Exact Mass: 197.9655

Exact Mass Matches: 197.9655

Found 322 metabolites which its exact mass value is equals to given mass value 197.9655, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Phosphoenol-4-deoxy-3-tetrulosonate

2-hydroxy-3-phosphonooxybut-3-enoic acid

C4H7O7P (197.9929)

2,4,5-trichlorocyclohexa-2,5-dien-1-ol

1-Hydroxyl-2,4,5-trichloro-2,5-cyclohexadiene

C6H5Cl3O (197.9406)

2-Oxopropyl-CoM

2-(2-Oxopropylthio)ethanesulfonate

C5H10O4S2 (198.002)

1-BROMO-2-PHENYLPROPANE

C9H11Br (198.0044)

Dihydroxyacetone Phosphate Acyl Ester

Dihydroxyacetone phosphoric acid acyl ester

C4H7O7P (197.9929)

1-acylglycerone 3-phosphate is found in the glycerophospholipid metabolism and ether lipid metabolism pathways. In the glycerophospholipid metabolism pathway, 1-acylglycerone 3-phosphate is created from glycerone phosphate, a reaction catalyzed by glyceronephosphate O-acyltransferase [EC:2.3.1.42]. 1-acylglycerone 3-phosphate is then converted to 1-acyl-sn-3-glycercol-phosphate or enters ether lipid metabolism. The conversion to 1-acyl-sn-3-glycercol-phosphate is catalyzed by 1-acylglycerone phosphate reductase [EC:1.1.1.101]. Within the ether lipid metabolism pathway, 1-acylglycerone 3-phosphate is converted to 1-alkyl-glycerone-3-phosphate through the action of alkyldihydroxyacetonephosphate synthase [EC:2.5.1.26]. 1-acylglycerone 3-phosphate is found in the glycerophospholipid metabolism and ether lipid metabolism pathways.

3-Bromosulfolane

Thiophene, tetrahydro-3-bromo-, 1,1-dioxide

C4H7BrO2S (197.935)

3-Bromosulfolane is a fungicide against black leg of sugar beet seedlings.

(±)-Sulfobutanedioic acid

Thiosuccinic acid, monoammonium salt

C4H6O7S (197.9834)

(±)-Sulfobutanedioic acid is present in can-end cements. Present in can-end cements

1-Iodopentane

C5H11I (197.9905)

1H,1'H-2,2'-Disulfanediyl-bis-imidazole

2-(1H-imidazol-2-yldisulfanyl)-1H-imidazole

C6H6N4S2 (198.0034)

7-Aminobenzo[d]isothiazol-3(2H)-one 1,1-dioxide

7-amino-2,3-dihydro-1lambda6,2-benzothiazole-1,1,3-trione

C7H6N2O3S (198.0099)

Sodium ascorbate

Sodium ascorbate; Sodium (2R)-2-[(1S)-1,2-dihydroxyethyl]-4-hydroxy-5-oxo-2,5-dihydrofuran-3-olate

C6H7O6.Na (198.014)

Minute crystals or white powder. pH of aqueous solutions 5.6 to 7.0 or even higher (a 10\\\\% solution, made from a commercial grade, may have a pH of 7.4 to 7.7). (NTP, 1992) Sodium ascorbate is an organic sodium salt resulting from the replacement of the proton from the 3-hydroxy group of ascorbic acid by a sodium ion. It has a role as a food antioxidant, a flour treatment agent, a coenzyme, a plant metabolite, a human metabolite, a Daphnia magna metabolite and a reducing agent. It is an organic sodium salt and a vitamin C. It contains a L-ascorbate. A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant. See also: Ascorbic Acid (has active moiety) ... View More ... An organic sodium salt resulting from the replacement of the proton from the 3-hydroxy group of ascorbic acid by a sodium ion. D020011 - Protective Agents > D000975 - Antioxidants D018977 - Micronutrients > D014815 - Vitamins L-Ascorbic acid sodium salt (Sodium ascorbate), an electron donor, is an endogenous antioxidant agent. L-Ascorbic acid sodium salt selectively inhibits Cav3.2 channels with an IC50 of 6.5 μM. L-Ascorbic acid sodium salt is also a collagen deposition enhancer and an elastogenesis inhibitor[1][2][3]. L-Ascorbic acid sodium salt (Sodium ascorbate), an electron donor, is an endogenous antioxidant agent. L-Ascorbic acid sodium salt selectively inhibits Cav3.2 channels with an IC50 of 6.5 μM. L-Ascorbic acid sodium salt is also a collagen deposition enhancer and an elastogenesis inhibitor[1][2][3].