Exact Mass: 810.179497

Exact Mass Matches: 810.179497

Found 17 metabolites which its exact mass value is equals to given mass value 810.179497, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Inositol nicotinate

2,3,4,5,6-pentakis(pyridine-3-carbonyloxy)cyclohexyl pyridine-3-carboxylate

C42H30N6O12 (810.192162)


C - Cardiovascular system > C04 - Peripheral vasodilators > C04A - Peripheral vasodilators > C04AC - Nicotinic acid and derivatives C78276 - Agent Affecting Digestive System or Metabolism > C29703 - Antilipidemic Agent > C98151 - Niacin-based Antilipidemic Agent D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents

   

Inositol nicotinate,BAN,INN

Inositol nicotinate,BAN,INN

C42H30N6O12 (810.192162)


   
   

Inositol niacinate

inositol nicotinate

C42H30N6O12 (810.192162)


C - Cardiovascular system > C04 - Peripheral vasodilators > C04A - Peripheral vasodilators > C04AC - Nicotinic acid and derivatives C78276 - Agent Affecting Digestive System or Metabolism > C29703 - Antilipidemic Agent > C98151 - Niacin-based Antilipidemic Agent D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents

   

Liensinine diperchlorate

4-[[(1R)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2-[[(1R)-1-[(4-hydroxyphenyl)methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-yl]oxy]phenol;perchloric acid

C37H44Cl2N2O14 (810.2169464000001)


Liensinine Diperchlor?ate is a major isoquinoline alkaloid, extracted from the seed embryo of Nelumbo nucifera Gaertn. Liensinine Diperchlor?ate inhibits late-stage autophagy/mitophagy through blocking autophagosome-lysosome fusion. Liensinine Diperchlor?ate has a wide range of biological activities, including anti-arrhythmias, anti-hypertension, anti-pulmonary fibrosis, relaxation on vascular smooth muscle, etc[1]. Liensinine Diperchlor?ate is a major isoquinoline alkaloid, extracted from the seed embryo of Nelumbo nucifera Gaertn. Liensinine Diperchlor?ate inhibits late-stage autophagy/mitophagy through blocking autophagosome-lysosome fusion. Liensinine Diperchlor?ate has a wide range of biological activities, including anti-arrhythmias, anti-hypertension, anti-pulmonary fibrosis, relaxation on vascular smooth muscle, etc[1].

   

inositol nicotinate

Inositol hexanicotinate

C42H30N6O12 (810.192162)


   

CATECHIN PENTABENZOATE

CATECHIN PENTABENZOATE

C50H34O11 (810.2101014)


   

HEXAKIS((4-METHYLPHENYL)THIO)BENZENE 9&

HEXAKIS((4-METHYLPHENYL)THIO)BENZENE 9&

C48H42S6 (810.1610652)


   

hexakis(benzylthio)benzene

hexakis(benzylthio)benzene

C48H42S6 (810.1610652)


   
   

(2'r,3s)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(1e)-2-[(2'r,3s)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxo-2'h-3,3'-spirobi[[1]benzofuran]-4-yl]ethenyl]-2'h-3,3'-spirobi[[1]benzofuran]-2-one

(2'r,3s)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(1e)-2-[(2'r,3s)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxo-2'h-3,3'-spirobi[[1]benzofuran]-4-yl]ethenyl]-2'h-3,3'-spirobi[[1]benzofuran]-2-one

C45H30O15 (810.158463)


   

(2'r,3r)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(1e)-2-[(2's,3s)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxo-2'h-3,3'-spirobi[[1]benzofuran]-4-yl]ethenyl]-2'h-3,3'-spirobi[[1]benzofuran]-2-one

(2'r,3r)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(1e)-2-[(2's,3s)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxo-2'h-3,3'-spirobi[[1]benzofuran]-4-yl]ethenyl]-2'h-3,3'-spirobi[[1]benzofuran]-2-one

C45H30O15 (810.158463)


   

(2'r,3r)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(1e)-2-[(2'r,3r)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxo-2'h-3,3'-spirobi[[1]benzofuran]-4-yl]ethenyl]-2'h-3,3'-spirobi[[1]benzofuran]-2-one

(2'r,3r)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(1e)-2-[(2'r,3r)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxo-2'h-3,3'-spirobi[[1]benzofuran]-4-yl]ethenyl]-2'h-3,3'-spirobi[[1]benzofuran]-2-one

C45H30O15 (810.158463)


   

4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-{2-[4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxo-2'h-3,3'-spirobi[[1]benzofuran]-4-yl]ethenyl}-2'h-3,3'-spirobi[[1]benzofuran]-2-one

4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-{2-[4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxo-2'h-3,3'-spirobi[[1]benzofuran]-4-yl]ethenyl}-2'h-3,3'-spirobi[[1]benzofuran]-2-one

C45H30O15 (810.158463)


   

(2'r,3s)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(1e)-2-[(2'r,3r)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxo-2'h-3,3'-spirobi[[1]benzofuran]-4-yl]ethenyl]-2'h-3,3'-spirobi[[1]benzofuran]-2-one

(2'r,3s)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(1e)-2-[(2'r,3r)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxo-2'h-3,3'-spirobi[[1]benzofuran]-4-yl]ethenyl]-2'h-3,3'-spirobi[[1]benzofuran]-2-one

C45H30O15 (810.158463)


   

(2'r,3s)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(1e)-2-[(2's,3s)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxo-2'h-3,3'-spirobi[[1]benzofuran]-4-yl]ethenyl]-2'h-3,3'-spirobi[[1]benzofuran]-2-one

(2'r,3s)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(1e)-2-[(2's,3s)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxo-2'h-3,3'-spirobi[[1]benzofuran]-4-yl]ethenyl]-2'h-3,3'-spirobi[[1]benzofuran]-2-one

C45H30O15 (810.158463)


   

(2'r,3r)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(1e)-2-[(2'r,3s)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxo-2'h-3,3'-spirobi[[1]benzofuran]-4-yl]ethenyl]-2'h-3,3'-spirobi[[1]benzofuran]-2-one

(2'r,3r)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(1e)-2-[(2'r,3s)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxo-2'h-3,3'-spirobi[[1]benzofuran]-4-yl]ethenyl]-2'h-3,3'-spirobi[[1]benzofuran]-2-one

C45H30O15 (810.158463)