Exact Mass: 387.00988100000006
Exact Mass Matches: 387.00988100000006
Found 72 metabolites which its exact mass value is equals to given mass value 387.00988100000006
,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Thifensulfuron-methyl
C12H13N5O6S2 (387.03072380000003)
CONFIDENCE standard compound; EAWAG_UCHEM_ID 124 CONFIDENCE standard compound; INTERNAL_ID 3688
dCDP
dCDP is a substrate for Uridine-cytidine kinase 1, Nucleoside diphosphate kinase (mitochondrial), Nucleoside diphosphate kinase homolog 5, Ribonucleoside-diphosphate reductase large subunit, Nucleoside diphosphate kinase A, Nucleoside diphosphate kinase 7, Ribonucleoside-diphosphate reductase M2 chain, Nucleoside diphosphate kinase B, Nucleoside diphosphate kinase 3, Nucleoside diphosphate kinase 6 and UMP-CMP kinase. [HMDB]. dCDP is found in many foods, some of which are oil palm, sweet bay, garden onion (variety), and italian sweet red pepper. dCDP is a substrate for Uridine-cytidine kinase 1, Nucleoside diphosphate kinase (mitochondrial), Nucleoside diphosphate kinase homolog 5, Ribonucleoside-diphosphate reductase large subunit, Nucleoside diphosphate kinase A, Nucleoside diphosphate kinase 7, Ribonucleoside-diphosphate reductase M2 chain, Nucleoside diphosphate kinase B, Nucleoside diphosphate kinase 3, Nucleoside diphosphate kinase 6 and UMP-CMP kinase. Acquisition and generation of the data is financially supported in part by CREST/JST.
benzylhydrochlorothiazide
C78275 - Agent Affecting Blood or Body Fluid > C448 - Diuretic > C49185 - Thiazide Diuretic Same as: D01246
5'-Hydroxylornoxicam
5-Hydroxylornoxicam is a metabolite of Tenoxicam. 5-hydroxylornoxicam belongs to the family of Thienothiazines. These are heterocyclic compounds containing a thiophene ring fused to a thiazine.
3',4'-Dichlorobenzamil
C13H12Cl3N7O (387.01688720000004)
2-Amino-5-[[1-[carboxymethyl(sulfo)amino]-1-oxo-3-sulfanylpropan-2-yl]amino]-5-oxopentanoic acid
2-{2-[3,5-Bis(trifluoromethyl)phenyl]hydrazono}-2-(propylsulfonyl)acetonitrile
glutathioselenol
A glutathione derivative that is glutathione in which the hydrogen attached to the sulfur is replaced by a selenol group.
5-Hydroxylornoxicam
Thiazolidine, 3-[(2,5-dichlorophenyl)sulfonyl]-2-(4-methylphenyl)- (9CI)
Thiazolidine, 2-(4-methylphenyl)-3-[[3-(trifluoromethyl)phenyl]sulfonyl]- (9CI)
5-bromo-3-[5-(morpholin-4-ylmethyl)-1H-pyridin-2-ylidene]-1H-indol-2-one
Thiazolidine, 3-[(3,4-dichlorophenyl)sulfonyl]-2-(4-methylphenyl)- (9CI)
6-BROMO-2-(2,4-DIMETHOXYPHENYL)QUINOLINE-4-CARBOXYLICACID
C18H14BrNO4 (387.01061440000007)
Benzenesulfonamide,N-(2,4-dinitro-1-naphthalenyl)-4-methyl-
C17H13N3O6S (387.05250380000007)
3-BOC-2-(4-BROMO-PHENYL)-THIAZOLIDINE-4-CARBOXYLIC ACID
C15H18BrNO4S (387.01398480000006)
Ethylenediaminetetraacetate-copper-ammonia complex
3-Bromo-N,N-dipropyl-5-(trifluoromethyl)benzenesulfonamide
C13H17BrF3NO2S (387.01153980000004)
2-CYANO-N-CYCLOPROPYL-N-((2-FLUORO-4-IODOPHENYL)CARBAMOYL)ACETAMIDE
6-amino-3-cyclopropyl-1-(2-fluoro-4-iodophenyl)pyrimidine-2,4(1H,3H)-dione
ISOPROPYL (2-IODO-4-METHYL-5-(TRIFLUOROMETHYL)PHENYL)CARBAMATE
7,8-Dimethoxy-3-(3-iodopropyl)-1,3-dihydro-2H-3-benzazepin-2-one
C15H18INO3 (387.0331388000001)
Benzenesulfonylchloride, 4-[2-[(5-chloro-2-methoxybenzoyl)amino]ethyl]-
C16H15Cl2NO4S (387.00988100000006)
tert-butyl 2-amino-5-iodo-4-(trifluoromethyl)benzoate
O-[3-chloro-4-(diethylsulfamoyl)phenyl] O,O-dimethyl phosphorothioate
4-[4-Bromo-3-[[(tetrahydro-2H-pyran-2-yl)oxy]methyl]phenoxy]benzonitrile
2-(4-Bromophenyl)-4,6-diphenyl-1,3,5-triazine
C21H14BrN3 (387.03710240000004)
2-(3-Bromophenyl)-4,6-diphenyl-1,3,5-triazine
C21H14BrN3 (387.03710240000004)
(4-chlorophenyl)-(3-methyl-1,3-benzothiazol-3-ium-2-yl)diazene,perchlorate
C14H11Cl2N3O4S (386.9847306000001)
Bromotris(dimethylamino)phosphonium hexafluorophosphate
C6H18BrF6N3P2 (387.00634599999995)
4-(4-Bromphenyl)-2,2:6,2-terpyridin
C21H14BrN3 (387.03710240000004)
3-Bromo-N-hexyl-5-(trifluoromethyl)benzenesulfonamide
C13H17BrF3NO2S (387.01153980000004)
2,4-dichloro-N-[5-(5,6,7,8-tetrahydronaphthalen-2-yl)-1,3,4-oxadiazol-2-yl]benzamide
5-(1H-benzimidazol-2-ylmethylidene)-3-(2-naphthalenyl)-2-sulfanylidene-4-thiazolidinone
2,3-Dihydroxybutanedioic acid--3-(5-nitrofuran-2-yl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole (1/1)
C13H13N3O9S (387.03724880000004)
[(2R,3S,4R,5S)-5-(2-amino-5-cyano-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-7-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate
C12H14N5O8P (387.05799740000003)
N-(4-bromo-2-methylphenyl)-3-(1,3-dioxo-2-pyrrolo[3,4-c]pyridinyl)propanamide
C17H14BrN3O3 (387.02184740000007)
3,5-diamino-N-[amino-[(2,4-dichlorophenyl)methylimino]methyl]-6-chloro-2-pyrazinecarboxamide
C13H12Cl3N7O (387.01688720000004)
2-[(2,4-dichlorophenoxy)acetyl]-N-(4-fluorophenyl)hydrazinecarbothioamide
N-{3-[3-(5-bromo-2-methoxyphenyl)acryloyl]phenyl}propanamide
[(3aR,4R,9bR)-8-bromo-4-(hydroxymethyl)-2,3,3a,4,5,9b-hexahydropyrrolo[3,2-c]quinolin-1-yl]-(2-pyridinyl)methanone
[(3aS,4S,9bS)-8-bromo-4-(hydroxymethyl)-2,3,3a,4,5,9b-hexahydropyrrolo[3,2-c]quinolin-1-yl]-(2-pyridinyl)methanone
[(3aR,4S,9bR)-8-bromo-4-(hydroxymethyl)-2,3,3a,4,5,9b-hexahydropyrrolo[3,2-c]quinolin-1-yl]-(2-pyridinyl)methanone
[(3aS,4R,9bS)-8-bromo-4-(hydroxymethyl)-2,3,3a,4,5,9b-hexahydropyrrolo[3,2-c]quinolin-1-yl]-(2-pyridinyl)methanone
[5-(2-amino-5-carbamoyl-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-7-yl)-3-hydroxy-2,5-dihydrofuran-2-yl]methyl dihydrogen phosphate
C12H14N5O8P (387.05799740000003)
Deoxycytidine diphosphate
A 2-deoxycytidine phosphate that is the 2- deoxy derivative of cytidine 5-diphosphate (CDP).
CCMI
CCMI (AVL-3288) is a potent and selective α7 nAChR-positive allosteric modulator, does not bind to or activate α7 nAChRs via the orthosteric site, and causes significant positive modulation of agonist-induced currents at α7 nAChRs. CCMI has potential in CNS diseases with cognitive dysfunction[1].
ERK5-IN-2
ERK5-IN-2 is an orally active, sub-micromolar, selective ERK5 inhibitor with IC50s of 0.82 μM, 3 μM for ERK5 and ERK5 MEF2D, respectively. ERK5-IN-2 does not interact with the BRD4 bromodomain. ERK5-IN-2 suppresses both tumor xenograft growth and basic fibroblast growth factor (bFGF) driven Matrigel plug angiogenesis[1].