NCBI Taxonomy: 316645

Mallotus philippensis (ncbi_taxid: 316645)

found 40 associated metabolites at species taxonomy rank level.

Ancestor: Mallotus

Child Taxonomies: Mallotus philippensis var. tomentosus

Bergenin

NCGC00346587-02_C14H16O9_Pyrano[3,2-c][2]benzopyran-6(2H)-one, 3,4,4a,10b-tetrahydro-3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-, (2R,3S,4S,4aR,10bS)-

C14H16O9 (328.0794)


Bergenin is a trihydroxybenzoic acid. It has a role as a metabolite. Bergenin is a natural product found in Ficus racemosa, Ardisia paniculata, and other organisms with data available. A natural product found in Cenostigma gardnerianum. C26170 - Protective Agent > C275 - Antioxidant Annotation level-1 Bergenin is a cytoprotective and antioxidative polyphenol found in many medicinal plants. Bergenin has a wide spectrum activities such as hepatoprotective, antiinflammatory, immunomodulatory, antitumor, antiviral, and antifungal properties[1][2]. Bergenin is a cytoprotective and antioxidative polyphenol found in many medicinal plants. Bergenin has a wide spectrum activities such as hepatoprotective, antiinflammatory, immunomodulatory, antitumor, antiviral, and antifungal properties[1][2].

   

Lupeol

(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol

C30H50O (426.3861)


Lupeol is a pentacyclic triterpenoid that is lupane in which the hydrogen at the 3beta position is substituted by a hydroxy group. It occurs in the skin of lupin seeds, as well as in the latex of fig trees and of rubber plants. It is also found in many edible fruits and vegetables. It has a role as an anti-inflammatory drug and a plant metabolite. It is a secondary alcohol and a pentacyclic triterpenoid. It derives from a hydride of a lupane. Lupeol has been investigated for the treatment of Acne. Lupeol is a natural product found in Ficus auriculata, Ficus septica, and other organisms with data available. See also: Calendula Officinalis Flower (part of). A pentacyclic triterpenoid that is lupane in which the hydrogen at the 3beta position is substituted by a hydroxy group. It occurs in the skin of lupin seeds, as well as in the latex of fig trees and of rubber plants. It is also found in many edible fruits and vegetables. D000893 - Anti-Inflammatory Agents Lupeol (Clerodol; Monogynol B; Fagarasterol) is an active pentacyclic?triterpenoid, has anti-oxidant, anti-mutagenic, anti-tumor and anti-inflammatory activity. Lupeol is a potent?androgen receptor (AR)?inhibitor and can be used for cancer research, especially prostate cancer of androgen-dependent phenotype (ADPC) and castration resistant phenotype (CRPC)[1]. Lupeol (Clerodol; Monogynol B; Fagarasterol) is an active pentacyclic?triterpenoid, has anti-oxidant, anti-mutagenic, anti-tumor and anti-inflammatory activity. Lupeol is a potent?androgen receptor (AR)?inhibitor and can be used for cancer research, especially prostate cancer of androgen-dependent phenotype (ADPC) and castration resistant phenotype (CRPC)[1].

   

Friedelin

3(2H)-PICENONE, EICOSAHYDRO-4,4A,6B,8A,11,11,12B,14A-OCTAMETHYL-, (4R-(4.ALPHA.,4A.ALPHA.,6A.BETA.,6B.ALPHA.,8A.ALPHA.,12A.ALPHA.,12B.BETA.,14A.ALPHA.,14B.BETA.))-

C30H50O (426.3861)


Friedelin is a pentacyclic triterpenoid that is perhydropicene which is substituted by an oxo group at position 3 and by methyl groups at the 4, 4a, 6b, 8a, 11, 11, 12b, and 14a-positions (the 4R,4aS,6aS,6bR,8aR,12aR,12bS,14aS,14bS-enantiomer). It is the major triterpenoid constituent of cork. It has a role as an anti-inflammatory drug, a non-narcotic analgesic, an antipyretic and a plant metabolite. It is a pentacyclic triterpenoid and a cyclic terpene ketone. Friedelin is a natural product found in Diospyros eriantha, Salacia chinensis, and other organisms with data available. A pentacyclic triterpenoid that is perhydropicene which is substituted by an oxo group at position 3 and by methyl groups at the 4, 4a, 6b, 8a, 11, 11, 12b, and 14a-positions (the 4R,4aS,6aS,6bR,8aR,12aR,12bS,14aS,14bS-enantiomer). It is the major triterpenoid constituent of cork. Friedelin is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Friedelin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Friedelin can be found in a number of food items such as pomegranate, sugar apple, apple, and mammee apple, which makes friedelin a potential biomarker for the consumption of these food products. Friedelin is a triterpenoid chemical compound found in Azima tetracantha, Orostachys japonica, and Quercus stenophylla. Friedelin is also found in the roots of the Cannabis plant .

   

Betulin

(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol

C30H50O2 (442.3811)


Betulin is found in black elderberry. Betulin is a constituent of Corylus avellana (filbert) and Vicia faba. Betulin (lup-20(29)-ene-3 ,28-diol) is an abundant naturally occurring triterpene. It is commonly isolated from the bark of birch trees and forms up to 30\\\\\% of the dry weight of the extractive. The purpose of the compound in the bark is not known. It can be converted to betulinic acid (the alcohol group replaced by a carboxylic acid group), which is biologically more active than betulin itself. Chemically, betulin is a triterpenoid of lupane structure. It has a pentacyclic ring structure, and hydroxyl groups in positions C3 and C28 Betulin is a pentacyclic triterpenoid that is lupane having a double bond at position 20(29) as well as 3beta-hydroxy and 28-hydroxymethyl substituents. It has a role as a metabolite, an antiviral agent, an analgesic, an anti-inflammatory agent and an antineoplastic agent. It is a pentacyclic triterpenoid and a diol. It derives from a hydride of a lupane. Betulin is a natural product found in Diospyros morrisiana, Euonymus carnosus, and other organisms with data available. A pentacyclic triterpenoid that is lupane having a double bond at position 20(29) as well as 3beta-hydroxy and 28-hydroxymethyl substituents. Constituent of Corylus avellana (filbert) and Vicia faba Betulin (Trochol), is a sterol regulatory element-binding protein (SREBP) inhibitor with an IC50 of 14.5 μM in K562 cell line. Betulin (Trochol), is a sterol regulatory element-binding protein (SREBP) inhibitor with an IC50 of 14.5 μM in K562 cell line. Betulin (Trochol), is a sterol regulatory element-binding protein (SREBP) inhibitor with an IC50 of 14.5 μM in K562 cell line.

   

Rottlerin

(2E) -1- [ 6- [ (3-Acetyl-2,4,6-trihydroxy-5-methylphenyl) methyl ] -5,7-dihydroxy-2,2-dimethyl-2H-1-benzopyran-8-yl ] -3-phenyl-2-propene-1-one

C30H28O8 (516.1784)


Rottlerin is a chromenol that is 2,2-dimethyl-2H-chromene substituted by hydroxy groups at positions 5 and 7, a 3-acetyl-2,4,6-trihydroxy-5-methylbenzyl group at position 6 and a (1E)-3-oxo-1-phenylprop-1-en-3-yl group at position 8. A potassium channel opener, it is isolated from Mallotus philippensis. It has a role as an antineoplastic agent, an apoptosis inducer, a metabolite, a K-ATP channel agonist, an antihypertensive agent and an anti-allergic agent. It is an enone, a chromenol, a benzenetriol, a methyl ketone and an aromatic ketone. Rottlerin is a natural product found in Mallotus philippensis with data available. A chromenol that is 2,2-dimethyl-2H-chromene substituted by hydroxy groups at positions 5 and 7, a 3-acetyl-2,4,6-trihydroxy-5-methylbenzyl group at position 6 and a (1E)-3-oxo-1-phenylprop-1-en-3-yl group at position 8. A potassium channel opener, it is isolated from Mallotus philippensis. D004791 - Enzyme Inhibitors relative retention time with respect to 9-anthracene Carboxylic Acid is 1.546 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.549 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.548 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.550 Rottlerin, a natural product purified from Mallotus Philippinensis, is a specific PKC inhibitor, with IC50 values for PKCδ of 3-6 μM, PKCα,β,γ of 30-42 μM, PKCε,η,ζ of 80-100 μM. Rottlerin acts as a direct mitochondrial uncoupler, and stimulates autophagy by targeting a signaling cascade upstream of mTORC1. Rottlerin induces apoptosis via caspase 3 activation[1][2][3]. Rottlerin inhibits HIV-1 integration and Rabies virus (RABV) infection[4][5]. Rottlerin, a natural product purified from Mallotus Philippinensis, is a specific PKC inhibitor, with IC50 values for PKCδ of 3-6 μM, PKCα,β,γ of 30-42 μM, PKCε,η,ζ of 80-100 μM. Rottlerin acts as a direct mitochondrial uncoupler, and stimulates autophagy by targeting a signaling cascade upstream of mTORC1. Rottlerin induces apoptosis via caspase 3 activation[1][2][3]. Rottlerin inhibits HIV-1 integration and Rabies virus (RABV) infection[4][5].

   

Friedelin

4,4a,6b,8a,11,11,12b,14a-octamethyl-docosahydropicen-3-one

C30H50O (426.3861)


Friedelin is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Friedelin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Friedelin can be found in a number of food items such as apple, pear, mammee apple, and sugar apple, which makes friedelin a potential biomarker for the consumption of these food products. Friedelin is a triterpenoid chemical compound found in Azima tetracantha, Orostachys japonica, and Quercus stenophylla. Friedelin is also found in the roots of the Cannabis plant .

   

Mallotophilippen B

Mallotophilippen B

C26H30O8 (470.1941)


A chromenol that is 2H-chromene-5,7-diol substituted by geminal methyl groups at position 2, a 2-methylbutanoyl group at position 8 and a 3-acetyl-2,4,6-trihydroxy-5-methylbenzyl group at position 6. Isolated from Mallotus philippensis, it exhibits anti-inflammatory activity.

   

Mallotophilippen A

Mallotophilippen A

C28H34O8 (498.2254)


A chromenol that is 2H-chromene-5,7-diol substituted by geminal methyl groups at position 2, a 2-methylbutanoyl group at position 8 and a 2,4,6-trihydroxy-3-methyl-5-(2-methylpropanoyl)benzyl group at position 6. Isolated from Mallotus philippensis, it exhibits anti-inflammatory activity.

   

lupeol

Lup-20(29)-en-3.beta.-ol

C30H50O (426.3861)


D000893 - Anti-Inflammatory Agents Lupeol (Clerodol; Monogynol B; Fagarasterol) is an active pentacyclic?triterpenoid, has anti-oxidant, anti-mutagenic, anti-tumor and anti-inflammatory activity. Lupeol is a potent?androgen receptor (AR)?inhibitor and can be used for cancer research, especially prostate cancer of androgen-dependent phenotype (ADPC) and castration resistant phenotype (CRPC)[1]. Lupeol (Clerodol; Monogynol B; Fagarasterol) is an active pentacyclic?triterpenoid, has anti-oxidant, anti-mutagenic, anti-tumor and anti-inflammatory activity. Lupeol is a potent?androgen receptor (AR)?inhibitor and can be used for cancer research, especially prostate cancer of androgen-dependent phenotype (ADPC) and castration resistant phenotype (CRPC)[1].

   

Betulin

NCGC00168803-04_C30H50O2_Lup-20(29)-ene-3,28-diol, (3beta)-

C30H50O2 (442.3811)


Betulin (Trochol), is a sterol regulatory element-binding protein (SREBP) inhibitor with an IC50 of 14.5 μM in K562 cell line. Betulin (Trochol), is a sterol regulatory element-binding protein (SREBP) inhibitor with an IC50 of 14.5 μM in K562 cell line. Betulin (Trochol), is a sterol regulatory element-binding protein (SREBP) inhibitor with an IC50 of 14.5 μM in K562 cell line.

   

3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one

3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one

C14H16O9 (328.0794)


   

3-hydroxy-4,4a,6b,8a,11,11,12b,14a-octamethyl-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-1h-picen-2-one

3-hydroxy-4,4a,6b,8a,11,11,12b,14a-octamethyl-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-1h-picen-2-one

C30H48O2 (440.3654)


   

3-phenyl-1-[7,9,15-trihydroxy-3,3,8,14,19,19-hexamethyl-16-(3-phenylprop-2-enoyl)-4,12,18-trioxapentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²¹]henicosa-5,7,9,13,15,17(21)-hexaen-6-yl]prop-2-en-1-one

3-phenyl-1-[7,9,15-trihydroxy-3,3,8,14,19,19-hexamethyl-16-(3-phenylprop-2-enoyl)-4,12,18-trioxapentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²¹]henicosa-5,7,9,13,15,17(21)-hexaen-6-yl]prop-2-en-1-one

C42H40O8 (672.2723)


   

10-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5-hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-2h,3h-pyrano[3,2-g]chromen-4-one

10-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5-hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-2h,3h-pyrano[3,2-g]chromen-4-one

C30H28O9 (532.1733)


   

3-hydroxy-4,4a,6b,8a,11,11,12b,14a-octamethyl-tetradecahydro-1h-picen-2-one

3-hydroxy-4,4a,6b,8a,11,11,12b,14a-octamethyl-tetradecahydro-1h-picen-2-one

C30H50O2 (442.3811)


   

5,7-dihydroxy-8-methyl-6-(3-methylbut-2-en-1-yl)-2-phenyl-2,3-dihydro-1-benzopyran-4-one

5,7-dihydroxy-8-methyl-6-(3-methylbut-2-en-1-yl)-2-phenyl-2,3-dihydro-1-benzopyran-4-one

C21H22O4 (338.1518)


   

3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-ol

3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-ol

C30H50O2 (442.3811)


   

(2e)-1-[(1r,2r,11s)-14-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-7,9,15-trihydroxy-3,3,8,19,19-pentamethyl-6-[(2e)-3-phenylprop-2-enoyl]-4,12,18-trioxapentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²¹]henicosa-5,7,9,13(21),14,16-hexaen-16-yl]-3-phenylprop-2-en-1-one

(2e)-1-[(1r,2r,11s)-14-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-7,9,15-trihydroxy-3,3,8,19,19-pentamethyl-6-[(2e)-3-phenylprop-2-enoyl]-4,12,18-trioxapentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²¹]henicosa-5,7,9,13(21),14,16-hexaen-16-yl]-3-phenylprop-2-en-1-one

C51H48O12 (852.3146)


   

1-(2-acetyl-1,3,6,8-tetrahydroxy-4,7,11,11-tetramethyl-11a,12-dihydro-5ah-5,10-dioxatetraphen-9-yl)-3-phenylprop-2-en-1-one

1-(2-acetyl-1,3,6,8-tetrahydroxy-4,7,11,11-tetramethyl-11a,12-dihydro-5ah-5,10-dioxatetraphen-9-yl)-3-phenylprop-2-en-1-one

C31H30O8 (530.1941)


   
   

(2e)-3-phenyl-1-[(1s,2s,11r)-7,9,15-trihydroxy-3,3,8,14,19,19-hexamethyl-16-[(2e)-3-phenylprop-2-enoyl]-4,12,18-trioxapentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²¹]henicosa-5,7,9,13,15,17(21)-hexaen-6-yl]prop-2-en-1-one

(2e)-3-phenyl-1-[(1s,2s,11r)-7,9,15-trihydroxy-3,3,8,14,19,19-hexamethyl-16-[(2e)-3-phenylprop-2-enoyl]-4,12,18-trioxapentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²¹]henicosa-5,7,9,13,15,17(21)-hexaen-6-yl]prop-2-en-1-one

C42H40O8 (672.2723)


   

1-{20-acetyl-26-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-13,15,21,27-tetrahydroxy-3,3,9,9,14,31,31-heptamethyl-12-(3-phenylprop-2-enoyl)-4,10,18,24,30-pentaoxaoctacyclo[23.7.1.0²,²³.0⁵,²².0⁶,¹⁹.0⁸,¹⁷.0¹¹,¹⁶.0²⁹,³³]tritriaconta-5,11,13,15,19,21,25(33),26,28-nonaen-28-yl}-3-phenylprop-2-en-1-one

1-{20-acetyl-26-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-13,15,21,27-tetrahydroxy-3,3,9,9,14,31,31-heptamethyl-12-(3-phenylprop-2-enoyl)-4,10,18,24,30-pentaoxaoctacyclo[23.7.1.0²,²³.0⁵,²².0⁶,¹⁹.0⁸,¹⁷.0¹¹,¹⁶.0²⁹,³³]tritriaconta-5,11,13,15,19,21,25(33),26,28-nonaen-28-yl}-3-phenylprop-2-en-1-one

C65H62O16 (1098.4038)


   

8-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-6-(3-methylbut-2-en-1-yl)-2-phenyl-2,3-dihydro-1-benzopyran-4-one

8-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-6-(3-methylbut-2-en-1-yl)-2-phenyl-2,3-dihydro-1-benzopyran-4-one

C30H30O8 (518.1941)


   

10-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5-hydroxy-8,8-dimethyl-2-phenyl-2h,3h-pyrano[3,2-g]chromen-4-one

10-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5-hydroxy-8,8-dimethyl-2-phenyl-2h,3h-pyrano[3,2-g]chromen-4-one

C30H28O8 (516.1784)


   

(2s,4r,4as,6as,6br,8ar,12ar,12bs,14as,14bs)-2-hydroxy-4,4a,6b,8a,11,11,12b,14a-octamethyl-tetradecahydro-1h-picen-3-one

(2s,4r,4as,6as,6br,8ar,12ar,12bs,14as,14bs)-2-hydroxy-4,4a,6b,8a,11,11,12b,14a-octamethyl-tetradecahydro-1h-picen-3-one

C30H50O2 (442.3811)


   

(2e)-3-phenyl-1-[(1r,2r,11s)-7,9,15-trihydroxy-3,3,8,14,19,19-hexamethyl-16-[(2e)-3-phenylprop-2-enoyl]-4,12,18-trioxapentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²¹]henicosa-5,7,9,13,15,17(21)-hexaen-6-yl]prop-2-en-1-one

(2e)-3-phenyl-1-[(1r,2r,11s)-7,9,15-trihydroxy-3,3,8,14,19,19-hexamethyl-16-[(2e)-3-phenylprop-2-enoyl]-4,12,18-trioxapentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²¹]henicosa-5,7,9,13,15,17(21)-hexaen-6-yl]prop-2-en-1-one

C42H40O8 (672.2723)


   

(2e)-1-[(1r,2r,8r,17r,23s)-20-acetyl-26-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-13,15,21,27-tetrahydroxy-3,3,9,9,14,31,31-heptamethyl-12-[(2e)-3-phenylprop-2-enoyl]-4,10,18,24,30-pentaoxaoctacyclo[23.7.1.0²,²³.0⁵,²².0⁶,¹⁹.0⁸,¹⁷.0¹¹,¹⁶.0²⁹,³³]tritriaconta-5,11,13,15,19,21,25(33),26,28-nonaen-28-yl]-3-phenylprop-2-en-1-one

(2e)-1-[(1r,2r,8r,17r,23s)-20-acetyl-26-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-13,15,21,27-tetrahydroxy-3,3,9,9,14,31,31-heptamethyl-12-[(2e)-3-phenylprop-2-enoyl]-4,10,18,24,30-pentaoxaoctacyclo[23.7.1.0²,²³.0⁵,²².0⁶,¹⁹.0⁸,¹⁷.0¹¹,¹⁶.0²⁹,³³]tritriaconta-5,11,13,15,19,21,25(33),26,28-nonaen-28-yl]-3-phenylprop-2-en-1-one

C65H62O16 (1098.4038)


   

(2e)-1-[(5ar,11as)-2-acetyl-1,3,6,8-tetrahydroxy-4,7,11,11-tetramethyl-11a,12-dihydro-5ah-5,10-dioxatetraphen-9-yl]-3-phenylprop-2-en-1-one

(2e)-1-[(5ar,11as)-2-acetyl-1,3,6,8-tetrahydroxy-4,7,11,11-tetramethyl-11a,12-dihydro-5ah-5,10-dioxatetraphen-9-yl]-3-phenylprop-2-en-1-one

C31H30O8 (530.1941)


   

(2r)-5-hydroxy-8,8,10-trimethyl-2-phenyl-2h,3h-pyrano[3,2-g]chromen-4-one

(2r)-5-hydroxy-8,8,10-trimethyl-2-phenyl-2h,3h-pyrano[3,2-g]chromen-4-one

C21H20O4 (336.1362)


   

(2s)-1-{6-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-2,2-dimethylchromen-8-yl}-2-methylbutan-1-one

(2s)-1-{6-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-2,2-dimethylchromen-8-yl}-2-methylbutan-1-one

C26H30O8 (470.1941)


   

1-{14-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-7,9,15-trihydroxy-3,3,8,19,19-pentamethyl-6-(3-phenylprop-2-enoyl)-4,12,18-trioxapentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²¹]henicosa-5,7,9,13(21),14,16-hexaen-16-yl}-3-phenylprop-2-en-1-one

1-{14-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-7,9,15-trihydroxy-3,3,8,19,19-pentamethyl-6-(3-phenylprop-2-enoyl)-4,12,18-trioxapentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²¹]henicosa-5,7,9,13(21),14,16-hexaen-16-yl}-3-phenylprop-2-en-1-one

C51H48O12 (852.3146)


   

(2r)-1-{6-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-2,2-dimethylchromen-8-yl}-2-methylbutan-1-one

(2r)-1-{6-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-2,2-dimethylchromen-8-yl}-2-methylbutan-1-one

C26H30O8 (470.1941)


   

(2s)-8-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-6-(3-methylbut-2-en-1-yl)-2-phenyl-2,3-dihydro-1-benzopyran-4-one

(2s)-8-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-6-(3-methylbut-2-en-1-yl)-2-phenyl-2,3-dihydro-1-benzopyran-4-one

C30H30O8 (518.1941)


   

(2r)-1-(5,7-dihydroxy-2,2-dimethyl-6-{[2,4,6-trihydroxy-3-methyl-5-(2-methylpropanoyl)phenyl]methyl}chromen-8-yl)-2-methylbutan-1-one

(2r)-1-(5,7-dihydroxy-2,2-dimethyl-6-{[2,4,6-trihydroxy-3-methyl-5-(2-methylpropanoyl)phenyl]methyl}chromen-8-yl)-2-methylbutan-1-one

C28H34O8 (498.2254)


   

(2r)-10-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5-hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-2h,3h-pyrano[3,2-g]chromen-4-one

(2r)-10-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5-hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-2h,3h-pyrano[3,2-g]chromen-4-one

C30H28O9 (532.1733)


   

(4as,6as,6br,8ar,12ar,12bs,14ar,14bs)-3-hydroxy-4,4a,6b,8a,11,11,12b,14a-octamethyl-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-1h-picen-2-one

(4as,6as,6br,8ar,12ar,12bs,14ar,14bs)-3-hydroxy-4,4a,6b,8a,11,11,12b,14a-octamethyl-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-1h-picen-2-one

C30H48O2 (440.3654)


   

(2s)-5,7-dihydroxy-8-methyl-6-(3-methylbut-2-en-1-yl)-2-phenyl-2,3-dihydro-1-benzopyran-4-one

(2s)-5,7-dihydroxy-8-methyl-6-(3-methylbut-2-en-1-yl)-2-phenyl-2,3-dihydro-1-benzopyran-4-one

C21H22O4 (338.1518)


   

(3s,4r,4as,6as,6br,8ar,12ar,12bs,14as,14bs)-3-hydroxy-4,4a,6b,8a,11,11,12b,14a-octamethyl-tetradecahydro-1h-picen-2-one

(3s,4r,4as,6as,6br,8ar,12ar,12bs,14as,14bs)-3-hydroxy-4,4a,6b,8a,11,11,12b,14a-octamethyl-tetradecahydro-1h-picen-2-one

C30H50O2 (442.3811)


   

(2s)-10-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5-hydroxy-8,8-dimethyl-2-phenyl-2h,3h-pyrano[3,2-g]chromen-4-one

(2s)-10-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5-hydroxy-8,8-dimethyl-2-phenyl-2h,3h-pyrano[3,2-g]chromen-4-one

C30H28O8 (516.1784)


   

5-hydroxy-8,8,10-trimethyl-2-phenyl-2h,3h-pyrano[3,2-g]chromen-4-one

5-hydroxy-8,8,10-trimethyl-2-phenyl-2h,3h-pyrano[3,2-g]chromen-4-one

C21H20O4 (336.1362)