Chemical Formula: C8H5NO2

Chemical Formula C8H5NO2

Found 41 metabolite its formula value is C8H5NO2

1H-Indole-2,3-dione

Indoline-2,3-dione;2,3-Dioxo-2,3-dihydroindole; Isatic acid lactam; Isotin

C8H5NO2 (147.032027)


Isatin is an indoledione that is the 2,3-diketo derivative of indole. It has a role as an EC 1.4.3.4 (monoamine oxidase) inhibitor and a plant metabolite. Isatin is an indole derivative first obtained by Erdman and Laurent in 1841 as an oxidation product of Indigo dye with nitric acid and chromic acids. The compound is found in many plants and Schiff bases of Isatin are have been investigated for pharmaceutical applications. Isatin is a natural product found in Isatis tinctoria, Alteromonas, and other organisms with data available. An indole-dione that is obtained by oxidation of indigo blue. It is a MONOAMINE OXIDASE INHIBITOR and high levels have been found in urine of PARKINSONISM patients. 1H-Indole-2,3-dione belongs to the class of organic compounds known as indolines. These are compounds containing an indole moiety, which consists of pyrrolidine ring fused to benzene to form 2,3-dihydroindole. An indoledione that is the 2,3-diketo derivative of indole. COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS [Raw Data] CB237_Isatin_pos_20eV_rep000005.txt [Raw Data] CB237_Isatin_pos_50eV_rep000005.txt [Raw Data] CB237_Isatin_pos_30eV_rep000005.txt [Raw Data] CB237_Isatin_pos_40eV_rep000005.txt [Raw Data] CB237_Isatin_pos_10eV_rep000005.txt KEIO_ID I019 Isatin (Indoline-2,3-dione) is a potent inhibitor of monoamine oxidase (MAO) with an IC50 of 3 μM. Also binds to central benzodiazepine receptors (IC50 against clonazepam, 123 μM)[1]. Also acts as an antagonist of both atrial natriuretic peptide stimulated and nitric oxide-stimulated guanylate cyclase activity[2]. Shows effect on the serotonergic system[3]. Isatin (Indoline-2,3-dione) is a potent inhibitor of monoamine oxidase (MAO) with an IC50 of 3 μM. Also binds to central benzodiazepine receptors (IC50 against clonazepam, 123 μM)[1]. Also acts as an antagonist of both atrial natriuretic peptide stimulated and nitric oxide-stimulated guanylate cyclase activity[2]. Shows effect on the serotonergic system[3].

   

Indole-5,6-quinone

5,6-dihydro-1H-indole-5,6-dione

C8H5NO2 (147.032027)


Indole-5,6-quinone is involved in the tyrosine metabolism pathway. More specifically, indole-5,6-quinone is an intermediate in the production of melanin. Indole-5,6-quinone is produced from 5,6-dihydroxyindole by tyrosinase [EC:1.14.18.1]. [HMDB] Indole-5,6-quinone is involved in the tyrosine metabolism pathway. More specifically, indole-5,6-quinone is an intermediate in the production of melanin. Indole-5,6-quinone is produced from 5,6-dihydroxyindole by tyrosinase [EC:1.14.18.1].

   

Agrocybin

8-hydroxyocta-2,4,6-triynimidic acid

C8H5NO2 (147.032027)


Agrocybin is found in mushrooms. Agrocybin is from Marasmius oreades (fairy ring mushroom

   

Phthalimide

Phthalimide calcium (2:1) salt

C8H5NO2 (147.032027)


   

Piperonylonitrile

Piperonylonitrile

C8H5NO2 (147.032027)


   

O-Phthalimide

1H-Isoindole-1,3(2H)-dione

C8H5NO2 (147.032027)


CONFIDENCE standard compound; INTERNAL_ID 20

   

4-Cyanobenzoic acid

4-Cyanobenzoic acid

C8H5NO2 (147.032027)


CONFIDENCE standard compound; INTERNAL_ID 1040; DATASET 20200303_ENTACT_RP_MIX502; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3135; ORIGINAL_PRECURSOR_SCAN_NO 3133 CONFIDENCE standard compound; INTERNAL_ID 1040; DATASET 20200303_ENTACT_RP_MIX502; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3123; ORIGINAL_PRECURSOR_SCAN_NO 3121 CONFIDENCE standard compound; INTERNAL_ID 1040; DATASET 20200303_ENTACT_RP_MIX502; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3164; ORIGINAL_PRECURSOR_SCAN_NO 3163 CONFIDENCE standard compound; INTERNAL_ID 1040; DATASET 20200303_ENTACT_RP_MIX502; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3178; ORIGINAL_PRECURSOR_SCAN_NO 3177 CONFIDENCE standard compound; INTERNAL_ID 1040; DATASET 20200303_ENTACT_RP_MIX502; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3132; ORIGINAL_PRECURSOR_SCAN_NO 3130

   

Agrocybin

8-hydroxyocta-2,4,6-triynamide

C8H5NO2 (147.032027)


   

3-Nitrophenylacetylene

3-Nitrophenylacetylene

C8H5NO2 (147.032027)


   

Benzo[d]oxazole-2-carbaldehyde

Benzo[d]oxazole-2-carbaldehyde

C8H5NO2 (147.032027)


   

2-Cyanobenzoic acid

2-Cyanobenzoic acid

C8H5NO2 (147.032027)


   

Benzonitrile,5-formyl-2-hydroxy-

Benzonitrile,5-formyl-2-hydroxy-

C8H5NO2 (147.032027)


   

4-formyl-2-hydroxybenzonitrile

4-formyl-2-hydroxybenzonitrile

C8H5NO2 (147.032027)


   

1,2-benzoxazole-5-carbaldehyde

1,2-benzoxazole-5-carbaldehyde

C8H5NO2 (147.032027)


   

3-Formyl-4-hydroxybenzonitrile

3-Formyl-4-hydroxybenzonitrile

C8H5NO2 (147.032027)


   

Benzo[d]oxazole-6-carbaldehyde

Benzo[d]oxazole-6-carbaldehyde

C8H5NO2 (147.032027)


   

Benzo[d][1,3]dioxole-4-carbonitrile

Benzo[d][1,3]dioxole-4-carbonitrile

C8H5NO2 (147.032027)


   

benzoyl isocyanate

benzoyl isocyanate

C8H5NO2 (147.032027)


   

Furo[2,3-b]pyridine-3-carboxaldehyde

Furo[2,3-b]pyridine-3-carboxaldehyde

C8H5NO2 (147.032027)


   

4-Nitrophenylacetylene

4-Nitrophenylacetylene

C8H5NO2 (147.032027)


   

1-Ethynyl-2-nitrobenzene

1-Ethynyl-2-nitrobenzene

C8H5NO2 (147.032027)


   

3-Cyanobenzoic acid

3-Cyanobenzoic acid

C8H5NO2 (147.032027)


   

1,3-Benzoxazole-5-carbaldehyde

1,3-Benzoxazole-5-carbaldehyde

C8H5NO2 (147.032027)


   

4-Cyano-2-hydroxybenzaldehyde

4-Cyano-2-hydroxybenzaldehyde

C8H5NO2 (147.032027)


   

pyrano[2,3-b]pyridin-4-one

pyrano[2,3-b]pyridin-4-one

C8H5NO2 (147.032027)


   

Furo[3,2-b]pyridine-5-carboxaldehyde

Furo[3,2-b]pyridine-5-carboxaldehyde

C8H5NO2 (147.032027)


   

2-Pyridinecarboxylic acid, 3-ethynyl- (9CI)

2-Pyridinecarboxylic acid, 3-ethynyl- (9CI)

C8H5NO2 (147.032027)


   

3-pyridin-3-ylprop-2-ynoic acid

3-pyridin-3-ylprop-2-ynoic acid

C8H5NO2 (147.032027)


   

Furo[3,2-b]pyridine-2-carboxaldehyde (9CI)

Furo[3,2-b]pyridine-2-carboxaldehyde (9CI)

C8H5NO2 (147.032027)


   

Furo[2,3-b]pyridine-2-carboxaldehyde (9CI)

Furo[2,3-b]pyridine-2-carboxaldehyde (9CI)

C8H5NO2 (147.032027)


   

Furo[3,2-c]pyridine-2-carboxaldehyde (9CI)

Furo[3,2-c]pyridine-2-carboxaldehyde (9CI)

C8H5NO2 (147.032027)


   

3-(Pyridin-2-yl)propiolic acid

3-(Pyridin-2-yl)propiolic acid

C8H5NO2 (147.032027)


   

Furo[2,3-b]pyridine-5-carboxaldehyde (9CI)

Furo[2,3-b]pyridine-5-carboxaldehyde (9CI)

C8H5NO2 (147.032027)


   

Furo[2,3-c]pyridine-5-carbaldehyde

Furo[2,3-c]pyridine-5-carbaldehyde

C8H5NO2 (147.032027)


   

Furo[3,2-b]pyridine-6-carbaldehyde

Furo[3,2-b]pyridine-6-carbaldehyde

C8H5NO2 (147.032027)


   

Furo[2,3-c]pyridine-2-carbaldehyde

Furo[2,3-c]pyridine-2-carbaldehyde

C8H5NO2 (147.032027)


   

2-Propynoic acid, 3-(4-pyridinyl)- (9CI)

2-Propynoic acid, 3-(4-pyridinyl)- (9CI)

C8H5NO2 (147.032027)


   

Indole-4,7-dione

Indole-4,7-dione

C8H5NO2 (147.032027)


   

5-Ethynylpicolinic acid

5-Ethynylpicolinic acid

C8H5NO2 (147.032027)


   

Isatin

InChI=1\C8H5NO2\c10-7-5-3-1-2-4-6(5)9-8(7)11\h1-4H,(H,9,10,11

C8H5NO2 (147.032027)


COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Isatin (Indoline-2,3-dione) is a potent inhibitor of monoamine oxidase (MAO) with an IC50 of 3 μM. Also binds to central benzodiazepine receptors (IC50 against clonazepam, 123 μM)[1]. Also acts as an antagonist of both atrial natriuretic peptide stimulated and nitric oxide-stimulated guanylate cyclase activity[2]. Shows effect on the serotonergic system[3]. Isatin (Indoline-2,3-dione) is a potent inhibitor of monoamine oxidase (MAO) with an IC50 of 3 μM. Also binds to central benzodiazepine receptors (IC50 against clonazepam, 123 μM)[1]. Also acts as an antagonist of both atrial natriuretic peptide stimulated and nitric oxide-stimulated guanylate cyclase activity[2]. Shows effect on the serotonergic system[3].

   

Indole-5,6-quinone

Indole-5,6-quinone

C8H5NO2 (147.032027)