| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4760595
Max Phase: Preclinical
Molecular Formula: C25H22N4O7S2
Molecular Weight: 554.61
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: O=C(c1cn(S(=O)(=O)c2cccc([N+](=O)[O-])c2)c2ccccc12)N1CCN(S(=O)(=O)c2ccccc2)CC1
Standard InChI: InChI=1S/C25H22N4O7S2/c30-25(26-13-15-27(16-14-26)37(33,34)20-8-2-1-3-9-20)23-18-28(24-12-5-4-11-22(23)24)38(35,36)21-10-6-7-19(17-21)29(31)32/h1-12,17-18H,13-16H2
Standard InChI Key: QBQQXGFQSPYSRL-UHFFFAOYSA-N
Associated Targets(Human)
Tumor necrosis factor ligand superfamily member 11 138 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: 554.61 | Molecular Weight (Monoisotopic): 554.0930 | AlogP: 2.93 | #Rotatable Bonds: 6 |
| Polar Surface Area: 139.90 | Molecular Species: NEUTRAL | HBA: 8 | HBD: 0 |
| #RO5 Violations: 1 | HBA (Lipinski): 11 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 2 |
| CX Acidic pKa: | CX Basic pKa: | CX LogP: 2.92 | CX LogD: 2.92 |
| Aromatic Rings: 4 | Heavy Atoms: 38 | QED Weighted: 0.26 | Np Likeness Score: -1.67 |
References
| 1. Rinotas V,Papakyriakou A,Violitzi F,Papaneophytou C,Ouzouni MD,Alexiou P,Strongilos A,Couladouros E,Kontopidis G,Eliopoulos E,Douni E. (2020) Discovery of Small-Molecule Inhibitors of Receptor Activator of Nuclear Factor-κB Ligand with a Superior Therapeutic Index., 63 (20.0): [PMID:32955874] [10.1021/acs.jmedchem.0c01316] |
Source
Source(1):