Exact Mass: 438.2012
Exact Mass Matches: 438.2012
Found 375 metabolites which its exact mass value is equals to given mass value 438.2012
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within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Kurarinone
(2S)-(-)-kurarinone is a trihydroxyflavanone that is (2S)-flavanone substituted by hydroxy groups at positions 7, 2 and 4, a lavandulyl group at position 8 and a methoxy group at position 5. Isolated from the roots of Sophora flavescens, it exhibits cytotoxicity against human myeloid leukemia HL-60 cells. It has a role as a metabolite and an antineoplastic agent. It is a trihydroxyflavanone, a monomethoxyflavanone and a member of 4-hydroxyflavanones. It is functionally related to a (2S)-flavanone. 7,2,4-Trihydroxy-8-lavandulyl-5-methoxyflavanone is a natural product found in Albizia julibrissin, Cunila, and other organisms with data available. A trihydroxyflavanone that is (2S)-flavanone substituted by hydroxy groups at positions 7, 2 and 4, a lavandulyl group at position 8 and a methoxy group at position 5. Isolated from the roots of Sophora flavescens, it exhibits cytotoxicity against human myeloid leukemia HL-60 cells. Kurarinone, a flavanoid derived from shrub Sophora flavescens, inhibits the process of experimental autoimmune encephalomyelitis via blocking Th1 and Th17 cell differentiation[1]. Kurarinone, a flavanoid derived from shrub Sophora flavescens, inhibits the process of experimental autoimmune encephalomyelitis via blocking Th1 and Th17 cell differentiation[1].
1-Hydroxy-3,6,7-trimethoxy-2,8-diprenylxanthone
1-Hydroxy-3,6,7-trimethoxy-2,8-diprenylxanthone is a member of xanthones. 3,6-Dimethylmangostin is a natural product found in Garcinia cowa, Cratoxylum arborescens, and Garcinia mangostana with data available. 1-Hydroxy-3,6,7-trimethoxy-2,8-diprenylxanthone is found in fruits. 1-Hydroxy-3,6,7-trimethoxy-2,8-diprenylxanthone is a constituent of Garcinia mangostana (mangosteen). Constituent of Garcinia mangostana (mangosteen). 1-Hydroxy-3,6,7-trimethoxy-2,8-diprenylxanthone is found in fruits. Fuscaxanthone C is an xanthone isolated from the stem bark of Garcinia fusca[1]. Fuscaxanthone C is an xanthone isolated from the stem bark of Garcinia fusca[1].
Kanzonol G
Kanzonol G is found in herbs and spices. Kanzonol G is a constituent of Glycyrrhiza uralensis (Chinese licorice). Constituent of Glycyrrhiza uralensis (Chinese licorice). Kanzonol G is found in herbs and spices.
Kurarinone
Isokurarinone
Isokurarinone is a natural product found in Sophora davidii and Sophora flavescens with data available.
25-O-Methylarugosin A
Exiguaflavanone B
A trihydroxyflavanone that is (2S)-flavanone substituted by hydroxy groups at positions 5, 2 and 6, a lavandulyl group at position 8 and a methoxy group at position 7. Isolated from Sophora exigua and Artemisia indica, it exhibits antimalarial activity.
Hiravanone
isosophoranone
Sophoraisoflavanone B
Amoradicin
(2S)-5,7,4-Trihydroxy-2-methoxy-8-prenyl-5-(1,1-dimethylallyl)flavanone
Homoflemingin
5,7,3-trihydroxy-4-methoxy-8,2-di(3-methyl-2-butenyl)-(2S)-flavanone
A trihydroxyflavanone that is (2S)-flavanone substituted by hydroxy groups at positions 5, 7 and 3, a methoxy group at position 4 and prenyl groups at positions 8 and 2. Isolated from Dendrolobium lanceolatum, it exhibits cytotoxic activity.
1-[3-(7-hydroperoxy-3,7-dimethylocta-2,5-dienyl)-2-hydroxy-4-methoxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one
3-lavandulyl-4-methoxyl-2,2,4,6-tetrahydroxylchalcone
1-[2,4-dihydroxy-6-methoxy-3-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)phenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one
1-[3-(6-hydroperoxy-3,7-dimethylocta-2,7-dienyl)-2-hydroxy-4-methoxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one
4,7-dihydroxy-5-methoxy-6,3-diprenylisoflavanquinone|licoriquinone B
3,4-Dihydro-5-hydroxy-7-methoxy-2,3-dimethyl-6-(3-methyl-2-butenyl)-4-oxo-beta-phenyl-2H-1-benzopyran-8-propanoic acid
3,5,7-Trihydroxy-2-(3-prenyl-4-methoxyphenyl)-8-prenyl-2,3-dihydro-4H-1-benzopyran-4-one
(2R,3R)-6-methyl-3-geranyl-2,3-trans-5,7,4-trihydroxyflavonol
2S-3-(2-hydroxy-3-methylbut-3-enyl)licoflavone-4-methyl ether
3-(3,7-dimethyl-octa-2,6-dienyl)-2,5,2,4-tetrahydroxy-5-methoxy-chalcone|3-(3,7-Dimethyl-octa-2,6-dienyl)-2,5,2,4-tetrahydroxy-5-methoxy-chalkon|Homoflemingin|Homoflemingin, 2.4-Dihydroxy-3-geranyl-5-<3-(2.5-dihydroxy-phenyl)-trans-acryloyl>-anisol
3,5,7-Trihydroxy-4-methoxy-5,6-diprenylisoflavanone
(1S,4aS,8aR)-7-[(1,4,4a,6,6,8a-Hexahydro-2,5,5,8a-tetramethyl-6-oxo-1-naphthalenyl)methoxy]-6,8-dimethoxy-2H-1-benzopyran-2-one
leachianoneA
Leachianone A is a trihydroxyflavanone that is (2S)-flavanone substituted by a lavandulyl group at position 8, hydroxy groups at positions 5, 7 and 4 and a methoxy group at position 2. Isolated from the roots of Sophora flavescens and Sophora leachiana, it exhibits antineoplastic and antimalarial activity. It has a role as a metabolite, an antineoplastic agent and an antimalarial. It is a monomethoxyflavanone, a trihydroxyflavanone and a member of 4-hydroxyflavanones. It is functionally related to a (2S)-flavanone. leachianone A is a natural product found in Sophora stenophylla, Sophora alopecuroides, and other organisms with data available. A trihydroxyflavanone that is (2S)-flavanone substituted by a lavandulyl group at position 8, hydroxy groups at positions 5, 7 and 4 and a methoxy group at position 2. Isolated from the roots of Sophora flavescens and Sophora leachiana, it exhibits antineoplastic and antimalarial activity. Leachianone A, isolated from Radix Sophorae, has anti-malarial, anti-inflammatory, and cytotoxic potent[1]. Leachianone A induces apoptosis involved both extrinsic and intrinsic pathways[2]. Leachianone A, isolated from Radix Sophorae, has anti-malarial, anti-inflammatory, and cytotoxic potent[1]. Leachianone A induces apoptosis involved both extrinsic and intrinsic pathways[2].
5,7-dihydroxy-3-[4-hydroxy-2-methoxy-5-(2-methylbut-3-en-2-yl)phenyl]-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
5,7-dihydroxy-3-[4-hydroxy-2-methoxy-3-(3-methylbut-2-enyl)phenyl]-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
Ferocaulicin
Origin: Plant, Coumarins, Coumarin terpenoids, Sesquiterpenoids, Ferula terpenoids
Ala Ala Phe Met
Ala Ala Met Phe
Ala Cys Phe Val
Ala Cys Val Phe
Ala Phe Ala Met
Ala Phe Cys Val
Ala Phe Met Ala
Ala Phe Val Cys
Ala Met Ala Phe
Ala Met Phe Ala
Ala Val Cys Phe
Ala Val Phe Cys
Cys Ala Phe Val
Cys Ala Val Phe
Cys Phe Ala Val
Cys Phe Gly Ile
Cys Phe Gly Leu
Cys Phe Ile Gly
Cys Phe Leu Gly
Cys Phe Val Ala
Cys Gly Phe Ile
Cys Gly Phe Leu
Cys Gly Ile Phe
Cys Gly Leu Phe
Cys Ile Phe Gly
Cys Ile Gly Phe
Cys Leu Phe Gly
Cys Leu Gly Phe
Cys Val Ala Phe
Cys Val Phe Ala
Phe Ala Ala Met
Phe Ala Cys Val
Phe Ala Met Ala
Phe Ala Val Cys
Phe Cys Ala Val
Phe Cys Gly Ile
Phe Cys Gly Leu
Phe Cys Ile Gly
Phe Cys Leu Gly
Phe Cys Val Ala
Phe Gly Cys Ile
Phe Gly Cys Leu
Phe Gly Ile Cys
Phe Gly Leu Cys
Phe Ile Cys Gly
Phe Ile Gly Cys
Phe Leu Cys Gly
Phe Leu Gly Cys
Phe Met Ala Ala
Phe Val Ala Cys
Phe Val Cys Ala
Gly Cys Phe Ile
Gly Cys Phe Leu
Gly Cys Ile Phe
Gly Cys Leu Phe
Gly Phe Cys Ile
Gly Phe Cys Leu
Gly Phe Ile Cys
Gly Phe Leu Cys
Gly Ile Cys Phe
Gly Ile Phe Cys
Gly Leu Cys Phe
Gly Leu Phe Cys
Ile Cys Phe Gly
Ile Cys Gly Phe
Ile Phe Cys Gly
Ile Phe Gly Cys
Ile Gly Cys Phe
Ile Gly Phe Cys
Leu Cys Phe Gly
Leu Cys Gly Phe
Leu Phe Cys Gly
Leu Phe Gly Cys
Leu Gly Cys Phe
Leu Gly Phe Cys
Met Ala Ala Phe
Met Ala Phe Ala
Met Phe Ala Ala
Val Ala Cys Phe
Val Ala Phe Cys
Val Cys Ala Phe
Val Cys Phe Ala
Val Phe Ala Cys
Val Phe Cys Ala
EPOXY (1,2α)-7-DEACETOXY-7-OXO-DEOXYDIHYDROGEDUNIN
Leachianone A
Leachianone A, isolated from Radix Sophorae, has anti-malarial, anti-inflammatory, and cytotoxic potent[1]. Leachianone A induces apoptosis involved both extrinsic and intrinsic pathways[2]. Leachianone A, isolated from Radix Sophorae, has anti-malarial, anti-inflammatory, and cytotoxic potent[1]. Leachianone A induces apoptosis involved both extrinsic and intrinsic pathways[2].
Fuscaxanthone C
Fuscaxanthone C is an xanthone isolated from the stem bark of Garcinia fusca[1]. Fuscaxanthone C is an xanthone isolated from the stem bark of Garcinia fusca[1].
Kanzonol G
glas#1
An ascarosyloxycarboxylic acid beta-D-glucopyranosyl ester resulting from the formal esterification of the carboxy group of ascr#1 with the anomeric hydroxy group of beta-D-glucopyranose. It is a metabolite of the nematode Caenorhabditis elegans.
5S-HYDROXY-6R-(S-(2-OXO-3-THIOPROPIONYL))-7E,9E,11Z,14Z-EICOSATETRAENOIC ACID
3,6-diethyl-1-N,4-N-bis(3-methoxyphenyl)-1,2,4,5-tetrazine-1,4-dicarboxamide
4-(4-((4-Chloro-4,4-dimethyl-3,4,5,6-tetrahydro-[1,1-biphenyl]-2-yl)methyl)piperazin-1-yl)benzoic acid
1,3-diisocyanato-2-methylbenzene,hexanedioic acid,hexane-1,6-diol
5-(2-(4-(2-(DIMETHYLAMINO)ETHOXY)PHENYL)-5-(PYRIDIN-4-YL)-1H-IMIDAZOL-4-YL)-2,3-DIHYDRO-1H-INDEN-1-ONE
butane-1,3-diol,2,2-dimethylpropane-1,3-diol,furan-2,5-dione,hexanedioic acid
3-(1H-Indol-3-YL)-4-(1-{2-[(2S)-1-methylpyrrolidinyl]ethyl}-1H-indol-3-YL)-1H-pyrrole-2,5-dione
3-(1h-Indol-3-Yl)-4-{1-[2-(1-Methylpyrrolidin-2-Yl)ethyl]-1h-Indol-3-Yl}-1h-Pyrrole-2,5-Dione
beta-D-glucopyranosyl (6R)-6-[(3,6-dideoxy-alpha-L-arabino-hexopyranosyl)oxy]heptanoate
10-[2-(morpholin-4-yl)ethyl]-12-phenyl-10,12-dihydro-11H-benzo[5,6]chromeno[2,3-d]pyrimidin-11-imine
3-[2-(1-adamantyl)ethylsulfamoyl]-N-phenylbenzamide
9-(2-Morpholin-4-yl-ethyl)-7-phenyl-7,9-dihydro-12-oxa-9,11-diaza-benzo[a]anthracen-8-ylideneamine
(1R)-N-(2-fluorophenyl)-1-(hydroxymethyl)-7-methoxy-1-spiro[1,2,3,9-tetrahydropyrido[3,4-b]indole-4,4-piperidine]carboxamide
2-[3-[(2,6-Dimethylphenoxy)methyl]phenyl]-3-(2-furanylmethyl)-1,2-dihydroquinazolin-4-one
N-[(2R,3S,6R)-2-(hydroxymethyl)-6-[2-[4-(2-methoxyphenyl)-1-triazolyl]ethyl]-3-oxanyl]-2-pyrazinecarboxamide
N-[(2S,3S,6R)-2-(hydroxymethyl)-6-[2-[4-(2-methoxyphenyl)-1-triazolyl]ethyl]-3-oxanyl]-2-pyrazinecarboxamide
N-[(2S,3R,6S)-2-(hydroxymethyl)-6-[2-[4-(2-methoxyphenyl)-1-triazolyl]ethyl]-3-oxanyl]-2-pyrazinecarboxamide
N-[(2S,3S,6S)-2-(hydroxymethyl)-6-[2-[4-(2-methoxyphenyl)-1-triazolyl]ethyl]-3-oxanyl]-2-pyrazinecarboxamide
N-[(2R,3S,6S)-2-(hydroxymethyl)-6-[2-[4-(2-methoxyphenyl)triazol-1-yl]ethyl]oxan-3-yl]pyrazine-2-carboxamide
N-[(2R,3R,6R)-2-(hydroxymethyl)-6-[2-[4-(2-methoxyphenyl)-1-triazolyl]ethyl]-3-oxanyl]-2-pyrazinecarboxamide
N-[(2R,3S,6R)-2-(hydroxymethyl)-6-[2-(4-propan-2-yl-1-triazolyl)ethyl]-3-oxanyl]-4-methoxybenzenesulfonamide
N-[(2R,3R,6R)-2-(hydroxymethyl)-6-[2-(4-propan-2-yl-1-triazolyl)ethyl]-3-oxanyl]-4-methoxybenzenesulfonamide
N-[(2R,3S,6S)-2-(hydroxymethyl)-6-[2-(4-propan-2-yl-1-triazolyl)ethyl]-3-oxanyl]-4-methoxybenzenesulfonamide
N-[(2S,3R,6R)-2-(hydroxymethyl)-6-[2-[4-(2-methoxyphenyl)-1-triazolyl]ethyl]-3-oxanyl]-2-pyrazinecarboxamide
N-[(2R,3R,6S)-2-(hydroxymethyl)-6-[2-[4-(2-methoxyphenyl)-1-triazolyl]ethyl]-3-oxanyl]-2-pyrazinecarboxamide
N-[(2S,3R,6S)-2-(hydroxymethyl)-6-[2-(4-propan-2-yl-1-triazolyl)ethyl]-3-oxanyl]-4-methoxybenzenesulfonamide
N-[(2S,3S,6S)-2-(hydroxymethyl)-6-[2-(4-propan-2-yl-1-triazolyl)ethyl]-3-oxanyl]-4-methoxybenzenesulfonamide
N-[(2S,3R,6R)-2-(hydroxymethyl)-6-[2-(4-propan-2-yl-1-triazolyl)ethyl]-3-oxanyl]-4-methoxybenzenesulfonamide
N-[(2S,3S,6R)-2-(hydroxymethyl)-6-[2-(4-propan-2-yl-1-triazolyl)ethyl]-3-oxanyl]-4-methoxybenzenesulfonamide
N-[(2R,3R,6S)-2-(hydroxymethyl)-6-[2-(4-propan-2-yl-1-triazolyl)ethyl]-3-oxanyl]-4-methoxybenzenesulfonamide
(1S)-N-(2-fluorophenyl)-1-(hydroxymethyl)-7-methoxy-1-spiro[1,2,3,9-tetrahydropyrido[3,4-b]indole-4,4-piperidine]carboxamide
(1R)-N-(4-fluorophenyl)-1-(hydroxymethyl)-7-methoxy-1-spiro[1,2,3,9-tetrahydropyrido[3,4-b]indole-4,4-piperidine]carboxamide
KT182
KT182 is a potent and selective inhibitor of α/β-hydrolase domain containing 6 (ABHD6), with an IC50 of 0.24 nM in Neuro2A cells[1].