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ID: ALA2058976
Max Phase: Preclinical
Molecular Formula: C22H25N3O2
Molecular Weight: 363.46
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: C=CCC12CCN(C)C1N(C)c1ccc(OC(=O)Nc3ccccc3)cc12
Standard InChI: InChI=1S/C22H25N3O2/c1-4-12-22-13-14-24(2)20(22)25(3)19-11-10-17(15-18(19)22)27-21(26)23-16-8-6-5-7-9-16/h4-11,15,20H,1,12-14H2,2-3H3,(H,23,26)
Standard InChI Key: TUYVEBCAXRVGSI-UHFFFAOYSA-N
Associated Targets(non-human)
Butyrylcholinesterase 745 Activities
Acetylcholinesterase 2577 Activities
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Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: Small molecule | 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 |
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Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Properties
| Molecular Weight: 363.46 | Molecular Weight (Monoisotopic): 363.1947 | AlogP: 4.22 | #Rotatable Bonds: 4 |
| Polar Surface Area: 44.81 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 12.86 | CX Basic pKa: 6.80 | CX LogP: 4.84 | CX LogD: 4.74 |
| Aromatic Rings: 2 | Heavy Atoms: 27 | QED Weighted: 0.83 | Np Likeness Score: 0.44 |
References
| 1. Shinada M, Narumi F, Osada Y, Matsumoto K, Yoshida T, Higuchi K, Kawasaki T, Tanaka H, Satoh M.. (2012) Synthesis of phenserine analogues and evaluation of their cholinesterase inhibitory activities., 20 (16): [PMID:22831800] [10.1016/j.bmc.2012.06.048] |
Source
Source(1):