| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4750116
Max Phase: Preclinical
Molecular Formula: C26H23N5O7S2
Molecular Weight: 581.63
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: CN(CCN(C)S(=O)(=O)c1ccc(C#N)cc1)C(=O)c1cn(S(=O)(=O)c2cccc([N+](=O)[O-])c2)c2ccccc12
Standard InChI: InChI=1S/C26H23N5O7S2/c1-28(14-15-29(2)39(35,36)21-12-10-19(17-27)11-13-21)26(32)24-18-30(25-9-4-3-8-23(24)25)40(37,38)22-7-5-6-20(16-22)31(33)34/h3-13,16,18H,14-15H2,1-2H3
Standard InChI Key: LNMBDKZTZYARJL-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: 581.63 | Molecular Weight (Monoisotopic): 581.1039 | AlogP: 3.05 | #Rotatable Bonds: 9 |
| Polar Surface Area: 163.69 | Molecular Species: NEUTRAL | HBA: 9 | HBD: 0 |
| #RO5 Violations: 1 | HBA (Lipinski): 12 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 2 |
| CX Acidic pKa: | CX Basic pKa: | CX LogP: 2.95 | CX LogD: 2.95 |
| Aromatic Rings: 4 | Heavy Atoms: 40 | QED Weighted: 0.21 | Np Likeness Score: -1.85 |
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):