Exact Mass: 214.0518
Exact Mass Matches: 214.0518
Found 134 metabolites which its exact mass value is equals to given mass value 214.0518,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Monolinuron
CONFIDENCE standard compound; INTERNAL_ID 955; DATASET 20200303_ENTACT_RP_MIX502; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8335; ORIGINAL_PRECURSOR_SCAN_NO 8330 CONFIDENCE standard compound; INTERNAL_ID 955; DATASET 20200303_ENTACT_RP_MIX502; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8309; ORIGINAL_PRECURSOR_SCAN_NO 8304
Amifostine
Amifostine is only found in individuals that have used or taken this drug. It is a phosphorothioate proposed as a radiation-protective agent. It causes splenic vasodilation and may block autonomic ganglia. [PubChem]The thiol metabolite is responsible for most of the cytoprotective and radioprotective properties of amifostine. It is readily taken up by cells where it binds to and detoxifies reactive metabolites of platinum and alkylating agents as well as scavenges free radicals. Other possible effects include inhibition of apoptosis, alteration of gene expression and modification of enzyme activity. V - Various > V03 - All other therapeutic products > V03A - All other therapeutic products > V03AF - Detoxifying agents for antineoplastic treatment C26170 - Protective Agent > C2459 - Chemoprotective Agent > C2080 - Cytoprotective Agent D020011 - Protective Agents > D011837 - Radiation-Protective Agents KEIO_ID A170 Amifostine (WR2721) is a broad-spectrum cytoprotective agent and a radioprotector. Amifostine selectively protects normal tissues from damage caused by radiation and chemotherapy. Amifostine is potent hypoxia-inducible factor-α1 (HIF-α1) and p53 inducer. Amifostine protects cells from damage by scavenging oxygen-derived free radicals. Amifostine reduces renal toxicity and has antiangiogenic action[1][2][3][4].
1-Methyl-3-(2-thiazolyl)-1H-indole
1-Methyl-3-(2-thiazolyl)-1H-indole is found in fruits. 1-Methyl-3-(2-thiazolyl)-1H-indole is from Capsella bursa-pastoris (shepherds purse) infected with Alternaria brassica From Capsella bursa-pastoris (shepherds purse) infected with Alternaria brassicae. 1-Methyl-3-(2-thiazolyl)-1H-indole is found in herbs and spices and fruits.
fluorobenzoylpropionic acid
fluorobenzoylpropionic acid is a metabolite of haloperidol. Haloperidol is a typical antipsychotic. It is in the butyrophenone class of antipsychotic medications and has pharmacological effects similar to the phenothiazines. Haloperidol is an older antipsychotic used in the treatment of schizophrenia and acute psychotic states and delirium. (Wikipedia)
Sulfaguanidine
A - Alimentary tract and metabolism > A07 - Antidiarrheals, intestinal antiinflammatory/antiinfective agents > A07A - Intestinal antiinfectives > A07AB - Sulfonamides C254 - Anti-Infective Agent > C29739 - Sulfonamide Anti-Infective Agent D000890 - Anti-Infective Agents > D013424 - Sulfanilamides
sulfaguanidine
A - Alimentary tract and metabolism > A07 - Antidiarrheals, intestinal antiinflammatory/antiinfective agents > A07A - Intestinal antiinfectives > A07AB - Sulfonamides C254 - Anti-Infective Agent > C29739 - Sulfonamide Anti-Infective Agent D000890 - Anti-Infective Agents > D013424 - Sulfanilamides CONFIDENCE standard compound; INTERNAL_ID 1012
Alloxazine
Alloxazine is a selective A2b antagonist. Alloxazine completely block 5’N-Ethylcarboxamido adenosine (NECA)-mediated cyclic AMP accumulation with an IC50 of 2.9 μM. Alloxazine can be used for the research of cancer[1][2].
methyl 3,5-dimethoxy-4-hydroxybenzoate|methyl syringate|RMS15
2--5-<5-hydroxy-penten-(3)-in-<1>-yl>-thiophen|5-(5-but-3-en-1-ynyl-thiophen-2-yl)-pent-2-en-4-yn-1-ol
2-(pent-1,3-diynyl)-5-(4-hydroxybut-1-ynyl)thiophene|2--5-<4-hydroxybut-1-ynyl>-thiophene|2--5-<4-hydroxy-butin-(1)-yl>-thiophen|4-(5-penta-1,3-diynyl-thiophen-2-yl)-but-3-yn-1-ol|4-[5-(1,3-Pentadiynyl)-7-thienyl]-3-butyn-1-ol
2-prop-1-inyl-5-(5,6-epoxyhex-3c-en-1-inyl)-thiophene
MONOLINURON
CONFIDENCE standard compound; EAWAG_UCHEM_ID 3173
2-(1h-1,2,4-triazol-5-yl)-1h-isoindole-1,3(2h)-dione
4H-Benzo[4,5]cyclohepta[1,2-b]thiophen-4-one,9,10-dihydro-
2,6-DIFLUORO-BETA-OXO-BENZENEPROPANOIC ACID METHYL ESTER
Pyrimidine, 4-ethyl-5-methyl-2,6-bis(methylthio)- (9CI)
2,3-DIHYDRO-1,4-BENZODIOXINE-2-CARBOXIMIDAMIDE HYDROCHLORIDE
2-(4-Carbamimidoylphenyl)acetic acid hydrochloride
6-(Aminomethyl)-2H-1,4-benzoxazin-3(4H)-one hydrochloride (1:1)
5-nitro-2,3-dihydro-1H-inden-2-amine,hydrochloride
6-(4-FLUOROPHENYL)-2-OXO-1,2-DIHYDROPYRIDINE-3-CARBONITRILE
(2E)-N-(3,4-DICHLOROPHENYL)-2-(HYDROXYIMINO)ACETAMIDE
6-(TRIFLUOROMETHYL)-2,3,4-TRIHYDRONAPHTHALEN-1-ONE
4,7-Dimethoxy-1H-pyrrolo[2,3-c]pyridine monohydrochloride
2-amino-5-methylsulfanyl-1H-pyrrole-3,4-dicarboxamide
1-(4-Fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carbonitrile
Magnesium acetate tetrahydrate
Acetic acid magnesium tetrahydrate is a hydrated form of anhydrous magnesium acetate salt. As a salt form of Magnesium, Magnesium acetate is one of the bioavailable forms of magnesium and forms a very water soluble compound. Acetic acid magnesium tetrahydrate can be used as an electrolyte supplementation or a reagent in molecular biology experiments[1].
N-(PIPERIDIN-4-YL)METHANESULFONAMIDE HYDROCHLORIDE
1-(4-Fluorophenyl)-2-oxo-1,2-dihydropyridine-4-carbonitrile
2-(1,3-Benzothiazol-2-yl)-3-methyl-2-butenenitrile
4-(2-Amino-1-hydroxyethyl)-5-nitrobenzene-1,2-diol
amifostine
V - Various > V03 - All other therapeutic products > V03A - All other therapeutic products > V03AF - Detoxifying agents for antineoplastic treatment C26170 - Protective Agent > C2459 - Chemoprotective Agent > C2080 - Cytoprotective Agent D020011 - Protective Agents > D011837 - Radiation-Protective Agents Amifostine (WR2721) is a broad-spectrum cytoprotective agent and a radioprotector. Amifostine selectively protects normal tissues from damage caused by radiation and chemotherapy. Amifostine is potent hypoxia-inducible factor-α1 (HIF-α1) and p53 inducer. Amifostine protects cells from damage by scavenging oxygen-derived free radicals. Amifostine reduces renal toxicity and has antiangiogenic action[1][2][3][4].
