1H-Indole-2,3-diol; (ξ)-Oxindole-form 

AlkaPlorer ID: AK302499

Synonym: None

IUPAC Name: 3-hydroxy-1,3-dihydroindol-2-one

Structure

SMILES: O=C1NC2=CC=CC=C2C1O

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InChI: InChI=1S/C8H7NO2/c10-7-5-3-1-2-4-6(5)9-8(7)11/h1-4,7,10H,(H,9,11)

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InChIKey: SGZFJWQQBHYNNF-UHFFFAOYSA-N

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Reference

PubChem CID: 6097

CAS: 61-71-2

COCONUT: CNP0273186.1

Source

Species Genus Family Order Class Phylum Kingdom Domain
Sphyraena japonica Sphyraena Sphyraenidae None Actinopteri Chordata Metazoa Eukaryota

Properties Information

Molecule Weight: 149.14899999999997

TPSA: 49.33

MolLogP: 0.6720999999999999

Number of H-Donors: 2

Number of H-Acceptors: 2

RingCount: 2

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi
Acinetobacter baumannii Acinetobacter baumannii Inhibition 0.09 % 10.6019/CHEMBL4513160
Homo sapiens D-amino-acid oxidase IC50 100000.0 nM 10.1021/ml300212a
Pseudomonas aeruginosa Pseudomonas aeruginosa Inhibition -3.58 % 10.6019/CHEMBL4513160
Pseudomonas aeruginosa Pseudomonas aeruginosa Inhibition 18.01 % 10.6019/CHEMBL4513160
None Unchecked Percent Effect -7.262 % 10.6019/CHEMBL3988442
None Unchecked Percent Effect 0.1265 % 10.6019/CHEMBL3988442
None Unchecked Percent Effect 4.302 % 10.6019/CHEMBL3988442

Metabolism Information

AKRT ID Reaction Reaction Link ID
AKRT004109 CC(=O)O.O=C1Nc2ccccc2C1O>>O=C(O)CC1(O)C(=O)Nc2ccccc21 MNXR176785
AKRT022725 O=C(O)CC1(O)C(=O)Nc2ccccc21>>O=C1Nc2ccccc2C1O RXN-3942
AKRT023589 O=C1Cc2ccccc2N1>>O=C1Nc2ccccc2C1O RXN-6682
AKRT023616 O=C1Nc2ccccc2C1=O>>O=C1Nc2ccccc2C1O 68608
AKRT023619 O=C1Nc2ccccc2C1O>>O=C1Nc2ccccc2C1=O RXN-3943
AKRT023620 O=C1Nc2ccccc2C1O>>O=C1Nc2ccccc2OC1O RXN-6683