Exact Mass: 358.9438580000001
Exact Mass Matches: 358.9438580000001
Found 27 metabolites which its exact mass value is equals to given mass value 358.9438580000001
,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Methyclothiazide
Methyclothiazide is only found in individuals that have used or taken this drug. It is a thiazide diuretic with properties similar to those of hydrochlorothiazide. (From Martindale, The Extra Pharmacopoeia, 30th ed, p825)Methyclothiazide appears to block the active reabsorption of chloride and possibly sodium in the ascending loop of Henle, altering electrolyte transfer in the proximal tubule. This results in excretion of sodium, chloride, and water and, hence, diuresis. As a diuretic, methyclothiazide inhibits active chloride reabsorption at the early distal tubule via the Na-Cl cotransporter, resulting in an increase in the excretion of sodium, chloride, and water. Thiazides like methyclothiazide also inhibit sodium ion transport across the renal tubular epithelium through binding to the thiazide sensitive sodium-chloride transporter. This results in an increase in potassium excretion via the sodium-potassium exchange mechanism. The antihypertensive mechanism of methyclothiazide is less well understood although it may be mediated through its action on carbonic anhydrases in the smooth muscle or through its action on the large-conductance calcium-activated potassium (KCa) channel, also found in the smooth muscle. C - Cardiovascular system > C03 - Diuretics > C03A - Low-ceiling diuretics, thiazides > C03AA - Thiazides, plain D045283 - Natriuretic Agents > D004232 - Diuretics > D049993 - Sodium Chloride Symporter Inhibitors C78275 - Agent Affecting Blood or Body Fluid > C448 - Diuretic > C49185 - Thiazide Diuretic D002317 - Cardiovascular Agents > D045283 - Natriuretic Agents D049990 - Membrane Transport Modulators
p-Chloromercuribenzoate; p-Chloromercuribenzoic acid; PCMB
methyclothiazide
C - Cardiovascular system > C03 - Diuretics > C03A - Low-ceiling diuretics, thiazides > C03AA - Thiazides, plain D045283 - Natriuretic Agents > D004232 - Diuretics > D049993 - Sodium Chloride Symporter Inhibitors C78275 - Agent Affecting Blood or Body Fluid > C448 - Diuretic > C49185 - Thiazide Diuretic D002317 - Cardiovascular Agents > D045283 - Natriuretic Agents D049990 - Membrane Transport Modulators
2-(4-Iodophenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione
C11H11BINO4 (358.98258660000005)
2-(3-iodophenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione
C11H11BINO4 (358.98258660000005)
7-AMINO-1,3-NAPHTHALENEDISULFONIC ACID, MONOPOTASSIUM SALT, HYDRATE
4-BROMO-2-(2,6-DICHLOROPHENYL)-7-FLUORO-1H-IMIDAZO[4,5-C]PYRIDINE
C12H5BrCl2FN3 (358.90279019999997)
methyl (2Z,4Z)-2-(bromomethyl)-5-chloro-5-(4-nitrophenyl)penta-2,4-dienoate
C13H11BrClNO4 (358.95599360000006)
8-Amino-1-naphthol-3,6-disulfonic acid monosodium salt monohydrate
2-(3-bromophenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione
C11H11BINO4 (358.98258660000005)
3-Bromo-N,N-diethyl-5-(trifluoromethyl)benzenesulfonamide
C11H13BrF3NO2S (358.98024140000007)
3-Bromo-N-butyl-5-(trifluoromethyl)benzenesulfonamide
C11H13BrF3NO2S (358.98024140000007)
4-Bromo-N-butyl-3-(trifluoromethyl)benzenesulfonamide
C11H13BrF3NO2S (358.98024140000007)
4-Bromo-N-(tert-butyl)-3-(trifluoromethyl)benzenesulfonamide
C11H13BrF3NO2S (358.98024140000007)
2-bromo-N-cyclopropyl-4-(trifluoromethoxy)benzenesulfonamide
C10H9BrF3NO3S (358.9438580000001)
4-Bromo-N,N-diethyl-3-(trifluoromethyl)benzenesulfonamide
C11H13BrF3NO2S (358.98024140000007)
Para-mercury-benzenesulfonic acid
C6H5HgO3S (358.96657200000004)
D010575 - Pesticides > D005659 - Fungicides, Industrial > D010663 - Phenylmercury Compounds
3-nitro-N-(2,4,6-trichlorophenyl)benzohydrazide
C13H8Cl3N3O3 (358.96312280000006)
Methyl 5-(2,4-dichloro-6-fluorophenoxy)-2-nitrobenzoate
Lipofermata
C15H10BrN3OS (358.97279100000003)
Lipofermata is a fatty acid transport protein 2 (FATP2) inhibitor. Lipofermata shows fatty acid transport inhibition with an IC50 of 4.84 μM in Caco-2 cells. Lipofermata, an analog of spiro-indoline-thadiazole, shows zinc-specific suppression of antibacterial activity. Lipofermata perturbs zinc homeostasis in E. coli K-12 with a MIC of 16 μM[1][2][3].