroazuleno[4,5-b]furan-4-yl 2-(4-hydroxyphenyl)acetate
(2e)-1-(5-hydroxy-2,2-dimethylchromen-6-yl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one
1,3-dihydroxy-7-[(6-hydroxy-3,7-dimethylocta-2,7-dien-1-yl)oxy]xanthen-9-one
4-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-1,3,5,6-tetrahydroxyxanthen-9-one
10,22-dihydroxy-7,7,18,18-tetramethyl-8,13,17-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁶,²¹]docosa-1(22),3,9,11,14,16(21)-hexaen-2-one
(2s)-4,8,9-trihydroxy-2,3,3-trimethyl-7-(3-methylbut-2-en-1-yl)-2h-furo[3,2-b]xanthen-5-one
2-[2,2-dimethyl-4-(prop-1-en-2-yl)cyclopentyl]-1,3,5,6-tetrahydroxyxanthen-9-one
4,8,9-trihydroxy-2,3,3-trimethyl-6-(3-methylbut-2-en-1-yl)-2h-furo[3,2-b]xanthen-5-one
4,8,9-trihydroxy-2,3,3-trimethyl-7-(3-methylbut-2-en-1-yl)-2h-furo[3,2-b]xanthen-5-one
(2r)-4,8,9-trihydroxy-2,3,3-trimethyl-11-(3-methylbut-2-en-1-yl)-2h-furo[3,2-b]xanthen-5-one
15,16-dihydroxy-4,5,5,9,10,10-hexamethyl-3,8,13-trioxapentacyclo[10.8.0.0²,⁶.0⁷,¹¹.0¹⁴,¹⁹]icosa-1,6,11,14,16,18-hexaen-20-one
(2s)-4,8,9-trihydroxy-2,3,3-trimethyl-11-(3-methylbut-2-en-1-yl)-2h-furo[3,2-b]xanthen-5-one
8-[3,5-dihydroxy-2-(3-methylbut-2-en-1-yl)benzoyl]-2,2-dimethylchromene-5,7-diol
3,6-dihydroxy-4,6,7,15,17,18-hexamethyl-8,11,19-trioxapentacyclo[10.7.1.0²,¹⁰.0⁵,⁹.0¹⁶,²⁰]icosa-1(20),2,4,9,12,15-hexaen-14-one
(5r)-3-(4-hydroxyphenyl)-4-{[2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]methyl}-5-methoxy-5h-furan-2-one
1-(5-hydroxy-2,2-dimethylchromen-6-yl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one
1,7-dihydroxy-3-{[(2e,6r)-6-hydroxy-3,7-dimethylocta-2,7-dien-1-yl]oxy}xanthen-9-one
3-(3,4-dimethoxyphenyl)-1-(5-hydroxy-8-methoxy-2,2-dimethylchromen-6-yl)prop-2-en-1-one
1,3,6,7-tetrahydroxy-5-(3-methylbut-2-en-1-yl)-2-(2-methylbut-3-en-2-yl)xanthen-9-one
6,8,12-trihydroxy-2,2-dimethyl-7-(3-methylbut-2-en-1-yl)-3,4-dihydro-1,10-dioxatetraphen-5-one
{2-[4-(hydroxymethyl)-2-[(2-methylpropanoyl)oxy]phenyl]oxiran-2-yl}methyl 3-phenylprop-2-enoate
(2s)-5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-4-(3-methylbut-2-en-1-yl)-1h,2h-furo[2,3-c]xanthen-6-one
(9s)-12-hydroxy-5-methoxy-2,2,9-trimethyl-11-oxo-8,10-dihydro-1-oxatetraphen-9-yl acetate
2-(3,4-dimethoxyphenyl)-6-methoxy-8,8-dimethyl-2h,3h-pyrano[2,3-f]chromen-4-one
methyl (2E)-2-[3-methoxy-4-(3-methylbutoxy)benzylidene]-3-oxo-2,3-dihydro-1-benzofuran-5-carboxylate
methyl (2Z)-2-(4-butoxy-3-ethoxybenzylidene)-3-oxo-2,3-dihydro-1-benzofuran-5-carboxylate
9-hydroxy-2,3-dimethoxy-8-(3-methylbut-2-enyl)-6a,12a-dihydro-6H-chromeno[3,4-b]chromen-12-one
9-hydroxy-2,3-dimethoxy-8-(3-methylbut-2-enyl)-6a,12a-dihydro-6H-chromeno[3,4-b]chromen-12-one has been reported in Amorpha fruticosa with data available.
