Chemical Formula: C8H7NO

Chemical Formula C8H7NO

Found 98 metabolite its formula value is C8H7NO

4-Hydroxyindole

4-Hydroxyindole

C8H7NO (133.0527612)


   

Indolin-2-one

1,3-dihydro-(2H)-indol-2-One

C8H7NO (133.0527612)


1,3-Dihydro-(2H)-indol-2-one, also known as 2-oxindole or 2-indolinone, belongs to the class of organic compounds known as indolines. Indolines are compounds containing an indole moiety, which consists of pyrrolidine ring fused to benzene to form 2,3-dihydroindole. CONFIDENCE standard compound; INTERNAL_ID 2508 COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Oxindole (Indolin-2-one) is an aromatic heterocyclic building block. 2-indolinone derivatives have become lead compounds in the research of kinase inhibitors. Oxindole (Indolin-2-one) is an aromatic heterocyclic building block. 2-indolinone derivatives have become lead compounds in the research of kinase inhibitors.

   

4-Hydroxybenzeneacetonitrile

4-Hydroxybenzylcyanide, 14C-labeled

C8H7NO (133.0527612)


Isolated from white mustard (Brassica alba) as a dec. product of 4-Hydroxybenzyl glucosinolate KZZ54-K. 4-Hydroxybenzeneacetonitrile is found in many foods, some of which are cucumber, strawberry, black-eyed pea, and jute. 4-Hydroxybenzeneacetonitrile is found in herbs and spices. 4-Hydroxybenzeneacetonitrile is isolated from white mustard (Brassica alba) as a decomposition product of 4-Hydroxybenzyl glucosinolate KZZ54-K 4-Hydroxybenzyl cyanide is an endogenous metabolite. 4-Hydroxybenzyl cyanide is an endogenous metabolite.

   

Mandelonitrile

(R)-(+)-ALPHA-HYDROXYBENZENE-ACETONITRILE

C8H7NO (133.0527612)


Mandelonitrile is a chemical compound of the cyanohydrin class. Small amounts of mandelonitrile occur in the pits of some fruits. (Wikipedia)

   

Indoxyl

1H-Indol-3-ol

C8H7NO (133.0527612)


Indoxyl, also known as 1H-indol-3-ol, belongs to the class of organic compounds known as hydroxyindoles. These are organic compounds containing an indole moiety that carries a hydroxyl group. Indoxyl is isomeric with oxindol and is obtained as an oily liquid. Indoxyl exists in all living organisms, ranging from bacteria to humans. Indoxyl is obtained from indican, which is a glycoside. Obermayers reagent is a dilute solution FeCl3 in hydrochloric acid. The hydrolysis of indican yields β-D-glucose and indoxyl. Indigo dye is a product of the reaction of indoxyl by a mild oxidizing agent such as atmospheric oxygen. In chemistry, indoxyl is a nitrogenous substance with the chemical formula: C8H7NO. Indoxyl can be found in urine and is titrated with Obermayers reagent. Indigo dye is a product of the reaction of indoxyl by a mild oxidizing agent, eg. atmospheric oxygen.

   

Mandelonitrile

InChI=1\C8H7NO\c9-6-8(10)7-4-2-1-3-5-7\h1-5,8,10

C8H7NO (133.0527612)


   

5-Hydroxyindole

5-Hydroxy-1H-indole

C8H7NO (133.0527612)


This compound belongs to the family of Indoles and Derivatives. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole. 5-Hydroxyindole, a hydroxylated indole, can be found in a vast array of pharmacologically active agents and natural products. 5-Hydroxyindole slows desensitization of the 5-HT3 receptor-mediated ion current in N1E-115 neuroblastoma cells[1][2]. 5-Hydroxyindole, a hydroxylated indole, can be found in a vast array of pharmacologically active agents and natural products. 5-Hydroxyindole slows desensitization of the 5-HT3 receptor-mediated ion current in N1E-115 neuroblastoma cells[1][2].

   

(±)-2-Hydroxy-2-phenylacetonitrile

(R)-(+)-ALPHA-HYDROXYBENZENE-ACETONITRILE

C8H7NO (133.0527612)


(±)-2-Hydroxy-2-phenylacetonitrile, also known as mandelonitrile, alpha-hydroxybenzeneacetonitrile or benzal dehyde cyanohydrin, belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene. Mandelonitrile is a chemical compound of the cyanohydrin class. Hydroxy-2-phenylacetonitrile is a potentially toxic compound. The primary mechanism of toxicity for organic nitriles is their production of toxic cyanide ions or hydrogen cyanide. Cyanide is also known produce some of its toxic effects by binding to catalase, glutathione peroxidase, methemoglobin, hydroxocobalamin, phosphatase, tyrosinase, ascorbic acid oxidase, xanthine oxidase, succinic dehydrogenase, and Cu/Zn superoxide dismutase. (±)-2-Hydroxy-2-phenylacetonitrile has been detected, but not quantified, in fruits. This could make (±)-2-hydroxy-2-phenylacetonitrile a potential biomarker for the consumption of these foods. (±)-2- Oxygen therapy can also be administered. Isolated from peach kernels (Prunus persica). (±)-2-Hydroxy-2-phenylacetonitrile is found in fruits.

   

2-Methyl-4,5-benzoxazole

2-Methyl-4,5-benzoxazole

C8H7NO (133.0527612)


2-Methyl-4,5-benzoxazole is used as a food additive [EAFUS] ("EAFUS: Everything Added to Food in the United States. [http://www.eafus.com/]") 2-Methylbenzoxazole is an endogenous metabolite. 2-Methylbenzoxazole is an endogenous metabolite.

   

1H-Indol-2-ol

1,3-dihydro-2h-indol-2-one

C8H7NO (133.0527612)


   

4h-Benzoxazine

4H-1,2-benzoxazine

C8H7NO (133.0527612)


   

Benzoxazine

2H-1,2-benzoxazine

C8H7NO (133.0527612)


   

Isoindolin-1-one

2,3-Dihydro-3-oxo-1H-isoindole

C8H7NO (133.0527612)


   

p-Tolyl isocyanate

Isocyanic acid, p-tolyl ester

C8H7NO (133.0527612)


   

indolol

6-Hydroxyindole, >=99.0\\% (GC)

C8H7NO (133.0527612)


   

5-Indolol

5-Hydroxyindole

C8H7NO (133.0527612)


A member of the class of hydroxyindoles that is 1H-indole in which the hydrogen at position 5 has been replaced by a hydroxy group. 5-Hydroxyindole, a hydroxylated indole, can be found in a vast array of pharmacologically active agents and natural products. 5-Hydroxyindole slows desensitization of the 5-HT3 receptor-mediated ion current in N1E-115 neuroblastoma cells[1][2]. 5-Hydroxyindole, a hydroxylated indole, can be found in a vast array of pharmacologically active agents and natural products. 5-Hydroxyindole slows desensitization of the 5-HT3 receptor-mediated ion current in N1E-115 neuroblastoma cells[1][2].

   

6-Methylbenzoxazole

6-METHYLBENZO[D]OXAZOLE

C8H7NO (133.0527612)


   

(Z)-form-4-(Tetrahydro-2-furylidene)-2-butynenitrile|4-(Tetrahydro-2-furyliden)but-2-in-nitril

(Z)-form-4-(Tetrahydro-2-furylidene)-2-butynenitrile|4-(Tetrahydro-2-furyliden)but-2-in-nitril

C8H7NO (133.0527612)


   

Nitrile-3-Methoxybenzoic acid

Nitrile-3-Methoxybenzoic acid

C8H7NO (133.0527612)


   

Nitrile-2-Hydroxyphenylacetic acid

Nitrile-2-Hydroxyphenylacetic acid

C8H7NO (133.0527612)


   

(E)-oct-6-ene-2,4-diynamide|agrocybyne D|Oct-6t-en-2,4-diinamid|oct-6t-ene-2,4-diynamide

(E)-oct-6-ene-2,4-diynamide|agrocybyne D|Oct-6t-en-2,4-diinamid|oct-6t-ene-2,4-diynamide

C8H7NO (133.0527612)


   

Nitrile-4-Methoxybenzoic acid

Nitrile-4-Methoxybenzoic acid

C8H7NO (133.0527612)


   

Indolin-2-one

InChI=1/C8H7NO/c10-8-5-6-3-1-2-4-7(6)9-8/h1-4H,5H2,(H,9,10

C8H7NO (133.0527612)


1,3-Dihydro-(2H)-indol-2-one, also known as 2-oxindole or 2-indolinone, belongs to the class of organic compounds known as indolines. Indolines are compounds containing an indole moiety, which consists of pyrrolidine ring fused to benzene to form 2,3-dihydroindole. Indolin-2-one is an indolinone carrying an oxo group at position 2. It is an indolinone and a gamma-lactam. Oxindole is a natural product found in Penicillium with data available. COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Oxindole (Indolin-2-one) is an aromatic heterocyclic building block. 2-indolinone derivatives have become lead compounds in the research of kinase inhibitors. Oxindole (Indolin-2-one) is an aromatic heterocyclic building block. 2-indolinone derivatives have become lead compounds in the research of kinase inhibitors.

   

indoxyl

1H-Indol-3-ol

C8H7NO (133.0527612)


   

4-Hydroxybenzylcyanide

4-Hydroxybenzylcyanide

C8H7NO (133.0527612)


   

Indoxyl sulfate

Indoxyl sulfate

C8H7NO (133.0527612)


   

2-Oxindole; AIF; CE0; CorrDec

2-Oxindole; AIF; CE0; CorrDec

C8H7NO (133.0527612)


   

2-Oxindole; AIF; CE10; CorrDec

2-Oxindole; AIF; CE10; CorrDec

C8H7NO (133.0527612)


   

2-Oxindole; AIF; CE30; CorrDec

2-Oxindole; AIF; CE30; CorrDec

C8H7NO (133.0527612)


   

2-Oxindole; AIF; CE0; MS2Dec

2-Oxindole; AIF; CE0; MS2Dec

C8H7NO (133.0527612)


   

2-Oxindole; AIF; CE10; MS2Dec

2-Oxindole; AIF; CE10; MS2Dec

C8H7NO (133.0527612)


   

2-Oxindole; AIF; CE30; MS2Dec

2-Oxindole; AIF; CE30; MS2Dec

C8H7NO (133.0527612)


   

2-Oxindole; LC-tDDA; CE10

2-Oxindole; LC-tDDA; CE10

C8H7NO (133.0527612)


   

2-Oxindole; LC-tDDA; CE20

2-Oxindole; LC-tDDA; CE20

C8H7NO (133.0527612)


   

2-Oxindole; LC-tDDA; CE30

2-Oxindole; LC-tDDA; CE30

C8H7NO (133.0527612)


   

2-Oxindole; LC-tDDA; CE40

2-Oxindole; LC-tDDA; CE40

C8H7NO (133.0527612)


   

3-HYDROXYINDOLE

3-HYDROXYINDOLE

C8H7NO (133.0527612)


   
   

5-Hydroxyindole

5-Hydroxyindole

C8H7NO (133.0527612)


   

2-Methylbenzoxazol

2-Methyl-4,5-benzoxazole

C8H7NO (133.0527612)


2-Methylbenzoxazole is an endogenous metabolite. 2-Methylbenzoxazole is an endogenous metabolite.

   

6-Hydroxyindole

6-Hydroxyindole

C8H7NO (133.0527612)


   

3-Methoxybenzonitrile

3-Methoxybenzonitrile

C8H7NO (133.0527612)


   

2-Hydroxy-3-methylbenzonitrile

2-Hydroxy-3-methylbenzonitrile

C8H7NO (133.0527612)


   

5-methylbenzoxazole

5-methylbenzoxazole

C8H7NO (133.0527612)


   

6,7-Dihydro-5H-cyclopenta[b]pyridin-5-one

6,7-Dihydro-5H-cyclopenta[b]pyridin-5-one

C8H7NO (133.0527612)


   

2-Ethynyl-5-methoxypyridine

2-Ethynyl-5-methoxypyridine

C8H7NO (133.0527612)


   

trans-3-(3-Pyridyl)acrolein

trans-3-(3-Pyridyl)acrolein

C8H7NO (133.0527612)


   

1h-indol-2-ol

1h-indol-2-ol

C8H7NO (133.0527612)


   

1-(PYRIDIN-4-YL)PROP-2-YN-1-OL

1-(PYRIDIN-4-YL)PROP-2-YN-1-OL

C8H7NO (133.0527612)


   

4-Hydroxy-2-methylbenzonitrile

4-Hydroxy-2-methylbenzonitrile

C8H7NO (133.0527612)


   

4-(Hydroxymethyl)benzonitrile

4-(Hydroxymethyl)benzonitrile

C8H7NO (133.0527612)


   

P-TOLYL ISOCYANATE

P-TOLYL ISOCYANATE

C8H7NO (133.0527612)


   

3-Hydroxy-2-methylbenzonitrile

3-Hydroxy-2-methylbenzonitrile

C8H7NO (133.0527612)


   

2-(Hydroxymethyl)benzonitrile

2-(Hydroxymethyl)benzonitrile

C8H7NO (133.0527612)


   

3-(Hydroxymethyl)benzonitrile

3-(Hydroxymethyl)benzonitrile

C8H7NO (133.0527612)


   

3-Methylfuro[2,3-b]pyridine

3-Methylfuro[2,3-b]pyridine

C8H7NO (133.0527612)


   

2-Hydroxy-6-methylbenzonitrile

2-Hydroxy-6-methylbenzonitrile

C8H7NO (133.0527612)


   

BENZOFURAN-5-AMINE

1-Benzofuran-5-amine

C8H7NO (133.0527612)


   

5,6-Dihydro-7H-cyclopenta[b]pyridin-7-one

5,6-Dihydro-7H-cyclopenta[b]pyridin-7-one

C8H7NO (133.0527612)


   

3-hydroxypheny acetonitrile

3-hydroxypheny acetonitrile

C8H7NO (133.0527612)


   

(2-Hydroxyphenyl)acetonitrile

(2-Hydroxyphenyl)acetonitrile

C8H7NO (133.0527612)


   

6-METHYLBENZO[D]ISOXAZOLE

6-METHYLBENZO[D]ISOXAZOLE

C8H7NO (133.0527612)


   

5-METHYL-1,2-BENZISOXAZOLE

5-METHYL-1,2-BENZISOXAZOLE

C8H7NO (133.0527612)


   

3-Hydroxy-4-methylbenzonitrile

3-Hydroxy-4-methylbenzonitrile

C8H7NO (133.0527612)


   

2-ETHYNYL-5-METHYLPYRIDINE1-OXIDE

2-ETHYNYL-5-METHYLPYRIDINE1-OXIDE

C8H7NO (133.0527612)


   

Phenoxyacetonitrile

Phenoxyacetonitrile

C8H7NO (133.0527612)


   

2-Methoxybenzonitrile

2-Methoxybenzonitrile

C8H7NO (133.0527612)


   

4-Methoxybenzonitrile

4-Methoxybenzonitrile

C8H7NO (133.0527612)


   

3-Indolinone

1,2-Dihydro-3H-indol-3-one

C8H7NO (133.0527612)


   

BENZOFURAN-2-AMINE

BENZOFURAN-2-AMINE

C8H7NO (133.0527612)


   

4-hydroxy-3-methylbenzonitrile

4-hydroxy-3-methylbenzonitrile

C8H7NO (133.0527612)


   

1H,3H-Cyclobuta[3,4]pyrrolo[1,2-c]oxazole(9CI)

1H,3H-Cyclobuta[3,4]pyrrolo[1,2-c]oxazole(9CI)

C8H7NO (133.0527612)


   

2-Propenal,3-(3-pyridinyl)-

2-Propenal,3-(3-pyridinyl)-

C8H7NO (133.0527612)


   

Benzene, 1-isocyano-3-methoxy- (9CI)

Benzene, 1-isocyano-3-methoxy- (9CI)

C8H7NO (133.0527612)


   

1-isocyano-4-methoxybenzene

1-isocyano-4-methoxybenzene

C8H7NO (133.0527612)


   
   

6-Ethynyl-2-Pyridinemethanol

6-Ethynyl-2-Pyridinemethanol

C8H7NO (133.0527612)


   

2-Hydroxy-4-methylbenzonitrile

2-Hydroxy-4-methylbenzonitrile

C8H7NO (133.0527612)


   

BENZOFURAN-7-AMINE

BENZOFURAN-7-AMINE

C8H7NO (133.0527612)


   

Isocyanatomethylbenzene

Isocyanatomethylbenzene

C8H7NO (133.0527612)


   

o-Tolyl isocyanate

1-Isocyanato-2-methylbenzene

C8H7NO (133.0527612)


   

6,7-Dihydro-5H-cyclopenta[c]pyridin-5-one

6,7-Dihydro-5H-cyclopenta[c]pyridin-5-one

C8H7NO (133.0527612)


   

3-Hydroxy-5-methylbenzonitrile

3-Hydroxy-5-methylbenzonitrile

C8H7NO (133.0527612)


   

1-benzofuran-4-amine

1-benzofuran-4-amine

C8H7NO (133.0527612)


   

5,6-Dihydro-7H-cyclopenta[c]pyridin-7-one

5,6-Dihydro-7H-cyclopenta[c]pyridin-7-one

C8H7NO (133.0527612)


   

m-Tolyl isocyanate

m-Isocyanatotoluene

C8H7NO (133.0527612)


   

CHEBI:18450

(R)-(+)-ALPHA-HYDROXYBENZENE-ACETONITRILE

C8H7NO (133.0527612)


   

95-21-6

InChI=1\C8H7NO\c1-6-9-7-4-2-3-5-8(7)10-6\h2-5H,1H

C8H7NO (133.0527612)


2-Methylbenzoxazole is an endogenous metabolite. 2-Methylbenzoxazole is an endogenous metabolite.

   

5-Indolol

5-21-03-00018 (Beilstein Handbook Reference)

C8H7NO (133.0527612)


5-Hydroxyindole, a hydroxylated indole, can be found in a vast array of pharmacologically active agents and natural products. 5-Hydroxyindole slows desensitization of the 5-HT3 receptor-mediated ion current in N1E-115 neuroblastoma cells[1][2]. 5-Hydroxyindole, a hydroxylated indole, can be found in a vast array of pharmacologically active agents and natural products. 5-Hydroxyindole slows desensitization of the 5-HT3 receptor-mediated ion current in N1E-115 neuroblastoma cells[1][2].

   

CHEBI:16667

ACETIC ACID,(4-HYDROXYPHENYL),NITRILE 4-HYDROXY-BENZYLCYANIDE

C8H7NO (133.0527612)


4-Hydroxybenzyl cyanide is an endogenous metabolite. 4-Hydroxybenzyl cyanide is an endogenous metabolite.

   

4-Hydroxybenzyl cyanide

(4-Hydroxyphenyl)acetonitrile

C8H7NO (133.0527612)


A hydroxynitrile that is phenylacetonitrile substituted by a hydroxy group at position 4. 4-Hydroxybenzyl cyanide is an endogenous metabolite. 4-Hydroxybenzyl cyanide is an endogenous metabolite.

   

(R)-Mandelonitrile

(R)-(+)-ALPHA-HYDROXYBENZENE-ACETONITRILE

C8H7NO (133.0527612)


   

2-methylbenzoxazole

2-methylbenzoxazole

C8H7NO (133.0527612)


2-Methylbenzoxazole is an endogenous metabolite. 2-Methylbenzoxazole is an endogenous metabolite.

   

Isoindolin-1-one

Isoindolin-1-one

C8H7NO (133.0527612)


   

Hydroxyindole

Hydroxyindole

C8H7NO (133.0527612)


   

Hydroxybenzeneacetonitrile

Hydroxybenzeneacetonitrile

C8H7NO (133.0527612)


   

Hydroxyphenylacetonitrile

Hydroxyphenylacetonitrile

C8H7NO (133.0527612)


   

Methylbenzoxazole

Methylbenzoxazole

C8H7NO (133.0527612)