Exact Mass: 238.063

Exact Mass Matches: 238.063

Found 93 metabolites which its exact mass value is equals to given mass value 238.063, within given mass tolerance error 0.001 dalton. Try search metabolite list with more accurate mass tolerance error 0.0002 dalton.

3-Hydroxyflavone

3-Hydroxy-2-phenyl-4H-1-benzopyran-4-one, 9CI

C15H10O3 (238.063)


Flavonol is a monohydroxyflavone that is the 3-hydroxy derivative of flavone. It is a monohydroxyflavone and a member of flavonols. It is a conjugate acid of a flavonol(1-). 3-Hydroxyflavone is a natural product found in Acacia retinodes, Acacia holosericea, and other organisms with data available. Constituent of cabbage. 3-Hydroxyflavone is found in many foods, some of which are red raspberry, brassicas, papaya, and pomegranate. 3-Hydroxyflavone is found in brassicas. 3-Hydroxyflavone is a constituent of cabbage Flavonol is an endogenous metabolite. Flavonol is an endogenous metabolite.

   

Primuliten

InChI=1/C15H10O3/c16-11-7-4-8-13-15(11)12(17)9-14(18-13)10-5-2-1-3-6-10/h1-9,16H

C15H10O3 (238.063)


5-Hydroxyflavone is a member of flavones. 5-Hydroxyflavone is a natural product found in Conchocarpus heterophyllus, Primula denticulata, and Lophomyrtus bullata with data available. relative retention time with respect to 9-anthracene Carboxylic Acid is 1.263 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.268 5-Hydroxyflavone, a flavonoid ligand, shows no cytotoxic activity against MCF-7, FaDU, MDA-MB-435S, U87, RPE-1, and HEK293 cells[1]. 5-Hydroxyflavone, a flavonoid ligand, shows no cytotoxic activity against MCF-7, FaDU, MDA-MB-435S, U87, RPE-1, and HEK293 cells[1].

   

7-Hydroxyflavone

7-Hydroxy-2-phenyl-4-benzopyrone

C15H10O3 (238.063)


[Raw Data] CB049_7-Hydroxyflavone_pos_10eV_CB000023.txt [Raw Data] CB049_7-Hydroxyflavone_pos_30eV_CB000023.txt [Raw Data] CB049_7-Hydroxyflavone_pos_50eV_CB000023.txt [Raw Data] CB049_7-Hydroxyflavone_pos_20eV_CB000023.txt [Raw Data] CB049_7-Hydroxyflavone_pos_40eV_CB000023.txt [Raw Data] CB049_7-Hydroxyflavone_neg_20eV_000015.txt [Raw Data] CB049_7-Hydroxyflavone_neg_10eV_000015.txt [Raw Data] CB049_7-Hydroxyflavone_neg_40eV_000015.txt [Raw Data] CB049_7-Hydroxyflavone_neg_30eV_000015.txt [Raw Data] CB049_7-Hydroxyflavone_neg_50eV_000015.txt 7-Hydroxyflavone is a flavonoid isolated from Clerodendrum phlomidis, with anti-inflammatory activity. 7-Hydroxyflavone protects renal cells from nicotine (NIC)-associated cytotoxicity via the ERK/Nrf2/HO-1 pathway[1][2]. 7-Hydroxyflavone is a flavonoid isolated from Clerodendrum phlomidis, with anti-inflammatory activity. 7-Hydroxyflavone protects renal cells from nicotine (NIC)-associated cytotoxicity via the ERK/Nrf2/HO-1 pathway[1][2]. 7-Hydroxyflavone is a flavonoid isolated from Clerodendrum phlomidis, with anti-inflammatory activity. 7-Hydroxyflavone protects renal cells from nicotine (NIC)-associated cytotoxicity via the ERK/Nrf2/HO-1 pathway[1][2].

   

6-Hydroxyflavone

6-Hydroxy-2-phenyl-4-benzopyrone

C15H10O3 (238.063)


6-Hydroxyflavone is a naturally occurring flavone, with anti-inflammatory activity. 6-Hydroxyflavone exhibits inhibitory effect towards bovine hemoglobin (BHb) glycation. 6-Hydroxyflavone can activate AKT, ERK 1/2, and JNK signaling pathways to effectively promote osteoblastic differentiation. 6-Hydroxyflavone inhibits the LPS-induced NO production[1] [2]. 6-Hydroxyflavone is a naturally occurring flavone, with anti-inflammatory activity. 6-Hydroxyflavone exhibits inhibitory effect towards bovine hemoglobin (BHb) glycation. 6-Hydroxyflavone can activate AKT, ERK 1/2, and JNK signaling pathways to effectively promote osteoblastic differentiation. 6-Hydroxyflavone inhibits the LPS-induced NO production[1] [2].

   

3-hydroxyflavone

2-(3-hydroxyphenyl)chromen-4-one

C15H10O3 (238.063)


   

2-Hydroxyisoflavone

2-Hydroxyisoflavone

C15H10O3 (238.063)


   

2-Hydroxymethylanthraquinone

2-(hydroxymethyl)-9,10-dihydroanthracene-9,10-dione

C15H10O3 (238.063)


2-hydroxymethylanthraquinone, also known as anthraquinone-2-methanol or hmaq-one, is a member of the class of compounds known as anthraquinones. Anthraquinones are organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone. 2-hydroxymethylanthraquinone is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 2-hydroxymethylanthraquinone can be found in turmeric, which makes 2-hydroxymethylanthraquinone a potential biomarker for the consumption of this food product. 2-(Hydroxymethyl)anthraquinone is used as a photoremovable protecting group (PRPG) to chemically cage sex pheromone (e.g. (Z)-11-hexadecen-1-ol (sex pheromone of?Chilo infuscatellussnellen))[1]. 2-(Hydroxymethyl)anthraquinone is used as a photoremovable protecting group (PRPG) to chemically cage sex pheromone (e.g. (Z)-11-hexadecen-1-ol (sex pheromone of?Chilo infuscatellussnellen))[1].

   

7-Hydroxyisoflavone

7-Hydroxyisoflavone

C15H10O3 (238.063)


   

5-Hydroxyflavone

5-Hydroxyflavone

C15H10O3 (238.063)


5-Hydroxyflavone, a flavonoid ligand, shows no cytotoxic activity against MCF-7, FaDU, MDA-MB-435S, U87, RPE-1, and HEK293 cells[1]. 5-Hydroxyflavone, a flavonoid ligand, shows no cytotoxic activity against MCF-7, FaDU, MDA-MB-435S, U87, RPE-1, and HEK293 cells[1].

   

4-Hydroxyflavone

4-Hydroxyflavone

C15H10O3 (238.063)


   

2-Hydroxyflavone

2-Hydroxyflavanone

C15H10O3 (238.063)


   

Cystathionine sulfoxide

[R-(R*,s*)]-2-amino-4-[(2-amino-2-carboxyethyl)sulfinyl]-butanoic acid

C7H14N2O5S (238.0623)


One of the unusual cystathionine metabolites found in the urine of patients with cystathioninuria [HMDB] One of the unusual cystathionine metabolites found in the urine of patients with cystathioninuria.

   

3,4-Flavandione

2-phenyl-3,4-dihydro-2H-1-benzopyran-3,4-dione

C15H10O3 (238.063)


   

PACHYBASIN

1-hydroxy-3-methyl-9,10-anthracenedione

C15H10O3 (238.063)


   

1-Hydroxy-2-methylanthraquinone

1-hydroxy-2-methyl-9,10-anthraquinone

C15H10O3 (238.063)


   

2-Hydroxyflavone

2-Hydroxyflavanone

C15H10O3 (238.063)


   

2-Isopropenyl naphtho[2,3-b]furan-4,9-quinone

2-Isopropenyl naphtho[2,3-b]furan-4,9-quinone

C15H10O3 (238.063)


   

Primuletin

5-HYDROXY-2-PHENYL-4H-1-BENZOPYRAN-4-ONE

C15H10O3 (238.063)


5-Hydroxyflavone, a flavonoid ligand, shows no cytotoxic activity against MCF-7, FaDU, MDA-MB-435S, U87, RPE-1, and HEK293 cells[1]. 5-Hydroxyflavone, a flavonoid ligand, shows no cytotoxic activity against MCF-7, FaDU, MDA-MB-435S, U87, RPE-1, and HEK293 cells[1].

   

1-(Hydroxymethyl)anthracene-9,10-dione

1-(Hydroxymethyl)anthracene-9,10-dione

C15H10O3 (238.063)


   

2-Hydroxy-3-methylanthraquinone

2-Hydroxy-3-methylanthraquinone

C15H10O3 (238.063)


   

2-isopropenylnaphtho[2,3-b]furan-4,9-dione

2-isopropenylnaphtho[2,3-b]furan-4,9-dione

C15H10O3 (238.063)


   

2-Methoxyanthraquinone

2-Methoxyanthraquinone

C15H10O3 (238.063)


   

stemophenanthrenene A

stemophenanthrenene A

C15H10O3 (238.063)


   

7-Hydroxy-2-methylanthraquinone

7-Hydroxy-2-methylanthraquinone

C15H10O3 (238.063)


   

1-hydroxy-6-methylanthracene-9,10-dione

1-hydroxy-6-methylanthracene-9,10-dione

C15H10O3 (238.063)


   

1-Methoxyanthraquinone

1-Methoxyanthraquinone

C15H10O3 (238.063)


   

SCHEMBL17975290

SCHEMBL17975290

C15H10O3 (238.063)


   

NSC609701

NSC609701

C15H10O3 (238.063)


   

1,3-bis(4-hydroxyphenyl)prop-2-yn-1-one|anemarchalconyn

1,3-bis(4-hydroxyphenyl)prop-2-yn-1-one|anemarchalconyn

C15H10O3 (238.063)


   

Barleriaquinone I

Barleriaquinone I

C15H10O3 (238.063)


   

1-Hydroxy-4-methylanthraquinone

1-Hydroxy-4-methylanthraquinone

C15H10O3 (238.063)


   

CZODYZFOLUNSFR-UHFFFAOYSA-N

1-hydroxy-2-methyl-9,10-dihydroanthracene-9,10-dione

C15H10O3 (238.063)


1-hydroxy-2-methyl-9,10-anthraquinone is a member of the class of hydroxyanthraquinones that is anthracene-9,10-dione substituted by a hydroxy group at position 1 and a methyl group at position 2. It has been isolated from the roots of Rubia yunnanensis. It has a role as a plant metabolite. 1-Hydroxy-2-methylanthraquinone is a natural product found in Prismatomeris tetrandra, Galium spurium, and other organisms with data available. A member of the class of hydroxyanthraquinones that is anthracene-9,10-dione substituted by a hydroxy group at position 1 and a methyl group at position 2. It has been isolated from the roots of Rubia yunnanensis.

   

7-Hydroxy-2-phenyl-4H-1-benzopyran-4-one

4H-1-Benzopyran-4-one, 7-hydroxy-2-phenyl-

C15H10O3 (238.063)


7-hydroxyflavone is a hydroxyflavonoid in which the flavone nucleus is substituted at position 7 by a hydroxy group. 7-Hydroxyflavone is a natural product found in Lawsonia inermis, Berberis dictyota, and other organisms with data available. 7-Hydroxyflavone is a flavonoid isolated from Clerodendrum phlomidis, with anti-inflammatory activity. 7-Hydroxyflavone protects renal cells from nicotine (NIC)-associated cytotoxicity via the ERK/Nrf2/HO-1 pathway[1][2]. 7-Hydroxyflavone is a flavonoid isolated from Clerodendrum phlomidis, with anti-inflammatory activity. 7-Hydroxyflavone protects renal cells from nicotine (NIC)-associated cytotoxicity via the ERK/Nrf2/HO-1 pathway[1][2]. 7-Hydroxyflavone. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=6665-86-7 (retrieved 2024-10-18) (CAS RN: 6665-86-7). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

6-Hydroxyflavone

4H-1-Benzopyran-4-one, 6-hydroxy-2-phenyl-

C15H10O3 (238.063)


6-Hydroxyflavone is a hydroxyflavonoid. 6-Hydroxyflavone is a natural product found in Scutellaria baicalensis with data available. 6-Hydroxyflavone is a naturally occurring flavone, with anti-inflammatory activity. 6-Hydroxyflavone exhibits inhibitory effect towards bovine hemoglobin (BHb) glycation. 6-Hydroxyflavone can activate AKT, ERK 1/2, and JNK signaling pathways to effectively promote osteoblastic differentiation. 6-Hydroxyflavone inhibits the LPS-induced NO production[1] [2]. 6-Hydroxyflavone is a naturally occurring flavone, with anti-inflammatory activity. 6-Hydroxyflavone exhibits inhibitory effect towards bovine hemoglobin (BHb) glycation. 6-Hydroxyflavone can activate AKT, ERK 1/2, and JNK signaling pathways to effectively promote osteoblastic differentiation. 6-Hydroxyflavone inhibits the LPS-induced NO production[1] [2].

   

HMAQ-one

2-(hydroxymethyl)-9,10-dihydroanthracene-9,10-dione

C15H10O3 (238.063)


2-(hydroxymethyl)anthraquinone is an anthraquinone. It has a role as a metabolite. 2-(Hydroxymethyl)anthraquinone is a natural product found in Rubia yunnanensis and Handroanthus impetiginosus with data available. 2-(Hydroxymethyl)anthraquinone is used as a photoremovable protecting group (PRPG) to chemically cage sex pheromone (e.g. (Z)-11-hexadecen-1-ol (sex pheromone of?Chilo infuscatellussnellen))[1]. 2-(Hydroxymethyl)anthraquinone is used as a photoremovable protecting group (PRPG) to chemically cage sex pheromone (e.g. (Z)-11-hexadecen-1-ol (sex pheromone of?Chilo infuscatellussnellen))[1].

   

7-Hydroxyflavone

7-Hydroxyflavone

C15H10O3 (238.063)


7-Hydroxyflavone is a flavonoid isolated from Clerodendrum phlomidis, with anti-inflammatory activity. 7-Hydroxyflavone protects renal cells from nicotine (NIC)-associated cytotoxicity via the ERK/Nrf2/HO-1 pathway[1][2]. 7-Hydroxyflavone is a flavonoid isolated from Clerodendrum phlomidis, with anti-inflammatory activity. 7-Hydroxyflavone protects renal cells from nicotine (NIC)-associated cytotoxicity via the ERK/Nrf2/HO-1 pathway[1][2]. 7-Hydroxyflavone is a flavonoid isolated from Clerodendrum phlomidis, with anti-inflammatory activity. 7-Hydroxyflavone protects renal cells from nicotine (NIC)-associated cytotoxicity via the ERK/Nrf2/HO-1 pathway[1][2].

   

3-Hydroxyflavone

3-Hydroxyflavone

C15H10O3 (238.063)


Flavonol is an endogenous metabolite. Flavonol is an endogenous metabolite.

   

4-Hydroxyflavone

4-Hydroxyflavone

C15H10O3 (238.063)


   

5-Hydroxyflavone

5-Hydroxyflavone

C15H10O3 (238.063)


5-Hydroxyflavone, a flavonoid ligand, shows no cytotoxic activity against MCF-7, FaDU, MDA-MB-435S, U87, RPE-1, and HEK293 cells[1]. 5-Hydroxyflavone, a flavonoid ligand, shows no cytotoxic activity against MCF-7, FaDU, MDA-MB-435S, U87, RPE-1, and HEK293 cells[1].

   

3-hydroxyflavone

2-(3-hydroxyphenyl)chromen-4-one

C15H10O3 (238.063)


   

5-hydroxy-2-phenylchromen-4-one

NCGC00095329-05!5-hydroxy-2-phenylchromen-4-one

C15H10O3 (238.063)


   

3-hydroxy-2-phenylchromen-4-one

NCGC00095653-05!3-hydroxy-2-phenylchromen-4-one

C15H10O3 (238.063)


   

7-hydroxy-2-phenylchromen-4-one

NCGC00163568-03!7-hydroxy-2-phenylchromen-4-one

C15H10O3 (238.063)


   

Primuletin (5-hydroxyflavone)

Primuletin (5-hydroxyflavone)

C15H10O3 (238.063)


   

7-hydroxy-2-phenylchromen-4-one [IIN-based: Match]

NCGC00163568-03!7-hydroxy-2-phenylchromen-4-one [IIN-based: Match]

C15H10O3 (238.063)


   

7-hydroxy-2-phenylchromen-4-one [IIN-based on: CCMSLIB00000849074]

NCGC00163568-03!7-hydroxy-2-phenylchromen-4-one [IIN-based on: CCMSLIB00000849074]

C15H10O3 (238.063)


   

Cystathionine sulfoxide

Cystathionine sulfoxide

C7H14N2O5S (238.0623)


   

(5-HYDROXYBENZOFURAN-3-YL)(PHENYL)METHANONE

(5-HYDROXYBENZOFURAN-3-YL)(PHENYL)METHANONE

C15H10O3 (238.063)


   

4-HYDROXY-3-PHENYLCOUMARIN

4-HYDROXY-3-PHENYLCOUMARIN

C15H10O3 (238.063)


   

2-Anthracenecarboxylicacid, 3-hydroxy-

2-Anthracenecarboxylicacid, 3-hydroxy-

C15H10O3 (238.063)


   

6-Chloro-9-(tetrahydro-2-pyranyl)purine

6-Chloro-9-(tetrahydro-2-pyranyl)purine

C10H11ClN4O (238.0621)


   

9H-Fluorene-4-carboxylicacid, 9-oxo-, methyl ester

9H-Fluorene-4-carboxylicacid, 9-oxo-, methyl ester

C15H10O3 (238.063)


   

8-Hydroxyflavone

8-Hydroxyflavone

C15H10O3 (238.063)


   

1-(3-METHOXYBENZOYL)-2-(1-NAPHTHOYL)-HYDRAZINE

1-(3-METHOXYBENZOYL)-2-(1-NAPHTHOYL)-HYDRAZINE

C9H16Cl2N2O (238.064)


   

4,5-Diphenyl-1,3-dioxol-2-one

4,5-Diphenyl-1,3-dioxol-2-one

C15H10O3 (238.063)


   

1H-Pyrazolo[3,4-d]pyrimidine,4-chloro-1-(tetrahydro-2H-pyran-2-yl)-

1H-Pyrazolo[3,4-d]pyrimidine,4-chloro-1-(tetrahydro-2H-pyran-2-yl)-

C10H11ClN4O (238.0621)


   

2,4-DIAMINO-5-METHYLPHENETOLE HCL

2,4-DIAMINO-5-METHYLPHENETOLE HCL

C9H16Cl2N2O (238.064)


   

6-hydroxy-3-phenylchromen-2-one

6-hydroxy-3-phenylchromen-2-one

C15H10O3 (238.063)


   

2-acetylxanthen-9-one

2-acetylxanthen-9-one

C15H10O3 (238.063)


   

1,2,3-Propanetrione,1,3-diphenyl-

1,2,3-Propanetrione,1,3-diphenyl-

C15H10O3 (238.063)


   

7-Hydroxy-4-phenylcoumarin

7-Hydroxy-4-phenylcoumarin

C15H10O3 (238.063)


   

2-phenyl-1-benzofuran-5-carboxylic acid

2-phenyl-1-benzofuran-5-carboxylic acid

C15H10O3 (238.063)


   

1-FURAN-2-YLMETHYL-PYRROLIDIN-3-YLAMINE DIHYDROCHLORIDE

1-FURAN-2-YLMETHYL-PYRROLIDIN-3-YLAMINE DIHYDROCHLORIDE

C9H16Cl2N2O (238.064)


   

3-(1-benzofuran-2-yl)benzoic acid

3-(1-benzofuran-2-yl)benzoic acid

C15H10O3 (238.063)


   

6-chloro-4-propan-2-yloxypyrido[3,2-d]pyrimidin-2-amine

6-chloro-4-propan-2-yloxypyrido[3,2-d]pyrimidin-2-amine

C10H11ClN4O (238.0621)


   

1-[(4-CHLORO-3-ETHYL-1-METHYL-1H-PYRAZOL-5-YL)CARBONYL]-1H-IMIDAZOLE

1-[(4-CHLORO-3-ETHYL-1-METHYL-1H-PYRAZOL-5-YL)CARBONYL]-1H-IMIDAZOLE

C10H11ClN4O (238.0621)


   

(S)-3-AMINO-3-(4-AMINOPHENYL)PROPAN-1-OL 2HCL

(S)-3-AMINO-3-(4-AMINOPHENYL)PROPAN-1-OL 2HCL

C9H16Cl2N2O (238.064)


   

[1,1-Biphenyl]-3,4,5-tricarboxaldehyde

[1,1-Biphenyl]-3,4,5-tricarboxaldehyde

C15H10O3 (238.063)


   

4-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-yl)morpholine

4-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-yl)morpholine

C10H11ClN4O (238.0621)


   

3-phenylumbelliferone

3-phenylumbelliferone

C15H10O3 (238.063)


   

4-Hydroxyisoflavone

4-Hydroxyisoflavone

C15H10O3 (238.063)


   

(4S)-4-{[(2S)-2-Amino-3-oxopropyl]sulfanyl}-L-homoserine

(4S)-4-{[(2S)-2-Amino-3-oxopropyl]sulfanyl}-L-homoserine

C7H14N2O5S (238.0623)


   

CHEBI:28649

4-08-00-02607 (Beilstein Handbook Reference)

C15H10O3 (238.063)


2-(Hydroxymethyl)anthraquinone is used as a photoremovable protecting group (PRPG) to chemically cage sex pheromone (e.g. (Z)-11-hexadecen-1-ol (sex pheromone of?Chilo infuscatellussnellen))[1]. 2-(Hydroxymethyl)anthraquinone is used as a photoremovable protecting group (PRPG) to chemically cage sex pheromone (e.g. (Z)-11-hexadecen-1-ol (sex pheromone of?Chilo infuscatellussnellen))[1].

   

AIDS-098137

9,10-Anthracenedione, 1-hydroxy-2-methyl-

C15H10O3 (238.063)


   

flavonol

4H-1-Benzopyran-4-one, 3-hydroxy-2-phenyl-

C15H10O3 (238.063)


Flavonol is an endogenous metabolite. Flavonol is an endogenous metabolite.

   

7-Hydroxyisoflavone

7-Hydroxyisoflavone

C15H10O3 (238.063)


The simplest member of the class of 7-hydroxyisoflavones that is isoflavone with a hydroxy substituent at position 7.

   

4'-Hydroxyisoflavone

4'-Hydroxyisoflavone

C15H10O3 (238.063)


   

Hydroxymethylanthraquinone

Hydroxymethylanthraquinone

C15H10O3 (238.063)


   

Hydroxyflavone

Hydroxyflavone

C15H10O3 (238.063)


   

2-(2-hydroxyphenyl)chromen-4-one

2-(2-hydroxyphenyl)chromen-4-one

C15H10O3 (238.063)


   

anemarchalconyn

anemarchalconyn

C15H10O3 (238.063)


   

1-methoxy-9,10-anthraquinone

1-methoxy-9,10-anthraquinone

C15H10O3 (238.063)


   

anemarchalconyn

NA

C15H10O3 (238.063)


{"Ingredient_id": "HBIN016044","Ingredient_name": "anemarchalconyn","Alias": "NA","Ingredient_formula": "C15H10O3","Ingredient_Smile": "C1=CC(=CC=C1C#CC(=O)C2=CC=C(C=C2)O)O","Ingredient_weight": "238.24 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "28678","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "44557158","DrugBank_id": "NA"}

   

anticancer flavonoid pmv70p691-94

NA

C15H10O3 (238.063)


{"Ingredient_id": "HBIN016343","Ingredient_name": "anticancer flavonoid pmv70p691-94","Alias": "NA","Ingredient_formula": "C15H10O3","Ingredient_Smile": "C1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "1419","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

2-hydroxy-7-methylanthracene-9,10-dione

2-hydroxy-7-methylanthracene-9,10-dione

C15H10O3 (238.063)


   

2-hydroxy-1-methylanthracene-9,10-dione

2-hydroxy-1-methylanthracene-9,10-dione

C15H10O3 (238.063)


   

2-hydroxy-6-methylanthracene-9,10-dione

2-hydroxy-6-methylanthracene-9,10-dione

C15H10O3 (238.063)


   

3-hydroxy-1-methylanthracene-9,10-dione

3-hydroxy-1-methylanthracene-9,10-dione

C15H10O3 (238.063)


   

2-hydroxy-3-methylanthracene-9,10-dione

2-hydroxy-3-methylanthracene-9,10-dione

C15H10O3 (238.063)


   

1-hydroxy-3-methylanthracene-9,10-dione

1-hydroxy-3-methylanthracene-9,10-dione

C15H10O3 (238.063)


   

2-(prop-1-en-2-yl)naphtho[2,3-b]furan-4,9-dione

2-(prop-1-en-2-yl)naphtho[2,3-b]furan-4,9-dione

C15H10O3 (238.063)


   

2-methoxy-9,10-anthracenedione

2-methoxy-9,10-anthracenedione

C15H10O3 (238.063)


   

3-methoxyphenanthrene-1,4-dione

3-methoxyphenanthrene-1,4-dione

C15H10O3 (238.063)