ID: ALA13204
Max Phase: Preclinical
Molecular Formula: C15H19NO2
Molecular Weight: 245.32
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: COc1ccc2c(c1)CC1(CCCCC1)[N+]([O-])=C2
Standard InChI: InChI=1S/C15H19NO2/c1-18-14-6-5-12-11-16(17)15(10-13(12)9-14)7-3-2-4-8-15/h5-6,9,11H,2-4,7-8,10H2,1H3
Standard InChI Key: OHGXCDCEUCQCQZ-UHFFFAOYSA-N
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 |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Properties
| Molecular Weight: 245.32 | Molecular Weight (Monoisotopic): 245.1416 | AlogP: 2.88 | #Rotatable Bonds: 1 |
| Polar Surface Area: 35.30 | Molecular Species: ACID | HBA: 2 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 3 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 2.16 | CX Basic pKa: | CX LogP: 0.11 | CX LogD: 2.13 |
| Aromatic Rings: 1 | Heavy Atoms: 18 | QED Weighted: 0.56 | Np Likeness Score: 0.48 |
References
| 1. Bernotas RC, Thomas CE, Carr AA, Nieduzak TR, Adams G, Ohlweiler DF, Hay DA. (1996) Synthesis and radical scavenging activity of 3,3-dialkyl-3,4-dihydro-isoquinoline 2-oxides, 6 (10): [10.1016/0960-894X(96)00181-3] |
Source
Source(1):