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ID: ALA593507
Max Phase: Preclinical
Molecular Formula: C15H11NO2
Molecular Weight: 237.26
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Oc1ccc(O)c2c1Cc1c-2[nH]c2ccccc12
Standard InChI: InChI=1S/C15H11NO2/c17-12-5-6-13(18)14-10(12)7-9-8-3-1-2-4-11(8)16-15(9)14/h1-6,16-18H,7H2
Standard InChI Key: ZYYKPVBVJWQNLK-UHFFFAOYSA-N
Associated Targets(Human)
Carbonic anhydrase I 13240 Activities
Carbonic anhydrase II 17698 Activities
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Carbonic anhydrase IV 2163 Activities
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Carbonic anhydrase VI 993 Activities
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Associated Targets(non-human)
Carbonic anhydrase 3 27 Activities
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Molecule Features
| 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 |
Drug Indications
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanisms of Action
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Properties
| Molecular Weight: 237.26 | Molecular Weight (Monoisotopic): 237.0790 | AlogP: 3.15 | #Rotatable Bonds: 0 |
| Polar Surface Area: 56.25 | Molecular Species: NEUTRAL | HBA: 2 | HBD: 3 |
| #RO5 Violations: 0 | HBA (Lipinski): 3 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 9.49 | CX Basic pKa: | CX LogP: 3.15 | CX LogD: 3.15 |
| Aromatic Rings: 3 | Heavy Atoms: 18 | QED Weighted: 0.41 | Np Likeness Score: 0.57 |
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] |
Source
Source(1):