Exact Mass: 410.1351
Exact Mass Matches: 410.1351
Found 258 metabolites which its exact mass value is equals to given mass value 410.1351
,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Lactupicrin
Lactucopicrin is an azulenofuran, a cyclic terpene ketone, an enone, a member of phenols, a sesquiterpene lactone and a primary alcohol. It has a role as a plant metabolite, a sedative and an antimalarial. It is functionally related to a 4-hydroxyphenylacetic acid and a lactucin. Lactupicrin is a natural product found in Cichorium endivia, Cichorium spinosum, and other organisms with data available. Constituent of Lactuca sativa (lettuce), Cichorium intybus (chicory) and Cichorium endivia (endive). Lactupicrin is found in many foods, some of which are endive, romaine lettuce, chicory, and lettuce. Lactupicrin is found in chicory. Lactupicrin is a constituent of Lactuca sativa (lettuce), Cichorium intybus (chicory) and Cichorium endivia (endive) Lactupicrin (Lactucopicrin) is a characteristic bitter sesquiterpene lactone that can relieve pain. Lactupicrin exhibits atheroprotective effect[1][2]. Lactupicrin (Lactucopicrin) is a characteristic bitter sesquiterpene lactone that can relieve pain. Lactupicrin exhibits atheroprotective effect[1][2].
Tephrosin
Tephrosin is a member of the class of rotenones that is 13,13a-dihydro-3H-chromeno[3,4-b]pyrano[2,3-h]chromen-7(7aH)-one substituted with geminal methyl groups at position 3, hydroxy group at position 7a and methoxy groups at positions 9 and 10 (the 7aR,13aR stereoisomer). It is isolated from the leaves and twigs of Antheroporum pierrei and exhibits antineoplastic and pesticidal activities. It has a role as a pesticide, an antineoplastic agent and a metabolite. It is an organic heteropentacyclic compound, an aromatic ether, a cyclic ketone and a member of rotenones. Tephrosin is a natural product found in Millettia ferruginea, Tephrosia vogelii, and other organisms with data available. A member of the class of rotenones that is 13,13a-dihydro-3H-chromeno[3,4-b]pyrano[2,3-h]chromen-7(7aH)-one substituted with geminal methyl groups at position 3, hydroxy group at position 7a and methoxy groups at positions 9 and 10 (the 7aR,13aR stereoisomer). It is isolated from the leaves and twigs of Antheroporum pierrei and exhibits antineoplastic and pesticidal activities.
(-)-cis-Rotenolone
(-)-cis-Rotenolone is found in jicama. (-)-cis-Rotenolone is isolated from Pachyrrhizus erosus (yam bean). Isolated from Pachyrrhizus erosus (yam bean). (-)-cis-Rotenolone is found in jicama and pulses.
(5a,6a,8a,11a)-8-Hydroxy-2-oxo-1(10),3-guaiadien-12,6-olide-15-al 8-(4-hydroxyphenylacetate)
(5a,6a,8a,11a)-8-Hydroxy-2-oxo-1(10),3-guaiadien-12,6-olide-15-al 8-(4-hydroxyphenylacetate) is found in coffee and coffee products. (5a,6a,8a,11a)-8-Hydroxy-2-oxo-1(10),3-guaiadien-12,6-olide-15-al 8-(4-hydroxyphenylacetate) is a constituent of Cichorium intybus (chicory). Constituent of Cichorium intybus (chicory). (5a,6a,8a,11a)-8-Hydroxy-2-oxo-1(10),3-guaiadien-12,6-olide-15-al 8-(4-hydroxyphenylacetate) is found in coffee and coffee products, herbs and spices, and green vegetables.
Epicocconone
Phenobarbital N-glucoside
Cratoxyarborenone D
An organic heterotetracyclic compound that is 2,3-dihydro-5H-furo[3,2-b]xanthen-5-one substituted by hydroxy groups at positions 4, 7, 8 and 9, an isoprenyl group at position 6 and a prop-1-en-2-yl group at position 2. It is isolated from Cratoxylum Sumatranum and exhibits cytotoxicity towards the KB (human oral epidermoid) cancer cell line. Cratoxyarborenone D has been reported in Cratoxylum and Cratoxylum sumatranum
Amorphispironone
Velloquercetin 3,5,3-trimethyl ether
brasixanthone C
A member of the class of pyranoxanthones that is 2H,6H-pyrano[3,2-b]xanthen-6-one substituted by a 2-hydroperoxy-3-methylbut-3-en-1-yl moiety at position 12, hydroxy groups at positions 5 and 8 and geminal methyl groups at position 2. It is isolated from the stem bark of Calophyllum brasiliense and exhibits significant inhibitory activity against 12-O-tetradecanoylphorbol-13-acetate induced Epstein-Barr virus early antigen activation in Raji cells.
Toxicarolisoflavone
Toxicarolisoflavone is a natural product found in Derris montana, Derris ovalifolia, and other organisms with data available.
Amorphigenin
Origin: Plant, Pyrans relative retention time with respect to 9-anthracene Carboxylic Acid is 1.086 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.088
Pongapinone A
(6S*,9aS*)-5,6-dihydro-3-[(1Z,4E,6E,8E)-1-hydroxy-3-oxo-1,4,6,8-decatetraenyl]-6-hydroxymethyl-9a-methyl-2H-furo[3,2-g]benzopyran-2-9(9H)-dione|epicocconone
4alpha-(2,4-dihydroxy-3-methoxyphenyl)-(-)-fisetinidol
3,4,8-Tri-Me ether-5,10-Dihydroxy-8-(3,4-dihydroxyphenyl)-2,2-dimethyl-2H,6H-benzo[1,2-b:5,4-b]dipyran-6-one
2,2-Dimethyl-5,8-dihydroxy-12-[hydroxy(3,3-dimethyloxiranyl)methyl]-2H,6H-pyrano[3,2-b]xanthene-6-one
(Rac)-Tephrosin
(1R,14R)-14-Hydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.0^{3,12.0^{4,9.0^{15,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one is a member of rotenones. (1R,14R)-14-hydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.0^{3,12.0^{4,9.0^{15,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one is a natural product found in Millettia ferruginea, Derris trifoliata, and other organisms with data available.
(2s,6as,12as)-6a-hydroxy-8,9-dimethoxy-2-(prop-1-en-2-yl)-1,2,12,12a-tetrahydrochromeno[3,4-b]furo[2,3-h]chromen-6(6ah)-one
Lactucopicrin
Lactupicrin (Lactucopicrin) is a characteristic bitter sesquiterpene lactone that can relieve pain. Lactupicrin exhibits atheroprotective effect[1][2]. Lactupicrin (Lactucopicrin) is a characteristic bitter sesquiterpene lactone that can relieve pain. Lactupicrin exhibits atheroprotective effect[1][2].
Ala Cys Met Ser
Ala Cys Ser Met
Ala Met Cys Ser
Ala Met Ser Cys
Ala Ser Cys Met
Ala Ser Met Cys
Cys Ala Met Ser
Cys Ala Ser Met
Cys Cys Ser Val
Cys Cys Val Ser
Cys Gly Met Thr
Cys Gly Thr Met
Cys Met Ala Ser
Cys Met Gly Thr
Cys Met Ser Ala
Cys Met Thr Gly
Cys Ser Ala Met
Cys Ser Cys Val
Cys Ser Met Ala
Cys Ser Val Cys
Cys Thr Gly Met
Cys Thr Met Gly
Cys Val Cys Ser
Cys Val Ser Cys
Asp Gly Gly Tyr
Asp Gly Tyr Gly
Asp Tyr Gly Gly
Gly Cys Met Thr
Gly Cys Thr Met
Gly Asp Gly Tyr
Gly Asp Tyr Gly
Gly Gly Asp Tyr
Gly Gly Tyr Asp
Gly Met Cys Thr
Gly Met Thr Cys
Gly Thr Cys Met
Gly Thr Met Cys
Gly Tyr Asp Gly
Gly Tyr Gly Asp
Met Ala Cys Ser
Met Ala Ser Cys
Met Cys Ala Ser
Met Cys Gly Thr
Met Cys Ser Ala
Met Cys Thr Gly
Met Gly Cys Thr
Met Gly Thr Cys
Met Ser Ala Cys
Met Ser Cys Ala
Met Thr Cys Gly
Met Thr Gly Cys
Ser Ala Cys Met
Ser Ala Met Cys
Ser Cys Ala Met
Ser Cys Cys Val
Ser Cys Met Ala
Ser Cys Val Cys
Ser Met Ala Cys
Ser Met Cys Ala
Ser Val Cys Cys
Thr Cys Gly Met
Thr Cys Met Gly
Thr Gly Cys Met
Thr Gly Met Cys
Thr Met Cys Gly
Thr Met Gly Cys
Val Cys Cys Ser
Val Cys Ser Cys
Val Ser Cys Cys
Tyr Asp Gly Gly
Tyr Gly Asp Gly
Tyr Gly Gly Asp
(5a,6a,8a,11a)-8-Hydroxy-2-oxo-1(10),3-guaiadien-12,6-olide-15-al 8-(4-hydroxyphenylacetate)
Solabegron
C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C87053 - Adrenergic Agonist D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D000322 - Adrenergic Agonists Solabegron (GW 427353) is a selective β3-adrenergic receptor agonist, stimulating cAMP accumulation in Chinese hamster ovary cells expressing the human β3-AR, with an EC50 value of 22 nM[1]. Solabegron (GW 427353) is being developed for the treatment of overactive bladder and irritable bowel syndrome[1].
Epicocconone
D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D049408 - Luminescent Agents D004396 - Coloring Agents > D005456 - Fluorescent Dyes
6-(2,5-dimethoxyphenyl)-3-(3-propan-2-yloxyphenyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine
N-[4-(1H-benzimidazol-2-yl)phenyl]-3-(2,5-dioxo-1-pyrrolidinyl)benzamide
(1)Benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(6aH)-one,1,2,12,12a-tetrahydro-6a-hydroxy-8,9-dimethoxy-2-(1-methylethenyl)-, (2S-(2alpha,6aalpha,12aalpha))-
1-(4-methylbenzenesulfonyl)-4-(5-phenyl-1H-pyrazole-3-carbonyl)piperazine
14-Hydroxy-17,18-dimethoxy-6,6-dimethyl-2,8,21-trioxahexacyclo[12.8.0.03,12.04,9.05,7.015,20]docosa-3(12),4(9),10,15,17,19-hexaen-13-one
5-Ethyl-5-phenyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3-diazinane-2,4,6-trione
6-(hydroxymethyl)-3-[(1Z,4E,6E,8E)-1-hydroxy-3-oxodeca-1,4,6,8-tetraenyl]-9a-methyl-5,6-dihydrofuro[3,2-g]isochromene-2,9-dione
N-[3-(4-methyl-1-piperidinyl)-1,4-dioxo-2-naphthalenyl]benzenesulfonamide
N-{2-[(2E)-2-(3,4-dimethoxybenzylidene)hydrazinyl]-4-(4-methylphenyl)-1,3-thiazol-5-yl}acetamide
Lactopicrin
Lactucopicrin is an azulenofuran, a cyclic terpene ketone, an enone, a member of phenols, a sesquiterpene lactone and a primary alcohol. It has a role as a plant metabolite, a sedative and an antimalarial. It is functionally related to a 4-hydroxyphenylacetic acid and a lactucin. Lactupicrin is a natural product found in Cichorium endivia, Cichorium spinosum, and other organisms with data available. Lactupicrin (Lactucopicrin) is a characteristic bitter sesquiterpene lactone that can relieve pain. Lactupicrin exhibits atheroprotective effect[1][2]. Lactupicrin (Lactucopicrin) is a characteristic bitter sesquiterpene lactone that can relieve pain. Lactupicrin exhibits atheroprotective effect[1][2].
7-(4-hydroxy-3-methoxyphenyl)-4,6-dimethoxy-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one
(4r,8s)-18-hydroxy-15-(3-hydroxy-3-methylbutyl)-2-methoxy-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1,3(10),5,11,14,16,18-heptaen-20-one
(2r)-7-(4-hydroxy-3-methoxyphenyl)-4,6-dimethoxy-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one
(6-acetyl-7-hydroxy-2-methylchromen-2-yl)methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
22-hydroxy-6,7-dimethoxy-18,18-dimethyl-10,13,17-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁶,²¹]docosa-1(14),4(9),5,7,15,19,21-heptaen-2-one
(1s,6s,13s,21s)-21-hydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one
12alpha-hudroxyrotenone
{"Ingredient_id": "HBIN000704","Ingredient_name": "12alpha-hudroxyrotenone","Alias": "NA","Ingredient_formula": "C23H22O7","Ingredient_Smile": "CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "31268","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
12α-hydroxyrotenone
{"Ingredient_id": "HBIN000713","Ingredient_name": "12\u03b1-hydroxyrotenone","Alias": "NA","Ingredient_formula": "C23H22O7","Ingredient_Smile": "CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "10679","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
1,3,7,8-tetrahydroxy xanthones
{"Ingredient_id": "HBIN001106","Ingredient_name": "1,3,7,8-tetrahydroxy xanthones","Alias": "NA","Ingredient_formula": "C23H22O7","Ingredient_Smile": "CC(=CCC1=C2C(=C(C(=C1O)O)O)OC3=CC4=C(CC(O4)C(=C)C)C(=C3C2=O)O)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "43025","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
anticancer flavonoid pmv70p691-105
{"Ingredient_id": "HBIN016333","Ingredient_name": "anticancer flavonoid pmv70p691-105","Alias": "NA","Ingredient_formula": "C23H22O7","Ingredient_Smile": "CC1(C=CC2=C(C(=C(C=C2O1)OC)C(=O)C=C(C3=CC4=C(C=C3)OCO4)O)OC)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "1408","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}