Exact Mass: 508.99405960000007

Exact Mass Matches: 508.99405960000007

Found 14 metabolites which its exact mass value is equals to given mass value 508.99405960000007, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Lignin

Disodium N-[8-oxo-7-(2-phenylhydrazin-1-ylidene)-6-sulphO-4-sulphonato-7,8-dihydronaphthalen-1-yl]ethanecarboximidic acid

C18H13N3Na2O8S2 (508.9939458)


Lignin is practically insoluble (in water) and an extremely strong acidic compound (based on its pKa). Lignin can be found in a number of food items such as evening primrose, carob, sunflower, and corn, which makes lignin a potential biomarker for the consumption of these food products. Lignin is a class of complex organic polymers that form important structural materials in the support tissues of vascular plants and some algae. Lignins are particularly important in the formation of cell walls, especially in wood and bark, because they lend rigidity and do not rot easily. Chemically, lignins are cross-linked phenolic polymers .

   

Lignin

disodium;4-acetamido-5-hydroxy-6-phenyldiazenylnaphthalene-1,7-disulfonate

C18H13N3Na2O8S2 (508.9939458)


The most abundant natural aromatic organic polymer found in all vascular plants. Lignin together with cellulose and hemicellulose are the major cell wall components of the fibers of all wood and grass species. Lignin is composed of coniferyl, p-coumaryl, and sinapyl alcohols in varying ratios in different plant species. (From Merck Index, 11th ed) Lignin is a class of complex organic polymers that form key structural materials in the support tissues of most plants.[1] Lignins are particularly important in the formation of cell walls, especially in wood and bark, because they lend rigidity and do not rot easily. Chemically, lignins are polymers made by cross-linking phenolic precursors.[2] Lignin was first mentioned in 1813 by the Swiss botanist A. P. de Candolle, who described it as a fibrous, tasteless material, insoluble in water and alcohol but soluble in weak alkaline solutions, and which can be precipitated from solution using acid.[3] He named the substance "lignine", which is derived from the Latin word lignum,[4] meaning wood. It is one of the most abundant organic polymers on Earth, exceeded only by cellulose and chitin. Lignin constitutes 30\% of terrestrial non-fossil organic carbon[5] on Earth, and 20 to 35\% of the dry mass of wood.[6] Lignin is present in red algae, which suggest that the common ancestor of plants and red algae also synthesised lignin. This finding also suggests that the original function of lignin was structural as it plays this role in the red alga Calliarthron, where it supports joints between calcified segments.[7]

   
   
   
   

Dicloxacillin Sodium

Dicloxacillin Sodium

C19H18Cl2N3NaO6S (509.0191028000001)


D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D047090 - beta-Lactams D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D010406 - Penicillins D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D007769 - Lactams C254 - Anti-Infective Agent > C258 - Antibiotic > C260 - Beta-Lactam Antibiotic

   

8-(4-chlorophenylthio)-cGMP.Na

8-(4-CHLOROPHENYLTHIO)GUANOSINE 3,5-CYCLIC MONOPHOSPHATE SODIUM SALT

C16H14ClN5NaO7PS (508.99377740000006)


   

2-[2-[(3-Chloro-1-benzothiophen-2-yl)-oxomethyl]imino-6-sulfamoyl-1,3-benzothiazol-3-yl]acetic acid ethyl ester

2-[2-[(3-Chloro-1-benzothiophen-2-yl)-oxomethyl]imino-6-sulfamoyl-1,3-benzothiazol-3-yl]acetic acid ethyl ester

C20H16ClN3O5S3 (508.99405960000007)


   
   

4-(4-chloro-3-nitrophenyl)-N-[2-(5,6-dichloro-1-propyl-2-benzimidazolyl)ethyl]-2-thiazolamine

4-(4-chloro-3-nitrophenyl)-N-[2-(5,6-dichloro-1-propyl-2-benzimidazolyl)ethyl]-2-thiazolamine

C21H18Cl3N5O2S (509.0246738)


   

Bicuculline methiodide

Bicuculline methiodide

C21H20INO6 (509.03353300000003)


Bicuculline methiodide is a potent GABA(A) receptors blocker. Bicuculline methiodide alters membrane properties and firing pattern. Bicuculline methiodide reduces the Apamin-sensitive afterhyperpolarization, while Apamin is a toxin isolated from bee venom to block small conductance Ca2+ -activated K+ channels. Bicuculline methiodide facilitates burst firing via blocking apamin-sensitive Ca2+ -activated K+ current[1].

   

(5r,10s)-7,9-dibromo-n-[(2r)-4-carbamimidamido-2-hydroxybutyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide

(5r,10s)-7,9-dibromo-n-[(2r)-4-carbamimidamido-2-hydroxybutyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide

C15H21Br2N5O5 (508.99093360000006)