Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA5218560
Max Phase: Preclinical
Molecular Formula: C20H21N3O3
Molecular Weight: 351.41
Associated Items:
ID: ALA5218560
Max Phase: Preclinical
Molecular Formula: C20H21N3O3
Molecular Weight: 351.41
Associated Items:
Canonical SMILES: COc1ccc(-c2ccc3c(N4CCOCC4)ncnc3c2)cc1OC
Standard InChI: InChI=1S/C20H21N3O3/c1-24-18-6-4-15(12-19(18)25-2)14-3-5-16-17(11-14)21-13-22-20(16)23-7-9-26-10-8-23/h3-6,11-13H,7-10H2,1-2H3
Standard InChI Key: UASZZKXYGRZHPF-UHFFFAOYSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
Molecule Type: | Topical: No | First In Class: No | Black Box: No |
Chirality: No | Availability: No | Prodrug: No |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 351.41 | Molecular Weight (Monoisotopic): 351.1583 | AlogP: 3.15 | #Rotatable Bonds: 4 |
Polar Surface Area: 56.71 | Molecular Species: NEUTRAL | HBA: 6 | HBD: 0 |
#RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: 4.53 | CX LogP: 3.24 | CX LogD: 3.24 |
Aromatic Rings: 3 | Heavy Atoms: 26 | QED Weighted: 0.72 | Np Likeness Score: -1.04 |
1. Callis TB, Garrett TR, Montgomery AP, Danon JJ, Kassiou M.. (2022) Recent Scaffold Hopping Applications in Central Nervous System Drug Discovery., 65 (20.0): [PMID:36206553] [10.1021/acs.jmedchem.2c00969] |
Source(1):