| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4749297
Max Phase: Preclinical
Molecular Formula: C13H16N2O
Molecular Weight: 216.28
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: Cc1c(CN(C)C)c(=O)[nH]c2ccccc12
Standard InChI: InChI=1S/C13H16N2O/c1-9-10-6-4-5-7-12(10)14-13(16)11(9)8-15(2)3/h4-7H,8H2,1-3H3,(H,14,16)
Standard InChI Key: JOHOURQSZIGKRQ-UHFFFAOYSA-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: 216.28 | Molecular Weight (Monoisotopic): 216.1263 | AlogP: 1.90 | #Rotatable Bonds: 2 |
| Polar Surface Area: 36.10 | Molecular Species: BASE | HBA: 2 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 3 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 13.46 | CX Basic pKa: 8.70 | CX LogP: 1.72 | CX LogD: 0.40 |
| Aromatic Rings: 2 | Heavy Atoms: 16 | QED Weighted: 0.83 | Np Likeness Score: -0.79 |
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):