Exact Mass: 182.9684

Exact Mass Matches: 182.9684

Found 193 metabolites which its exact mass value is equals to given mass value 182.9684, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Se-Methylselenocysteine

selenomethylselenocysteine, (L)-isomer, 75Se-labeled

C4H9NO2Se (182.9798)


Se-Methylselenocysteine (SeMSC) is a naturally occurring seleno-amino acid that is synthesized by plants such as garlic, astragalus, onions, and broccoli. It cannot be synthesized by higher animals. Unlike selenomethionine, which is incorporated into proteins in place of methionine, SeMSC is not incorporated into any proteins, thereby being fully available for the synthesis of selenium-containing enzymes such as glutathione peroxidase. Selenomethionine is the major seleno-compound in cereal grains (wheat grain, maize, and rice), soybeans, and enriched yeast. Seleno-compounds present in plants may have a profound effect upon the health of animals and human subjects. It is now known that the total Se content cannot be used as an indication of its efficacy, but knowledge of individual selenocompounds is necessary to fully assess the significance. Thus, speciation of the seleno-compounds has moved to the forefront. Since animals and man are dependent upon plants for their nutritional requirements, this makes the types of seleno-compounds in plants even more critical. Se enters the food chain through incorporation into plant proteins, mostly as selenocysteine and selenomethionine at normal Se levels. There are two possible pathways for the catabolism of selenomethionine: (1) a transsulfuration pathway via selenocystathionine to produce selenocysteine, which in turn is degraded to H2Se by the enzyme beta-lyase and (2) a transamination-decarboxylation pathway. It was estimated that 90\\\\% of methionine is metabolized through this pathway and thus could be also the major route for selenomethionine catabolism (PMID: 14748935 , Br J Nutr. 2004 Jan;91(1):11-28.). Selenomethionine is an amino acid containing selenium. The L-isomer of selenomethionine, known as Se-met and Sem, is a common natural food source of selenium. In vivo, selenomethionine is randomly incorporated instead of methionine and is readily oxidized. Its antioxidant activity arises from its ability to deplete reactive species. Selenium and sulfur are chalcogen elements that share many chemical properties and the substitution of methionine to selenomethionine may have no effect on protein structure and function. However, the incorporation of selenomethionine into tissue proteins and keratin in horses causes alkali disease. Alkali disease is characterized by emaciation, loss of hair, deformation and shedding of hooves, loss of vitality, and erosion of the joints of long bones. Se-methyl-L-selenocysteine is an L-alpha-amino acid compound having methylselanylmethyl as the side-chain. It has a role as an antineoplastic agent. It is a Se-methylselenocysteine, a non-proteinogenic L-alpha-amino acid and a L-selenocysteine derivative. It is a conjugate base of a Se-methyl-L-selenocysteinium. It is a conjugate acid of a Se-methyl-L-selenocysteinate. It is an enantiomer of a Se-methyl-D-selenocysteine. It is a tautomer of a Se-methyl-L-selenocysteine zwitterion. Methylselenocysteine has been used in trials studying the prevention of Prostate Carcinoma and No Evidence of Disease. Se-Methylselenocysteine is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Methylselenocysteine is a naturally occurring organoselenium compound found in many plants, including garlic, onions, and broccoli, with potential antioxidant and chemopreventive activities. Se-Methyl-seleno-L-cysteine (MSC) is an amino acid analogue of cysteine in which a methylselenium moiety replaces the sulphur atom of cysteine. This agent acts as an antioxidant when incorporated into glutathione peroxidase and has been shown to exhibit potent chemopreventive activity in animal models. Se-Methylselenocysteine (SeMSC) is a naturally occurring seleno-amino acid that is synthesized by plants such as garlic, astragalus, onions and broccoli. Unlike selenomethionine, which is incorporated into proteins in place of methionine, SeMSC is not incorporated into any proteins, thereby being fully available for the synthesis of selenium-containing enzymes such as glutathione peroxidase. 3-(Methylseleno)alanine is found in many foods, some of which are common cabbage, white cabbage, lima bean, and cauliflower. D020011 - Protective Agents > D016588 - Anticarcinogenic Agents C26170 - Protective Agent > C275 - Antioxidant D000970 - Antineoplastic Agents Se-Methylselenocysteine, a precursor of Methylselenol, has potent cancer chemopreventive activity and anti-oxidant activity. Se-Methylselenocysteine is orally bioavailable, and induces apoptosis[1][2]. Se-Methylselenocysteine, a precursor of Methylselenol, has potent cancer chemopreventive activity and anti-oxidant activity. Se-Methylselenocysteine is orally bioavailable, and induces apoptosis[1][2].

   

Acephate

N-[methoxy(methylsulfanyl)phosphoryl]ethanimidic acid

C4H10NO3PS (183.0119)


CONFIDENCE standard compound; INTERNAL_ID 702; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1493; ORIGINAL_PRECURSOR_SCAN_NO 1491 CONFIDENCE standard compound; INTERNAL_ID 702; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3008; ORIGINAL_PRECURSOR_SCAN_NO 3003 CONFIDENCE standard compound; INTERNAL_ID 702; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1469; ORIGINAL_PRECURSOR_SCAN_NO 1467 CONFIDENCE standard compound; INTERNAL_ID 702; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1489; ORIGINAL_PRECURSOR_SCAN_NO 1488 CONFIDENCE standard compound; INTERNAL_ID 702; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3023; ORIGINAL_PRECURSOR_SCAN_NO 3020 CONFIDENCE standard compound; INTERNAL_ID 702; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3022; ORIGINAL_PRECURSOR_SCAN_NO 3018 CONFIDENCE standard compound; INTERNAL_ID 702; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3000; ORIGINAL_PRECURSOR_SCAN_NO 2996 CONFIDENCE standard compound; INTERNAL_ID 702; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1491; ORIGINAL_PRECURSOR_SCAN_NO 1488 CONFIDENCE standard compound; INTERNAL_ID 702; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1478; ORIGINAL_PRECURSOR_SCAN_NO 1476 CONFIDENCE standard compound; INTERNAL_ID 702; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3021; ORIGINAL_PRECURSOR_SCAN_NO 3018 CONFIDENCE standard compound; INTERNAL_ID 702; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3035; ORIGINAL_PRECURSOR_SCAN_NO 3030 CONFIDENCE standard compound; INTERNAL_ID 702; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1488; ORIGINAL_PRECURSOR_SCAN_NO 1486 C471 - Enzyme Inhibitor > C47792 - Acetylcholinesterase Inhibitor CONFIDENCE standard compound; INTERNAL_ID 3111 D010575 - Pesticides > D007306 - Insecticides D016573 - Agrochemicals

   

Saccharin

1,1-dioxo-1,2-dihydro-1Lambda*6*-benzo[D]isothiazol-3-one

C7H5NO3S (182.999)


Saccharin, ammonium salt is used as a food additive [EAFUS] (EAFUS: Everything Added to Food in the United States). Saccharin belongs to the family of aromatic homomonocyclic compounds. These are aromatic compounds containing only one ring, which is homocyclic. Widely-used sweetening agent. All salts intensely sweet. Permitted in foods at levels of 80-1200 ppm in EU D000074385 - Food Ingredients > D005503 - Food Additives D010592 - Pharmaceutic Aids > D005421 - Flavoring Agents CONFIDENCE standard compound; INTERNAL_ID 8670 COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

Selenohomocysteine

(2S)-2-Amino-4-selenylbutanoic acid

C4H9NO2Se (182.9798)


Selenohomocysteine is the precursor of selenocysteine, which is synthesized by catalysis of cystathionine beta-synthase (EC 4.2.1.22) and cystathionine gamma-lyase (EC 4.4.1.1), in mammalian systems (both enzymes require pyridoxal phosphate). Selenohomocysteine (lactone) has been found to be a competitive and irreversible inhibitor of lysyl oxidase; this may relate to the development of connective tissue defects seen in homocystinuria. L-Selenohomocysteine also can serve as a substituent donor in the beta-replacement reaction to yield selenocystathionine. (PMID: 10609891, 9405445, 6456763, 3338973) [HMDB]. Selenohomocysteine is found in many foods, some of which are alaska wild rhubarb, kai-lan, towel gourd, and vanilla. Selenohomocysteine (CAS: 29412-93-9) is the precursor of selenocysteine, which is synthesized by the catalysis of cystathionine beta-synthase (EC 4.2.1.22) and cystathionine gamma-lyase (EC 4.4.1.1) in mammalian systems (both enzymes require pyridoxal phosphate). Selenohomocysteine (lactone) has been found to be a competitive and irreversible inhibitor of lysyl oxidase; this may relate to the development of connective tissue defects seen in homocystinuria. L-Selenohomocysteine also can serve as a substituent donor in the beta-replacement reaction to yield selenocystathionine (PMID: 10609891, 9405445, 6456763, 3338973).

   

5-Nitrosalicylate

2-Hydroxy-5-nitrobenzoate

C7H5NO5 (183.0168)


   

4-Fluoro-7-nitrobenzofurazan

7-Fluoro-4-nitrobenzo-2-oxa-1,3-diazole

C6H2FN3O3 (183.008)


D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D049408 - Luminescent Agents D004396 - Coloring Agents > D005456 - Fluorescent Dyes

   

S-(2-Chloroethyl)cysteine

2-Amino-3-[(2-chloroethyl)sulphanyl]propanoic acid

C5H10ClNO2S (183.0121)


   

2-phospho-D-glycerate

3-hydroxy-2-(phosphonatooxy)propanoate

C3H4O7P (182.9695)


2-phospho-d-glycerate, also known as 2-phosphonatoglyceric acid(3-), belongs to sugar acids and derivatives class of compounds. Those are compounds containing a saccharide unit which bears a carboxylic acid group. 2-phospho-d-glycerate is soluble (in water) and an extremely strong acidic compound (based on its pKa). 2-phospho-d-glycerate can be found in a number of food items such as wasabi, sea-buckthornberry, black chokeberry, and sweet potato, which makes 2-phospho-d-glycerate a potential biomarker for the consumption of these food products.

   

Enaminomycin A

4-Amino-2,5-dioxo-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic acid

C7H5NO5 (183.0168)


   

3-(Methylseleno)alanine

Se-Methyl-L-selenocysteine

C4H9NO2Se (182.9798)


   

methylselenocysteine

3-(Methylseleno)alanine

C4H9NO2Se (182.9798)


D020011 - Protective Agents > D016588 - Anticarcinogenic Agents D000970 - Antineoplastic Agents Se-Methylselenocysteine, a precursor of Methylselenol, has potent cancer chemopreventive activity and anti-oxidant activity. Se-Methylselenocysteine is orally bioavailable, and induces apoptosis[1][2]. Se-Methylselenocysteine, a precursor of Methylselenol, has potent cancer chemopreventive activity and anti-oxidant activity. Se-Methylselenocysteine is orally bioavailable, and induces apoptosis[1][2].

   

Antiphenicol

Antiphenicol

C7H5NO5 (183.0168)


   

saccharin

Saccharin, ammonium salt

C7H5NO3S (182.999)


D000074385 - Food Ingredients > D005503 - Food Additives D010592 - Pharmaceutic Aids > D005421 - Flavoring Agents COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS It is used as a food additive . CONFIDENCE standard compound; EAWAG_UCHEM_ID 2816

   

acephate

Pesticide1_Acephate_C4H10NO3PS_O,S-Dimethyl acetylphosphoramidothioate

C4H10NO3PS (183.0119)


C471 - Enzyme Inhibitor > C47792 - Acetylcholinesterase Inhibitor D010575 - Pesticides > D007306 - Insecticides D016573 - Agrochemicals CONFIDENCE standard compound; INTERNAL_ID 3111

   

Saccharin; LC-tDDA; CE10

Saccharin; LC-tDDA; CE10

C7H5NO3S (182.999)


   

Saccharin; LC-tDDA; CE20

Saccharin; LC-tDDA; CE20

C7H5NO3S (182.999)


   

Saccharin; LC-tDDA; CE30

Saccharin; LC-tDDA; CE30

C7H5NO3S (182.999)


   

Saccharin; LC-tDDA; CE40

Saccharin; LC-tDDA; CE40

C7H5NO3S (182.999)


   

Selenomethyl selenocysteine

2-amino-3-(methylselanyl)propanoic acid

C4H9NO2Se (182.9798)


Selenomethionine is an amino acid containing selenium that cannot be synthesized by higher animals, but can be obtained from plant material. Selenomethionine is the major seleno-compound in cereal grains (wheat grain, maize and rice), soybeans and enriched yeast. Seleno-compounds present in plants may have a profound effect upon the health of animals and human subjects. It is now known that the total Se content cannot be used as an indication of its efficacy, but knowledge of individual selenocompounds is necessary to fully assess the significance. Thus, speciation of the seleno-compounds has moved to the forefront. Since animals and man are dependent upon plants for their nutritional requirements, this makes the types of seleno-compounds in plants even more critical. Se enters the food chain through incorporation into plant proteins, mostly as selenocysteine and selenomethionine at normal Se levels. There are two possible pathways for the catabolism of selenomethionine. One is the transsulfuration pathway via selenocystathionine to produce selenocysteine, which in turn is degraded to H2Se by the enzyme b-lyase. The other pathway is the transamination-decarboxylation pathway. It was estimated that 90\\% of methionine is metabolized through this pathway and thus could be also the major route for selenomethionine catabolism. (PMID: 14748935, Br J Nutr. 2004 Jan;91(1):11-28.); Selenomethionine is an amino acid containing selenium. The L-isomer of selenomethionine, known as Se-met and Sem, is a common natural food source of selenium. In vivo, selenomethionine is randomly incorporated instead of methionine and is readily oxidized. Its antioxidant activity arises from its ability to deplete reactive species. Selenium and sulfur are chalcogen elements that share many chemical properties and the substitution of methionine to selenomethionine may have no effect on protein structure and function. However, the incorporation of selenomethionine into tissue proteins and keratin in horses causes alkali disease. Alkali disease is characterized by emaciation, loss of hair, deformation and shedding of hooves, loss of vitality and erosion of the joints of long bones. Selenomethyl selenocysteine is found in garden onion.

   

Imidazo[2,1-b]thiazole-5-carbonitrile,6-chloro-

Imidazo[2,1-b]thiazole-5-carbonitrile,6-chloro-

C6H2ClN3S (182.9658)


   

5-CHLORO-1,3-DIHYDRO-INDOLE-2-THIONE

5-CHLORO-1,3-DIHYDRO-INDOLE-2-THIONE

C8H6ClNS (182.9909)


   

2-Bromopyrimidine-4-carbonitrile

2-Bromopyrimidine-4-carbonitrile

C5H2BrN3 (182.9432)


   

DICHLOROETHOXYOXOVANADIUM (V)

DICHLOROETHOXYOXOVANADIUM (V)

C2H6Cl2O2V (182.9184)


   

Cobalt(II) Oxalate Dihydrate

Cobalt(II) Oxalate Dihydrate

C2H4CoO6 (182.934)


   

2,6-Pyridinedicarboxylic acid, 1-oxide

2,6-Pyridinedicarboxylic acid, 1-oxide

C7H5NO5 (183.0168)


   

2-Amino-5-(2-thienyl)-1,3,4-thiadiazole

2-Amino-5-(2-thienyl)-1,3,4-thiadiazole

C6H5N3S2 (182.9925)


   

(5-chlorothiophen-2-yl)methanamine hydrochloride

(5-chlorothiophen-2-yl)methanamine hydrochloride

C5H7Cl2NS (182.9676)


   

7-Chloro-3-methylthieno[3,2-b]pyridine

7-Chloro-3-methylthieno[3,2-b]pyridine

C8H6ClNS (182.9909)


   

(4-chlorophenylthio)acetonitrile

(4-chlorophenylthio)acetonitrile

C8H6ClNS (182.9909)


   

5-Hydroxy-2-nitrobenzoic Acid

5-Hydroxy-2-nitrobenzoic Acid

C7H5NO5 (183.0168)


   

2,3,4,5,6-Pentafluoroaniline

2,3,4,5,6-Pentafluoroaniline

C6H2F5N (183.0107)


   

2-chlorobenzyl isothiocyanate

2-chlorobenzyl isothiocyanate

C8H6ClNS (182.9909)


   

2-Chloro-6-methylphenyl isothiocyanate

2-Chloro-6-methylphenyl isothiocyanate

C8H6ClNS (182.9909)


   

2-chloro-4-methylphenyl isothiocyanate

2-chloro-4-methylphenyl isothiocyanate

C8H6ClNS (182.9909)


   

3-Chlorobenzyl isothiocyanate

3-Chlorobenzyl isothiocyanate

C8H6ClNS (182.9909)


   

B-Trichloroborazine

B-Trichloroborazine

B3Cl3H3N3 (182.9672)


   

Borazine,2,4,6-trichloro-

Borazine,2,4,6-trichloro-

B3Cl3H3N3 (182.9672)


   

(2-(TRIFLUOROMETHYL)THIAZOL-4-YL)METHANOL

(2-(TRIFLUOROMETHYL)THIAZOL-4-YL)METHANOL

C5H4F3NOS (182.9966)


   

3-Chloro-5-nitropicolinonitrile

3-Chloro-5-nitropicolinonitrile

C6H2ClN3O2 (182.9836)


   

3-AMINO-TETRAHYDRO-THIOPHENE-3-CARBOXYLIC ACID HYDROCHLORIDE

3-AMINO-TETRAHYDRO-THIOPHENE-3-CARBOXYLIC ACID HYDROCHLORIDE

C5H10ClNO2S (183.0121)


   

3-Hydroxy-2-nitrobenzoic acid

3-Hydroxy-2-nitrobenzoic acid

C7H5NO5 (183.0168)


   

3-CHLORO-2,5,6-TRIFLUORO-4-PYRIDINOL

3-CHLORO-2,5,6-TRIFLUORO-4-PYRIDINOL

C5HClF3NO (182.9699)


   

3-(5-Nitro-2-furyl)acrylic Acid

3-(5-Nitro-2-furyl)acrylic Acid

C7H5NO5 (183.0168)


   

3,4-dichloropyridine hcl

3,4-dichloropyridine hcl

C5H4Cl3N (182.9409)


   

2-Bromo-6-cyanopyrazine

2-Bromo-6-cyanopyrazine

C5H2BrN3 (182.9432)


   

3-Cyano-4-fluorobenzoyl chloride

3-Cyano-4-fluorobenzoyl chloride

C8H3ClFNO (182.9887)


   

BENZONITRILE, 3-CHLORO-4-HYDROXY-5-METHOXY-

BENZONITRILE, 3-CHLORO-4-HYDROXY-5-METHOXY-

C8H6ClNO2 (183.0087)


   

5-Bromo-4-pyrimidinecarbonitrile

5-Bromo-4-pyrimidinecarbonitrile

C5H2BrN3 (182.9432)


   

2-CHLORO-4-METHYLBENZOTHIAZOLE

2-CHLORO-4-METHYLBENZOTHIAZOLE

C8H6ClNS (182.9909)


   

Phosphonic acid,P-(4-cyanophenyl)-

Phosphonic acid,P-(4-cyanophenyl)-

C7H6NO3P (183.0085)


   

5-BROMO-2-VINYLPYRIDINE

5-BROMO-2-VINYLPYRIDINE

C7H6BrN (182.9684)


   

1,2,4-trichloro-3,5,6-trideuteriobenzene

1,2,4-trichloro-3,5,6-trideuteriobenzene

C6Cl3D3 (182.9489)


   

trans-3-chloro-beta-nitrostyrene

trans-3-chloro-beta-nitrostyrene

C8H6ClNO2 (183.0087)


   

5-Bromopyrazine-2-carbonitrile

5-Bromopyrazine-2-carbonitrile

C5H2BrN3 (182.9432)


   

5-Chloro-2-cyano-3-nitropyridine

5-Chloro-2-cyano-3-nitropyridine

C6H2ClN3O2 (182.9836)


   

2-CHLORO-5-METHYLBENZO[D]THIAZOLE

2-CHLORO-5-METHYLBENZO[D]THIAZOLE

C8H6ClNS (182.9909)


   

2,4-DICHLORO-5-THIAZOLEMETHANOL

2,4-DICHLORO-5-THIAZOLEMETHANOL

C4H3Cl2NOS (182.9312)


   

(2E)-3-(6-Chloro-3-pyridinyl)acrylic acid

(2E)-3-(6-Chloro-3-pyridinyl)acrylic acid

C8H6ClNO2 (183.0087)


   

4-Chloro-β-nitrostyrene

4-Chloro-β-nitrostyrene

C8H6ClNO2 (183.0087)


   

1-(2-Chlorophenyl)-2-nitroethylene

1-(2-Chlorophenyl)-2-nitroethylene

C8H6ClNO2 (183.0087)


   

1-chloro-3-(2-nitrovinyl)benzene

1-chloro-3-(2-nitrovinyl)benzene

C8H6ClNO2 (183.0087)


   

2-chloro-6-methylbenzo[d]thiazole

2-chloro-6-methylbenzo[d]thiazole

C8H6ClNS (182.9909)


   

Thiazolo[5,4-d]pyrimidine-5,7(4H,6H)-dione,2-methyl-

Thiazolo[5,4-d]pyrimidine-5,7(4H,6H)-dione,2-methyl-

C6H5N3O2S (183.0102)


   

2-bromo-2-nitropropan-1-ol

2-bromo-2-nitropropan-1-ol

C3H6BrNO3 (182.9531)


   

6-hydroxy-2-sulfanylidene-1,7-dihydropyrrolo[2,3-d]pyrimidin-4-one

6-hydroxy-2-sulfanylidene-1,7-dihydropyrrolo[2,3-d]pyrimidin-4-one

C6H5N3O2S (183.0102)


   

N-dimethoxyphosphinothioylacetamide

N-dimethoxyphosphinothioylacetamide

C4H10NO3PS (183.0119)


   

2-(Chloromethyl)-1,3-Benzothiazole

2-(Chloromethyl)-1,3-Benzothiazole

C8H6ClNS (182.9909)


   

Benzenecarboperoxoicacid, 4-nitro-

Benzenecarboperoxoicacid, 4-nitro-

C7H5NO5 (183.0168)


   

2-Hydroxy-6-nitrobenzoic acid

2-Hydroxy-6-nitrobenzoic acid

C7H5NO5 (183.0168)


   

4,7-Difluoro-1H-indole-2,3-dione

4,7-Difluoro-1H-indole-2,3-dione

C8H3F2NO2 (183.0132)


   

(4R)-4-mercapto-L-proline hydrochloride

(4R)-4-mercapto-L-proline hydrochloride

C5H10ClNO2S (183.0121)


   

4-bromopyrimidine-2-carbonitrile

4-bromopyrimidine-2-carbonitrile

C5H2BrN3 (182.9432)


   

1,3-Thiazole-2-sulfonyl chloride

1,3-Thiazole-2-sulfonyl chloride

C3H2ClNO2S2 (182.9216)


   

7-Chloro-2-Methyl-thieno[3,2-b]pyridine

7-Chloro-2-Methyl-thieno[3,2-b]pyridine

C8H6ClNS (182.9909)


   

2,4-dihydroxy-5-nitrobenzaldehyde

2,4-dihydroxy-5-nitrobenzaldehyde

C7H5NO5 (183.0168)


   

3,4-Dihydroxy-6-nitrobenzaldehyde

3,4-Dihydroxy-6-nitrobenzaldehyde

C7H5NO5 (183.0168)


   

3-HYDROXY-4-NITROBENZOIC ACID

3-HYDROXY-4-NITROBENZOIC ACID

C7H5NO5 (183.0168)


   

2-(Methylamino)-5-(trifluoromethyl)-1,3,4-thiadiazole

2-(Methylamino)-5-(trifluoromethyl)-1,3,4-thiadiazole

C4H4F3N3S (183.0078)


   

chelidamic acid

4-hydroxypyridine-2,6-dicarboxylic acid

C7H5NO5 (183.0168)


   

3-chloro-4-fluorobenzoyl cyanide

3-chloro-4-fluorobenzoyl cyanide

C8H3ClFNO (182.9887)


   

Benzenesulfonyl isocyanate

Benzenesulfonyl isocyanate

C7H5NO3S (182.999)


   

4-Cyano-2,6-difluorobenzoic acid

4-Cyano-2,6-difluorobenzoic acid

C8H3F2NO2 (183.0132)


   

4-Chloro-2-methylthieno[3,2-c]pyridine

4-Chloro-2-methylthieno[3,2-c]pyridine

C8H6ClNS (182.9909)


   

METHYL THIAZOLIDINE-2-CARBOXYLATE HYDROCHLORIDE

METHYL THIAZOLIDINE-2-CARBOXYLATE HYDROCHLORIDE

C5H10ClNO2S (183.0121)


   

4,6-Difluoro-1H-indole-2,3-dione

4,6-Difluoro-1H-indole-2,3-dione

C8H3F2NO2 (183.0132)


   

phenylselenocyanate

phenylselenocyanate

C7H5NSe (182.9587)


   

2,2-DIFLUOROBENZO[D][1,3]DIOXOLE-5-CARBONITRILE

2,2-DIFLUOROBENZO[D][1,3]DIOXOLE-5-CARBONITRILE

C8H3F2NO2 (183.0132)


   

3-Hydroxy-5-nitrobenzoic acid

3-Hydroxy-5-nitrobenzoic acid

C7H5NO5 (183.0168)


   

5-Bromo-2-pyrimidinecarbonitrile

5-Bromo-2-pyrimidinecarbonitrile

C5H2BrN3 (182.9432)


   

1,3,5-Trichloro(2H3)benzene

1,3,5-Trichloro(2H3)benzene

C6Cl3D3 (182.9489)


   

7-Fluoro-4-methoxy-1,2-benzothiazole

7-Fluoro-4-methoxy-1,2-benzothiazole

C8H6FNOS (183.0154)


   

(5-Fluoro-1,3-benzothiazol-2-yl)methanol

(5-Fluoro-1,3-benzothiazol-2-yl)methanol

C8H6FNOS (183.0154)


   

2-Bromo-5-pyrimidinecarbonitrile

2-Bromo-5-pyrimidinecarbonitrile

C5H2BrN3 (182.9432)


   

methyl 2-isocyanatothiophene-3-carboxylate(SALTDATA: FREE)

methyl 2-isocyanatothiophene-3-carboxylate(SALTDATA: FREE)

C7H5NO3S (182.999)


   

5,6-Difluoroisatin

5,6-Difluoroisatin

C8H3F2NO2 (183.0132)


   

Thiomorpholine-3-carboxylic acid hydrochloride

Thiomorpholine-3-carboxylic acid hydrochloride

C5H10ClNO2S (183.0121)


   

(6-FLUOROBENZO[D]THIAZOL-2-YL)METHANOL

(6-FLUOROBENZO[D]THIAZOL-2-YL)METHANOL

C8H6FNOS (183.0154)


   

3-vinyl-5-bromo-pyridine

3-vinyl-5-bromo-pyridine

C7H6BrN (182.9684)


   

2-(CHLOROMETHYL)-5-METHYLTHIAZOLE

2-(CHLOROMETHYL)-5-METHYLTHIAZOLE

C5H7Cl2NS (182.9676)


   

4-CHLOROMETHYL-2-METHYLTHIAZOLE HYDROCHLORIDE

4-CHLOROMETHYL-2-METHYLTHIAZOLE HYDROCHLORIDE

C5H7Cl2NS (182.9676)


   

2-chloro-5-nitronicotinonitrile

2-chloro-5-nitronicotinonitrile

C6H2ClN3O2 (182.9836)


   

4-Thiazolidinecarboxylicacid, methyl ester, hydrochloride (1:1)

4-Thiazolidinecarboxylicacid, methyl ester, hydrochloride (1:1)

C5H10ClNO2S (183.0121)


   

3-hydroxypyridine-2,6-dicarboxylic acid

3-hydroxypyridine-2,6-dicarboxylic acid

C7H5NO5 (183.0168)


   

5-CHLORO-6-METHYLBENZO[D]OXAZOL-2(3H)-ONE

5-CHLORO-6-METHYLBENZO[D]OXAZOL-2(3H)-ONE

C8H6ClNO2 (183.0087)


   

5,7-Difluoro-1H-indole-2,3-dione

5,7-Difluoro-1H-indole-2,3-dione

C8H3F2NO2 (183.0132)


   

4-CHLORO-2-METHYLBENZO[D]THIAZOLE

4-CHLORO-2-METHYLBENZO[D]THIAZOLE

C8H6ClNS (182.9909)


   

4-cyano-2,5-difluoro-benzoic acid

4-cyano-2,5-difluoro-benzoic acid

C8H3F2NO2 (183.0132)


   

(4-fluoro-1,3-benzothiazol-2-yl)methanol

(4-fluoro-1,3-benzothiazol-2-yl)methanol

C8H6FNOS (183.0154)


   

4-Hydroxy-3-nitrobenzoic acid

4-Hydroxy-3-nitrobenzoic acid

C7H5NO5 (183.0168)


   

5-chloro-2-methylphenyl isothiocyanate

5-chloro-2-methylphenyl isothiocyanate

C8H6ClNS (182.9909)


   

4-chloro-2-methylphenyl isothiocyanate

4-chloro-2-methylphenyl isothiocyanate

C8H6ClNS (182.9909)


   

3-chloro-4-methylphenyl isothiocyanate

3-chloro-4-methylphenyl isothiocyanate

C8H6ClNS (182.9909)


   

2-Hydroxy-3-nitrobenzoic acid

2-Hydroxy-3-nitrobenzoic acid

C7H5NO5 (183.0168)


   

[4-(trifluoromethyl)-1,3-thiazol-2-yl]hydrazine

[4-(trifluoromethyl)-1,3-thiazol-2-yl]hydrazine

C4H4F3N3S (183.0078)


   

4-Hydroxy-2-nitrobenzoic acid

4-Hydroxy-2-nitrobenzoic acid

C7H5NO5 (183.0168)


   

4-Methyl-5-(trifluoromethyl)-1,2,4-triazolin-3(2H)-thione

4-Methyl-5-(trifluoromethyl)-1,2,4-triazolin-3(2H)-thione

C4H4F3N3S (183.0078)


   

2-Aminohexafluoropropan-2-ol

2-Aminohexafluoropropan-2-ol

C3H3F6NO (183.0119)


   

7-Chloro-2H-benzo[b][1,4]oxazin-3(4H)-one

7-Chloro-2H-benzo[b][1,4]oxazin-3(4H)-one

C8H6ClNO2 (183.0087)


   

[4-(trifluoromethyl)-1,3-thiazol-2-yl]methanol

[4-(trifluoromethyl)-1,3-thiazol-2-yl]methanol

C5H4F3NOS (182.9966)


   

4-Cyano-2,3-difluorobenzoic acid

4-Cyano-2,3-difluorobenzoic acid

C8H3F2NO2 (183.0132)


   

(5-chlorothiophen-3-yl)methanamine,hydrochloride

(5-chlorothiophen-3-yl)methanamine,hydrochloride

C5H7Cl2NS (182.9676)


   

3,4-Dihydroxy-5-nitrobenzaldehyde

3,4-Dihydroxy-5-nitrobenzaldehyde

C7H5NO5 (183.0168)


   

6-chloro-2h-1,4-benzoxazin-3(4h)-one

6-chloro-2h-1,4-benzoxazin-3(4h)-one

C8H6ClNO2 (183.0087)


   

4-CHLORO-6-FLUOROPYRIDO[3,4-D]PYRIMIDINE

4-CHLORO-6-FLUOROPYRIDO[3,4-D]PYRIMIDINE

C7H3ClFN3 (183)


   

4-chloro-7-fluoropyrido[4,3-d]pyrimidine

4-chloro-7-fluoropyrido[4,3-d]pyrimidine

C7H3ClFN3 (183)


   

3-chloro-2-methylphenyl isothiocyanate

3-chloro-2-methylphenyl isothiocyanate

C8H6ClNS (182.9909)


   

3-CHLORO-4-METHOXYPHENYL ISOCYANATE

3-CHLORO-4-METHOXYPHENYL ISOCYANATE

C8H6ClNO2 (183.0087)


   

Benzene,1-chloro-4-(isothiocyanatomethyl)-

Benzene,1-chloro-4-(isothiocyanatomethyl)-

C8H6ClNS (182.9909)


   

3-(CHLOROMETHYL)-5-(2-FURYL)ISOXAZOLE

3-(CHLOROMETHYL)-5-(2-FURYL)ISOXAZOLE

C8H6ClNO2 (183.0087)


   

2-(PHENYLTHIO)ETHANETHIOAMIDE

2-(PHENYLTHIO)ETHANETHIOAMIDE

C8H9NS2 (183.0176)


   

Ruthenium red

Ruthenium red

C8H6ClNS (182.9909)


   

6-Oxo-1,6-dihydro-2,5-pyridinedicarboxylic acid

6-Oxo-1,6-dihydro-2,5-pyridinedicarboxylic acid

C7H5NO5 (183.0168)


   

2-Chloro-4-methyl-benzothiozole

2-Chloro-4-methyl-benzothiozole

C8H6ClNS (182.9909)


   

6,7-Difluoro-1H-Indole-2,3-Dione

6,7-Difluoro-1H-Indole-2,3-Dione

C8H3F2NO2 (183.0132)


   

2,6-Difluorobenzoyl isocyanate

2,6-Difluorobenzoyl isocyanate

C8H3F2NO2 (183.0132)


   

(2-CHLORO-PHENYL)-OXO-ACETALDEHYDE OXIME

(2-CHLORO-PHENYL)-OXO-ACETALDEHYDE OXIME

C8H6ClNO2 (183.0087)


   

2,3-Difluoro-5-(trifluoromethyl)pyridine

2,3-Difluoro-5-(trifluoromethyl)pyridine

C6H2F5N (183.0107)


   

3,5-Dichloro-2,6-difluoropyridine

3,5-Dichloro-2,6-difluoropyridine

C5HCl2F2N (182.9454)


   

6-Chloro-2-cyano-3-nitropyridine

6-Chloro-2-cyano-3-nitropyridine

C6H2ClN3O2 (182.9836)


   

5-chloro-2-methoxyphenyl isocyanate

5-chloro-2-methoxyphenyl isocyanate

C8H6ClNO2 (183.0087)


   

2-metyl-5-chloro-benzothiazole

2-metyl-5-chloro-benzothiazole

C8H6ClNS (182.9909)


   

5,6-Difluoroindoline-2,3-dione

5,6-Difluoroindoline-2,3-dione

C8H3F2NO2 (183.0132)


   

2-(1-BROMOVINYL)-PYRIDINE

2-(1-BROMOVINYL)-PYRIDINE

C7H6BrN (182.9684)


   

2,2-Difluoro-1,3-benzodioxole-4-carbonitrile

2,2-Difluoro-1,3-benzodioxole-4-carbonitrile

C8H3F2NO2 (183.0132)


   

4-Nitrosalicylic Acid

4-Nitrosalicylic Acid

C7H5NO5 (183.0168)


   

Piperidine-1-sulfonyl chloride

Piperidine-1-sulfonyl chloride

C5H10ClNO2S (183.0121)


   

2,4-Dinitrophenolate

2,4-Dinitrophenolate

C6H3N2O5- (183.0042)


   

Methyl phenyldithiocarbamate

Methyl phenyldithiocarbamate

C8H9NS2 (183.0176)


   

(2R)-2-ammonio-3-(methylselanyl)propanoate

(2R)-2-ammonio-3-(methylselanyl)propanoate

C4H9NO2Se (182.9798)


   

3-Phospho-L-serine

3-Phospho-L-serine

C3H6NO6P-2 (182.9933)


   

3-phosphonato-D-glycerate(3-)

3-phosphonato-D-glycerate(3-)

C3H4O7P-3 (182.9695)


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2-phosphonato-D-glycerate(3-)

2-phosphonato-D-glycerate(3-)

C3H4O7P-3 (182.9695)


   

3-Carboxy-cis,cis-muconate

3-Carboxy-cis,cis-muconate

C7H3O6-3 (182.993)


   

O-phosphonatooxy-D-serine(2-)

O-phosphonatooxy-D-serine(2-)

C3H6NO6P-2 (182.9933)


   

2-Carboxy-cis,cis-muconate

2-Carboxy-cis,cis-muconate

C7H3O6-3 (182.993)


   

2-oxoethyl-CoM

2-oxoethyl-CoM

C4H7O4S2- (182.9786)


   

5-chloro-5-deoxy-D-ribonate

5-chloro-5-deoxy-D-ribonate

C5H8ClO5- (183.006)


   

(3E)-buta-1,3-diene-1,1,4-tricarboxylate

(3E)-buta-1,3-diene-1,1,4-tricarboxylate

C7H3O6-3 (182.993)


   

(2Z,4E)-5-amino-2-formylhexa-2,4-dienedioate

(2Z,4E)-5-amino-2-formylhexa-2,4-dienedioate

C7H5NO5-2 (183.0168)


   

2-Carboxyethyldimethylselenonium

2-Carboxyethyldimethylselenonium

C5H11O2Se+ (182.9924)


   

2-Phosphoglycerate(3-)

2-Phosphoglycerate(3-)

C3H4O7P-3 (182.9695)


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Se-methyl-D-selenocysteine

Se-methyl-D-selenocysteine

C4H9NO2Se (182.9798)


A D-alpha-amino acid compound having methylselanylmethyl as the side-chain. D020011 - Protective Agents > D016588 - Anticarcinogenic Agents D000970 - Antineoplastic Agents

   

cis,cis-2-Amino-3-(3-oxoprop-1-enyl)but-2-enedioate

cis,cis-2-Amino-3-(3-oxoprop-1-enyl)but-2-enedioate

C7H5NO5-2 (183.0168)


   

5-Hydroxyisouric acid anion

5-Hydroxyisouric acid anion

C5H3N4O4- (183.0154)


The conjugate base of 5-hydroxyisouric acid.

   

3-Phosphoglycerate(3-)

3-Phosphoglycerate(3-)

C3H4O7P-3 (182.9695)


   

Arsonoacetic acid anion

Arsonoacetic acid anion

C2H4AsO5- (182.9275)


   

2-Isothiocyanatoethyl phosphate

2-Isothiocyanatoethyl phosphate

C3H6NO4PS (182.9755)


   

2-Amino-3-(3-oxoprop-1-enyl)but-2-enedioate

2-Amino-3-(3-oxoprop-1-enyl)but-2-enedioate

C7H5NO5-2 (183.0168)


   

2-(Carboxylatomethyl)-5-oxo-2,5-dihydrofuran-2-ide-3-carboxylate

2-(Carboxylatomethyl)-5-oxo-2,5-dihydrofuran-2-ide-3-carboxylate

C7H3O6-3 (182.993)


   

(2Z,4E)-4-amino-6-oxohepta-2,4-dienedioate

(2Z,4E)-4-amino-6-oxohepta-2,4-dienedioate

C7H5NO5-2 (183.0168)


   

O-phosphonatooxyserine(2-)

O-phosphonatooxyserine(2-)

C3H6NO6P-2 (182.9933)


   

Methyl 1,3-thiazolane-2-carboxylate hydrochloride

Methyl 1,3-thiazolane-2-carboxylate hydrochloride

C5H10ClNO2S (183.0121)


   

4-deoxy-4-sulfo-D-erythrose

4-deoxy-4-sulfo-D-erythrose

C4H7O6S- (182.9963)


   

4-deoxy-4-sulfo-D-erythrulose

4-deoxy-4-sulfo-D-erythrulose

C4H7O6S- (182.9963)


   

tetraaquasilver(II)

tetraaquasilver(II)

AgH12O4+4 (182.9787)


   

5-Nitrosalicylic acid

Salicylic acid, 5-nitro-

C7H5NO5 (183.0168)


A monohydroxybenzoic acid in which the hydroxy group is ortho- to the carboxylic acid group and which has a nitro substituent para- to the phenolic hydroxy group.

   

O-phosphonato-L-serine(2-)

O-phosphonato-L-serine(2-)

C3H6NO6P (182.9933)


An O-phosphonatooxyserine(2-) that is the conjugate base of O-phospho-L-serine.

   

Se-methyl-L-selenocysteine zwitterion

Se-methyl-L-selenocysteine zwitterion

C4H9NO2Se (182.9798)


Zwitterionic form of Se-methyl-L-selenocysteine.

   

2,4-dinitrophenol(1-)

2,4-dinitrophenol(1-)

C6H3N2O5 (183.0042)


A phenolate anion obtained from 2,4-dinitrophenol. It is the major microspecies at pH 7.3 (according to Marvin v 6.2.0.).

   

3-phosphonato-D-glycerate(3-)

3-phosphonato-D-glycerate(3-)

C3H4O7P (182.9695)


An organophosphate oxoanion arising from deprotonation of the carboxy and phosphate OH groups of 3-phospho-D-glyceric acid; major species at pH 7.3.

   

selenohomocysteine

L-Selenohomocysteine

C4H9NO2Se (182.9798)


A selenoamino acid that is the selenium analogue of L-homocysteine.

   

2-Phosphoglycerate(3-)

2-Phosphoglycerate(3-)

C3H4O7P (182.9695)


A phosphoglycerate obtained by deprotonation of the carboxy and phosphate OH groups of 2-phosphoglyceric acid.

   

3-Phosphoglycerate(3-)

3-Phosphoglycerate(3-)

C3H4O7P (182.9695)


Trianion of 3-phosphoglyceric acid arising from deprotonation of the carboxy and phosphate groups; major species at pH 7.3.

   

2-Amino-3-(3-oxoprop-1-enyl)but-2-enedioate

2-Amino-3-(3-oxoprop-1-enyl)but-2-enedioate

C7H5NO5 (183.0168)


   

O-phosphonatooxyserine(2-)

O-phosphonatooxyserine(2-)

C3H6NO6P (182.9933)


An organophosphate oxoanion that is the dianionic form of O-phosphoserine having anionic phosphate and carboxy functions and a protonated amino group.

   

Se-Methyl-L-selenocysteine

Se-Methyl-L-selenocysteine

C4H9NO2Se (182.9798)


An L-alpha-amino acid compound having methylselanylmethyl as the side-chain.

   

O-phosphonatooxy-D-serine(2-)

O-phosphonatooxy-D-serine(2-)

C3H6NO6P (182.9933)


An O-phosphonatooxyserine(2-) that is the dianion of O-phospho-D-serine.

   

Se-Methylselenocysteine

Se-Methylselenocysteine

C4H9NO2Se (182.9798)


An alpha-amino acid compound having methylselanylmethyl as the side-chain.

   

cis,cis-2-Amino-3-(3-oxoprop-1-enyl)but-2-enedioate

cis,cis-2-Amino-3-(3-oxoprop-1-enyl)but-2-enedioate

C7H5NO5 (183.0168)


The cis,cis-isomer of 2-amino-3-(3-oxoprop-1-enyl)but-2-enedioate.

   

2-phosphonato-D-glycerate(3-)

2-phosphonato-D-glycerate(3-)

C3H4O7P (182.9695)


An organophosphate oxoanion arising from deprotonation of the phosphate OH and carboxy groups of 2-phospho-D-glyceric acid; major species at pH 7.3.

   

L-selenohomocysteine zwitterion

L-selenohomocysteine zwitterion

C4H9NO2Se (182.9798)


An L-alpha-amino acid zwitterion obtained from L-selenohomocysteine by transfer of a proton from the carboxy group to the amino group. It is the major species at pH 7.3.

   

(1s,6r)-2-hydroxy-4-imino-5-oxo-7-oxabicyclo[4.1.0]hept-2-ene-3-carboxylic acid

(1s,6r)-2-hydroxy-4-imino-5-oxo-7-oxabicyclo[4.1.0]hept-2-ene-3-carboxylic acid

C7H5NO5 (183.0168)


   

(1s)-4-amino-2,5-dioxo-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic acid

(1s)-4-amino-2,5-dioxo-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic acid

C7H5NO5 (183.0168)