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ID: ALA5178466
Max Phase: Preclinical
Molecular Formula: C22H26N4OS
Molecular Weight: 394.54
Associated Items:
Representations
Canonical SMILES: Cc1ccccc1N1CCN(CCC(=O)Nc2nc3c(C)cccc3s2)CC1
Standard InChI: InChI=1S/C22H26N4OS/c1-16-6-3-4-8-18(16)26-14-12-25(13-15-26)11-10-20(27)23-22-24-21-17(2)7-5-9-19(21)28-22/h3-9H,10-15H2,1-2H3,(H,23,24,27)
Standard InChI Key: CZYWSXAIWGJPTD-UHFFFAOYSA-N
Associated Targets(Human)
ACHE Tclin Acetylcholinesterase (18204 Activities)
BCHE Tclin Butyrylcholinesterase (7174 Activities)
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GRIN2B Tclin Glutamate [NMDA] receptor subunit epsilon 2 (467 Activities)
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Associated Targets(non-human)
SIGMAR1 Sigma-1 receptor (3326 Activities)
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Tmem97 Sigma intracellular receptor 2 (922 Activities)
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Molecule Features
| 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 |
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: 394.54 | Molecular Weight (Monoisotopic): 394.1827 | AlogP: 4.06 | #Rotatable Bonds: 5 |
| Polar Surface Area: 48.47 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 8.09 | CX Basic pKa: 7.30 | CX LogP: 4.53 | CX LogD: 4.51 |
| Aromatic Rings: 3 | Heavy Atoms: 28 | QED Weighted: 0.71 | Np Likeness Score: -2.33 |
References
| 1. Turgutalp B, Bhattarai P, Ercetin T, Luise C, Reis R, Gurdal EE, Isaak A, Biriken D, Dinter E, Sipahi H, Schepmann D, Junker A, Wünsch B, Sippl W, Gulcan HO, Kizil C, Yarim M.. (2022) Discovery of Potent Cholinesterase Inhibition-Based Multi-Target-Directed Lead Compounds for Synaptoprotection in Alzheimer's Disease., 65 (18.0): [PMID:36084304] [10.1021/acs.jmedchem.2c01003] |
Source
Source(1):