Chemical Formula: C6H7NO

Chemical Formula C6H7NO

Found 79 metabolite its formula value is C6H7NO

aminophenol

o-Hydroxyaniline

C6H7NO (109.0527612)


The aminophenol which has the single amino substituent located ortho to the phenolic -OH group. CONFIDENCE standard compound; INTERNAL_ID 8011 KEIO_ID A114

   

3-Aminophenol

3-Aminophenol monopotassium salt

C6H7NO (109.0527612)


   

4-Aminophenol

4-Aminophenol monopotassium salt

C6H7NO (109.0527612)


4-aminophenol is considered a minor nephrotoxic metabolite of phenacetin and acetaminophen (paracetamol) in man. 4-Aminophenol can undergo autoxidations and metal-catalyzed and enzymatic oxidations in man to produce reactive oxygen species. (PMID 1713494). 4-aminophenol is considered a minor nephrotoxic metabolite of phenacetin and acetaminophen (paracetamol) in man. CONFIDENCE standard compound; INTERNAL_ID 8255 D009676 - Noxae > D009153 - Mutagens

   

Hydroxylaminobenzene

(Hydroxyamino)benzene

C6H7NO (109.0527612)


   

2-Acetylpyrrole

1-(1H-Pyrrol-2-yl)ethanone (acetylpyrrole)

C6H7NO (109.0527612)


2-acetylpyrrole, also known as 1-(1h-pyrrol-2-yl)1-ethanone or 2-pyrrolyl methyl ketone, is a member of the class of compounds known as aryl alkyl ketones. Aryl alkyl ketones are ketones have the generic structure RC(=O)R, where R = aryl group and R=alkyl group. 2-acetylpyrrole is soluble (in water) and a very weakly acidic compound (based on its pKa). 2-acetylpyrrole is a bread, coumarin, and licorice tasting compound and can be found in a number of food items such as green vegetables, tea, nuts, and white mustard, which makes 2-acetylpyrrole a potential biomarker for the consumption of these food products. 2-Acetylpyrrole, also known as fema 3202 or pyrrole, 2-acetyl, belongs to the class of organic compounds known as aryl alkyl ketones. These are ketones have the generic structure RC(=O)R, where R = aryl group and R=alkyl group. 2-Acetylpyrrole is a bread, nut, and walnut tasting compound. 2-Acetylpyrrole has been detected, but not quantified, in tea. This could make 2-acetylpyrrole a potential biomarker for the consumption of these foods. A pyrrole carrying an acetyl substituent at the 2-position. 2-Acetylpyrrole is a product of model browning systems, and has been isolated as a major flavour component of many foods[1]. 2-Acetylpyrrole has been used in the synthesis of 2-acetyl-1-pyrroline[2]. 2-Acetylpyrrole is a product of model browning systems, and has been isolated as a major flavour component of many foods[1]. 2-Acetylpyrrole has been used in the synthesis of 2-acetyl-1-pyrroline[2].

   

1-Methyl-2-pyrrolecarboxaldehyde

1-Methyl-1H-pyrrole-2-carboxaldehyde

C6H7NO (109.0527612)


1-Methyl-2-pyrrolecarboxaldehyde is a maillard product. Maillard product

   

Piconol

(pyridin-2-yl)methanol

C6H7NO (109.0527612)


   

3-Pyridinemethanol

Hydrofluoride, nicomethanol

C6H7NO (109.0527612)


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 C78274 - Agent Affecting Cardiovascular System > C29707 - Vasodilating Agent D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents

   

Carbapenem

1-azabicyclo[3.2.0]hept-2-en-7-one

C6H7NO (109.0527612)


D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D047090 - beta-Lactams D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D007769 - Lactams

   

O-Phenylhydroxylamine

O-Phenylhydroxylamine

C6H7NO (109.0527612)


   

3-Methoxypyridine

3-methyoxypyridine

C6H7NO (109.0527612)


3-methoxypyridine is a member of the class of compounds known as alkyl aryl ethers. Alkyl aryl ethers are organic compounds containing the alkyl aryl ether functional group with the generic formula R-O-R , where R is an alkyl group and R is an aryl group. 3-methoxypyridine is soluble (in water) and a strong basic compound (based on its pKa). 3-methoxypyridine can be found in tea, which makes 3-methoxypyridine a potential biomarker for the consumption of this food product.

   

4-Hydroxy-2-methylpyridine

4-Hydroxy-2-methylpyridine

C6H7NO (109.0527612)


   

2-Methoxypyridine

2-Methoxypyridine

C6H7NO (109.0527612)


   

3-Hydroxy-2-methylpyridine

3-Hydroxy-2-methylpyridine

C6H7NO (109.0527612)


3-Hydroxy-2-methylpyridine, isolated from alkaline extracts of cocoa, is used in the synthesis of pyrimidine[1]. 3-Hydroxy-2-methylpyridine, isolated from alkaline extracts of cocoa, is used in the synthesis of pyrimidine[1].

   

Nicotinyl alcohol

3-PYRIDINEMETHANOL

C6H7NO (109.0527612)


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 C78274 - Agent Affecting Cardiovascular System > C29707 - Vasodilating Agent D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents

   

5-Methyl-1H-pyrrole-2-carbaldehyde

5-Methyl-1H-pyrrole-2-carbaldehyde

C6H7NO (109.0527612)


   

N-Acetylpyrrole

N-Acetylpyrrole

C6H7NO (109.0527612)


   

4-PYRIDINEMETHANOL

4-PYRIDINEMETHANOL

C6H7NO (109.0527612)


   

3-Hydroxy-5-picoline

3-Hydroxy-5-picoline

C6H7NO (109.0527612)


   

5-Hydroxy-2-methylpyridine

5-Hydroxy-2-methylpyridine

C6H7NO (109.0527612)


   

3-METHOXYPYRIDINE

3-METHOXYPYRIDINE

C6H7NO (109.0527612)


   

2methylpyridin-3-ol

3-Hydroxy-2-methylpyridine, 99\\%

C6H7NO (109.0527612)


3-Hydroxy-2-methylpyridine is a natural product found in Astragalus mongholicus, Streptomyces, and Salvia divinorum with data available. 3-Hydroxy-2-methylpyridine, isolated from alkaline extracts of cocoa, is used in the synthesis of pyrimidine[1]. 3-Hydroxy-2-methylpyridine, isolated from alkaline extracts of cocoa, is used in the synthesis of pyrimidine[1].

   

4-aminophenol

4-aminophenol

C6H7NO (109.0527612)


An amino phenol (one of the three possible isomers) which has the single amino substituent located para to the phenolic -OH group. D009676 - Noxae > D009153 - Mutagens MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; PLIKAWJENQZMHA-UHFFFAOYSA-N_STSL_0197_4-Aminophenol_0125fmol_180831_S2_L02M02_46; 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.

   

2-Aminophenol

2-Aminophenol

C6H7NO (109.0527612)


MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; CDAWCLOXVUBKRW-UHFFFAOYSA-N_STSL_0192_2-Aminophenol_0031fmol_180831_S2_L02M02_10; 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.

   

3-Pyridinemthanol

3-Pyridinemthanol

C6H7NO (109.0527612)


   

2-Aminophenol; LC-tDDA; CE10

2-Aminophenol; LC-tDDA; CE10

C6H7NO (109.0527612)


   

2-Aminophenol; LC-tDDA; CE20

2-Aminophenol; LC-tDDA; CE20

C6H7NO (109.0527612)


   

3-Aminophenol; AIF; CE0; CorrDec

3-Aminophenol; AIF; CE0; CorrDec

C6H7NO (109.0527612)


   

3-Aminophenol; AIF; CE10; CorrDec

3-Aminophenol; AIF; CE10; CorrDec

C6H7NO (109.0527612)


   

3-Aminophenol; AIF; CE30; CorrDec

3-Aminophenol; AIF; CE30; CorrDec

C6H7NO (109.0527612)


   

3-Aminophenol; AIF; CE0; MS2Dec

3-Aminophenol; AIF; CE0; MS2Dec

C6H7NO (109.0527612)


   

3-Aminophenol; AIF; CE10; MS2Dec

3-Aminophenol; AIF; CE10; MS2Dec

C6H7NO (109.0527612)


   

3-Aminophenol; AIF; CE30; MS2Dec

3-Aminophenol; AIF; CE30; MS2Dec

C6H7NO (109.0527612)


   

3-Aminophenol; LC-tDDA; CE10

3-Aminophenol; LC-tDDA; CE10

C6H7NO (109.0527612)


   

3-Aminophenol; LC-tDDA; CE20

3-Aminophenol; LC-tDDA; CE20

C6H7NO (109.0527612)


   

3-Aminophenol; LC-tDDA; CE30

3-Aminophenol; LC-tDDA; CE30

C6H7NO (109.0527612)


   

3-Aminophenol; LC-tDDA; CE40

3-Aminophenol; LC-tDDA; CE40

C6H7NO (109.0527612)


   

3-Hydroxy-N-methylpyridinium

3-Hydroxy-N-methylpyridinium

C6H7NO (109.0527612)


   

Nicotinyl alcohol

Nicotinyl alcohol

C6H7NO (109.0527612)


   

2-ACETYLPYRROLE

2-Acetyl-1H-pyrrole

C6H7NO (109.0527612)


2-Acetylpyrrole is a product of model browning systems, and has been isolated as a major flavour component of many foods[1]. 2-Acetylpyrrole has been used in the synthesis of 2-acetyl-1-pyrroline[2]. 2-Acetylpyrrole is a product of model browning systems, and has been isolated as a major flavour component of many foods[1]. 2-Acetylpyrrole has been used in the synthesis of 2-acetyl-1-pyrroline[2].

   

1-Methylformylpyrrole

1-Methyl-1H-pyrrole-2-carboxaldehyde

C6H7NO (109.0527612)


   

6-Methyl-3-pyridinol

6-Methyl-3-pyridinol

C6H7NO (109.0527612)


   

3,6-dihydro-2h-pyran-4-carbonitrile

3,6-dihydro-2h-pyran-4-carbonitrile

C6H7NO (109.0527612)


   

2-Hydroxy-5-picoline

2-Hydroxy-5-methylpyridine

C6H7NO (109.0527612)


   

2-oxocyclopentanecarbonitrile

2-oxocyclopentanecarbonitrile

C6H7NO (109.0527612)


   

4-picoline n-oxide

4-picoline n-oxide

C6H7NO (109.0527612)


   

2-Azabicyclo[2.2.1]hept-5-en-3-one

2-Azabicyclo[2.2.1]hept-5-en-3-one

C6H7NO (109.0527612)


   

1-Methyl-1H-pyrrole-3-carbaldehyde

1-Methyl-1H-pyrrole-3-carbaldehyde

C6H7NO (109.0527612)


   

3-methyl-2-pyridone

2-Hydroxy-3-methylpyridine

C6H7NO (109.0527612)


   

3-ACETYLPYRROLE

3-ACETYLPYRROLE

C6H7NO (109.0527612)


   

Propanenitrile,3-(2-propyn-1-yloxy)-

Propanenitrile,3-(2-propyn-1-yloxy)-

C6H7NO (109.0527612)


   

3-Cyclopropyl-3-oxopropanenitrile

3-Cyclopropyl-3-oxopropanenitrile

C6H7NO (109.0527612)


   

5-Methylpyrrole-2-carbaldehyde

5-Methylpyrrole-2-carbaldehyde

C6H7NO (109.0527612)


   

2-Picoline 1-oxide

2-Methylpyridine 1-oxide

C6H7NO (109.0527612)


   

3,4-Dihydro-2H-pyran-6-carbonitrile

3,4-Dihydro-2H-pyran-6-carbonitrile

C6H7NO (109.0527612)


   

(1S)-(+)-2-Azabicyclo[2.2.1]hept-5-en-3-one

(1S)-(+)-2-Azabicyclo[2.2.1]hept-5-en-3-one

C6H7NO (109.0527612)


   

6-methylpyridin-2-ol

6-methylpyridin-2-ol

C6H7NO (109.0527612)


   

2-Hydroxy-4-picoline

2-Hydroxy-4-methylpyridine

C6H7NO (109.0527612)


   

4-Methyl-3-pyridinol

4-Methyl-3-pyridinol

C6H7NO (109.0527612)


   

3-Methylpyridin-4-ol

3-Methylpyridin-4-ol

C6H7NO (109.0527612)


   

1-Methyl-2-pyridone

1-Methyl-2-pyridone

C6H7NO (109.0527612)


   

4-Methoxypyridine

4-Methoxypyridine

C6H7NO (109.0527612)


   

4-Methyl-1H-pyrrole-2-carbaldehyde

4-Methyl-1H-pyrrole-2-carbaldehyde

C6H7NO (109.0527612)


   

5-Methyl-3-pyridinol

5-Methyl-3-pyridinol

C6H7NO (109.0527612)


   

3-cyclopropylisoxazole

3-cyclopropylisoxazole

C6H7NO (109.0527612)


   

3-picoline n-oxide

3-picoline n-oxide

C6H7NO (109.0527612)


   

3-methyl-1h-pyrrole-2-carbaldehyde

3-methyl-1h-pyrrole-2-carbaldehyde

C6H7NO (109.0527612)


   

(1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one

(1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one

C6H7NO (109.0527612)


   

3-Oxocyclopentanecarbonitrile

3-Oxocyclopentanecarbonitrile

C6H7NO (109.0527612)


   

AIDS-019597

InChI=1\C6H7NO\c1-5(8)6-3-2-4-7-6\h2-4,7H,1H

C6H7NO (109.0527612)


2-Acetylpyrrole is a product of model browning systems, and has been isolated as a major flavour component of many foods[1]. 2-Acetylpyrrole has been used in the synthesis of 2-acetyl-1-pyrroline[2]. 2-Acetylpyrrole is a product of model browning systems, and has been isolated as a major flavour component of many foods[1]. 2-Acetylpyrrole has been used in the synthesis of 2-acetyl-1-pyrroline[2].

   

Zoba eg

InChI=1\C6H7NO\c7-5-2-1-3-6(8)4-5\h1-4,8H,7H

C6H7NO (109.0527612)


   

Zoba 3GA

InChI=1\C6H7NO\c7-5-3-1-2-4-6(5)8\h1-4,8H,7H

C6H7NO (109.0527612)


   

Citol

InChI=1\C6H7NO\c7-5-1-3-6(8)4-2-5\h1-4,8H,7H

C6H7NO (109.0527612)


D009676 - Noxae > D009153 - Mutagens

   

Carbapenem

Carbapenem

C6H7NO (109.0527612)


An organic heterobicyclic compound that consists of (5R)-1-azabicyclo[3.2.0]hept-2-ene bearing a 7-keto substituent. The parent of the class of carbapenems. D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D047090 - beta-Lactams D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D007769 - Lactams

   

3-Aminophenol

3-Aminophenol

C6H7NO (109.0527612)


   

N-PHENYLHYDROXYLAMINE

N-PHENYLHYDROXYLAMINE

C6H7NO (109.0527612)


   
   

1-Methylpyrrole-2-carboxaldehyde

1-Methylpyrrole-2-carboxaldehyde

C6H7NO (109.0527612)


   

Acetylpyrrole

Acetylpyrrole

C6H7NO (109.0527612)