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5,10-Dihydroindeno[1,2-b]indol-3-ol ID: ALA611504
Chembl Id: CHEMBL611504
PubChem CID: 46225656
Max Phase: Preclinical
Molecular Formula: C15H11NO
Molecular Weight: 221.26
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: Oc1ccc2c(c1)-c1[nH]c3ccccc3c1C2
Standard InChI: InChI=1S/C15H11NO/c17-10-6-5-9-7-13-11-3-1-2-4-14(11)16-15(13)12(9)8-10/h1-6,8,16-17H,7H2
Standard InChI Key: PGXKTNKPMOJOOZ-UHFFFAOYSA-N
Associated Targets(Human) Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 221.26Molecular Weight (Monoisotopic): 221.0841AlogP: 3.44#Rotatable Bonds: ┄Polar Surface Area: 36.02Molecular Species: NEUTRALHBA: 1HBD: 2#RO5 Violations: ┄HBA (Lipinski): 2HBD (Lipinski): 2#RO5 Violations (Lipinski): ┄CX Acidic pKa: 9.88CX Basic pKa: ┄CX LogP: 3.45CX LogD: 3.45Aromatic Rings: 3Heavy Atoms: 17QED Weighted: 0.47Np Likeness Score: 0.62
References 1. Talaz O, Gülçin I, Göksu S, Saracoglu N.. (2009) Antioxidant activity of 5,10-dihydroindeno[1,2-b]indoles containing substituents on dihydroindeno part., 17 (18): [PMID:19683932 ] [10.1016/j.bmc.2009.07.077 ] 2. Ekinci D, Cavdar H, Durdagi S, Talaz O, Sentürk M, Supuran CT.. (2012) Structure-activity relationships for the interaction of 5,10-dihydroindeno[1,2-b]indole derivatives with human and bovine carbonic anhydrase isoforms I, II, III, IV and VI., 49 [PMID:22245047 ] [10.1016/j.ejmech.2011.12.022 ]