Exact Mass: 530.2125
Exact Mass Matches: 530.2125
Found 225 metabolites which its exact mass value is equals to given mass value 530.2125
,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Gomisin D
Gomisin D is a natural product found in Schisandra chinensis with data available. Gomisin D, a lignan compound isolated from Fructus Schisandra, is a potential antidiabetic and anti-Alzheimer’s agent. Gomisin D inhibits UDP-Glucuronosyltransferases activity and scavenges ABTS(+) radicals. Gomisin D is used as a quality marker of Shengmai San and shenqi Jiangtang Granule[1]. Gomisin D, a lignan compound isolated from Fructus Schisandra, is a potential antidiabetic and anti-Alzheimer’s agent. Gomisin D inhibits UDP-Glucuronosyltransferases activity and scavenges ABTS(+) radicals. Gomisin D is used as a quality marker of Shengmai San and shenqi Jiangtang Granule[1].
7-Acetoxy-6-hydroxylimonin
7-Acetoxy-6-hydroxylimonin is found in herbs and spices. 7-Acetoxy-6-hydroxylimonin is a constituent of Ruta graveolens (rue). Constituent of Ruta graveolens (rue). 7-Acetoxy-6-hydroxylimonin is found in herbs and spices.
Peliglitazar
Gomisin
Gomisin D is a natural product found in Schisandra chinensis with data available. Gomisin D, a lignan compound isolated from Fructus Schisandra, is a potential antidiabetic and anti-Alzheimer’s agent. Gomisin D inhibits UDP-Glucuronosyltransferases activity and scavenges ABTS(+) radicals. Gomisin D is used as a quality marker of Shengmai San and shenqi Jiangtang Granule[1]. Gomisin D, a lignan compound isolated from Fructus Schisandra, is a potential antidiabetic and anti-Alzheimer’s agent. Gomisin D inhibits UDP-Glucuronosyltransferases activity and scavenges ABTS(+) radicals. Gomisin D is used as a quality marker of Shengmai San and shenqi Jiangtang Granule[1].
(2R,3R),(2S,3S)-2,3-divanillyl-1,4-butandiol tetraacetate|Secoisolarcinoltetraacetat|Tetra-Ac-Secoisolariciresinol
Taiwanschirin D
An organic heterotetracyclic compound isolated from the stems of Kadsura matsudai.
{6-O-[(4-oxo-4H-pyran-3-yloxy)-O-beta?D-glucopyranosyl]}-4-hydroxy-3,5-bis(3-methyl-2-butenyl)benzoate
Ala Phe Met Tyr
Ala Phe Tyr Met
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Phe Ala Met Tyr
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Phe Cys Val Tyr
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Phe Phe Met Ser
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Phe Met Phe Ser
Phe Met Ser Phe
Phe Met Tyr Ala
Phe Ser Phe Met
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Phe Val Cys Tyr
Phe Val Tyr Cys
Phe Tyr Ala Met
Phe Tyr Cys Val
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His Asp Pro Tyr
His Asp Tyr Pro
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Met Ala Phe Tyr
Met Ala Tyr Phe
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Met Phe Phe Ser
Met Phe Ser Phe
Met Phe Tyr Ala
Met Ser Phe Phe
Met Tyr Ala Phe
Met Tyr Phe Ala
Asn Asp Pro Trp
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Ser Phe Phe Met
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Val Cys Phe Tyr
Val Cys Tyr Phe
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Trp Asp Asn Pro
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Tyr Ala Phe Met
Tyr Ala Met Phe
Tyr Cys Phe Val
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Tyr Asp Pro His
Tyr Phe Ala Met
Tyr Phe Cys Val
Tyr Phe Met Ala
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7-Acetoxy-6-hydroxylimonin
2-(chloromethyl)oxirane,formaldehyde,4-[2-(4-hydroxyphenyl)propan-2-yl]phenol,2-methylprop-2-enoic acid,phenol
AC480 (BMS-599626)
C274 - Antineoplastic Agent > C2189 - Signal Transduction Inhibitor > C129824 - Antineoplastic Protein Inhibitor C274 - Antineoplastic Agent > C163758 - Targeted Therapy Agent > C163952 - EGFR-targeting Agent C471 - Enzyme Inhibitor > C1404 - Protein Kinase Inhibitor > C1967 - Tyrosine Kinase Inhibitor C471 - Enzyme Inhibitor > C129825 - Antineoplastic Enzyme Inhibitor
1-(5-O-(DIMETHOXYTRITYL)-BETA-D-2-DEOXYRIBOFURANOSYL)-3-NITROPYRROLE
5-O-(4,4-Dimethoxytrityl)-2-deoxyuridine
5'-O-(4,4'-Dimethoxytrityl)-2'-deoxyuridine (5'-O-DMT-dU) is a competitive inhibitor of E. coli dUTP nucleotidohydrolase (dUTPase), with the Ki higher than 1000 μM. 5'-O-(4,4'-Dimethoxytrityl)-2'-deoxyuridine can be used in machine-assisted DNA synthesis by synthesizing nucleosidic phosphoramidite blocks[1][2].
[(2R)-2-hexanoyloxy-3-[hydroxy-[(2S,3S,5R,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphoryl]oxypropyl] hexanoate
13-Dihydrodaunorubicin(1+)
An organic cation that is the conjugate acid of 13-dihydrodaunorubicin, obtained by protonation of the primary amino function.
Ananolignan G
A lignan with a dibenzocyclooctadiene skeleton isolated from Kadsura ananosma.