| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4172107
Max Phase: Preclinical
Molecular Formula: C15H10Cl2N2O3S
Molecular Weight: 369.23
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: O=S(=O)(Nc1cccc2ncccc12)c1cc(Cl)cc(Cl)c1O
Standard InChI: InChI=1S/C15H10Cl2N2O3S/c16-9-7-11(17)15(20)14(8-9)23(21,22)19-13-5-1-4-12-10(13)3-2-6-18-12/h1-8,19-20H
Standard InChI Key: CULXGCRNHXTGHB-UHFFFAOYSA-N
Associated Targets(non-human)
Beta-glucuronidase 291 Activities
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: 369.23 | Molecular Weight (Monoisotopic): 367.9789 | AlogP: 4.05 | #Rotatable Bonds: 3 |
| Polar Surface Area: 79.29 | Molecular Species: ACID | HBA: 4 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 5.47 | CX Basic pKa: 4.86 | CX LogP: 2.94 | CX LogD: 1.63 |
| Aromatic Rings: 3 | Heavy Atoms: 23 | QED Weighted: 0.73 | Np Likeness Score: -1.58 |
References
| 1. Bano B, Arshia, Khan KM, Kanwal, Fatima B, Taha M, Ismail NH, Wadood A, Ghufran M, Perveen S.. (2017) Synthesis, in vitro β-glucuronidase inhibitory potential and molecular docking studies of quinolines., 139 [PMID:28865280] [10.1016/j.ejmech.2017.08.052] |
Source
Source(1):