| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA5287265
Max Phase: Preclinical
Molecular Formula: C24H23N5O3
Molecular Weight: 429.48
Associated Items:
Representations
Canonical SMILES: O=C(Nc1ccccc1)Nc1ccc2n(c1=O)C[C@@H]1C[C@H]2CN(C(=O)c2ccccn2)C1
Standard InChI: InChI=1S/C24H23N5O3/c30-22(19-8-4-5-11-25-19)28-13-16-12-17(15-28)21-10-9-20(23(31)29(21)14-16)27-24(32)26-18-6-2-1-3-7-18/h1-11,16-17H,12-15H2,(H2,26,27,32)/t16-,17+/m1/s1
Standard InChI Key: YMADCEPSWWDWLO-SJORKVTESA-N
Associated Targets(Human)
Proteasome Macropain subunit MB1 2451 Activities
Molecule Features
| Natural Product: Yes | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: | 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: 429.48 | Molecular Weight (Monoisotopic): 429.1801 | AlogP: 3.15 | #Rotatable Bonds: 3 |
| Polar Surface Area: 96.33 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 8 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 12.09 | CX Basic pKa: 2.07 | CX LogP: 1.19 | CX LogD: 1.19 |
| Aromatic Rings: 3 | Heavy Atoms: 32 | QED Weighted: 0.67 | Np Likeness Score: -1.59 |
References
| 1. Allardyce D, Adu Mantey P, Szalecka M, Nkwo R, Loizidou EZ.. (2023) Identification of a new class of proteasome inhibitors based on a naphthyl-azotricyclic-urea-phenyl scaffold., 14 (3): [PMID:36970145] [10.1039/d2md00404f] |
Source
Source(1):