| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4785759
Max Phase: Preclinical
Molecular Formula: C13H13NO2
Molecular Weight: 215.25
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: CCO/C=C/c1cc(=O)c2ccccc2[nH]1
Standard InChI: InChI=1S/C13H13NO2/c1-2-16-8-7-10-9-13(15)11-5-3-4-6-12(11)14-10/h3-9H,2H2,1H3,(H,14,15)/b8-7+
Standard InChI Key: BFTQPHKOPCKETP-BQYQJAHWSA-N
Associated Targets(non-human)
Bacillus spizizenii 1898 Activities
Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: Unknown | 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: 215.25 | Molecular Weight (Monoisotopic): 215.0946 | AlogP: 2.54 | #Rotatable Bonds: 3 |
| Polar Surface Area: 42.09 | Molecular Species: NEUTRAL | HBA: 2 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 3 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 0.42 | CX LogP: 2.41 | CX LogD: 2.41 |
| Aromatic Rings: 2 | Heavy Atoms: 16 | QED Weighted: 0.80 | Np Likeness Score: 0.18 |
References
| 1. Li J,Clark BR. (2020) Synthesis of Natural and Unnatural Quinolones Inhibiting the Growth and Motility of Bacteria., 83 (10): [PMID:33047958] [10.1021/acs.jnatprod.0c00865] |
Source
Source(1):