Exact Mass: 224.0909362
Exact Mass Matches: 224.0909362
Found 214 metabolites which its exact mass value is equals to given mass value 224.0909362,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Flavanone
Flavonoids (or bioflavonoids) (from the Latin word flavus meaning yellow), also collectively known as Vitamin P and citrin, are a class of plant secondary metabolites or yellow pigments having a structure similar to that of flavones. Flavonoids is found in many foods, some of which are blackcurrant, wild celery, rose hip, and turmeric. Flavanone is a naturally occurring flavone. Flavanone has inhibitory activity for human estrogen synthetase (aromatase)[1]. Flavanone is a naturally occurring flavone. Flavanone has inhibitory activity for human estrogen synthetase (aromatase)[1].
4-Hydroxychalcone
4'-Hydroxychalcone is a chalcone isolated from licorice root, with hepatoprotective activity. 4'-Hydroxychalcone inhibits TNFα-induced NF-κB activation via proteasome inhibition. 4'-Hydroxychalcone induces a rapid potassium release from mitochondrial vesicles and causes deterioration of respiratory control and oxidative phosphorylation of isolated rat liver mitochondria[1][2][3].
4-Hydroxychalcone
4-Hydroxychalcone is found in herbs and spices. 4-Hydroxychalcone is a constituent of Glycyrrhiza glabra (licorice) roots 4-Hydroxychalcone is a chalcone metabolite with anti-angiogenic and anti-inflammatory activities. 4-Hydroxychalcone suppresses angiogenesis by suppression of growth factor pathway with no signs of cytotoxicity[1]. 4-Hydroxychalcone inhibits TNF-α induced NF-κB pathway activation and activates BMP signaling, reduces resistant hypertension (RH) by attenuating hyperaldosteronism and renal injury in mice[2].
Flavanone
Annotation level-1 Flavanone is a naturally occurring flavone. Flavanone has inhibitory activity for human estrogen synthetase (aromatase)[1]. Flavanone is a naturally occurring flavone. Flavanone has inhibitory activity for human estrogen synthetase (aromatase)[1].
Flavanone
Flavanone is the simplest member of the class of flavanones that consists of flavan bearing an oxo substituent at position 4. It derives from a hydride of a flavan. Flavanone is a natural product found in Annona muricata, Ginkgo biloba, and other organisms with data available. The simplest member of the class of flavanones that consists of flavan bearing an oxo substituent at position 4. Flavanone is a naturally occurring flavone. Flavanone has inhibitory activity for human estrogen synthetase (aromatase)[1]. Flavanone is a naturally occurring flavone. Flavanone has inhibitory activity for human estrogen synthetase (aromatase)[1].
N-Methoxy-1-vinyl-beta-carboline
C14H12N2O (224.09495819999998)
N-Methoxy-1-vinyl-beta-carboline is an alkaloid from Picrasma excelsa (Jamaican quassiawood
Temurin
Temurin is a methyl derivative of uric acid, found occasionally in human urine. Temurin is one of the purine components in urinary calculi. Methylated purines originate from the metabolism of methylxanthines (caffeine, theophylline and theobromine). Methyluric acids are indistinguishable from uric acid by simple methods routinely used in clinical laboratories, requiring the use of high-performance liquid chromatography (HPLC). Purine derivatives in urinary calculi could be considered markers of abnormal purine metabolism. The content of a purine derivative in stone depends on its average urinary excretion in the general population, similarity to the chemical structure of uric acid, and content of the latter in stone. This suggests that purines in stones represent a solid solution with uric acid as solvent. It is also plausible that methylxanthines, ubiquitous components of the diet and drugs, are involved in the pathogenesis of urolithiasis. (PMID: 11712316, 15833286, 3506820, 15013152). Isolated from tea
6-[(1Z,2Z)-3-Hydroxy-3-phenyl-2-propene-1-ylidene]-2,4-cyclohexadiene-1-one
8-(2-Hydroxyethyl)theophyline
Dibenzoylmethane
Dibenzoylmethane, a minor ingredient in licorice, activates Nrf2 and prevents various cancers and oxidative damage. Dibenzoylmethane, an analog of curcumin, results in dissociation from Keap1 and nuclear translocation of Nrf2[1]. Dibenzoylmethane, a minor ingredient in licorice, activates Nrf2 and prevents various cancers and oxidative damage. Dibenzoylmethane, an analog of curcumin, results in dissociation from Keap1 and nuclear translocation of Nrf2[1].
Isoflavanone
Isoflavone in which the double bond between positions 2 and 3 has been reduced to a single bond.
Dibenzoylmethane
Dibenzoylmethane is a beta-diketone that is acetylacetone (acac) in which both methyl groups have been replaced by phenyl groups. It is a minor constituent of the root extract of licorice (Glycyrrhiza glabra) and exhibits antimutagenic and anticancer effects. It has a role as an antineoplastic agent, a metabolite and an antimutagen. It is a beta-diketone and an aromatic ketone. Dibenzoylmethane is a natural product found in Acca sellowiana with data available. A beta-diketone that is acetylacetone (acac) in which both methyl groups have been replaced by phenyl groups. It is a minor constituent of the root extract of licorice (Glycyrrhiza glabra) and exhibits antimutagenic and anticancer effects. Dibenzoylmethane, a minor ingredient in licorice, activates Nrf2 and prevents various cancers and oxidative damage. Dibenzoylmethane, an analog of curcumin, results in dissociation from Keap1 and nuclear translocation of Nrf2[1]. Dibenzoylmethane, a minor ingredient in licorice, activates Nrf2 and prevents various cancers and oxidative damage. Dibenzoylmethane, an analog of curcumin, results in dissociation from Keap1 and nuclear translocation of Nrf2[1].
7-(2-Hydroxyethyl)theophylline
D019141 - Respiratory System Agents > D018927 - Anti-Asthmatic Agents > D001993 - Bronchodilator Agents D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents C471 - Enzyme Inhibitor > C744 - Phosphodiesterase Inhibitor CONFIDENCE Reference Standard (Level 1); HBM4EU - science and policy for a healthy future (https://www.hbm4eu.eu); Flow Injection CONFIDENCE Reference Standard (Level 1); HBM4EU - science and policy for a healthy future (https://www.hbm4eu.eu)
(beta,beta-Dihydroxy-isopropyl)-beta-D-xylopyranosid|(beta,beta-dihydroxy-isopropyl)-beta-D-xylopyranoside|2-Desoxyglycer-2-yl-beta-D-xylopyranosid|2-O-beta-D-Xylopyranosylglycerin|<2-Hydroxy-1-hydroxymethyl-aethyl>-beta-D-xylopyranosid
7-acetoxy-1-phenylhept-5E-ene-1,3-diyne|Ac-(E)-7-Phenyl-2-heptene-4,6-diyn-1-ol|Acetat des 1-Phenyl-hepten-(5)-trans-diin-(1.3)-ols-(7)|acetic acid-(7-phenyl-hept-2t-ene-4,6-diynyl ester)|Essigsaeure-(7-phenyl-hept-2t-en-4,6-diinylester)|trans-1-Phenyl-hepten-(5)-diin-(1,3)-yl-(7)-acetat
cis,cis-Tridecatrien-(2,10,12)-triin-(4,6,8)-yl-acetat
azuleno[6,5-b]furan-5-carboxaldehyde, 3,8-dimethyl-
3,5-Dimethyl-4-methylenenaphtho[2,3-b]furan-9(4H)-one
Chalcone, 3
4-hydroxychalcone is a member of the class of chalcones that is trans-chalcone substituted by a hydroxy group at position 4. It has a role as a plant metabolite and an antihypertensive agent. It is a member of chalcones and a member of phenols. It is functionally related to a trans-chalcone. A member of the class of chalcones that is trans-chalcone substituted by a hydroxy group at position 4. 4-Hydroxychalcone is a chalcone metabolite with anti-angiogenic and anti-inflammatory activities. 4-Hydroxychalcone suppresses angiogenesis by suppression of growth factor pathway with no signs of cytotoxicity[1]. 4-Hydroxychalcone inhibits TNF-α induced NF-κB pathway activation and activates BMP signaling, reduces resistant hypertension (RH) by attenuating hyperaldosteronism and renal injury in mice[2].
TOB-10
C14H12N2O (224.09495819999998)
Dehydrocrenatine is a natural product found in Picrasma quassioides and Picrasma javanica with data available.
Spectrum5_000333
4-hydroxychalcone is a member of the class of chalcones that is trans-chalcone substituted by a hydroxy group at position 4. It has a role as an anti-inflammatory agent and an antineoplastic agent. It is a member of chalcones and a member of phenols. 4'-Hydroxychalcone is a chalcone isolated from licorice root, with hepatoprotective activity. 4'-Hydroxychalcone inhibits TNFα-induced NF-κB activation via proteasome inhibition. 4'-Hydroxychalcone induces a rapid potassium release from mitochondrial vesicles and causes deterioration of respiratory control and oxidative phosphorylation of isolated rat liver mitochondria[1][2][3].
2-Hydroxychalcone
2-hydroxychalcone, a natural flavonoid, is a potent antioxidant, inhibiting lipid peroxidation. 2-Hydroxychalcone induces apoptosis by Bcl-2 downregulation. 2-Hydroxychalcone inhibits the activation of NF-kB[1][2][3]. 2-hydroxychalcone, a natural flavonoid, is a potent antioxidant, inhibiting lipid peroxidation. 2-Hydroxychalcone induces apoptosis by Bcl-2 downregulation. 2-Hydroxychalcone inhibits the activation of NF-kB[1][2][3].
(4S,5Z,6S)-4-(2-methoxy-2-oxoethyl)-5-[2-[(E)-3-phenylprop-2-enoyl]oxyethylidene]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylic acid
N-Methoxy-1-vinyl-b-carboline
C14H12N2O (224.09495819999998)
[3-(1H-benzimidazol-2-yl)phenyl]methanol
C14H12N2O (224.09495819999998)
6-(BENZYLOXY)-1H-PYRROLO[2,3-B]PYRIDINE
C14H12N2O (224.09495819999998)
(2E)-1-(4-aminophenyl)-3-pyridin-3-ylprop-2-en-1-one
C14H12N2O (224.09495819999998)
Benzenamine,4-(5-methyl-2-benzoxazolyl)-
C14H12N2O (224.09495819999998)
5-(benzyloxy)-1H-pyrrolo[3,2-b]pyridine
C14H12N2O (224.09495819999998)
5-FLUORO-7,8-DIMETHOXY-3,4-DIHYDRONAPHTHALEN-1(2H)-ONE
2-amino-4,5,6,7,8,9-hexahydrocycloocta[b]thiophene-3-carboxamide
C11H16N2OS (224.09832859999997)
(2-([1,1-BIPHENYL]-4-YL)VINYL)BORONIC ACID
C14H13BO2 (224.10085480000004)
4-(4-FLUOROPHENYL)TETRAHYDRO-2H-PYRAN-4-CARBOXYLIC ACID
Acetic acid,2-[[4-(1,1-dimethylethyl)phenyl]thio]-
7-(BENZYLOXY)-1H-PYRROLO[3,2-B]PYRIDINE
C14H12N2O (224.09495819999998)
4-(Benzyloxy)-1H-pyrrolo[2,3-b]pyridine
C14H12N2O (224.09495819999998)
2-HYDROXY-10,11-DIHYDRO-5H-DIBENZO[A,D][7]ANNULEN-5-ONE
6-Methoxy-2-phenylimidazo[1,2-a]pyridine
C14H12N2O (224.09495819999998)
1-(2-Methoxyethyl)-2-pyrrolidinone
C14H12N2O (224.09495819999998)
6-(3-Pyridinyl)-3,4-dihydro-2(1H)-quinolinone
C14H12N2O (224.09495819999998)
5-amino-2-methyl-10h-acridin-9-one
C14H12N2O (224.09495819999998)
1,2-Ethanedione,1,2-diphenyl-, 1-hydrazone
C14H12N2O (224.09495819999998)
5-Benzooxazol-2-yl-2-methyl-phenylamine
C14H12N2O (224.09495819999998)
1-(3-METHOXYBIPHENYL-4-YL)ETHANONE
C14H12N2O (224.09495819999998)
1,2,3,6-TETRAHYDROINDOLIZINO[6,7-B]INDOL-5-ONE
C14H12N2O (224.09495819999998)
(R)-3-AMINO-N-METHYL-4-(PHENYLTHIO)BUTANAMIDE
C11H16N2OS (224.09832859999997)
8-(Benzyloxy)imidazo[1,5-a]pyridine
C14H12N2O (224.09495819999998)
(3-HYDROXY-BENZYL)-CARBAMICACIDTERT-BUTYLESTER
C14H12N2O (224.09495819999998)
1-benzyl-3H-pyrrolo[2,3-b]pyridin-2-one
C14H12N2O (224.09495819999998)
6-BENZYL-6,7-DIHYDROPYRROLO[3,4-B]PYRIDIN-5-ONE
C14H12N2O (224.09495819999998)
5-(6-METHOXY-2-NAPHTHYL)-1H-PYRAZOLE
C14H12N2O (224.09495819999998)
2-amino-n-ethyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide
C11H16N2OS (224.09832859999997)
Phenol,2-(6-methyl-1H-benzimidazol-2-yl)-
C14H12N2O (224.09495819999998)
1H-Benzimidazole,2-(4-methoxyphenyl)-
C14H12N2O (224.09495819999998)
azanium,2-methyl-2-(prop-2-enoylamino)propane-1-sulfonate
3-ETHYL-5-PYRAZOLCARBOXYLICACIDMETHYLESTER
C9H18Cl2N2 (224.08469680000002)
4-(3-Fluorophenyl)tetrahydro-2H-pyran-4-carboxylic acid
3H-Indazol-3-one,1,2-dihydro-2-(phenylmethyl)-
C14H12N2O (224.09495819999998)
[3-(1H-pyrrolo[2,3-b]pyridin-4-yl)phenyl]methanol
C14H12N2O (224.09495819999998)
1-Benzyl-1,2-dihydro-3H-indazol-3-one
C14H12N2O (224.09495819999998)
2-(4-Methoxy-phenyl)-imidazo[1,2-a]pyridine
C14H12N2O (224.09495819999998)
1-Benzyl-1,3-dihydro-2H-benzimidazole-2-one
C14H12N2O (224.09495819999998)
2 4-BIS(DIMETHYLAMINO)-6-CHLOROPYRIDINE-3-CARBONITRILE
2-Fluoro-2-methyl-3-oxo-3-phenyl-propionic acid ethyl ester
methyl 3-(4-fluorophenyl)pyrazolidine-4-carboxylate
6-pyridin-3-yl-3,4-dihydro-1H-quinolin-2-one
C14H12N2O (224.09495819999998)
1-BENZYL-2-FURAN-2-YL-1H-IMIDAZOLE
C14H12N2O (224.09495819999998)
8-(Benzyloxy)imidazo[1,2-a]pyridine
C14H12N2O (224.09495819999998)
(S)-(-)-2-(4-phenyl-4,5-dihydro-1,3-oxazol-2-yl)pyridine
C14H12N2O (224.09495819999998)
5-Amino-2-(4-aminophenyl)benzofuran
C14H12N2O (224.09495819999998)
(2-((Dimethylamino)methyl)-5-nitrophenyl)boronic acid
N-(3-CYANOPHENYL)-N-(4-METHOXYPHENYL)AMINE
C14H12N2O (224.09495819999998)
2-(1-NAPHTHYL)-4-(HYDROXYMETHYL)IMIDAZOLE
C14H12N2O (224.09495819999998)
3-Phenyl-N-pyridin-3-yl-acrylamide
C14H12N2O (224.09495819999998)
3-(4-Methoxyphenyl)imidazo[1,5-a]pyridine
C14H12N2O (224.09495819999998)
1H-indol-3-yl(pyridin-2-yl)methanol
C14H12N2O (224.09495819999998)
Benzoic acid, 2-[(trimethylsilyl)oxy]-, methyl ester
Phosphonic acid, methyl-, 2-methylpropyl trimethylsilyl ester
3-Pyridinecarboxamide, 1,6-dihydro-1-methyl-6-oxo-N-(trimethylsilyl)-
(5R)-4-Hydroxy-3,5-dimethyl-5-[(1E,3E)-2-methylpenta-1,3-dienyl]thiophen-2(5H)-one
Karenzu DK2
Dibenzoylmethane, a minor ingredient in licorice, activates Nrf2 and prevents various cancers and oxidative damage. Dibenzoylmethane, an analog of curcumin, results in dissociation from Keap1 and nuclear translocation of Nrf2[1]. Dibenzoylmethane, a minor ingredient in licorice, activates Nrf2 and prevents various cancers and oxidative damage. Dibenzoylmethane, an analog of curcumin, results in dissociation from Keap1 and nuclear translocation of Nrf2[1].
AI3-00855
2-hydroxychalcone, a natural flavonoid, is a potent antioxidant, inhibiting lipid peroxidation. 2-Hydroxychalcone induces apoptosis by Bcl-2 downregulation. 2-Hydroxychalcone inhibits the activation of NF-kB[1][2][3]. 2-hydroxychalcone, a natural flavonoid, is a potent antioxidant, inhibiting lipid peroxidation. 2-Hydroxychalcone induces apoptosis by Bcl-2 downregulation. 2-Hydroxychalcone inhibits the activation of NF-kB[1][2][3].
2,3-Dihydroxybutanedioic acid;propane-1,3-diamine
C7H16N2O6 (224.10083160000002)
2-(butylthio)-3,5,6,7-tetrahydro-4H-cyclopenta[d]pyrimidin-4-one
C11H16N2OS (224.09832859999997)
(4S,5S)-2-(2-Chloroethyl)-4,5-bis(methoxymethyl)-1,3-dioxolane
Tetramethyluric acid
An oxopurine that is uric acid in which the hydrogens at positions 1,3,7 and 9 are replaced by methyl groups. It is a purine alkaloid that is found in Chinese tea known as kucha (Camellia assamica var. kucha) and exhibits anti-inflammatory and analgesic properties.
2-[(1s)-1-phenylprop-2-en-1-yl]cyclohexa-2,5-diene-1,4-dione
4-[2-(phenylmethylidene)hydrazin-1-yl]benzaldehyde
C14H12N2O (224.09495819999998)