ID: ALA593972
Chembl Id: CHEMBL593972
PubChem CID: 46225646
Max Phase: Preclinical
Molecular Formula: C15H11NO
Molecular Weight: 221.26
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: Oc1ccc2c(c1)Cc1c-2[nH]c2ccccc12
Standard InChI: InChI=1S/C15H11NO/c17-10-5-6-11-9(7-10)8-13-12-3-1-2-4-14(12)16-15(11)13/h1-7,16-17H,8H2
Standard InChI Key: AECQYBVEPFXPNZ-UHFFFAOYSA-N
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| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: Small molecule | Topical: No | First In Class: No | Black Box: No |
| Chirality: No | Availability: No | Prodrug: No |
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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| Molecular Weight: 221.26 | Molecular Weight (Monoisotopic): 221.0841 | AlogP: 3.44 | #Rotatable Bonds: ┄ |
| Polar Surface Area: 36.02 | Molecular Species: NEUTRAL | HBA: 1 | HBD: 2 |
| #RO5 Violations: ┄ | HBA (Lipinski): 2 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): ┄ |
| CX Acidic pKa: 10.04 | CX Basic pKa: ┄ | CX LogP: 3.45 | CX LogD: 3.45 |
| Aromatic Rings: 3 | Heavy Atoms: 17 | QED Weighted: 0.47 | Np Likeness Score: 0.51 |
| 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] |
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