Exact Mass: 95.9612

Exact Mass Matches: 95.9612

Found 55 metabolites which its exact mass value is equals to given mass value 95.9612, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Mesylate

Methanesulfonic acid solution

CH4SO3 (95.9881)


Mesylate, also known as methanesulfonate or mesylic acid, belongs to the class of organic compounds known as organosulfonic acids. Organosulfonic acids are compounds containing the sulfonic acid group, which has the general structure RS(=O)2OH (R is not a hydrogen atom). Mesylate exists as a solid, soluble (in water), and an extremely strong acidic compound (based on its pKa). Mesylate is also a parent compound for other transformation products, including but not limited to, methanesulfonates, S-methyl methanethiosulfonate, and (Z)-11-methyl-N-(methylsulfonyl)dodec-2-enamide. KEIO_ID M135 KEIO_ID M021

   

Methaneselenol

Methylselenium(II)

CH4Se (95.9478)


Methaneselenol, commonly referred to as methylselenol, is an organoselenium compound that is a selenium analogue of methanol. It consists of a methyl group covalently bound to a selenol group. Methylselenol is a naturally produced metabolite of selenium (Se), an essential trace element (PMID: 25258323). Inorganic selenium is mainly represented by selenate and selenite, whereas the organic selenium forms are represented by the selenoamino acids: selenomethionine (SeMet), selenocysteine (SeCys) and selenium methylselenocysteine (MSC) (PMID: 25258323). SeMet and MSC can be found in vegetables such as garlic and onions. Selenite is reduced in the presence of glutathione to selenide (H2Se). SeMet and selenocysteine (SeCys2) are also primarily converted to selenide and incorporated into selenoproteins or selenosugars. On the other hand, MSC (a natural metabolite) and the antineoplastic drug methylselenic acid (MSA) are converted to methylselenol by the enzyme beta-lyase (PMID: 25258323). Both selenide and methylselenol are highly reactive and both can interconvert through methylation/demethylation activities. Methylselenol is thought to be most significant in the anticancer activity of Se compounds (PMID: 30241340). Redox active Se compounds such as methylselenol have gained significant attention in the past decade as potential cancer therapeutic agents. Methylselenol is known for its action to selectively kill transformed cells through mechanisms that include increased formation of reactive oxygen species, induction of DNA damage, triggering of apoptosis, and inhibition of angiogenesis. Methylselenol also regulates the expression of ligands that trigger immune activation through the lymphocyte receptor NKG2D. The expression of NKG2D ligands is induced by stress-associated pathways that occur early during malignant transformation and enable the recognition and elimination of tumors by activating the lymphocyte receptor NKG2D (PMID: 25258323). This suggests that the application of selenium compounds that are metabolized to CH3SeH could improve NKG2D-based immune therapy for cancer treatment.

   

1,2-Dichloroethene

trans-Acetylene dichloride

C2H2Cl2 (95.9534)


   

Methylphosphonic acid

Dihydrogen methylphosphonate

CH5O3P (95.9976)


   

Vinylidene chloride

Vinylidene dichloride

C2H2Cl2 (95.9534)


   

cis-Acetylene dichloride

cis-1,2-Dichloroethylene

C2H2Cl2 (95.9534)


   

1,2-Dichloroethylene

1,2-Dichloroethylene, (e)-isomer

C2H2Cl2 (95.9534)


   

2-Chloroethane-1,1-diol

Chloroacetaldehyde hydrate

C2H5ClO2 (95.9978)


   

Sulfamide

Imidosulphamic acid

H4N2O2S (95.9993)


   

Magnesium chloride; Magnesium chloride anhydrous

Magnesium chloride; Magnesium chloride anhydrous

H2Cl2Mg+2 (95.9384)


   

Kieselsaeure

Silicon hydroxide (Si(OH)4)

H4O4Si (95.9879)


   

Chloromethyl Methyl Sulfide

Chloromethyl Methyl Sulfide

C2H5ClS (95.98)


   

Vinylidene chloride

Polyvinyl Dichloride

C2H2Cl2 (95.9534)


   
   

lithium oxalate

lithium oxalate

C2HLiO4 (96.0035)


   

Difluoroacetic acid

Difluoroacetic acid

C2H2F2O2 (96.0023)


   

Dichloroethene

Dichloroethene

C2H2Cl2 (95.9534)


   

Fluoroacetyl chloride

Fluoroacetyl chloride

C2H2ClFO (95.9778)


   

Zinc dioxidanediide

Zinc dioxidanediide

O2Zn (95.919)


   

sodium glyoxylate

sodium glyoxylate

C2HNaO3 (95.9823)


An organic sodium salt that is the monosodium salt of glyoxylic acid.

   

chromium silicon monoxide

chromium silicon monoxide

CrOSi (95.9124)


   

Calcium silicide(CaSi2)

Calcium silicide(CaSi2)

CaSi2 (95.9164)


   

2-chloroethane-1,1-diol

2-chloroethane-1,1-diol

C2H5ClO2 (95.9978)


   

Algeldrate

Algeldrate

H5AlO4 (96.0003)


   

soda lime

soda lime

CaHNaO2 (95.95)


   

SULFAMIDE

SULFAMIDE

H4N2O2S (95.9993)


   

Dimethylchlorophosphine

Dimethylchlorophosphine

C2H6ClP (95.9896)


   

Sulfate Ion

Sulfate Ion

O4S-2 (95.9517)


   

Algeldrate

Algeldrate

AlH5O4 (96.0003)


C29629 - Combination Medication > C29633 - Antacid Preparation

   

Hydrogen phosphate

Hydrogen phosphate

HO4P-2 (95.9612)


   

Sulfamate

Sulfamate

H2NO3S- (95.9755)


D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents D010575 - Pesticides > D006540 - Herbicides D016573 - Agrochemicals

   

Hypobromous acid

Hypobromous acid

BrHO (95.9211)


   

Trisulfur

Trisulfur

S3 (95.9162)


   

Trisulfide(2-)

Trisulfide(2-)

S3-2 (95.9162)


   

SO4 radical anion

SO4 radical anion

O4S- (95.9517)


   

sulfate

sulfate

O4S-- (95.9517)


The sulfate ion is a polyatomic anion with the empirical formula SO42- and a molecular mass of 96.06 daltons; it consists of one central sulfur atom surrounded by four equivalent oxygen atoms in a tetrahedral arrangement. The sulfate ion carries a negative two charge and is the conjugate base of the hydrogen sulfate ion, HSO4-, which is the conjugate base of H2SO4, sulfuric acid. In inorganic chemistry, a sulfate (IUPAC-recommended spelling; also sulphate in British English) is a salt of sulfuric acid. Sulfate aerosols can act as cloud condensation nuclei and this leads to greater numbers of smaller droplets of water. Lots of smaller droplets can diffuse light more efficiently than just a few larger droplets. [HMDB]. Sulfate is found in many foods, some of which are grass pea, groundcherry, garden tomato (variety), and garden tomato.

   

CID 10313078

CID 10313078

AlH2NaOSi (95.9588)


   

Thiosulfite

Thiosulfite

O2S2-2 (95.934)


   

Diaminozinc

Diaminozinc

H4N2Zn (95.9666)


   

CID 6857654

CID 6857654

HO4P- (95.9612)


   

Peroxybis(sulfanide)

Peroxybis(sulfanide)

O2S2-2 (95.934)


   

Disulfanediolate(2-)

Disulfanediolate(2-)

O2S2-2 (95.934)


   

Trisulfanidyl

Trisulfanidyl

S3- (95.9162)


   

CID 20491310

CID 20491310

HO4P (95.9612)


   

1,2-dichloroethylene

trans-1,2-Dichloroethylene

C2H2Cl2 (95.9534)


   

cis-1,2-Dichloroethylene

cis-1,2-Dichloroethylene

C2H2Cl2 (95.9534)


   

Methylphosphonic acid

Methylphosphonic acid

CH5O3P (95.9976)


   

1,1-DCE

1,1-Dichloroethylene

C2H2Cl2 (95.9534)


   

Methanesulfonate

METHANESULFONIC ACID

CH4SO3 (95.9881)


An alkanesulfonic acid in which the alkyl group directly linked to the sulfo functionality is methyl.

   

OrthosilicicAcid

Orthosilicic acid

H4O4Si (95.9879)


   

hydroxidotrioxidophosphate(.1-)

hydroxidotrioxidophosphate(.1-)

HO4P (95.9612)


   

hydrogenphosphate

hydrogenphosphate

HO4P (95.9612)


A phosphate ion that is the conjugate base of dihydrogenphosphate.

   

Methylselenol

Methylselenol

CH4Se (95.9478)


An organoselenium compound that is a selenium analogue of methanol, comprising a methyl group covalently bound to a selenol group.

   

sulfate

sulfate

O4S (95.9517)


A sulfur oxoanion obtained by deprotonation of both OH groups of sulfuric acid.

   

1,1-dichloroethene

1,1-dichloroethene

C2H2Cl2 (95.9534)


A member of the class of chloroethenes that is ethene in which both of the hydrogens attached to one of the carbons are replaced by chlorines.