Exact Mass: 346.225631
Exact Mass Matches: 346.225631
Found 119 metabolites which its exact mass value is equals to given mass value 346.225631
,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
(-)-Chimonanthine
(-)-chimonanthine is the (3aS,3aS,8aS,8aS)-stereoisomer of chimonanthine. It is an enantiomer of a (+)-chimonanthine. (-)-Chimonanthine is a natural product found in Eumachia forsteriana, Chimonanthus praecox, and Idiospermum australiense with data available. meso-Chimonanthine is found in herbs and spices. meso-Chimonanthine is an alkaloid from Calycanthus floridus (Carolina allspice
(+)-Calycanthine
(+)-Calycanthine is found in herbs and spices. (+)-Calycanthine is an alkaloid from Calycanthus floridus (Carolina allspice) and other Calycanthus specie Calycanthine, the principal alkaloid of the order Calycanthaceae, has been isolated from a species of the genus Psychotria, and is a central nervous system toxin, causing convulsions[1][2]. Calycanthine, the principal alkaloid of the order Calycanthaceae, has been isolated from a species of the genus Psychotria, and is a central nervous system toxin, causing convulsions[1][2].
Sorbitan laurate
Sorbitan laurate is a food emulsifier, solubiliser, crystallisation retarder, dough improver, antifoam agent, stabilise Food emulsifier, solubiliser, crystallisation retarder, dough improver, antifoam agent, stabiliser
21-Fluoro-16-ethyl-19-norprogesterone
C22H31FO2 (346.23079579999995)
Calycanthine
Calycanthine is the principal alkaloid of the plant family Calycanthaceae. It is a calycanthaceous alkaloid, an aminal and an organonitrogen heterocyclic compound. It derives from a hydride of a calycanine. Calycanthine is a natural product found in Chimonanthus praecox, Idiospermum australiense, and other organisms with data available. The principal alkaloid of the plant family Calycanthaceae. Annotation level-1 Calycanthine, the principal alkaloid of the order Calycanthaceae, has been isolated from a species of the genus Psychotria, and is a central nervous system toxin, causing convulsions[1][2]. Calycanthine, the principal alkaloid of the order Calycanthaceae, has been isolated from a species of the genus Psychotria, and is a central nervous system toxin, causing convulsions[1][2].
N-methyl-1-[(3aS,8aR)-2,3,8,8a-tetrahydro-1-methylpyrrol[2,3-b]indol-3a(1H)-yl]-1Hindole-3-ethanamine|psychohenin|psychotriasine|rel-N-methyl-1-[(3aR,8aS)-2,3,8,8a-tetrahydro-1-methylpyrrolo[2,3-b]indol-3a(1H)-yl]-1H-indole-3-ethanamine
(-)-(6Xi,7Xi)-13-((1S,2Xi,3Xi)-2,3-dihydroxy-cyclopentyl)-6,7-dihydroxy-tridecanoic acid ; tetrahydroxy-dihydro-chaulmoogric acid|(-)-(6Xi,7Xi)-13-((1S,2Xi,3Xi)-2,3-Dihydroxy-cyclopentyl)-6,7-dihydroxy-tridecansaeure; Tetrahydroxy-dihydro-chaulmoograsaeure|7.8-Dihydroxy-1-(2.3-dihydroxy-cyclopentyl)-tridecansaeure-(13)
2-methyl-6-methylene-n-decan-2-olyl-beta-D-glucopyranoside|2-methyl-6-methylene-n-decan-2-yl-beta-D-glucopyranoside|malvanoyl glucoside
11beta-Hydroxy-3alpha-ureido-androst-4-en-17-on|Ureasteron
Chimonanthine
A ring assembly that is 2,2,3,3,8,8,8a,8a-octahydro-1H,1H-3a,3a-bipyrrolo[2,3-b]indole substituted by methyl groups at positions 1 and 1.
9-hydroperoxy-12,13-dihydroxy-10-octadecenoic acid
9,10-dihydroxy-13-hydroperoxy-11-octadecenoic acid
ascr#20
An (omega-1)-hydroxy fatty acid ascaroside obtained by formal condensation of the alcoholic hydroxy group of (11R)-11-hydroxylauric acid with ascarylopyranose (the alpha anomer). It is a metabolite of the nematode Caenorhabditis elegans.
oscr#20
An omega-hydroxy fatty acid ascaroside obtained by formal condensation of the alcoholic hydroxy group of 12-hydroxydodecanoic acid with ascarylopyranose (the alpha anomer). It is a metabolite of the nematode Caenorhabditis elegans.
trans,trans-4-Fluorophenyl 4-propylbicyclohexyl-4-carboxylate
C22H31FO2 (346.23079579999995)
octadecadienyl dihydrogen phosphate
C18H35O4P (346.22728400000005)
1-[(4-Ethoxyphenyl)ethynyl]-4-(4-propylcyclohexyl)benzene
trans-1-Ethoxy-4-(2-(4-(4-propylcyclohexyl)phenyl)ethynyl)benzene
TRANS-1-(2-(4-(4-BUTYLCYCLOHEXYL)PHENYL)ETHYNYL)-4-METHOXYBENZENE
1,3-Propanediamine,N3-(1,2-diphenylethyl)-N1,N1-diethyl-, hydrochloride (1:2)
(11R)-11-[(3,6-dideoxy-alpha-L-arabino-hexopyranosyl)oxy]dodecanoic acid
12-[(3,6-dideoxy-alpha-L-arabino-hexopyranosyl)oxy]dodecanoic acid
CHEBI:38953
[(4R)-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] (E)-2-methylbut-2-enoate
[3-Carboxy-2-(9-carboxynonanoyloxy)propyl]-trimethylazanium
[3-Carboxy-2-(8-carboxy-3-methyloctanoyl)oxypropyl]-trimethylazanium
N-methyl-2-(4-methylphenyl)-N-(1-methylpiperidin-4-yl)quinazolin-4-amine
[(2R)-3-carboxy-2-(9-carboxynonanoyloxy)propyl]-trimethylazanium
(3aS,8bS)-8b-[(3aS,8bS)-3-methyl-1,2,3a,4-tetrahydropyrrolo[2,3-b]indol-8b-yl]-3-methyl-1,2,3a,4-tetrahydropyrrolo[2,3-b]indole
(-)-chimonanthine is the (3aS,3aS,8aS,8aS)-stereoisomer of chimonanthine. It is an enantiomer of a (+)-chimonanthine. (-)-Chimonanthine is a natural product found in Eumachia forsteriana, Chimonanthus praecox, and Idiospermum australiense with data available. The (3aS,3aS,8aS,8aS)-stereoisomer of chimonanthine.