Chemical Formula: C19H18O8

Chemical Formula C19H18O8

Found 235 metabolite its formula value is C19H18O8

Chrysosplenetin

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

C19H18O8 (374.1001628)


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].

   

Skullcapflavone II

5-hydroxy-2-(2-hydroxy-6-methoxyphenyl)-6,7,8-trimethoxy-4H-chromen-4-one

C19H18O8 (374.1001628)


Skullcapflavone II, a flavonoid derived from Scutellaria baicalensis, has anti-inflammatory, anti-microbial activities. Skullcapflavone II regulates osteoclast differentiation, survival, and function. Skullcapflavone II exerts potent antimicrobial activity against M. aurum and M. bovis BCG[1][2]. Skullcapflavone II, a flavonoid derived from Scutellaria baicalensis, has anti-inflammatory, anti-microbial activities. Skullcapflavone II regulates osteoclast differentiation, survival, and function. Skullcapflavone II exerts potent antimicrobial activity against M. aurum and M. bovis BCG[1][2].

   

Casticin

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

C19H18O8 (374.1001628)


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.

   

Methylrosmarinic acid

Benzenepropanoic acid, .alpha.-[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-3,4-dihydroxy-, methyl ester, (.alpha.R)-

C19H18O8 (374.1001628)


Methyl rosmarinate is a hydroxycinnamic acid. Methyl rosmarinate is a natural product found in Dimetia scandens, Bourreria pulchra, and other organisms with data available. Methylrosmarinic acid is found in herbs and spices. Methylrosmarinic acid is isolated from Salvia (sage) species. Isolated from Salvia (sage) subspecies Methyl rosmarinate is found in herbs and spices. Methyl rosmarinate is a noncompetitive tyrosinase inhibitor which is isolated from Rabdosia serra, with an IC50 of 0.28 mM for mushroom tyrosinase, and also inhibits a-glucosidase[1]. Methyl rosmarinate is a noncompetitive tyrosinase inhibitor which is isolated from Rabdosia serra, with an IC50 of 0.28 mM for mushroom tyrosinase, and also inhibits a-glucosidase[1].

   

Neobaicalein

4H-1-Benzopyran-4-one, 5-hydroxy-2-(2-hydroxy-6-methoxyphenyl)-6,7,8-trimethoxy-

C19H18O8 (374.1001628)


Scullcapflavone II is a tetramethoxyflavone that is flavone substituted by methoxy groups at positions 6, 7, 8 and 6 and hydroxy groups at positons 5 and 2 respectively. It has a role as a plant metabolite and an anti-asthmatic drug. It is a tetramethoxyflavone and a dihydroxyflavone. It is functionally related to a flavone. Skullcapflavone II is a natural product found in Lagochilus leiacanthus, Scutellaria guatemalensis, and other organisms with data available. A tetramethoxyflavone that is flavone substituted by methoxy groups at positions 6, 7, 8 and 6 and hydroxy groups at positons 5 and 2 respectively. Skullcapflavone II, a flavonoid derived from Scutellaria baicalensis, has anti-inflammatory, anti-microbial activities. Skullcapflavone II regulates osteoclast differentiation, survival, and function. Skullcapflavone II exerts potent antimicrobial activity against M. aurum and M. bovis BCG[1][2]. Skullcapflavone II, a flavonoid derived from Scutellaria baicalensis, has anti-inflammatory, anti-microbial activities. Skullcapflavone II regulates osteoclast differentiation, survival, and function. Skullcapflavone II exerts potent antimicrobial activity against M. aurum and M. bovis BCG[1][2].

   

5,8-Dihydroxy-3,3',4',7-tetramethoxyflavone

2-(3,4-dimethoxyphenyl)-5,8-dihydroxy-3,7-dimethoxy-4H-chromen-4-one

C19H18O8 (374.1001628)


5,8-Dihydroxy-3,3,4,7-tetramethoxyflavone is found in citrus. 5,8-Dihydroxy-3,3,4,7-tetramethoxyflavone is isolated from sweet orange oi

   

3-O-Methylrosmarinic acid

2-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-3-(4-hydroxy-3-methoxyphenyl)propanoic acid

C19H18O8 (374.1001628)


3-O-Methylrosmarinic acid is a polyphenol metabolite detected in biological fluids (PMID: 20428313). A polyphenol metabolite detected in biological fluids [PhenolExplorer]

   
   

3,5-Dihydroxy-6,7,8,4-tetramethoxyflavone

3,5-Dihydroxy-6,7,8,4-tetramethoxyflavone

C19H18O8 (374.1001628)


   

Comosin

3-[(Acetyloxy)methyl]-2,3-dihydro-5,7-dihydroxy-3-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one, 9ci

C19H18O8 (374.1001628)


Comosin is found in herbs and spices. Comosin is a constituent of Muscari comosum (tassel hyacinth). Constituent of Muscari comosum (tassel hyacinth). Comosin is found in herbs and spices.

   

3-(3,4-dihydroxyphenyl)-2-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propanoic acid

3-(3,4-dihydroxyphenyl)-2-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propanoic acid

C19H18O8 (374.1001628)


   
   

Pebrellin

2-(3,4-Dimethoxyphenyl)-5,6-dihydroxy-7,8-dimethoxy-4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


Constituent of Mentha piperita and Thymus piperella. Pebrellin is found in many foods, some of which are spearmint, peppermint, pot marjoram, and herbs and spices. Pebrellin is found in herbs and spices. Pebrellin is a constituent of Mentha piperita and Thymus piperella

   

Hymenoxin

2-(3,4-Dimethoxyphenyl)-5,7-dihydroxy-6,8-dimethoxy-4H-1-benzopyran-4-one, 9ci

C19H18O8 (374.1001628)


Isolated from Mentha piperita (peppermint). Hymenoxin is found in sunflower, peppermint, and herbs and spices. Hymenoxin is found in herbs and spices. Hymenoxin is isolated from Mentha piperita (peppermint).

   

4',5-Dihydroxy-3',5',7,8-tetramethoxyflavone

5-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-7,8-dimethoxy-4H-chromen-4-one

C19H18O8 (374.1001628)


4,5-Dihydroxy-3,5,7,8-tetramethoxyflavone is isolated from Lepidium sativum (garden cress). Isolated from Lepidium sativum (garden cress).

   

Menadiol disuccinate

4-({4-[(3-carboxypropanoyl)oxy]-2-methylnaphthalen-1-yl}oxy)-4-oxobutanoic acid

C19H18O8 (374.1001628)


Prothrombogenic vitamin. Prothrombogenic vitamin

   

clauslactone D

(+)-Clauslactone D

C19H18O8 (374.1001628)


   

Parmelin

Usnarin acid

C19H18O8 (374.1001628)


Atranorin is a lichen secondary metabolite. Atranorin inhibits lung cancer cell motility and tumorigenesis by affecting AP-1, Wnt, and STAT signaling and suppressing RhoGTPase activity[1][2]. Atranorin is a lichen secondary metabolite. Atranorin inhibits lung cancer cell motility and tumorigenesis by affecting AP-1, Wnt, and STAT signaling and suppressing RhoGTPase activity[1][2]. Atranorin is a lichen secondary metabolite. Atranorin inhibits lung cancer cell motility and tumorigenesis by affecting AP-1, Wnt, and STAT signaling and suppressing RhoGTPase activity[1][2].

   

Irisjaponin B

5,7-Dihydroxy-6,2,3,4-tetramethoxyisoflavone

C19H18O8 (374.1001628)


   
   

6-Deoxyclitoriacetal

6-Deoxyclitoriacetal

C19H18O8 (374.1001628)


   

Dihydrostemonal

6,11-Dihydroxy-2,3,9-trimethoxyrotenone

C19H18O8 (374.1001628)


   

11-Deoxyclitoriacetal

(6aR,12aR)-6,12a-Dihydroxy-2,3,9-trimethoxyrotenone

C19H18O8 (374.1001628)


   

6-(3-Oxobutyl)taxifolin

3,5,7,3,4-Pentahydroxy-6-(3-oxobutyl)flavanone

C19H18O8 (374.1001628)


   

3,5,2-Trihydroxy-7,8-dimethoxyflavanone 2-acetate

3,5,2-Trihydroxy-7,8-dimethoxyflavanone 2-acetate

C19H18O8 (374.1001628)


   

(2R,3R)-5,2-Dihydroxy-7,8-dimethoxy-3-O-acetylflavanone

(2R,3R)-5,2-Dihydroxy-7,8-dimethoxy-3-O-acetylflavanone

C19H18O8 (374.1001628)


   

Bracteaxanthone V

Bracteaxanthone V

C19H18O8 (374.1001628)


   

7-Methylsudachitin

5-Hydroxy-2- (4-hydroxy-3-methoxyphenyl) -6,7,8-trimethoxy-4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

Gardenin D

5-Hydroxy-2- (3-hydroxy-4-methoxyphenyl) -6,7,8-trimethoxy-4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

5,4-Dihidroxy-6,7,3,5-tetramethoxyflavone

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

C19H18O8 (374.1001628)


   

5,3-Dihydroxy-6,7,4,5-tetramethoxyflavone

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

C19H18O8 (374.1001628)


   

3,4,5-Trimethoxywogonin

5,7-Dihydroxy-8-methoxy-2- (3,4,5-trimethoxyphenyl) -4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

Calycopterin

5-Hydroxy-2- (4-hydroxyphenyl) -3,6,7,8-tetramethoxy-4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

Araneosol

5,7-Dihydroxy-3,6,8-trimethoxy-2- (4-methoxyphenyl) -4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

Bonanzin

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

C19H18O8 (374.1001628)


   

Quercetagetin 6,7,34-tetramethyl ether

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

C19H18O8 (374.1001628)


   

Ternatin

5-Hydroxy-2- (4-hydroxy-3-methoxyphenyl) -3,7,8-trimethoxy-4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

Gossypetin 3,7,8,4-tetramethyl ether

5-Hydroxy-2- (3-hydroxy-4-methoxyphenyl) -3,7,8-trimethoxy-4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

Myricetin 3,3,4,5-tetramethyl ether

5,7-Dihydroxy-3-methoxy-2- (3,4,5-trimethoxyphenyl) -4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

8-C-Methylquercetagetin 3,6,7-trimethyl ether

2- (3,4-Dihydroxyphenyl) -5-hydroxy-3,6,7-trimethoxy-8-methyl-4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

8-C-Methylquercetagetin 3,6,3-trimethyl ether

5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-8-methyl-4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

5,4-Dihydroxy-7,2,3,5-tetramethoxyflavone

5-Hydroxy-2- (4-hydroxy-2,3,5-trimethoxyphenyl) -7-methoxy-4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

5,7-Dihydroxy-2,3,4,5-tetramethoxyflavone

5,7-Dihydroxy-2- (2,3,4,5-tetramethoxyphenyl) -4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

3,5-Dihydroxy-6,7,8,4-tetramethoxyflavone

3,5-Dihydroxy-6,7,8-trimethoxy-2- (4-methoxyphenyl) -4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

3,5-Dihydroxy-7,3,4,5-tetramethoxyflavone

3,5-Dihydroxy-7-methoxy-2- (3,4,5-trimethoxyphenyl) -4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

5,3-Dihydroxy-7,8,4,5-tetramethoxyflavone

5,3-Dihydroxy-7,8,4,5-tetramethoxyflavone

C19H18O8 (374.1001628)


   

5,3-Dihydroxy-7,2,4,5-tetramethoxyflavone

5,3-Dihydroxy-7,2,4,5-tetramethoxyflavone

C19H18O8 (374.1001628)


   

Quercetagetin 3,7,3,4-tetramethyl ether

5,6-Dihydroxy-3,3,4,7-tetramethoxyflavone

C19H18O8 (374.1001628)


   

5,4-Dihydroxy-3,7,8,2-tetramethoxyflavone

5,4-Dihydroxy-3,7,8,2-tetramethoxyflavone

C19H18O8 (374.1001628)


   

5,5-Dihydroxy-3,7,8,2-tetramethoxyflavone

5,5-Dihydroxy-3,7,8,2-tetramethoxyflavone

C19H18O8 (374.1001628)


   

Myricetin 3,7,3,4-tetramethyl ether

3,5-dihydroxy-3,4,5,7-tetramethoxyflavone

C19H18O8 (374.1001628)


   

6,5-Dihydroxy-3,7,2,4-tetramethoxyflavone

6,5-Dihydroxy-3,7,2,4-tetramethoxyflavone

C19H18O8 (374.1001628)


   

Caviunin

5,7-Dihydroxy-6,2,4,5-tetramethoxyisoflavone

C19H18O8 (374.1001628)


   

Junipegenin C

5,7-Dihydroxy-6,3,4,5-tetramethoxyisoflavone

C19H18O8 (374.1001628)


   

Isocaviunin

5,7-Dihydroxy-8,2,4,5-tetramethoxyisoflavone

C19H18O8 (374.1001628)


   

5,3-Dihydroxy-6,7,8,2-tetramethoxyisoflavone

5,3-Dihydroxy-6,7,8,2-tetramethoxyisoflavone

C19H18O8 (374.1001628)


   

8,3-Dihydroxy-5,6,7,4-tetramethoxyflavone

8,3-Dihydroxy-5,6,7,4-tetramethoxyflavone

C19H18O8 (374.1001628)


   

5,5-Dihydroxy-3,7,3,4-tetramethoxyflavone

5,5-Dihydroxy-3,7,3,4-tetramethoxyflavone

C19H18O8 (374.1001628)


   

Quercetagetin 3,5,6,3-tetramethyl ether

Quercetagetin 3,5,6,3-tetramethyl ether

C19H18O8 (374.1001628)


   

Quercetagetin 3,5,7,3-tetramethyl ether

6,4-Dihydroxy-3,5,7,3-tetramethoxyflavone

C19H18O8 (374.1001628)


   

Quercetagetin 3,5,7,4-tetramethyl ether

Quercetagetin 3,5,7,4-tetramethyl ether

C19H18O8 (374.1001628)


   

Gossypetin 3,8,3,4-tetramethyl ether

5,7-Dihydroxy-3,8,3,4-tetramethoxyflavone

C19H18O8 (374.1001628)


   

Gossypetin 7,8,3,4-tetramethyl ether

Gossypetin 7,8,3,4-tetramethyl ether

C19H18O8 (374.1001628)


   

Myricetin 3,7,3,5-tetramethyl ether

Myricetin 3,7,3,5-tetramethyl ether

C19H18O8 (374.1001628)


   

6,8-Di-C-methylmyricetin 3,4-dimethyl ether

5,7,3,5-Tetrahydroxy-3,4-dimethoxy-6,8-dimethylflavone

C19H18O8 (374.1001628)


   

5-O-Methyloxyayanin-A

2,5-Dihydroxy-3,4,5,7-tetramethoxyflavone

C19H18O8 (374.1001628)


   

Arteanoflavone

5,7-Dihydroxy-6-methoxy-2- (3,4,5-trimethoxyphenyl) -4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


Arteanoflavone is a natural product found in Artemisia lucentica with data available.

   

5,4-Dihidroxy-7,8,2,3-tetramethoxyflavone

5,4-Dihidroxy-7,8,2,3-tetramethoxyflavone

C19H18O8 (374.1001628)


   

Chrysosplenol E

5,2-Dihydroxy-3,7,4,5-tetramethoxyflavone

C19H18O8 (374.1001628)


   

Chrysosplin

4,5-Dihydroxy-2,3,6,7-tetramethoxyflavone

C19H18O8 (374.1001628)


   

Tabularin

5,7-Dihydroxy-6,2,4,5-tetramethoxyflavone

C19H18O8 (374.1001628)


   

Eriostemin

3,8-Dihydroxy-5,6,7-trimethoxy-2- (4-methoxyphenyl) -4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

EUPATORETIN

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

C19H18O8 (374.1001628)


   

Polycladin

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

C19H18O8 (374.1001628)


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].

   

Hymenoxin

2- (3,4-Dimethoxyphenyl) -5,7-dihydroxy-6,8-dimethoxy-4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

Pebrellin

2- (3,4-Dimethoxyphenyl) -5,6-dihydroxy-7,8-dimethoxy-4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

Casticin

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

C19H18O8 (374.1001628)


[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.

   

Neobaicalein

2,5-DIHYDROXY-6,6,7,8-TETRAMETHOXYFLAVONE

C19H18O8 (374.1001628)


Skullcapflavone II, a flavonoid derived from Scutellaria baicalensis, has anti-inflammatory, anti-microbial activities. Skullcapflavone II regulates osteoclast differentiation, survival, and function. Skullcapflavone II exerts potent antimicrobial activity against M. aurum and M. bovis BCG[1][2]. Skullcapflavone II, a flavonoid derived from Scutellaria baicalensis, has anti-inflammatory, anti-microbial activities. Skullcapflavone II regulates osteoclast differentiation, survival, and function. Skullcapflavone II exerts potent antimicrobial activity against M. aurum and M. bovis BCG[1][2].

   

3,5-dihydroxy-3,4,5,7-tetramethoxyflavone

3,5-dihydroxy-3,4,5,7-tetramethoxyflavone

C19H18O8 (374.1001628)


A tetramethoxyflavone that is myricetin in which the hydroxy groups at positions 3, 7, 4 and 5 have been replaced by methoxy groups. It has been isolated from Combretum quadrangulare.

   
   
   

3,4-deoxypsorospermin-3,4,5-triol

3,4-deoxypsorospermin-3,4,5-triol

C19H18O8 (374.1001628)


   

2,5-Dihydroxy-3,6,7,8-tetramethoxyflavone

2,5-Dihydroxy-3,6,7,8-tetramethoxyflavone

C19H18O8 (374.1001628)


   

4-Hydroxybenzophenone glucuronide|O1-(4-benzoyl-phenyl)-beta-D-glucopyranuronic acid|O1-(4-Benzoyl-phenyl)-beta-D-glucopyranuronsaeure

4-Hydroxybenzophenone glucuronide|O1-(4-benzoyl-phenyl)-beta-D-glucopyranuronic acid|O1-(4-Benzoyl-phenyl)-beta-D-glucopyranuronsaeure

C19H18O8 (374.1001628)


   
   
   

5-hydroxy-2-(4-hydroxy-2,3,5-trimethoxyphenyl)-7-methoxychromen-4-one

5-hydroxy-2-(4-hydroxy-2,3,5-trimethoxyphenyl)-7-methoxychromen-4-one

C19H18O8 (374.1001628)


   
   

quercetagetin-3,5,7,3-tetramethyl ether

quercetagetin-3,5,7,3-tetramethyl ether

C19H18O8 (374.1001628)


   
   

4-O-methylconhypoprotocetraric acid

4-O-methylconhypoprotocetraric acid

C19H18O8 (374.1001628)


   
   
   

8-Methoxycirsilineol

8-Methoxycirsilineol

C19H18O8 (374.1001628)


   

Quercetagetin-6,7-3,4-tetramethyl Ether

Quercetagetin-6,7-3,4-tetramethyl Ether

C19H18O8 (374.1001628)


   

4,5-Dihydroxy-3,5,6,7-tetramethoxyflavone

4,5-Dihydroxy-3,5,6,7-tetramethoxyflavone

C19H18O8 (374.1001628)


   

Diplotrin A

Diplotrin A

C19H18O8 (374.1001628)


A dihydroxyflavone that is flavone substituted by hydroxy groups at positions 2 and 5 and methoxy groups at positions 3, 7, 8 and 4. It has been isolated from the aerial parts of Mimosa diplotricha.

   
   

shimobashiric acid B

shimobashiric acid B

C19H18O8 (374.1001628)


   

5-hydroxy-2-(2-hydroxy-3,4,5-trimethoxy-phenyl)-7-methoxy-chromen-4-one

5-hydroxy-2-(2-hydroxy-3,4,5-trimethoxy-phenyl)-7-methoxy-chromen-4-one

C19H18O8 (374.1001628)


   

Isothymonin 4-methyl ether

Isothymonin 4-methyl ether

C19H18O8 (374.1001628)


   
   

7-Hydroxy-2-(3-methoxy-4-hydroxyphenyl)-3,5,8-trimethoxy-4H-1-benzopyran-4-one

7-Hydroxy-2-(3-methoxy-4-hydroxyphenyl)-3,5,8-trimethoxy-4H-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

casticin|vitexicarpin

casticin|vitexicarpin

C19H18O8 (374.1001628)


   

6,2-dihydroxy-5,7,8,6-tetramethoxyflavone

6,2-dihydroxy-5,7,8,6-tetramethoxyflavone

C19H18O8 (374.1001628)


   

3,7-diacetoxy epicatechin|3,7-diacetyl (-) epicatechin|3,7-O-diacetyl-(-)-epicatechin

3,7-diacetoxy epicatechin|3,7-diacetyl (-) epicatechin|3,7-O-diacetyl-(-)-epicatechin

C19H18O8 (374.1001628)


   

5,7-Dihydroxy-6,8,2,3-tetramethoxyflavone

5,7-Dihydroxy-6,8,2,3-tetramethoxyflavone

C19H18O8 (374.1001628)


   

Atranorin

methyl 1-(3-formyl-2,4-dihydroxy-6-methylphenylcarbonyloxy)-3-hydroxy-2,5-dimethyl-4-benzenecarboxylate

C19H18O8 (374.1001628)


Atranorin is a carbonyl compound. Atranorin is a natural product found in Candelaria concolor, Loxospora elatina, and other organisms with data available. Atranorin is a lichen secondary metabolite. Atranorin inhibits lung cancer cell motility and tumorigenesis by affecting AP-1, Wnt, and STAT signaling and suppressing RhoGTPase activity[1][2]. Atranorin is a lichen secondary metabolite. Atranorin inhibits lung cancer cell motility and tumorigenesis by affecting AP-1, Wnt, and STAT signaling and suppressing RhoGTPase activity[1][2]. Atranorin is a lichen secondary metabolite. Atranorin inhibits lung cancer cell motility and tumorigenesis by affecting AP-1, Wnt, and STAT signaling and suppressing RhoGTPase activity[1][2].

   

3,5-Dihydroxy-4,5,6,7-tetramethoxyflavone

3,5-Dihydroxy-4,5,6,7-tetramethoxyflavone

C19H18O8 (374.1001628)


   
   
   

6-(Hydroxymethyl)-1,2,3,5-tetramethoxy-8-hydroxy-9,10-anthraquinone

6-(Hydroxymethyl)-1,2,3,5-tetramethoxy-8-hydroxy-9,10-anthraquinone

C19H18O8 (374.1001628)


   
   

6-Methoxyboeravinone|6-Methoxyboeravinone C

6-Methoxyboeravinone|6-Methoxyboeravinone C

C19H18O8 (374.1001628)


   

2,3,5,7-Tetra-Me ether-2,3,5,5,6,7-Hexahydroxyflavone|6,5-dihydroxy-3,5,7,2-tetramethoxyflavone

2,3,5,7-Tetra-Me ether-2,3,5,5,6,7-Hexahydroxyflavone|6,5-dihydroxy-3,5,7,2-tetramethoxyflavone

C19H18O8 (374.1001628)


   

4,5-Dihydroxy-3,3,7,8-tetramethoxyflavone

4,5-Dihydroxy-3,3,7,8-tetramethoxyflavone

C19H18O8 (374.1001628)


   

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

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

C19H18O8 (374.1001628)


   

3,4,7-Tri-Me ether-3,3,4,5,5,7-Hexahydroxy-8-methylflavone

3,4,7-Tri-Me ether-3,3,4,5,5,7-Hexahydroxy-8-methylflavone

C19H18O8 (374.1001628)


   
   

7,5-dihydroxy-5,6,3,4-tetramethoxyflavone

7,5-dihydroxy-5,6,3,4-tetramethoxyflavone

C19H18O8 (374.1001628)


   

2-hydroxy 3,7,3,4-tetramethylquercetin

2-hydroxy 3,7,3,4-tetramethylquercetin

C19H18O8 (374.1001628)


   

4-Hydroxy-6,7,8,3-tetramethoxyflavonol

4-Hydroxy-6,7,8,3-tetramethoxyflavonol

C19H18O8 (374.1001628)


   

5-hydroxy-2-(2-hydroxy-6-methoxyphenyl)-6,7,8-trimethoxychromen-4-one

NCGC00385229-01!5-hydroxy-2-(2-hydroxy-6-methoxyphenyl)-6,7,8-trimethoxychromen-4-one

C19H18O8 (374.1001628)


   

5-hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-3,7-dimethoxychromen-4-one

NCGC00169183-02!5-hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-3,7-dimethoxychromen-4-one

C19H18O8 (374.1001628)


   

Skullcapflavone II

Skullcapflavone II

C19H18O8 (374.1001628)


   

5-hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-3,7-dimethoxychromen-4-one [IIN-based: Match]

NCGC00169183-02!5-hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-3,7-dimethoxychromen-4-one [IIN-based: Match]

C19H18O8 (374.1001628)


   

5-hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-3,7-dimethoxychromen-4-one [IIN-based on: CCMSLIB00000848808]

NCGC00169183-02!5-hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-3,7-dimethoxychromen-4-one [IIN-based on: CCMSLIB00000848808]

C19H18O8 (374.1001628)


   

5-hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-3,7-dimethoxy-4H-chromen-4-one

5-hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-3,7-dimethoxy-4H-chromen-4-one

C19H18O8 (374.1001628)


   

2-(3,4-dimethoxyphenyl)-5,7-dihydroxy-3,6-dimethoxy-4H-chromen-4-one

2-(3,4-dimethoxyphenyl)-5,7-dihydroxy-3,6-dimethoxy-4H-chromen-4-one

C19H18O8 (374.1001628)


   

Gossypetin 3,7,3,4-tetramethyl ether

Gossypetin 3,7,3,4-tetramethyl ether

C19H18O8 (374.1001628)


   

Comosin

3-[(Acetyloxy)methyl]-2,3-dihydro-5,7-dihydroxy-3-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one, 9ci

C19H18O8 (374.1001628)


   

4',5-Dihydroxy-3',5',7,8-tetramethoxyflavone

5-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-7,8-dimethoxy-4H-chromen-4-one

C19H18O8 (374.1001628)


   

Kapathrom

4-({4-[(3-carboxypropanoyl)oxy]-2-methylnaphthalen-1-yl}oxy)-4-oxobutanoic acid

C19H18O8 (374.1001628)


   

Methyl rosmarinate

3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl (2Z)-3-(3,4-dihydroxyphenyl)prop-2-enoate

C19H18O8 (374.1001628)


Methyl rosmarinate is a noncompetitive tyrosinase inhibitor which is isolated from Rabdosia serra, with an IC50 of 0.28 mM for mushroom tyrosinase, and also inhibits a-glucosidase[1]. Methyl rosmarinate is a noncompetitive tyrosinase inhibitor which is isolated from Rabdosia serra, with an IC50 of 0.28 mM for mushroom tyrosinase, and also inhibits a-glucosidase[1].

   

3-O-Methylrosmarinic acid

2-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-3-(4-hydroxy-3-methoxyphenyl)propanoic acid

C19H18O8 (374.1001628)


   

Ethyl 4,5,8-triacetoxy-2-naphthoate

Ethyl 4,5,8-triacetoxy-2-naphthoate

C19H18O8 (374.1001628)


   

NCI60_040650

4H-1-Benzopyran-4-one, 5-hydroxy-2-(2-hydroxy-6-methoxyphenyl)-6,7,8-trimethoxy-

C19H18O8 (374.1001628)


Skullcapflavone II, a flavonoid derived from Scutellaria baicalensis, has anti-inflammatory, anti-microbial activities. Skullcapflavone II regulates osteoclast differentiation, survival, and function. Skullcapflavone II exerts potent antimicrobial activity against M. aurum and M. bovis BCG[1][2]. Skullcapflavone II, a flavonoid derived from Scutellaria baicalensis, has anti-inflammatory, anti-microbial activities. Skullcapflavone II regulates osteoclast differentiation, survival, and function. Skullcapflavone II exerts potent antimicrobial activity against M. aurum and M. bovis BCG[1][2].

   

603-56-5

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

C19H18O8 (374.1001628)


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].

   

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

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

C19H18O8 (374.1001628)


   

5-[(3-Formyl-2-hydroxy-4-methoxy-6-methylphenyl)-oxomethoxy]-2-hydroxy-3,6-dimethylbenzoic acid

5-[(3-Formyl-2-hydroxy-4-methoxy-6-methylphenyl)-oxomethoxy]-2-hydroxy-3,6-dimethylbenzoic acid

C19H18O8 (374.1001628)


   

Chrysosplenetin

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

C19H18O8 (374.1001628)


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].

   

5,7-Dihydroxy-3,3,4,5-tetramethoxyflavone

5,7-Dihydroxy-3,3,4,5-tetramethoxyflavone

C19H18O8 (374.1001628)


   

3,7,3,4-TETRAMETHYLGOSSYPETIN

2-(3,4-dimethoxyphenyl)-5,8-dihydroxy-3,7-dimethoxychromen-4-one

C19H18O8 (374.1001628)


   

Menadiol disuccinate

Menadiol disuccinate

C19H18O8 (374.1001628)


   

4,5-Dihydroxy-3,5,7,8-tetramethoxyflavone

4,5-Dihydroxy-3,5,7,8-tetramethoxyflavone

C19H18O8 (374.1001628)


   

5,3-Dihydroxy-3,7,8,4-tetramethoxyflavone

5,3-Dihydroxy-3,7,8,4-tetramethoxyflavone

C19H18O8 (374.1001628)


   

3,3,4,5-tetramethylmyricetin

3,3,4,5-tetramethylmyricetin

C19H18O8 (374.1001628)


A tetramethoxyflavone that is myricetin in which the hydroxy groups at positions 3, 3, 4 and 5 are replaced by methoxy groups. It is isolated from Bridelia ferruginea, a subtropical medicinal plant widely used in traditional African medicine.

   

3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl 3-(3,4-dihydroxyphenyl)prop-2-enoate

3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl 3-(3,4-dihydroxyphenyl)prop-2-enoate

C19H18O8 (374.1001628)


   

3,5-dihydroxy-6,7,8-trimethoxy-2-(4-methoxyphenyl)chromen-4-one

3,5-dihydroxy-6,7,8-trimethoxy-2-(4-methoxyphenyl)chromen-4-one

C19H18O8 (374.1001628)


   

5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-3,7,8-trimethoxychromen-4-one

5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-3,7,8-trimethoxychromen-4-one

C19H18O8 (374.1001628)


   

(5r,5's,9s)-5'-(furan-3-yl)-2',3,6-trioxo-4,7,8,9-tetrahydro-1h-spiro[cycloocta[c]furan-5,3'-oxolan]-9-yl acetate

(5r,5's,9s)-5'-(furan-3-yl)-2',3,6-trioxo-4,7,8,9-tetrahydro-1h-spiro[cycloocta[c]furan-5,3'-oxolan]-9-yl acetate

C19H18O8 (374.1001628)


   

10-hydroxy-5-methoxy-2-(1,2,3-trihydroxypropan-2-yl)-1h,2h-furo[2,3-c]xanthen-6-one

10-hydroxy-5-methoxy-2-(1,2,3-trihydroxypropan-2-yl)-1h,2h-furo[2,3-c]xanthen-6-one

C19H18O8 (374.1001628)


   

5-hydroxy-2-(3-hydroxy-2,4,5-trimethoxyphenyl)-7-methoxychromen-4-one

5-hydroxy-2-(3-hydroxy-2,4,5-trimethoxyphenyl)-7-methoxychromen-4-one

C19H18O8 (374.1001628)


   

(5r)-5-[(2r)-2-hydroxy-2-[(2s)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one

(5r)-5-[(2r)-2-hydroxy-2-[(2s)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one

C19H18O8 (374.1001628)


   

3-(acetyloxy)-2-(3,4-dihydroxyphenyl)-5-hydroxy-3,4-dihydro-2h-1-benzopyran-7-yl acetate

3-(acetyloxy)-2-(3,4-dihydroxyphenyl)-5-hydroxy-3,4-dihydro-2h-1-benzopyran-7-yl acetate

C19H18O8 (374.1001628)


   

2-(3,4-dimethoxyphenyl)-3,5-dihydroxy-7,8-dimethoxychromen-4-one

2-(3,4-dimethoxyphenyl)-3,5-dihydroxy-7,8-dimethoxychromen-4-one

C19H18O8 (374.1001628)


   

5-hydroxy-3-(3-hydroxy-2-methoxyphenyl)-6,7,8-trimethoxychromen-4-one

5-hydroxy-3-(3-hydroxy-2-methoxyphenyl)-6,7,8-trimethoxychromen-4-one

C19H18O8 (374.1001628)


   

5-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3,7-dimethoxychromen-4-one

5-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3,7-dimethoxychromen-4-one

C19H18O8 (374.1001628)


   

(1s)-1-(3,4-dihydroxyphenyl)-3-methoxy-3-oxopropyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

(1s)-1-(3,4-dihydroxyphenyl)-3-methoxy-3-oxopropyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

C19H18O8 (374.1001628)


   

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

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

C19H18O8 (374.1001628)


   

methyl 5-hydroxy-4-methoxy-2-[4-methoxy-2-(methoxycarbonyl)benzoyl]benzoate

methyl 5-hydroxy-4-methoxy-2-[4-methoxy-2-(methoxycarbonyl)benzoyl]benzoate

C19H18O8 (374.1001628)


   

2-(3,4-dimethoxyphenyl)-5,7-dihydroxy-3,8-dimethoxychromen-4-one

2-(3,4-dimethoxyphenyl)-5,7-dihydroxy-3,8-dimethoxychromen-4-one

C19H18O8 (374.1001628)


   

5,3'-dihydroxy-3,7,4',5'-tetramethoxyflavone

NA

C19H18O8 (374.1001628)


{"Ingredient_id": "HBIN011018","Ingredient_name": "5,3'-dihydroxy-3,7,4',5'-tetramethoxyflavone","Alias": "NA","Ingredient_formula": "C19H18O8","Ingredient_Smile": "COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3OC)OC)O)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "6146","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

6-methoxyboeravinone c

NA

C19H18O8 (374.1001628)


{"Ingredient_id": "HBIN012518","Ingredient_name": "6-methoxyboeravinone c","Alias": "NA","Ingredient_formula": "C19H18O8","Ingredient_Smile": "CC1=C(C=C2C(=C1O)C(=O)C3(C(O2)C(OC4=C3C=CC=C4O)OC)O)OC","Ingredient_weight": "374.3 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "13853","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "487169","DrugBank_id": "NA"}

   

ariseminone

NA

C19H18O8 (374.1001628)


{"Ingredient_id": "HBIN016751","Ingredient_name": "ariseminone","Alias": "NA","Ingredient_formula": "C19H18O8","Ingredient_Smile": "NA","Ingredient_weight": "374.34","OB_score": "NA","CAS_id": "149575-60-0","SymMap_id": "NA","TCMID_id": "NA","TCMSP_id": "NA","TCM_ID_id": "6679","PubChem_id": "NA","DrugBank_id": "NA"}

   

5-(2-hydroxy-2-{9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl}propyl)-3-(hydroxymethyl)-5h-furan-2-one

5-(2-hydroxy-2-{9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl}propyl)-3-(hydroxymethyl)-5h-furan-2-one

C19H18O8 (374.1001628)


   

methyl 5-hydroxy-3-methoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)pyran-3-carbonyl]benzoate

methyl 5-hydroxy-3-methoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)pyran-3-carbonyl]benzoate

C19H18O8 (374.1001628)


   

5-hydroxy-2-(2-hydroxy-3-methoxyphenyl)-6,7,8-trimethoxychromen-4-one

5-hydroxy-2-(2-hydroxy-3-methoxyphenyl)-6,7,8-trimethoxychromen-4-one

C19H18O8 (374.1001628)


   

4,11,12a-trihydroxy-6,9-dimethoxy-10-methyl-6,6a-dihydro-5,7-dioxatetraphen-12-one

4,11,12a-trihydroxy-6,9-dimethoxy-10-methyl-6,6a-dihydro-5,7-dioxatetraphen-12-one

C19H18O8 (374.1001628)


   

(6r,6ar,12as)-6,11-dihydroxy-2,3,9-trimethoxy-6a,12a-dihydro-6h-5,7-dioxatetraphen-12-one

(6r,6ar,12as)-6,11-dihydroxy-2,3,9-trimethoxy-6a,12a-dihydro-6h-5,7-dioxatetraphen-12-one

C19H18O8 (374.1001628)


   

(6r,6ar,12ar)-4,11,12a-trihydroxy-6,9-dimethoxy-10-methyl-6,6a-dihydro-5,7-dioxatetraphen-12-one

(6r,6ar,12ar)-4,11,12a-trihydroxy-6,9-dimethoxy-10-methyl-6,6a-dihydro-5,7-dioxatetraphen-12-one

C19H18O8 (374.1001628)


   

5-hydroxy-2-(5-hydroxy-2-methoxyphenyl)-3,7,8-trimethoxychromen-4-one

5-hydroxy-2-(5-hydroxy-2-methoxyphenyl)-3,7,8-trimethoxychromen-4-one

C19H18O8 (374.1001628)


   

methyl 3,5-dimethoxy-2-{5-methyl-7-oxo-5h,6h-furo[3,2-b]pyran-3-carbonyl}benzoate

methyl 3,5-dimethoxy-2-{5-methyl-7-oxo-5h,6h-furo[3,2-b]pyran-3-carbonyl}benzoate

C19H18O8 (374.1001628)


   

5,7-dihydroxy-3-methoxy-2-(3,4,5-trimethoxyphenyl)chromen-4-one

5,7-dihydroxy-3-methoxy-2-(3,4,5-trimethoxyphenyl)chromen-4-one

C19H18O8 (374.1001628)


   

5-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-3,7,8-trimethoxychromen-4-one

5-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-3,7,8-trimethoxychromen-4-one

C19H18O8 (374.1001628)


   

methyl 3,5-dimethoxy-2-[(1s,6r)-5-oxo-3-[(1e)-prop-1-en-1-yl]-2,7-dioxabicyclo[4.1.0]hept-3-ene-6-carbonyl]benzoate

methyl 3,5-dimethoxy-2-[(1s,6r)-5-oxo-3-[(1e)-prop-1-en-1-yl]-2,7-dioxabicyclo[4.1.0]hept-3-ene-6-carbonyl]benzoate

C19H18O8 (374.1001628)


   

[(3r)-5,7-dihydroxy-3-(3-hydroxy-4-methoxyphenyl)-4-oxo-2h-1-benzopyran-3-yl]methyl acetate

[(3r)-5,7-dihydroxy-3-(3-hydroxy-4-methoxyphenyl)-4-oxo-2h-1-benzopyran-3-yl]methyl acetate

C19H18O8 (374.1001628)


   

5-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-6,7-dimethoxychromen-4-one

5-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-6,7-dimethoxychromen-4-one

C19H18O8 (374.1001628)


   

5-hydroxy-2-(4-hydroxy-2,3-dimethoxyphenyl)-7,8-dimethoxychromen-4-one

5-hydroxy-2-(4-hydroxy-2,3-dimethoxyphenyl)-7,8-dimethoxychromen-4-one

C19H18O8 (374.1001628)


   

2-(3,4-dihydroxyphenyl)-5-hydroxy-3,6,7-trimethoxy-8-methylchromen-4-one

2-(3,4-dihydroxyphenyl)-5-hydroxy-3,6,7-trimethoxy-8-methylchromen-4-one

C19H18O8 (374.1001628)


   

5-hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-6,7-dimethoxychromen-4-one

5-hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-6,7-dimethoxychromen-4-one

C19H18O8 (374.1001628)


   

methyl 3,5-dimethoxy-2-[5-oxo-3-(prop-1-en-1-yl)-2,7-dioxabicyclo[4.1.0]hept-3-ene-6-carbonyl]benzoate

methyl 3,5-dimethoxy-2-[5-oxo-3-(prop-1-en-1-yl)-2,7-dioxabicyclo[4.1.0]hept-3-ene-6-carbonyl]benzoate

C19H18O8 (374.1001628)


   

(2r)-3-(3,4-dihydroxyphenyl)-2-{[(2e)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxy}propanoic acid

(2r)-3-(3,4-dihydroxyphenyl)-2-{[(2e)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxy}propanoic acid

C19H18O8 (374.1001628)


   

2-(3,4-dimethoxyphenyl)-3,5-dihydroxy-6,7-dimethoxychromen-4-one

2-(3,4-dimethoxyphenyl)-3,5-dihydroxy-6,7-dimethoxychromen-4-one

C19H18O8 (374.1001628)


   

6-hydroxy-2-(2-hydroxy-6-methoxyphenyl)-5,7,8-trimethoxychromen-4-one

6-hydroxy-2-(2-hydroxy-6-methoxyphenyl)-5,7,8-trimethoxychromen-4-one

C19H18O8 (374.1001628)


   

(2s)-3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

(2s)-3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

C19H18O8 (374.1001628)


   

5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-8-methylchromen-4-one

5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-8-methylchromen-4-one

C19H18O8 (374.1001628)


   

(2r)-3-(3,4-dihydroxyphenyl)-2-{[3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxy}propanoic acid

(2r)-3-(3,4-dihydroxyphenyl)-2-{[3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxy}propanoic acid

C19H18O8 (374.1001628)


   

(2s)-10-hydroxy-5-methoxy-2-(1,2,3-trihydroxypropan-2-yl)-1h,2h-furo[2,3-c]xanthen-6-one

(2s)-10-hydroxy-5-methoxy-2-(1,2,3-trihydroxypropan-2-yl)-1h,2h-furo[2,3-c]xanthen-6-one

C19H18O8 (374.1001628)


   

(2r)-3-(3,4-dihydroxyphenyl)-2-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propanoic acid

(2r)-3-(3,4-dihydroxyphenyl)-2-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propanoic acid

C19H18O8 (374.1001628)


   

(7as,9s)-2,4,5,6,7a-pentahydroxy-1,8,8,9-tetramethyl-9h-phenaleno[1,2-b]furan-3,7-dione

(7as,9s)-2,4,5,6,7a-pentahydroxy-1,8,8,9-tetramethyl-9h-phenaleno[1,2-b]furan-3,7-dione

C19H18O8 (374.1001628)


   

(5s,5's,9s)-5'-(furan-3-yl)-2',3,6-trioxo-4,7,8,9-tetrahydro-1h-spiro[cycloocta[c]furan-5,3'-oxolan]-9-yl acetate

(5s,5's,9s)-5'-(furan-3-yl)-2',3,6-trioxo-4,7,8,9-tetrahydro-1h-spiro[cycloocta[c]furan-5,3'-oxolan]-9-yl acetate

C19H18O8 (374.1001628)


   

5,7-dihydroxy-6-methoxy-3-(2,3,4-trimethoxyphenyl)chromen-4-one

5,7-dihydroxy-6-methoxy-3-(2,3,4-trimethoxyphenyl)chromen-4-one

C19H18O8 (374.1001628)


   

5-hydroxy-2-(2-hydroxy-3,4,5-trimethoxyphenyl)-7-methoxychromen-4-one

5-hydroxy-2-(2-hydroxy-3,4,5-trimethoxyphenyl)-7-methoxychromen-4-one

C19H18O8 (374.1001628)


   

2-(3,4-dimethoxyphenyl)-5,6-dihydroxy-3,7-dimethoxychromen-4-one

2-(3,4-dimethoxyphenyl)-5,6-dihydroxy-3,7-dimethoxychromen-4-one

C19H18O8 (374.1001628)


   

(2s,3s,4ar,12br)-2,3,4a,8,12b-pentahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione

(2s,3s,4ar,12br)-2,3,4a,8,12b-pentahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione

C19H18O8 (374.1001628)


   

7,10,13,18-tetrahydroxy-15-methyl-19-oxapentacyclo[13.3.1.0¹,¹⁰.0³,⁸.0¹³,¹⁸]nonadeca-3,5,7-triene-2,9,17-trione

7,10,13,18-tetrahydroxy-15-methyl-19-oxapentacyclo[13.3.1.0¹,¹⁰.0³,⁸.0¹³,¹⁸]nonadeca-3,5,7-triene-2,9,17-trione

C19H18O8 (374.1001628)


   

(2r,3r)-3-(acetyloxy)-2-(3,4-dihydroxyphenyl)-5-hydroxy-3,4-dihydro-2h-1-benzopyran-7-yl acetate

(2r,3r)-3-(acetyloxy)-2-(3,4-dihydroxyphenyl)-5-hydroxy-3,4-dihydro-2h-1-benzopyran-7-yl acetate

C19H18O8 (374.1001628)


   

(6s,6as,12ar)-6,12a-dihydroxy-2,3,9-trimethoxy-6,6a-dihydro-5,7-dioxatetraphen-12-one

(6s,6as,12ar)-6,12a-dihydroxy-2,3,9-trimethoxy-6,6a-dihydro-5,7-dioxatetraphen-12-one

C19H18O8 (374.1001628)


   

3-{[(5e)-6-(3,8-dihydroxy-1,4-dioxonaphthalen-2-yl)hex-5-en-1-yl]oxy}-3-oxopropanoic acid

3-{[(5e)-6-(3,8-dihydroxy-1,4-dioxonaphthalen-2-yl)hex-5-en-1-yl]oxy}-3-oxopropanoic acid

C19H18O8 (374.1001628)


   

3',4',5'-trimethoxywogonin

3',4',5'-trimethoxywogonin

C19H18O8 (374.1001628)


   

(2r,3r)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-(3-oxobutyl)-2,3-dihydro-1-benzopyran-4-one

(2r,3r)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-(3-oxobutyl)-2,3-dihydro-1-benzopyran-4-one

C19H18O8 (374.1001628)


   

3-{[6-(3,8-dihydroxy-1,4-dioxonaphthalen-2-yl)hex-5-en-1-yl]oxy}-3-oxopropanoic acid

3-{[6-(3,8-dihydroxy-1,4-dioxonaphthalen-2-yl)hex-5-en-1-yl]oxy}-3-oxopropanoic acid

C19H18O8 (374.1001628)


   

methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1e)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate

methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1e)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate

C19H18O8 (374.1001628)


   

6-hydroxy-7-(hydroxymethyl)-14-methoxy-4,12,15-trimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-5-carboxylic acid

6-hydroxy-7-(hydroxymethyl)-14-methoxy-4,12,15-trimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-5-carboxylic acid

C19H18O8 (374.1001628)


   

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

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

C19H18O8 (374.1001628)


   

(6r,6as,12ar)-6,12a-dihydroxy-2,3,9-trimethoxy-6,6a-dihydro-5,7-dioxatetraphen-12-one

(6r,6as,12ar)-6,12a-dihydroxy-2,3,9-trimethoxy-6,6a-dihydro-5,7-dioxatetraphen-12-one

C19H18O8 (374.1001628)


   

(6ar,12ar)-11,12a-dihydroxy-2,3,9-trimethoxy-6,6a-dihydro-5,7-dioxatetraphen-12-one

(6ar,12ar)-11,12a-dihydroxy-2,3,9-trimethoxy-6,6a-dihydro-5,7-dioxatetraphen-12-one

C19H18O8 (374.1001628)


   

methyl 3,5-dimethoxy-2-[(2r)-2-methyl-7-oxo-2h,3h-furo[3,2-b]pyran-6-carbonyl]benzoate

methyl 3,5-dimethoxy-2-[(2r)-2-methyl-7-oxo-2h,3h-furo[3,2-b]pyran-6-carbonyl]benzoate

C19H18O8 (374.1001628)


   

4-(3-formyl-2-hydroxy-4-methoxy-6-methylbenzoyloxy)-2-hydroxy-3,6-dimethylbenzoic acid

4-(3-formyl-2-hydroxy-4-methoxy-6-methylbenzoyloxy)-2-hydroxy-3,6-dimethylbenzoic acid

C19H18O8 (374.1001628)


   

2-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-3-(4-hydroxy-3-methoxyphenyl)propanoic acid

2-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-3-(4-hydroxy-3-methoxyphenyl)propanoic acid

C19H18O8 (374.1001628)


   

(5r)-5-[(2r)-2-hydroxy-2-[(2r)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one

(5r)-5-[(2r)-2-hydroxy-2-[(2r)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one

C19H18O8 (374.1001628)


   

(2r)-3-(3,4-dihydroxyphenyl)-2-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propanoic acid

(2r)-3-(3,4-dihydroxyphenyl)-2-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propanoic acid

C19H18O8 (374.1001628)


   

(1r,10s,13s,15s,18r)-7,10,13,18-tetrahydroxy-15-methyl-19-oxapentacyclo[13.3.1.0¹,¹⁰.0³,⁸.0¹³,¹⁸]nonadeca-3,5,7-triene-2,9,17-trione

(1r,10s,13s,15s,18r)-7,10,13,18-tetrahydroxy-15-methyl-19-oxapentacyclo[13.3.1.0¹,¹⁰.0³,⁸.0¹³,¹⁸]nonadeca-3,5,7-triene-2,9,17-trione

C19H18O8 (374.1001628)


   

8-hydroxy-6-(hydroxymethyl)-1,2,3,5-tetramethoxyanthracene-9,10-dione

8-hydroxy-6-(hydroxymethyl)-1,2,3,5-tetramethoxyanthracene-9,10-dione

C19H18O8 (374.1001628)


   

(4r,5as,13br)-4,5a,9,13b-tetrahydroxy-4-methyl-3h,5h,6h,7h-anthra[1,2-b]oxepine-2,8,13-trione

(4r,5as,13br)-4,5a,9,13b-tetrahydroxy-4-methyl-3h,5h,6h,7h-anthra[1,2-b]oxepine-2,8,13-trione

C19H18O8 (374.1001628)


   

(2r)-3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl 3-(3,4-dihydroxyphenyl)prop-2-enoate

(2r)-3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl 3-(3,4-dihydroxyphenyl)prop-2-enoate

C19H18O8 (374.1001628)


   

(2r)-2-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-3-(4-hydroxy-3-methoxyphenyl)propanoic acid

(2r)-2-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-3-(4-hydroxy-3-methoxyphenyl)propanoic acid

C19H18O8 (374.1001628)


   

1-(3,4-dihydroxyphenyl)-3-methoxy-3-oxopropyl 3-(3,4-dihydroxyphenyl)prop-2-enoate

1-(3,4-dihydroxyphenyl)-3-methoxy-3-oxopropyl 3-(3,4-dihydroxyphenyl)prop-2-enoate

C19H18O8 (374.1001628)


   

3-{[(5e)-6-(1,8-dihydroxy-3,4-dioxonaphthalen-2-yl)hex-5-en-1-yl]oxy}-3-oxopropanoic acid

3-{[(5e)-6-(1,8-dihydroxy-3,4-dioxonaphthalen-2-yl)hex-5-en-1-yl]oxy}-3-oxopropanoic acid

C19H18O8 (374.1001628)


   

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

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

C19H18O8 (374.1001628)


   

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

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

C19H18O8 (374.1001628)


   

5-hydroxy-2-(5-hydroxy-2,3-dimethoxyphenyl)-6,7-dimethoxychromen-4-one

5-hydroxy-2-(5-hydroxy-2,3-dimethoxyphenyl)-6,7-dimethoxychromen-4-one

C19H18O8 (374.1001628)


   

(1r)-1-(3,4-dihydroxyphenyl)-3-methoxy-3-oxopropyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

(1r)-1-(3,4-dihydroxyphenyl)-3-methoxy-3-oxopropyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

C19H18O8 (374.1001628)


   

5,7-dihydroxy-2-(2,3,4,5-tetramethoxyphenyl)chromen-4-one

5,7-dihydroxy-2-(2,3,4,5-tetramethoxyphenyl)chromen-4-one

C19H18O8 (374.1001628)


   

3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

C19H18O8 (374.1001628)


   

methyl 3-(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)-6-hydroxy-2,5-dimethylbenzoate

methyl 3-(3-formyl-2,4-dihydroxy-6-methylbenzoyloxy)-6-hydroxy-2,5-dimethylbenzoate

C19H18O8 (374.1001628)


   

11,12a-dihydroxy-2,3,9-trimethoxy-6,6a-dihydro-5,7-dioxatetraphen-12-one

11,12a-dihydroxy-2,3,9-trimethoxy-6,6a-dihydro-5,7-dioxatetraphen-12-one

C19H18O8 (374.1001628)


   

(6as,12ar)-6,12a-dihydroxy-2,3,9-trimethoxy-6,6a-dihydro-5,7-dioxatetraphen-12-one

(6as,12ar)-6,12a-dihydroxy-2,3,9-trimethoxy-6,6a-dihydro-5,7-dioxatetraphen-12-one

C19H18O8 (374.1001628)


   

5'-(furan-3-yl)-2',3,6-trioxo-4,7,8,9-tetrahydro-1h-spiro[cycloocta[c]furan-5,3'-oxolan]-9-yl acetate

5'-(furan-3-yl)-2',3,6-trioxo-4,7,8,9-tetrahydro-1h-spiro[cycloocta[c]furan-5,3'-oxolan]-9-yl acetate

C19H18O8 (374.1001628)


   

7-hydroxy-3-(4-hydroxy-3-methoxyphenyl)-2,6,8-trimethoxychromen-4-one

7-hydroxy-3-(4-hydroxy-3-methoxyphenyl)-2,6,8-trimethoxychromen-4-one

C19H18O8 (374.1001628)


   

methyl 3,5-dimethoxy-2-[(1r,6s)-5-oxo-3-[(1e)-prop-1-en-1-yl]-2,7-dioxabicyclo[4.1.0]hept-3-ene-6-carbonyl]benzoate

methyl 3,5-dimethoxy-2-[(1r,6s)-5-oxo-3-[(1e)-prop-1-en-1-yl]-2,7-dioxabicyclo[4.1.0]hept-3-ene-6-carbonyl]benzoate

C19H18O8 (374.1001628)


   

6,12a-dihydroxy-2,3,9-trimethoxy-6,6a-dihydro-5,7-dioxatetraphen-12-one

6,12a-dihydroxy-2,3,9-trimethoxy-6,6a-dihydro-5,7-dioxatetraphen-12-one

C19H18O8 (374.1001628)


   

methyl 3,5-dimethoxy-2-[(2s)-2-methyl-7-oxo-2h,3h-furo[3,2-b]pyran-6-carbonyl]benzoate

methyl 3,5-dimethoxy-2-[(2s)-2-methyl-7-oxo-2h,3h-furo[3,2-b]pyran-6-carbonyl]benzoate

C19H18O8 (374.1001628)