| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4784661
Max Phase: Preclinical
Molecular Formula: C13H15NO3
Molecular Weight: 233.27
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: COC(OC)c1c(C)c2ccccc2[nH]c1=O
Standard InChI: InChI=1S/C13H15NO3/c1-8-9-6-4-5-7-10(9)14-12(15)11(8)13(16-2)17-3/h4-7,13H,1-3H3,(H,14,15)
Standard InChI Key: NSSIUYHYTCOYGR-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: 233.27 | Molecular Weight (Monoisotopic): 233.1052 | AlogP: 2.13 | #Rotatable Bonds: 3 |
| Polar Surface Area: 51.32 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 13.06 | CX Basic pKa: | CX LogP: 1.93 | CX LogD: 1.93 |
| Aromatic Rings: 2 | Heavy Atoms: 17 | QED Weighted: 0.83 | Np Likeness Score: -0.19 |
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):