Exact Mass: 122.98472140000001

Exact Mass Matches: 122.98472140000001

Found 97 metabolites which its exact mass value is equals to given mass value 122.98472140000001, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Nicotinic acid

pyridine-3-carboxylic acid

C6H5NO2 (123.032027)


Nicotinic acid is an odorless white crystalline powder with a feebly acid taste. pH (saturated aqueous solution) 2.7. pH (1.3\\\\\% solution) 3-3.5. (NTP, 1992) Nicotinic acid is a pyridinemonocarboxylic acid that is pyridine in which the hydrogen at position 3 is replaced by a carboxy group. It has a role as an antidote, an antilipemic drug, a vasodilator agent, a metabolite, an EC 3.5.1.19 (nicotinamidase) inhibitor, an Escherichia coli metabolite, a mouse metabolite, a human urinary metabolite and a plant metabolite. It is a vitamin B3, a pyridinemonocarboxylic acid and a pyridine alkaloid. It is a conjugate acid of a nicotinate. Niacin is a B vitamin used to treat vitamin deficiencies as well as hyperlipidemia, dyslipidemia, hypertriglyceridemia, and to reduce the risk of myocardial infarctions. Nicotinic acid is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Niacin is a Nicotinic Acid. Niacin, also known as nicotinic acid and vitamin B3, is a water soluble, essential B vitamin that, when given in high doses, is effective in lowering low density lipoprotein (LDL) cholesterol and raising high density lipoprotein (HDL) cholesterol, which makes this agent of unique value in the therapy of dyslipidemia. Niacin can cause mild-to-moderate serum aminotransferase elevations and high doses and certain formulations of niacin have been linked to clinically apparent, acute liver injury which can be severe as well as fatal. Niacin is a water-soluble vitamin belonging to the vitamin B family, which occurs in many animal and plant tissues, with antihyperlipidemic activity. Niacin is converted to its active form niacinamide, which is a component of the coenzymes nicotinamide adenine dinucleotide (NAD) and its phosphate form, NADP. These coenzymes play an important role in tissue respiration and in glycogen, lipid, amino acid, protein, and purine metabolism. Although the exact mechanism of action by which niacin lowers cholesterol is not fully understood, it may act by inhibiting the synthesis of very low density lipoproteins (VLDL), inhibiting the release of free fatty acids from adipose tissue, increasing lipoprotein lipase activity, and reducing the hepatic synthesis of VLDL-C and LDL-C. Nicotinic acid, also known as niacin or vitamin B3, is a water-soluble vitamin whose derivatives such as NADH, NAD, NAD+, and NADP play essential roles in energy metabolism in the living cell and DNA repair. The designation vitamin B3 also includes the amide form, nicotinamide or niacinamide. Severe lack of niacin causes the deficiency disease pellagra, whereas a mild deficiency slows down the metabolism decreasing cold tolerance. The recommended daily allowance of niacin is 2-12 mg a day for children, 14 mg a day for women, 16 mg a day for men, and 18 mg a day for pregnant or breast-feeding women. It is found in various animal and plant tissues and has pellagra-curative, vasodilating, and antilipemic properties. The liver can synthesize niacin from the essential amino acid tryptophan (see below), but the synthesis is extremely slow and requires vitamin B6; 60 mg of tryptophan are required to make one milligram of niacin. Bacteria in the gut may also perform the conversion but are inefficient. A water-soluble vitamin of the B complex occurring in various animal and plant tissues. It is required by the body for the formation of coenzymes NAD and NADP. It has PELLAGRA-curative, vasodilating, and antilipemic properties. Nicotinic acid, also known as niacin or vitamin B3, is a water-soluble vitamin whose derivatives such as NADH, NAD, NAD+, and NADP play essential roles in energy metabolism in the living cell and DNA repair. The designation vitamin B3 also includes the amide form, nicotinamide or niacinamide. Severe lack of niacin causes the deficiency disease pellagra, whereas a mild deficiency slows down the metabolism decreasing cold tolerance. The recommended daily allowance of niacin is 2-12 mg a day for children, 14 mg a day for women, 16 mg a day for men, and 18 mg a day for pregnant or breast-feeding women. It is found in various animal and plant tissues and has pellagra-curative, vasodilating, and antilipemic properties. The liver can synthesize niacin from the essential amino acid tryptophan, but the synthesis is extremely slow and requires vitamin B6; 60 mg of tryptophan are required to make one milligram of niacin. Bacteria in the gut may also perform the conversion but are inefficient. Nicotinic acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=59-67-6 (retrieved 2024-06-29) (CAS RN: 59-67-6). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Niacin (Vitamin B3) is an orally active water-soluble B3 vitamin that is an essential nutrient for humans. Niacin (Vitamin B3) plays a key role in energy metabolism, cell signaling cascades regulating gene expression and apoptosis. Niacin (Vitamin B3) is also used in the study of cardiovascular diseases[1][2]. Niacin (Vitamin B3) is an orally active water-soluble B3 vitamin that is an essential nutrient for humans. Niacin (Vitamin B3) plays a key role in energy metabolism, cell signaling cascades regulating gene expression and apoptosis. Niacin (Vitamin B3) is also used in the study of cardiovascular diseases[1][2].

   

Isonicotinic acid

Pyridine-4-carboxylic Acid; Nicotinic Acid Imp. E (EP); Isonicotinic Acid; Isoniazid Impurity A; Nicotinic Acid Impurity E

C6H5NO2 (123.032027)


Isonicotinic acid is a pyridinemonocarboxylic acid in which the carboxy group is at position 4 of the pyridine ring. It has a role as a human metabolite and an algal metabolite. It is a conjugate acid of an isonicotinate. Isonicotinic acid is a natural product found in Aloe africana, Chlamydomonas reinhardtii, and other organisms with data available. Heterocyclic acids that are derivatives of 4-pyridinecarboxylic acid (isonicotinic acid). Isonicotinic acid is a metabolite of isoniazid. Isonicotinic acid is an organic compound with a carboxyl group on a pyridine ring. It is an isomer of nicotinic acid. The carboxyl group for isonicotinic acid is on the 4-position instead of the 3-position for nicotinic acid (Wikipedia). A pyridinemonocarboxylic acid in which the carboxy group is at position 4 of the pyridine ring. Acquisition and generation of the data is financially supported in part by CREST/JST. KEIO_ID I017 Isonicotinic acid is a metabolite of Isoniazid. Isoniazid is converted to Isonicotinic acid by hydrazinolysis, with the Isoniazid to Isonicotinic acid biotransformation also to be catalyzed by cytochrome P450 (CYP) enzymes, e.g., CYP2C[1].

   

Picolinic acid

5-Aminopyridine-2-carboxylic acid

C6H5NO2 (123.032027)


Picolinic acid is a metabolite of the tryptophan catabolism. Picolinic acid is produced under inflammatory conditions and a costimulus with interferon-gamma (IFNgamma) of macrophage (Mphi) effector functions, is a selective inducer of the Mphi inflammatory protein-1alpha (MIP-1alpha) and -1beta (MIPs), two chemokines/cytokines involved in the elicitation of the inflammatory reactions and in the development of the Th1 responses. IFNgamma and picolinic acid have reciprocal effects on the production of MIPs chemokines and the expression of their receptor. The concerted action of IFNgamma and picolinic acid on MIP-1alpha/beta chemokine/receptor system is likely to be of pathophysiological significance and to represent an important regulatory mechanism for leukocyte recruitment and distribution into damaged tissues during inflammatory responses. Picolinic acid has an effect on the production of L-arginine-derived reactive nitrogen intermediates in macrophages, by augmenting IFN-gamma-induced NO2- production, and acts synergistically with IFN-gamma in activating macrophages. Children with acrodermatitis enteropathica (AE) are treated with oral zinc dipicolinate (zinc-PA). The concentration of picolinic acid in the plasma of asymptomatic children with AE was significantly less than that of normal children. However, oral treatment with PA alone is ineffective. The results support the hypothesis that the genetic defect in AE is in the tryptophan pathway, although the role of PA in zinc metabolism remains to be defined. (PMID:15206716, 8473748, 1701787, 6694049). Picolinic acid is a metabolite of the tryptophan catabolism. Picolinic acid is produced under inflammatory conditions and a costimulus with interferon-gamma (IFNgamma) of macrophage (Mphi) effector functions, is a selective inducer of the Mphi inflammatory protein-1alpha (MIP-1alpha) and -1beta (MIPs), two chemokines/cytokines involved in the elicitation of the inflammatory reactions and in the development of the Th1 responses. IFNgamma and picolinic acid have reciprocal effects on the production of MIPs chemokines and the expression of their receptor. The concerted action of IFNgamma and picolinic acid on MIP-1alpha/beta chemokine/receptor system is likely to be of pathophysiological significance and to represent an important regulatory mechanism for leukocyte recruitment and distribution into damaged tissues during inflammatory responses. Picolinic acid has an effect on the production of L-arginine-derived reactive nitrogen intermediates in macrophages, by augmenting IFN-gamma-induced NO2- production, and acts synergistically with IFN-gamma in activating macrophages. D064449 - Sequestering Agents > D002614 - Chelating Agents > D007502 - Iron Chelating Agents [Raw Data] CBA16_Picolinic-acid_pos_10eV_1-8_01_816.txt [Raw Data] CBA16_Picolinic-acid_pos_20eV_1-8_01_817.txt KEIO_ID P045 Picolinic acid (PCL 016) is a topical antiviral agent, which inhibits adenovirus replication in rabbits.

   

Nitrobenzene

Hydroxy(phenyl)azane oxide (acd/name 4.0)

C6H5NO2 (123.032027)


Approximately 95\\% of nitrobenzene is consumed in the production of aniline, which is a precursor to rubber chemicals, pesticides, dyes, explosives, and pharmaceuticals. Nitrobenzene is an organic compound with the chemical formula C6H5NO2. It is a water-insoluble pale yellow oil with an almond-like odor. It freezes to give greenish-yellow crystals. It is produced on a large scale from benzene as a precursor to aniline. In the laboratory, it is occasionally used as a solvent, especially for electrophilic reagents. Nitrobenzene is prepared by nitration of benzene with a mixture of concentrated sulfuric acid, water, and nitric acid. This mixture is sometimes called mixed acid. The production of nitrobenzene is one of the most dangerous processes conducted in the chemical industry because of the exothermicity of the reaction ( delta H = 117 kJ/mol).

   

3-Chloroalanine

3-Chloro-D-alanine

C3H6ClNO2 (123.0087046)


   

2-Thiopheneacetonitrile

2-Thiopheneacetonitrile

C6H5NS (123.014269)


   
   

2-Hydroxy-4-imino-2,5-cyclohexadienone

2-hydroxy-4-iminocyclohexa-2,5-dien-1-one

C6H5NO2 (123.032027)


2-Hydroxy-4-imino-2,5-cyclohexadienone is found in mushrooms. Red pigment found in the sporulating gill tissue of the mushroom Agaricus bisporus (button mushroom

   

3-Chloro-D-alanine

3-Chloroalanine hydrochloride, (DL-ala)-isomer

C3H6ClNO2 (123.0087046)


   

2-Chloro-L-alanine

2-amino-2-chloropropanoic acid

C3H6ClNO2 (123.0087046)


   
   

nicotinate

Nicotinic acid

C6H5NO2 (123.032027)


Niacin (Vitamin B3) is an orally active water-soluble B3 vitamin that is an essential nutrient for humans. Niacin (Vitamin B3) plays a key role in energy metabolism, cell signaling cascades regulating gene expression and apoptosis. Niacin (Vitamin B3) is also used in the study of cardiovascular diseases[1][2]. Niacin (Vitamin B3) is an orally active water-soluble B3 vitamin that is an essential nutrient for humans. Niacin (Vitamin B3) plays a key role in energy metabolism, cell signaling cascades regulating gene expression and apoptosis. Niacin (Vitamin B3) is also used in the study of cardiovascular diseases[1][2].

   

Nicotinic acid

Nicotinic acid

C6H5NO2 (123.032027)


CONFIDENCE standard compound; INTERNAL_ID 488; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 706; ORIGINAL_PRECURSOR_SCAN_NO 705 C - Cardiovascular system > C10 - Lipid modifying agents > C10A - Lipid modifying agents, plain > C10AD - Nicotinic acid and derivatives C - Cardiovascular system > C04 - Peripheral vasodilators > C04A - Peripheral vasodilators > C04AC - Nicotinic acid and derivatives D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents D018977 - Micronutrients > D014815 - Vitamins D009676 - Noxae > D000963 - Antimetabolites COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS CONFIDENCE standard compound; INTERNAL_ID 488; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 699; ORIGINAL_PRECURSOR_SCAN_NO 697 CONFIDENCE standard compound; INTERNAL_ID 488; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 707; ORIGINAL_PRECURSOR_SCAN_NO 706 CONFIDENCE standard compound; INTERNAL_ID 488; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1277; ORIGINAL_PRECURSOR_SCAN_NO 1275 CONFIDENCE standard compound; INTERNAL_ID 488; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1271; ORIGINAL_PRECURSOR_SCAN_NO 1269 CONFIDENCE standard compound; INTERNAL_ID 488; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1283; ORIGINAL_PRECURSOR_SCAN_NO 1281 CONFIDENCE standard compound; INTERNAL_ID 488; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 1265; ORIGINAL_PRECURSOR_SCAN_NO 1263 MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; PVNIIMVLHYAWGP_STSL_0169_Nicotinic acid_0125fmol_180506_S2_LC02_MS02_96; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. MS2 deconvoluted using CorrDec from all ion fragmentation data, MetaboLights identifier MTBLS1040; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. Niacin (Vitamin B3) is an orally active water-soluble B3 vitamin that is an essential nutrient for humans. Niacin (Vitamin B3) plays a key role in energy metabolism, cell signaling cascades regulating gene expression and apoptosis. Niacin (Vitamin B3) is also used in the study of cardiovascular diseases[1][2]. Niacin (Vitamin B3) is an orally active water-soluble B3 vitamin that is an essential nutrient for humans. Niacin (Vitamin B3) plays a key role in energy metabolism, cell signaling cascades regulating gene expression and apoptosis. Niacin (Vitamin B3) is also used in the study of cardiovascular diseases[1][2].

   

Isonicotinic acid

Isonicotinic acid

C6H5NO2 (123.032027)


Isonicotinic acid is a metabolite of Isoniazid. Isoniazid is converted to Isonicotinic acid by hydrazinolysis, with the Isoniazid to Isonicotinic acid biotransformation also to be catalyzed by cytochrome P450 (CYP) enzymes, e.g., CYP2C[1].

   

picolinic acid

2-Pyridinecarboxylic acid

C6H5NO2 (123.032027)


A pyridinemonocarboxylic acid in which the carboxy group is located at position 2. It is an intermediate in the metabolism of tryptophan. D064449 - Sequestering Agents > D002614 - Chelating Agents > D007502 - Iron Chelating Agents Picolinic acid (PCL 016) is a topical antiviral agent, which inhibits adenovirus replication in rabbits.

   
   

Nicotinic acid; LC-tDDA; CE10

Nicotinic acid; LC-tDDA; CE10

C6H5NO2 (123.032027)


   

Nicotinic acid; LC-tDDA; CE20

Nicotinic acid; LC-tDDA; CE20

C6H5NO2 (123.032027)


   
   

Nicotinic Acid-13C6

Nicotinic Acid-13C6

C6H5NO2 (123.032027)


   

Dimethylcarbamothioic chloride

Dimethylcarbamothioic chloride

C3H6ClNS (122.9909466)


   

2,3-Dichloropropanenitrile

2,3-Dichloropropanenitrile

C3H3Cl2N (122.9642538)


   

3-Hydroxy-2-pyridinecarbaldehyde

3-Hydroxy-2-pyridinecarbaldehyde

C6H5NO2 (123.032027)


   

3-FORMYLPYRIDINE 1-OXIDE

3-FORMYLPYRIDINE 1-OXIDE

C6H5NO2 (123.032027)


   

6-Hydroxynicotinaldehyde

6-Hydroxynicotinaldehyde

C6H5NO2 (123.032027)


   

Nitrobenzene-13C6

Nitrobenzene-13C6

C6H5NO2 (123.032027)


   

4-methylthiophene-3-carbonitrile

4-methylthiophene-3-carbonitrile

C6H5NS (123.014269)


   

3-Methyl-2-thiophenecarbonitrile

3-Methyl-2-thiophenecarbonitrile

C6H5NS (123.014269)


   

Propane,1-chloro-1-nitro-

Propane,1-chloro-1-nitro-

C3H6ClNO2 (123.0087046)


   

2-Oxo-1,2-dihydropyridine-3-carbaldehyde

2-Oxo-1,2-dihydropyridine-3-carbaldehyde

C6H5NO2 (123.032027)


   

Propane,1-chloro-2-nitro-

Propane,1-chloro-2-nitro-

C3H6ClNO2 (123.0087046)


   

5-methylthiophene-3-carbonitrile

5-methylthiophene-3-carbonitrile

C6H5NS (123.014269)


   
   

2-Chloroethyl carbamate

2-Chloroethyl carbamate

C3H6ClNO2 (123.0087046)


   

5-Fluoro-2-pyrimidinecarbonitrile

5-Fluoro-2-pyrimidinecarbonitrile

C5H2FN3 (123.02327439999999)


   

[oxido(oxo)azaniumyl]benzene

[oxido(oxo)azaniumyl]benzene

C6H5NO2 (123.032027)


   
   

3-Hydroxyisonicotinaldehyde

3-Hydroxyisonicotinaldehyde

C6H5NO2 (123.032027)


   
   

5-Hydroxypicolinaldehyde

5-Hydroxypicolinaldehyde

C6H5NO2 (123.032027)


   

5-hydroxynicotinaldehyde

5-hydroxynicotinaldehyde

C6H5NO2 (123.032027)


   

N-Methylolchloroacetamide

N-Methylolchloroacetamide

C3H6ClNO2 (123.0087046)


   

Sodium 1H-1,2,3-triazole-4-thiolate

Sodium 1H-1,2,3-triazole-4-thiolate

C2H2N3NaS (122.9867132)


   

3-FORMYL-4(1H)-PYRIDONE

3-FORMYL-4(1H)-PYRIDONE

C6H5NO2 (123.032027)


   

4-Ethynyl-2-methylthiazole

4-Ethynyl-2-methylthiazole

C6H5NS (123.014269)


   

N-methoxy-N-methylcarbamoyl chloride

N-methoxy-N-methylcarbamoyl chloride

C3H6ClNO2 (123.0087046)


   

4-Benzoquinone Monoxime

4-Benzoquinone Monoxime

C6H5NO2 (123.032027)


   

2,2-dichloropropanenitrile

2,2-dichloropropanenitrile

C3H3Cl2N (122.9642538)


   

4-Nitrosophenol

4-Nitrosophenol

C6H5NO2 (123.032027)


   
   

2-Hydroxypyridine-4-carbaldehyde

2-Hydroxypyridine-4-carbaldehyde

C6H5NO2 (123.032027)


   

4-Methylthiophene-2-carbonitrile

4-Methylthiophene-2-carbonitrile

C6H5NS (123.014269)


   

1,3]DIOXOLO[4,5-B]PYRIDINE

1,3]DIOXOLO[4,5-B]PYRIDINE

C6H5NO2 (123.032027)


   

Propane,2-chloro-2-nitro-

Propane,2-chloro-2-nitro-

C3H6ClNO2 (123.0087046)


   

5-mercapto-1,2,3-triazole monosodium salt

5-mercapto-1,2,3-triazole monosodium salt

C2H2N3NaS (122.9867132)


   

3-Thienylacetonitrile

3-Thienylacetonitrile

C6H5NS (123.014269)


   

2-PYRIDONE-6-CARBOXALDEHYDE

2-PYRIDONE-6-CARBOXALDEHYDE

C6H5NO2 (123.032027)


   
   
   

1H-1,2,3-Triazole-4-ThiolSodiumSalt

1H-1,2,3-Triazole-4-ThiolSodiumSalt

C2H2N3NaS (122.9867132)


   

2-isocyanato-3-methylfuran

2-isocyanato-3-methylfuran

C6H5NO2 (123.032027)


   

4-Pyridinecarboxaldehyde N-oxide

4-Pyridinecarboxaldehyde N-oxide

C6H5NO2 (123.032027)


   

5-amino-1h-tetrazole potassium salt

5-amino-1h-tetrazole potassium salt

CH2KN5 (122.9947272)


   

5-(hydroxymethyl)furan-2-carbonitrile

5-(hydroxymethyl)furan-2-carbonitrile

C6H5NO2 (123.032027)


   

FURFURYL ISOCYANATE

FURFURYL ISOCYANATE

C6H5NO2 (123.032027)


   

4-HYDROXYPYRIDINE-2-CARBALDEHYDE

4-HYDROXYPYRIDINE-2-CARBALDEHYDE

C6H5NO2 (123.032027)


   

1H-Pyrrole-2,5-dicarbaldehyde

1H-Pyrrole-2,5-dicarbaldehyde

C6H5NO2 (123.032027)


   

3-FLUORO-5-CARBOXYPYRIDINE

3-FLUORO-5-CARBOXYPYRIDINE

C6H5NO2 (123.032027)


   

(R)-(2-Furyl)hydroxyacetonitrile

(R)-(2-Furyl)hydroxyacetonitrile

C6H5NO2 (123.032027)


   
   

Linic

InChI=1\C6H5NO2\c8-6(9)5-2-1-3-7-4-5\h1-4H,(H,8,9

C6H5NO2 (123.032027)


C - Cardiovascular system > C10 - Lipid modifying agents > C10A - Lipid modifying agents, plain > C10AD - Nicotinic acid and derivatives C - Cardiovascular system > C04 - Peripheral vasodilators > C04A - Peripheral vasodilators > C04AC - Nicotinic acid and derivatives D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents D018977 - Micronutrients > D014815 - Vitamins D009676 - Noxae > D000963 - Antimetabolites COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Niacin (Vitamin B3) is an orally active water-soluble B3 vitamin that is an essential nutrient for humans. Niacin (Vitamin B3) plays a key role in energy metabolism, cell signaling cascades regulating gene expression and apoptosis. Niacin (Vitamin B3) is also used in the study of cardiovascular diseases[1][2]. Niacin (Vitamin B3) is an orally active water-soluble B3 vitamin that is an essential nutrient for humans. Niacin (Vitamin B3) plays a key role in energy metabolism, cell signaling cascades regulating gene expression and apoptosis. Niacin (Vitamin B3) is also used in the study of cardiovascular diseases[1][2].

   

Pyrazine-2-carboxylate

Pyrazine-2-carboxylate

C5H3N2O2- (123.0194518)


A monocarboxylic acid anion that is the conjugate base of pyrazine-2-carboxylic acid, obtained by deprotonation of the carboxy group.

   

Sulfonatoacetaldehyde

Sulfonatoacetaldehyde

C2H3O4S- (122.9752058)


   

Phosphonoacetaldehyde(1-)

Phosphonoacetaldehyde(1-)

C2H4O4P- (122.98472140000001)


An organophosphonate oxoanion that is the conjugate base of phosphonoacetaldehyde, arising from deprotonation of one of the two phosphonate OH groups; major species at pH 7.3.

   

3,6-Dioxocyclohexa-1,4-dien-1-olate

3,6-Dioxocyclohexa-1,4-dien-1-olate

C6H3O3- (123.00821880000001)


Conjugate base of 2-hydroxy-1,4-benzoquinone

   

(2R)-2-azaniumyl-3-chloropropanoate

(2R)-2-azaniumyl-3-chloropropanoate

C3H6ClNO2 (123.0087046)


   

1-Propanesulfonate

1-Propanesulfonate

C3H7O3S- (123.0115892)


   

Propanephosphonic acid

Propanephosphonic acid

C3H8O3P- (123.0211048)


   

2-Chloro-2-hydroxypropanoate

2-Chloro-2-hydroxypropanoate

C3H4ClO3- (122.9848964)


   
   
   

Imino dimethylene phosphonic acid

Imino dimethylene phosphonic acid

C2H6NO3P (123.00852960000002)


   

2-Azaniumyl-3-chloropropanoate

2-Azaniumyl-3-chloropropanoate

C3H6ClNO2 (123.0087046)


   
   
   

nitrobenzene-d5

nitrobenzene-d5

C6H5NO2 (123.032027)


   
   

Propane-2-sulfonate

Propane-2-sulfonate

C3H7O3S- (123.0115892)


   

Nicotinic-d4 Acid

Nicotinic-d4 Acid

C6H5NO2 (123.032027)


   

(S)-(3-Furyl)hydroxyacetonitrile

(S)-(3-Furyl)hydroxyacetonitrile

C6H5NO2 (123.032027)


   
   
   

2-Hydroxy-4-imino-2,5-cyclohexadienone

2-Hydroxy-4-imino-2,5-cyclohexadienone

C6H5NO2 (123.032027)


   

3-chloro-D-alanine zwitterion

3-chloro-D-alanine zwitterion

C3H6ClNO2 (123.0087046)


Zwitterionic form of 3-chloro-D-alanine having an anionic carboxy group and a protonated amino group; major species at pH 7.3.

   

3-chloro-L-alanine zwitterion

3-chloro-L-alanine zwitterion

C3H6ClNO2 (123.0087046)


Zwitterionic form of 3-chloro-L-alanine arising from transfer of a proton from the carboxy to the amino group; major species at pH 7.3