Chemical Formula: C14H10O5

Chemical Formula C14H10O5

Found 110 metabolite its formula value is C14H10O5

Mesuaxanthone A

1,5-Dihydroxy-3-methoxyxanthone; 1,5-Hydroxy-3-methoxyxanthone

C14H10O5 (258.052821)


Mesuaxanthone A is a member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at bpositions 1 and 5 and a methoxy group at position 3. It has a role as a plant metabolite. It is a member of xanthones, a polyphenol and an aromatic ether. Mesuaxanthone A is a natural product found in Calophyllum inophyllum, Hypericum chinense, and other organisms with data available. A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at bpositions 1 and 5 and a methoxy group at position 3.

   

Norlichexanthone

1,3,6-Trihydroxy-8-methyl-9H-xanthen-9-one

C14H10O5 (258.052821)


   

Gentisin

1,7-dihydroxy-3-methoxy-9H-xanthen-9-one

C14H10O5 (258.052821)


Gentisin is found in alcoholic beverages. Gentisin is a pigment from root of Gentiana lutea (yellow gentian

   

Isogentisin

9H-Xanthen-9-one, 1,3-dihydroxy-7-methoxy- (9ci)

C14H10O5 (258.052821)


Isogentisin is found in alcoholic beverages. Isogentisin is isolated from roots of Gentiana lutea (yellow gentian

   
   

5,6,8-Trihydroxy-2-methylbenzo[g]chromen-4-one

5,6,8-Trihydroxy-2-methyl-4H-naphtho[2,3-b]pyran-4-one

C14H10O5 (258.052821)


5,6,8-Trihydroxy-2-methylbenzo[g]chromen-4-one is found in coffee and coffee products. 5,6,8-Trihydroxy-2-methylbenzo[g]chromen-4-one is isolated from seeds of Cassia tora (charota). Isolated from seeds of Cassia tora (charota). Norrubrofusarin is found in coffee and coffee products, herbs and spices, and pulses.

   

3-CARBETHOXYPSORALEN

3-CARBETHOXYPSORALEN

C14H10O5 (258.052821)


D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins

   

Alternariol

3,4,4-Trihydroxy-6-methyl-2-biphenylcarboxylic acid gamma-lactone

C14H10O5 (258.052821)


Alternariol is found in mushrooms. Alternariol occurs in mycelium of Alternaria tenuis responsible for alternaria cone disorder in hops and fruit spot on papaya (Carica papaya) and Passiflora species.Alternariol is a toxic metabolite of Alternaria fungi. It is an important contaminant in cereals and fruits D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D002800 - Cholinesterase Inhibitors D004791 - Enzyme Inhibitors

   

Salsalate

Salsalate

C14H10O5 (258.052821)


N - Nervous system > N02 - Analgesics > N02B - Other analgesics and antipyretics > N02BA - Salicylic acid and derivatives D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D018501 - Antirheumatic Agents

   

Alfafuran

2-(3,5-Dihydroxyphenyl)-5,6-benzofurandiol, 9ci

C14H10O5 (258.052821)


Alfafuran is found in pulses. Alfafuran is a stress metabolite of Medicago sativa (alfalfa). Stress metabolite of Medicago sativa (alfalfa). Alfafuran is found in pulses.

   

(±)-2-(3,4-Dihydroxyphenyl)-1,3-benzodioxole-5-carboxaldehyde

(±)-2-(3,4-Dihydroxyphenyl)-1,3-benzodioxole-5-carboxaldehyde

C14H10O5 (258.052821)


(±)-2-(3,4-Dihydroxyphenyl)-1,3-benzodioxole-5-carboxaldehyde is found in herbs and spices. (±)-2-(3,4-Dihydroxyphenyl)-1,3-benzodioxole-5-carboxaldehyde is a constituent of Melissa officinalis (lemon balm). Constituent of Melissa officinalis (lemon balm). (±)-2-(3,4-Dihydroxyphenyl)-1,3-benzodioxole-5-carboxaldehyde is found in tea and herbs and spices.

   

Salsalate

Benzoic acid, 2-hydroxy-, 2-carboxyphenyl ester

C14H10O5 (258.052821)


Salsalate is a nonsteroidal anti-inflammatory agent for oral administration. Salsalates mode of action as an anti-inflammatory and antirheumatic agent may be due to inhibition of synthesis and release of prostaglandins. The usefulness of salicylic acid, the active in vivo product of salsalate, in the treatment of arthritic disorders has been established. In contrast to aspirin, salsalate causes no greater fecal gastrointestinal blood loss than placebo. Salsalate is readily soluble in the small intestine where it is partially hydrolyzed to two molecules of salicylic acid. A significant portion of the parent compound is absorbed unchanged and undergoes rapid esterase hydrolysis in the body. The parent compound has an elimination half-life of about 1 hour. Salicylic acid (the active metabolite) biotransformation is saturated at anti-inflammatory doses of salsalate. Such capacity limited biotransformation results in an increase in the half-life of salicylic acid from 3.5 to 16 or more hours. N - Nervous system > N02 - Analgesics > N02B - Other analgesics and antipyretics > N02BA - Salicylic acid and derivatives D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D018501 - Antirheumatic Agents

   

Porric acid C

4,11-dihydroxy-13-methyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),2(7),3,5,9,11-hexaene-6-carboxylic acid

C14H10O5 (258.052821)


Porric acid C is found in onion-family vegetables. Porric acid C is a constituent of the bulbs of Allium porrum (leek)

   

Gentisin

1,7-Dihydroxy-3-methoxyxanthone; 1,7-Dihydroxy-3-methoxyxanthen-9-one

C14H10O5 (258.052821)


Gentisin is a member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1 and 7 and a methoxy group at position 3. It has a role as a plant metabolite. It is a member of xanthones, a polyphenol and an aromatic ether. Gentisin is a natural product found in Pterocarpus santalinus, Gentiana orbicularis, and other organisms with data available. See also: Menyanthes trifoliata leaf (part of). A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1 and 7 and a methoxy group at position 3. Gentisin is found in alcoholic beverages. Gentisin is a pigment from root of Gentiana lutea (yellow gentian

   

1,5-Dihydroxy-6-methoxyxanthone

1,5-Dihydroxy-6-methoxyxanthone

C14H10O5 (258.052821)


   

1,3-Dihydroxy-5-methoxy-xanthone

1,3-Dihydroxy-5-methoxy-xanthone

C14H10O5 (258.052821)


   

2,8-Dihydroxy-1-methoxyxanthone

2,8-Dihydroxy-1-methoxyxanthone

C14H10O5 (258.052821)


   

Buchanaxanthone

1,6-Dihydroxy-5-methoxyxanthone

C14H10O5 (258.052821)


   

1,2,5-TRIHYDROXY-7-METHOXYFLUOREN-9-ONE

1,2,5-TRIHYDROXY-7-METHOXYFLUOREN-9-ONE

C14H10O5 (258.052821)


   

3,5-Dihydroxy-1-methoxyxanthone

3,5-Dihydroxy-1-methoxyxanthone

C14H10O5 (258.052821)


   

1,7-Dihydroxy-6-methoxyxanthone

1,7-Dihydroxy-6-methoxyxanthone

C14H10O5 (258.052821)


   

1,3-Dihydroxy-2-methoxyxanthone

1,3-Dihydroxy-2-methoxyxanthone

C14H10O5 (258.052821)


   
   

Arthoniafuron B

Arthoniafuron B

C14H10O5 (258.052821)


   

Porric acid C

4,11-dihydroxy-13-methyl-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(13),2,4,6,9,11-hexaene-6-carboxylic acid

C14H10O5 (258.052821)


   

Mesuaxanthone A

1,5-Dihydroxy-3-methoxyxanthone

C14H10O5 (258.052821)


   

2,5-Dihydroxy-1-methoxyxanthone

2,5-Dihydroxy-1-methoxyxanthone

C14H10O5 (258.052821)


   

1,7-Dihydroxy-4-methoxyxanthone

1,7-Dihydroxy-4-methoxyxanthone

C14H10O5 (258.052821)


A member of the class of xanthones that is 9H-xanthene substituted by hydroxy groups at positions 1 and 7, a methoxy group at position 4 and an oxo group at position 9. It has been isolated from the stems of Cratoxylum cochinchinense.

   
   

3,7-dihydroxy-1-methoxyxanthone

3,7-dihydroxy-1-methoxyxanthone

C14H10O5 (258.052821)


   

CRATOXYARBORENONE F

CRATOXYARBORENONE F

C14H10O5 (258.052821)


A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1 and 6 and a methoxy group at position 4. It is isolated from Cratoxylum Sumatranum and exhibits cytotoxicity towards the KB (human oral epidermoid) cancer cell line.

   
   

1-Me ether-1,5,6-Trihydroxyxanthone|5,6-dihydroxy-1-methoxyxanthone

1-Me ether-1,5,6-Trihydroxyxanthone|5,6-dihydroxy-1-methoxyxanthone

C14H10O5 (258.052821)


   
   

3,4-dihydroxy-2-methoxyxanthone

3,4-dihydroxy-2-methoxyxanthone

C14H10O5 (258.052821)


   
   

calophymembranol B

calophymembranol B

C14H10O5 (258.052821)


   

1,7-Dihydroxy-2-methoxyxanthone

1,7-Dihydroxy-2-methoxyxanthone

C14H10O5 (258.052821)


   

7-benzoyloxy-6-oxo-2,4Z-heptadiene-1,4-olide

7-benzoyloxy-6-oxo-2,4Z-heptadiene-1,4-olide

C14H10O5 (258.052821)


   

3,5-dihydroxy-4-methoxy-xanthen-9-one

3,5-dihydroxy-4-methoxy-xanthen-9-one

C14H10O5 (258.052821)


   

2,7-dihydroxy-3-methoxyxanthone

2,7-dihydroxy-3-methoxyxanthone

C14H10O5 (258.052821)


   

1,5-dihydroxy-8-methoxyxanthone

1,5-dihydroxy-8-methoxyxanthone

C14H10O5 (258.052821)


   

1,3-dihydroxy-5-methoxy-9H-xanthen-9-one

1,3-dihydroxy-5-methoxy-9H-xanthen-9-one

C14H10O5 (258.052821)


   
   

1-Methoxy-2,3-dihydroxyxanthone

1-Methoxy-2,3-dihydroxyxanthone

C14H10O5 (258.052821)


   

5-hydroxy-2-(1-hydroxyethyl)naphtho[2,3-b]furan-4,9-dione

5-hydroxy-2-(1-hydroxyethyl)naphtho[2,3-b]furan-4,9-dione

C14H10O5 (258.052821)


   

1,5,8-Trihydroxy-3-methylxanthone

1,5,8-Trihydroxy-3-methylxanthone

C14H10O5 (258.052821)


   

1-Methoxy-3,4-dihydroxy-9H-xanthene-9-one

1-Methoxy-3,4-dihydroxy-9H-xanthene-9-one

C14H10O5 (258.052821)


   

1,6-Dihydroxy-7-methoxyxanthone

1,6-Dihydroxy-7-methoxyxanthone

C14H10O5 (258.052821)


   

4,5-dihydroxy-3-methoxyxanthone

4,5-dihydroxy-3-methoxyxanthone

C14H10O5 (258.052821)


   

4,4-Oxydibenzoic acid

4,4-Oxydibenzoic acid

C14H10O5 (258.052821)


   

1,8-Dihydroxy-3-methoxyxanthone

1,8-Dihydroxy-3-methoxyxanthone

C14H10O5 (258.052821)


   

1,4,5-trihydroxy-7-methoxyfluoren-9-one

1,4,5-trihydroxy-7-methoxyfluoren-9-one

C14H10O5 (258.052821)


   
   

1-methoxy-4,7-dihydroxyxanthone

1-methoxy-4,7-dihydroxyxanthone

C14H10O5 (258.052821)


   

Caesalpiniaphenol C

Caesalpiniaphenol C

C14H10O5 (258.052821)


   

3,9-Dihydroxy-8-methoxy-6H-dibenzo[b,d]pyran-6-one

3,9-Dihydroxy-8-methoxy-6H-dibenzo[b,d]pyran-6-one

C14H10O5 (258.052821)


   
   

3,6-Dihydroxy-2-methoxy-9H-xanthen-9-one

3,6-Dihydroxy-2-methoxy-9H-xanthen-9-one

C14H10O5 (258.052821)


   

Gentisin (Dihydroxy-1,7-methoxy-3-xanthon)

Gentisin (Dihydroxy-1,7-methoxy-3-xanthon)

C14H10O5 (258.052821)


   

Globosuxanthone C

Globosuxanthone C

C14H10O5 (258.052821)


A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy group at positions 1 and 8 and a methoxy group at position 2. It has been isolated from Chaetomium globosum.( Compound class : xanthenone)

   
   

1-Methyl-5-methoxy-8-hydroxynaphtho[2,3-c]furan-4,9-dione

1-Methyl-5-methoxy-8-hydroxynaphtho[2,3-c]furan-4,9-dione

C14H10O5 (258.052821)


   

9-propionyloxy-furo[3,2-g]chromen-7-one

9-propionyloxy-furo[3,2-g]chromen-7-one

C14H10O5 (258.052821)


   

1,5-Dihydroxy-2-methoxyxanthone

1,5-Dihydroxy-2-methoxyxanthone

C14H10O5 (258.052821)


   

6-O-Demethyl-5-deoxyanhydrofusarubin

6-O-Demethyl-5-deoxyanhydrofusarubin

C14H10O5 (258.052821)


   

1,7-DIHYDROXY-6-METHOXY-9H-XANTHEN-9-ONE

1,7-DIHYDROXY-6-METHOXY-9H-XANTHEN-9-ONE

C14H10O5 (258.052821)


   

9H-Xanthen-9-one,1,3-dihydroxy-6-methoxy-

9H-Xanthen-9-one,1,3-dihydroxy-6-methoxy-

C14H10O5 (258.052821)


   
   

Isogentisin

1,3-Dihydroxy-7-methoxyxanthone

C14H10O5 (258.052821)


A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1 and 3 and a methoxy group at position 7.

   

9H-Xanthen-9-one, 1,3-dihydroxy-2-methoxy-

9H-Xanthen-9-one, 1,3-dihydroxy-2-methoxy-

C14H10O5 (258.052821)


   

crataequinone A

crataequinone A

C14H10O5 (258.052821)


   

1-Methyl-5-hydroxy-8-methoxynaphtho[2,3-c]furan-4,9-dione

1-Methyl-5-hydroxy-8-methoxynaphtho[2,3-c]furan-4,9-dione

C14H10O5 (258.052821)


   

1,4-Dihydroxy-7-methoxy-xanthen-9-on|1,4-dihydroxy-7-methoxy-xanthen-9-one|1,4-dihydroxy-7-methoxyxanthone

1,4-Dihydroxy-7-methoxy-xanthen-9-on|1,4-dihydroxy-7-methoxy-xanthen-9-one|1,4-dihydroxy-7-methoxyxanthone

C14H10O5 (258.052821)


   

Hydroxycyperaquinone

Hydroxycyperaquinone

C14H10O5 (258.052821)


   

2,6,7-Trihydroxy-9-methylxanthen-3-one

2,6,7-Trihydroxy-9-methylxanthen-3-one

C14H10O5 (258.052821)


   

STAT3-IN-14

5-hydroxy-2-[(1S)-1-hydroxyethyl]benzo[f][1]benzofuran-4,9-dione

C14H10O5 (258.052821)


5-hydroxy-2-(1-hydroxyethyl)naphtho[2,3-b]furan-4,9-dione is a naphthofuran that is naphtho[2,3-b]furan-4,9-dione substituted by a hydroxy group at position 5 and a 1-hydroxyethyl group at position 2 (the S stereoisomer). Isolated from Tabebuia impetiginosa and Tabebuia avellanedae, it exhibits antineoplastic activity. It has a role as a metabolite and an antineoplastic agent. It is a naphthofuran, a member of phenols, a secondary alcohol and a member of p-quinones. 5-Hydroxy-2-(1-hydroxyethyl)naphtho[2,3-b]furan-4,9-dione is a natural product found in Handroanthus impetiginosus with data available. A naphthofuran that is naphtho[2,3-b]furan-4,9-dione substituted by a hydroxy group at position 5 and a 1-hydroxyethyl group at position 2 (the S stereoisomer). Isolated from Tabebuia impetiginosa and Tabebuia avellanedae, it exhibits antineoplastic activity.

   

Fusarindin

3,6,8-Trihydroxy-1-methylxanthone; Fusarindin

C14H10O5 (258.052821)


Norlichexanthone is a member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3 and 6 and a methyl group at position 8. It has been isolated from Wardomyces anomalus. It has a role as an antimalarial and a fungal metabolite. It is a member of xanthones and a polyphenol. It is a conjugate acid of a norlichexanthone(1-). Norlichexanthone is a natural product found in Arthrinium, Wardomyces anomalus, 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 and 6 and a methyl group at position 8. It has been isolated from Wardomyces anomalus.

   

5,6-Dimethoxynaphtol[2,3-b]furan-4,9-dione

5,6-Dimethoxynaphtol[2,3-b]furan-4,9-dione

C14H10O5 (258.052821)


[Raw Data] CB136_5; 6-Dimethoxynaphtol[2,3-b]furan-4; 9-dione_pos_50eV_CB000048.txt [Raw Data] CB136_5; 6-Dimethoxynaphtol[2,3-b]furan-4; 9-dione_pos_40eV_CB000048.txt [Raw Data] CB136_5; 6-Dimethoxynaphtol[2,3-b]furan-4; 9-dione_pos_30eV_CB000048.txt [Raw Data] CB136_5; 6-Dimethoxynaphtol[2,3-b]furan-4; 9-dione_pos_20eV_CB000048.txt [Raw Data] CB136_5; 6-Dimethoxynaphtol[2,3-b]furan-4; 9-dione_pos_10eV_CB000048.txt

   

Alternariol

Alternariol 3,4,5-Trihydroxy-6-methyl-dibenzo[a]pyrone

C14H10O5 (258.052821)


A benzochromenone that is 6H-benzo[c]chromen-6-one which is substituted by a methyl group at position 1 and by hydroxy groups at positions 3, 7, and 9. It is the most important mycotoxin produced by the black mould Alternaria species, which are the most common mycoflora infecting small grain cereals worldwide. D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D002800 - Cholinesterase Inhibitors D004791 - Enzyme Inhibitors CONFIDENCE Reference Standard (Level 1)

   

3,7,9-trihydroxy-1-methylbenzo[c]chromen-6-one

NCGC00180653-03!3,7,9-trihydroxy-1-methylbenzo[c]chromen-6-one

C14H10O5 (258.052821)


   

1,3,6-trihydroxy-8-methylxanthen-9-one

NCGC00169665-03!1,3,6-trihydroxy-8-methylxanthen-9-one

C14H10O5 (258.052821)


   

1,6-dihydroxy-5-methoxyxanthen-9-one

NCGC00385584-01!1,6-dihydroxy-5-methoxyxanthen-9-one

C14H10O5 (258.052821)


   

3,6-dihydroxy-1-methoxyxanthen-9-one

NCGC00380439-01!3,6-dihydroxy-1-methoxyxanthen-9-one

C14H10O5 (258.052821)


   

norlichexanthone_major

norlichexanthone_major

C14H10O5 (258.052821)


   

2-(3,4-dihydroxyphenyl)-2H-1,3-benzodioxole-5-carbaldehyde

(±)-2-(3,4-Dihydroxyphenyl)-1,3-benzodioxole-5-carboxaldehyde

C14H10O5 (258.052821)


   

Alfafuran

2-(3,5-Dihydroxyphenyl)-5,6-benzofurandiol, 9ci

C14H10O5 (258.052821)


   

2-PHENOXY-TEREPHTHALIC ACID

2-PHENOXY-TEREPHTHALIC ACID

C14H10O5 (258.052821)


   

3-(BENZO[D][1,3]DIOXOL-5-YL)-5-HYDROXYBENZOIC ACID

3-(BENZO[D][1,3]DIOXOL-5-YL)-5-HYDROXYBENZOIC ACID

C14H10O5 (258.052821)


   

2-(2,4-Dihydroxybenzoyl)benzoic acid

2-(2,4-Dihydroxybenzoyl)benzoic acid

C14H10O5 (258.052821)


   

4,4-Oxybisbenzoic acid

4,4-Oxybisbenzoic acid

C14H10O5 (258.052821)


   

3-(BENZOYLOXY)-2-HYDROXYBENZOIC ACID

3-(BENZOYLOXY)-2-HYDROXYBENZOIC ACID

C14H10O5 (258.052821)


   

3H-Xanthen-3-one,2,6,7-trihydroxy-9-methyl-

3H-Xanthen-3-one,2,6,7-trihydroxy-9-methyl-

C14H10O5 (258.052821)


   

2-(3,4-Dihydroxyphenyl)-1,3-benzodioxole-5-carboxaldehyde

2-(3,4-Dihydroxyphenyl)-1,3-benzodioxole-5-carboxaldehyde

C14H10O5 (258.052821)


   

8-Hydroxy-2-(1-hydroxyethyl)benzo[f][1]benzofuran-4,9-dione

8-Hydroxy-2-(1-hydroxyethyl)benzo[f][1]benzofuran-4,9-dione

C14H10O5 (258.052821)


   

Gentisin

5-18-04-00497 (Beilstein Handbook Reference)

C14H10O5 (258.052821)


   

5,6-Dimethoxynaphtho[2,3-b]furan-4,9-dione

5,6-Dimethoxynaphtho[2,3-b]furan-4,9-dione

C14H10O5 (258.052821)


   

3-Methyl-7,9,10-trihydroxy-1H-naphtho[2,3-c]pyran-1-one

3-Methyl-7,9,10-trihydroxy-1H-naphtho[2,3-c]pyran-1-one

C14H10O5 (258.052821)


   

3,6-Dihydroxy-1-methoxyxanthen-9-one

3,6-Dihydroxy-1-methoxyxanthen-9-one

C14H10O5 (258.052821)


   

Norrubrofusarin

Norrubrofusarin

C14H10O5 (258.052821)


A member of the class of benzochromenones that is 4H-benzo[g]chromen-4-one carrying a methyl group at position 2 and a hydroxy group at positions 5, 6 and 8, respectively.

   

8-hydroxy-2-(1-hydroxyethyl)naphtho-[2,3-b]-furan-4,9-dione

8-hydroxy-2-(1-hydroxyethyl)naphtho-[2,3-b]-furan-4,9-dione

C14H10O5 (258.052821)


A naphthofuran that is naphtho[2,3-b]furan-4,9-dione substituted by a hydroxy group at position 8 and a 1-hydroxyethyl group at position 2. Isolated from Tabebuia impetiginosa and Kigelia pinnata, it exhibits antineoplastic activity.

   

nor-toralactone

nor-toralactone

C14H10O5 (258.052821)


A naphtho-gamma-pyrone that is 1H-benzo[g]isochromen-1-one substituted by a methyl group at position 3 and hydroxy groups at positions 7, 9 and 10.

   

hydroxyethyl furanhydroxynaphthoquinone

hydroxyethyl furanhydroxynaphthoquinone

C14H10O5 (258.052821)


   

5,6-dihydroxy-1-methoxyxanthen-9-one

5,6-dihydroxy-1-methoxyxanthen-9-one

C14H10O5 (258.052821)


   

5-hydroxy-2-[(1r)-1-hydroxyethyl]naphtho[2,3-b]furan-4,9-dione

5-hydroxy-2-[(1r)-1-hydroxyethyl]naphtho[2,3-b]furan-4,9-dione

C14H10O5 (258.052821)


   

8-hydroxy-2-(1-hydroxyethyl)naphtho[2,3-b]furan-4,9-dione

8-hydroxy-2-(1-hydroxyethyl)naphtho[2,3-b]furan-4,9-dione

C14H10O5 (258.052821)


   

(9r)-3-acetyl-5,9-dihydroxy-9h-naphtho[2,3-c]furan-4-one

(9r)-3-acetyl-5,9-dihydroxy-9h-naphtho[2,3-c]furan-4-one

C14H10O5 (258.052821)


   

(9s)-3-acetyl-5,9-dihydroxy-9h-naphtho[2,3-c]furan-4-one

(9s)-3-acetyl-5,9-dihydroxy-9h-naphtho[2,3-c]furan-4-one

C14H10O5 (258.052821)


   

4,8,10-trihydroxy-5-methylbenzo[h]chromen-2-one

4,8,10-trihydroxy-5-methylbenzo[h]chromen-2-one

C14H10O5 (258.052821)


   

3,4-dihydroxy-2-methoxyxanthen-9-one

3,4-dihydroxy-2-methoxyxanthen-9-one

C14H10O5 (258.052821)