Exact Mass: 294.1358

Exact Mass Matches: 294.1358

Found 117 metabolites which its exact mass value is equals to given mass value 294.1358, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

UNII-TMB86QZP1J

2-[3-Ethyl-5-(4-methoxyphenyl)-1H-pyrazol-4-yl]phenol

C18H18N2O2 (294.1368)

WP 155

TRIAMIPHOS

C12H19N6OP (294.1358)

5,10-dihydro-9-dimethylallylphenazine-1-carboxylic acid

C18H18N2O2 (294.1368)

A member of the class of phenazines that is 5,10-dihydrophenazine substituted at positions 1 and 9 by carboxy and dimethylallyl groups respectively.

Ethyl (S)-3-hydroxybutyrate glucoside

Ethyl 3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanoic acid

C12H22O8 (294.1315)

Ethyl (S)-3-hydroxybutyrate glucoside is found in fruits. Ethyl (S)-3-hydroxybutyrate glucoside is a constituent of the fruit of mountain papaya Carica pubescens

Ginsenoyne B

10-chloroheptadeca-1,16-dien-4,6-diyne-3,9-diol

C17H23ClO2 (294.1386)

Ginsenoyne B is found in tea. Ginsenoyne B is present in ginseng root. Present in ginseng root. Ginsenoyne B is found in tea.

Nigellidine

6,7,8,9-Tetrahydro-1-hydroxy-11-(4-hydroxyphenyl)-3-methylpyridazino[1,2-a]indazol-5-ium inner salt, 9ci

C18H18N2O2 (294.1368)

Nigellidine is found in herbs and spices. Nigellidine is an alkaloid from seeds of Nigella sativa (black cumin). Alkaloid from seeds of Nigella sativa (black cumin). Nigellidine is found in herbs and spices.

4-[(E)-5,6-Dihydro-2,3'-bipyridin-3(4H)-ylidenemethyl]-3-methoxyphenol

3-methoxy-4-({3,4,5,6-tetrahydro-[2,3-bipyridine]-3-ylidene}methyl)phenol

C18H18N2O2 (294.1368)

Puromycin aminonucleoside

4-amino-2-[6-(dimethylamino)-9H-purin-9-yl]-5-(hydroxymethyl)oxolan-3-ol

C12H18N6O3 (294.144)

relative retention time with respect to 9-anthracene Carboxylic Acid is 0.738 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.734

Q63408720

C12H22O8 (294.1315)

C12H22O8

C12H22O8 (294.1315)

(3Z,9Z,12E)-7-acetoxy-6-chloropentadeca-3,9,12-trien-1-yne

C17H23ClO2 (294.1386)

3,6-dibenzylpiperazine-2,5-dione

C18H18N2O2 (294.1368)

(6R,7R)-3-cis,9-cis,12-cis,6-acetoxy,7-chloro-pentadeca-3,9,12-trien-1-yne|6(R),7(R)-3-cis-9-cis-12-cis-6-acetoxy-7-chloropentadeca-3,9,12-trien-1-yne

C17H23ClO2 (294.1386)

Stophanthobiose

C12H22O8 (294.1315)

2,2,6-Trimethyl-4-(acetoxymethyl)-5-(2-chloroethyl)indan

C17H23ClO2 (294.1386)

5-Hydroxy-4-methylpentansaeure-5-O-beta-glucosid|gamma-methyl-delta-hydroxy-pentanoic acid beta-D-glucopyranoside|gamma-Methyl-delta-hydroxy-pentansaeureglucosid

C12H22O8 (294.1315)

5-Ethyl-7,12-etheno-6,5-(iminoethano)-2,3,4,5-tetrahydro-1H-1-benzoazonine-2,13-dione

C18H18N2O2 (294.1368)

herdmanine H

C13H18N4O4 (294.1328)

Nigellidine

10-(4-hydroxyphenyl)-7-methyl-1H,2H,3H,4H-5000000,11000000$l^{5}-pyridazino[1,2-a]indazol-11-ylium-9-olate

C18H18N2O2 (294.1368)

Dicarboxyl-2Et-A4EO3

C12H22O8 (294.1315)

Literature spectrum; CONFIDENCE Tentative identification: isomers possible (Level 3); Could be alkyl homologue of given structure; Digitised from figure: approximate intensities

PHOP

1-oxazolo[4,5-b]pyridin-2-yl-6-phenyl-1-hexanone

C18H18N2O2 (294.1368)

Ethyl (S)-3-hydroxybutyrate glucoside

ethyl 3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanoate

C12H22O8 (294.1315)

Ginsenoyne B

10-chloroheptadeca-1,16-dien-4,6-diyne-3,9-diol

C17H23ClO2 (294.1386)

Ethyl 3-O-beta-D-glucopyranosyl-butanoate

C12H22O8 (294.1315)

Ginsenoyne B

10-chloro-heptadeca-1,16-dien-4,6-diyne-3,9-diol

C17H23O2Cl (294.1386)

Heptanal,2-(2,4-dinitrophenyl)hydrazone

C13H18N4O4 (294.1328)

2,6-dimorpholinopyrimidine-4-carboxylic acid

C13H18N4O4 (294.1328)

Puromycin aminonucleoside

Stylomycin aminonucleoside

C12H18N6O3 (294.144)

D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents Puromycin aminonucleoside (NSC 3056) is the aminonucleoside portion of the antibiotic puromycin, and used in nephrosis animal models[1]. Puromycin aminonucleoside induces apoptosis[2]. Puromycin aminonucleoside is a reversible inhibitor of dipeptidyl peptidase II and cytosol alanyl aminopeptidase[3]. Puromycin aminonucleoside induces secretion of cell migrasome[4].

D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents

4-[(E)-5,6-Dihydro-2,3-bipyridin-3(4H)-ylidenemethyl]-3-methoxyphenol

C18H18N2O2 (294.1368)

6-methoxy-3-[(3-methylanilino)methyl]-1H-quinolin-2-one

C18H18N2O2 (294.1368)

N-(1-acetyl-2,3-dihydroindol-5-yl)-4-methylbenzamide

C18H18N2O2 (294.1368)

4-[2-(4-hydroxyphenyl)-4-propyl-1H-pyrazol-5-ylidene]-1-cyclohexa-2,5-dienone

C18H18N2O2 (294.1368)

4-Methoxy-2-(4-propoxyphenyl)quinazoline

C18H18N2O2 (294.1368)

2-(3-Methoxyphenyl)-4-propan-2-yloxyquinazoline

C18H18N2O2 (294.1368)

(1-Methyl-2-imidazolyl)-(4-phenylmethoxyphenyl)methanol

C18H18N2O2 (294.1368)

N-(3-methoxyphenyl)-2-(1-methyl-3-indolyl)acetamide

C18H18N2O2 (294.1368)

(2R,3S,4S)-4-(hydroxymethyl)-3-[4-(2-methoxyphenyl)phenyl]-2-azetidinecarbonitrile

C18H18N2O2 (294.1368)

Ac-D-His-Pro

C13H18N4O4 (294.1328)

(2S,3R,4S)-4-(hydroxymethyl)-3-[4-(2-methoxyphenyl)phenyl]-2-azetidinecarbonitrile

C18H18N2O2 (294.1368)

(2S,3S,4S)-4-(hydroxymethyl)-3-[4-(2-methoxyphenyl)phenyl]-2-azetidinecarbonitrile

C18H18N2O2 (294.1368)

(2R,3R,4R)-4-(hydroxymethyl)-3-[4-(2-methoxyphenyl)phenyl]-2-azetidinecarbonitrile

C18H18N2O2 (294.1368)

(2S,3R,4R)-4-(hydroxymethyl)-3-[4-(2-methoxyphenyl)phenyl]-2-azetidinecarbonitrile

C18H18N2O2 (294.1368)

(2R,3R,4S)-4-(hydroxymethyl)-3-[4-(2-methoxyphenyl)phenyl]-2-azetidinecarbonitrile

C18H18N2O2 (294.1368)

8-(1,2-dideoxy-1-D-ribityl)-7-methyllumazine

C13H18N4O4 (294.1328)

8-(1,4-dideoxy-1-D-ribityl)-7-methyllumazine

C13H18N4O4 (294.1328)

N-[(E)-2-Bicyclo[2.2.1]heptanylideneamino]-3-hydroxynaphthalene-2-carboxamide

C18H18N2O2 (294.1368)

4-[[(2S,5S)-5-[(4-hydroxyphenyl)methyl]-2,5-dihydropyrazin-2-yl]methyl]phenol

C18H18N2O2 (294.1368)

2-[3-Ethyl-5-(4-methoxyphenyl)-1H-pyrazol-4-yl]phenol

C18H18N2O2 (294.1368)

A pyrazole that is 1H-pyrazole bearing an ethyl group at position 3, a 2-hydroxyphenyl group at position 2, and a 4-methoxyphenyl group at position 5.