Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA5221103
Max Phase: Preclinical
Molecular Formula: C20H17N3O2
Molecular Weight: 331.38
Associated Items:
ID: ALA5221103
Max Phase: Preclinical
Molecular Formula: C20H17N3O2
Molecular Weight: 331.38
Associated Items:
Canonical SMILES: COc1ccc(-c2cnc3c(-c4ccccc4)cnn3c2)cc1OC
Standard InChI: InChI=1S/C20H17N3O2/c1-24-18-9-8-15(10-19(18)25-2)16-11-21-20-17(12-22-23(20)13-16)14-6-4-3-5-7-14/h3-13H,1-2H3
Standard InChI Key: SROJXRFDGZDDJC-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: 331.38 | Molecular Weight (Monoisotopic): 331.1321 | AlogP: 4.08 | #Rotatable Bonds: 4 |
Polar Surface Area: 48.65 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 0 |
#RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: 0.99 | CX LogP: 3.63 | CX LogD: 3.63 |
Aromatic Rings: 4 | Heavy Atoms: 25 | QED Weighted: 0.57 | Np Likeness Score: -0.97 |
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):