Exact Mass: 366.13462680000004
Exact Mass Matches: 366.13462680000004
Found 119 metabolites which its exact mass value is equals to given mass value 366.13462680000004,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
4-[4-(Dimethylamino)phenylazo]benzoic acid N-succinimidyl ester
C19H18N4O4 (366.13279880000005)
Semilepidinoside B
Semilepidinoside B is found in brassicas. Semilepidinoside B is an alkaloid from the seeds of Lepidium sativum (garden cress). Alkaloid from the seeds of Lepidium sativum (garden cress). Semilepidinoside B is found in garden cress and brassicas.
7-beta-D-Glucopyranosyloxybutylidenephthalide
7-beta-D-Glucopyranosyloxybutylidenephthalide is found in herbs and spices. 7-beta-D-Glucopyranosyloxybutylidenephthalide is isolated from elicitor-treated cultures of Petroselinum crispum (parsley Isolated from elicitor-treated cultures of Petroselinum crispum (parsley). 7-Hydroxybutylidenephthalide 7-glucoside is found in herbs and spices.
1-(1,2,3,4,5-Pentahydroxypent-1-yl)-1,2,3,4-tetrahydro-beta-carboline-3-carboxylate
The novel carbohydrate-derived b-carboline, 1-pentahydroxypentyl-1,2,3,4-tetrahydro-b-carboline-3-carboxylic acid, was identified in fruit- and vegetable-derived products such as juices, jams, and tomato sauces. This compound occurred as two diastereoisomers, a cis isomer (the major compound) and a trans isomer, ranging from undetectable amounts to 6.5 ug/g. Grape, tomato, pineapple, and tropical juices exhibited the highest amount of this alkaloid (up to 3.8 mg/L), whereas apple, banana, and peach juices showed very low or nondetectable levels. This tetrahydro-b-carboline was also found in jams (up to 0.45 ug/g), and a relative high amount was present in tomato concentrate (6.5 ug/g) and sauce (up to 1.8 ug/g). This b-carboline occurred in fruit-derived products as a glycoconjugate from a chemical condensation of d-glucose and l-tryptophan that is highly favored at low pH values and high temperature. Production, processing treatments, and storage of fruit juices and jams can then release this b-carboline. Fruit-derived products and other foods containing this compound might be an exogenous dietary source of this glucose-derived tetrahydro-b-carboline.(PMID: 12137498).
C-glycosyltryptophan
Tryptophan 2-C-mannoside, also known as 2-alpha-D-mannopyranosyl-L-tryptophan or C-mannosyltryptophan, belongs to the class of organic compounds known as indolyl carboxylic acids and derivatives. Indolyl carboxylic acids and derivatives are compounds containing a carboxylic acid chain (of at least 2 carbon atoms) linked to an indole ring. It is an L-tryptophan derivative and a C-glycosyl compound in which the hydrogen at position 2 on the indole portion has been replaced by an alpha-mannosyl residue. Tryptophan 2-C-mannoside is a very strong basic compound (based on its pKa). Tryptophan 2-C-mannoside has been identified in blood and urine and is a marker of kidney function (PMID: 29234020).
2-(beta-D-Mannopyranosyl)-L-tryptophan
5,7-Dihydroxy-2-isopropylchromone-8-beta-D-glucoside
2-{2-[5-(ethoxycarbonyl)-2-morpholinoanilino]-2-oxoethoxy}acetic acid
6-deoxy-4-O-[(2E)-3-(4-methoxyphenyl)-1-oxoprop-2-en-1-yl]-alpha-L-mannopyranose 3-acetate|asiatiside A
3-(3,4-dihydro-4-oxoquinazolin-2-yl)propyl beta-D-glucopyranoside|pegamine beta-D-glucopyranoside
2-alpha-D-C-mannopyranosyl-L-tryptophan|2-alpha-D-mannopyranosyl-L-tryptophan|alpha-C-Mannosyltryptophan|C2-alpha-D-mannosylpyranosyl-L-tryptophan|C2-alpha-D-mannosylpyranosyltryptophan
(+)-(7S,8S)-1,4-dihydroxy-3,3,5-trimethoxy-7,8,9-trinor-8,4-oxyneolignan-7,9-diol
A lignan that consists of propane-1,3-diol substituted by a 4-hydroxy-3-methoxyphenyl substituent at position 1 and a 4-hydroxy-2,6-dimethoxyphenoxy substituent at position 2. It has been isolated from the stems of Sinocalamus affinis.
3-O-acetyl-2-O-p-methoxycinnamoyl-alpha-L-rhamnopyranose|ningposide D
6-deoxy-4-O-[(2E)-3-(4-methoxyphenyl)-1-oxoprop-2-en-1-yl]-alpha-L-mannopyranose 2-acetate|asiatiside D
Ser Ser Ser Ser
Tetrahydropentoxyline
A member of the class of beta-carbolines that is 2,3,4,9-tetrahydro-1H-beta-carboline in which a hydrogen at positions 1 and 3 have been replaced by a (5S)-D-arabinityl and carboxy groups, respectively. It is a metabolite found in human urine.
Semilepidinoside B
7-b-D-Glucopyranosyloxybutylidenephthalide
3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl 2-(prop-1-en-2-yl)-2,3-dihydrobenzofuran-5-carboxylate
1-(4-Methoxybenzyl)-6-((trimethylsilyl)ethynyl)-1H-pyrido[2,3-b][1,4]oxazin-2(3H)-one
C20H22N2O3Si (366.13996219999996)
1-(1,4-DIHYDROXY-3-PHENYLNAPHTHALEN-2-YL)-3-PHENYLPROP-2-EN-1-ONE
3-[(2,4-dihydro-2,4-dimethyl-3H-1,2,4-triazol-3-ylidene)hydrazono]-1-methyl-2-phenyl-3H-indolium chloride
(1S,2S)-(+)-N-(4-Toluenesulfonyl)-1,2-Diphenylethylenediamine
N-((1R,2R)-2-Amino-1,2-diphenylethyl)-4-methylbenzenesulfonamide
3-(3-BIPHENYL-4-YL-1-PHENYL-1H-PYRAZOL-4-YL)-ACRYLIC ACID
C24H18N2O2 (366.13682079999995)
(1R,5R,7S,8S)-7-(Acetyloxy)-8-(phenylmethoxy)-3,6-dioxabicyclo[3.2.1]octane-5-methanol 5-acetate
ETHYL 7-((4-CHLORO-7-METHOXYQUINAZOLIN-6-YL)OXY)HEPTANOATE
C18H23ClN2O4 (366.13462680000004)
Rovatirelin
C16H22N4O4S (366.13616920000004)
C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C76367 - Thyrotropin-Releasing Hormone Analogue D000890 - Anti-Infective Agents > D023303 - Oxazolidinones
1-(Phenethylamino)-3H-naphtho[1,2,3-de]quinoline-2,7-dione
C24H18N2O2 (366.13682079999995)
BRD7389 is a specific RSK family kinase inhibitor with IC50s of 1.5 μM, 2.4 μM, and 1.2 μM for RSK1, RSK2, and RSK3, respectively. BRD7389 is a small-molecule inducer of insulin expression in pancreatic α-cells[1].
N-[2-(4-methylphenoxy)-1-oxoethyl]-2-(5-phenyl-2-tetrazolyl)acetohydrazide
1alpha,5alpha-Epidithio-17a-oxa-D-homoandrostan-3,17-dione
(2,5-Dimethylbenzene-1,4-Diyl)dimethanediyl Bis(N-Carbamimidoylcarbamimidothioate)
(1R)-1,5-anhydro-1-{3-[(2S)-2-azaniumyl-2-carboxylatoethyl]-1H-indol-2-yl}-D-mannitol
tryptophan N-glucoside
A L-tryptophan derivative that is L-tryptophan in which the hydrogen attached to the indole nitrogen replaced by a beta-D-glucosyl residue.
1-(2-Furanylmethyl)-7,7-dimethyl-2-(4-methylphenyl)-5,8-dihydropyrano[4,3-d]pyrimidine-4-thione
N-(2,6-dimethylphenyl)-2-[(6-methoxy-2-methyl-4-quinolinyl)thio]acetamide
13-(pyridin-3-ylmethyl)-11,15-dihydro-9H-9,10-[3,4]epipyrroloanthracene-12,14(10H,13H)-dione
C24H18N2O2 (366.13682079999995)
Ethyl 2-[5-hydroxy-4-(trifluoromethyl)biphenyl-3-yl]pentanoate
C20H21F3O3 (366.14427120000005)
6-{[5-(p-Nitrophenoxy)-5-oxopentanoyl]amino}hexanoic acid
(2S)-4-(1H-indol-3-yl)-2-({[(3S,4S,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl}amino)butanoic acid
2,6-Bis(methylphenylsilyl)naphthalene
C24H22Si2 (366.12599720000003)
2,7-Bis(methylphenylsilyl)naphthalene
C24H22Si2 (366.12599720000003)
1,4-Bis(methylphenylsilyl)naphthalene
C24H22Si2 (366.12599720000003)
1,5-Bis[methyl(phenyl)silyl]naphthalene
C24H22Si2 (366.12599720000003)
2-alpha-mannosyl-L-tryptophan
A C-glycosyl compound that is L-tryptophan in which the hydrogen at position 2 on the indole protion has been replaced by an alpha-mannosyl residue.
1-(1,2,3,4,5-Pentahydroxypent-1-yl)-1,2,3,4-tetrahydro-beta-carboline-3-carboxylate
beta-D-galactosyl-(1->3)-N-acetyl-D-galactosaminyl group
2-alpha-mannosyl-L-tryptophan zwitterion
An L-alpha-amino acid zwitterion that is 2-alpha-mannosyl-L-tryptophan in which a proton has been transferred from the carboxy group to the amino group. It is the major species at pH 7.3.
ML327
C19H18N4O4 (366.13279880000005)
ML327 is a blocker of MYC which can also de-repress E-cadherin transcription and reverse Epithelial-to-Mesenchymal Transition (EMT).
methyl (2r)-3-[(1r)-6-ethyl-1,5-dihydroxy-2,7-dimethoxy-4-oxonaphthalen-1-yl]-2-hydroxypropanoate
(2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-[4-(1h-imidazol-2-ylmethyl)-2-methoxyphenoxy]oxane-3,4,5-triol
methyl (2r,4r)-4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoate
(3as,4r,6ar)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-hydroxy-tetrahydrocyclopenta[c]furan-1-one
3-(acetyloxy)-2,5-dihydroxy-6-methyloxan-4-yl 3-(4-methoxyphenyl)prop-2-enoate
(2s,3r,4s,5s,6r)-2-[(2-hydroxy-3-methoxy-8-methylnaphthalen-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
(3ar,4s,6as)-6a-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3a-(dimethoxymethyl)-4-hydroxy-tetrahydrocyclopenta[c]furan-1-one
2-{[(1r,5r,6s)-4,5-dihydroxy-6-methoxy-3,6-dimethyl-2-oxocyclohex-3-en-1-yl]oxy}-4-hydroxy-3,6-dimethylbenzoic acid
2,5-bis(acetyloxy)-8-[(2z)-5-oxofuran-2-ylidene]oct-6-en-3-yl acetate
(2s,3r,4r,5r,6r)-5-(acetyloxy)-4,6-dihydroxy-2-methyloxan-3-yl (2e)-3-(4-methoxyphenyl)prop-2-enoate
(2r,3r,4r,5s,6s)-4-(acetyloxy)-2,5-dihydroxy-6-methyloxan-3-yl (2e)-3-(4-methoxyphenyl)prop-2-enoate
5-(acetyloxy)-4,6-dihydroxy-2-methyloxan-3-yl 3-(4-methoxyphenyl)prop-2-enoate
4-(acetyloxy)-5,6-dihydroxy-2-methyloxan-3-yl 3-(4-methoxyphenyl)prop-2-enoate
(2r,3r,4r,5s,6s)-3-(acetyloxy)-2,5-dihydroxy-6-methyloxan-4-yl (2z)-3-(4-methoxyphenyl)prop-2-enoate
2-[(2-hydroxy-3-methoxy-8-methylnaphthalen-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
(2s,3r,4s,5s,6r)-2-[(1-hydroxy-3-methoxy-8-methylnaphthalen-2-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
(2s,3r,5s,6z)-2,5-bis(acetyloxy)-8-[(2e)-5-oxofuran-2-ylidene]oct-6-en-3-yl acetate
{16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁵,²⁰]henicosa-1,4(8),9,14,16,18,20-heptaen-3-ylidene}(methyl)oxidanium
[C21H20NO5]+ (366.13414100000006)