| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA151428
Max Phase: Preclinical
Molecular Formula: C17H24N4S
Molecular Weight: 316.47
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: c1ccc(CC2CCN(CCCSc3nc[nH]n3)CC2)cc1
Standard InChI: InChI=1S/C17H24N4S/c1-2-5-15(6-3-1)13-16-7-10-21(11-8-16)9-4-12-22-17-18-14-19-20-17/h1-3,5-6,14,16H,4,7-13H2,(H,18,19,20)
Standard InChI Key: VVFBLNODTINYDD-UHFFFAOYSA-N
Associated Targets(Human)
Glutamate [NMDA] receptor subunit epsilon 1 112 Activities
Glutamate [NMDA] receptor subunit epsilon 2 467 Activities
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Glutamate [NMDA] receptor subunit epsilon 3 47 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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 |
|---|
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: 316.47 | Molecular Weight (Monoisotopic): 316.1722 | AlogP: 3.24 | #Rotatable Bonds: 7 |
| Polar Surface Area: 44.81 | Molecular Species: BASE | HBA: 4 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 10.08 | CX Basic pKa: 9.11 | CX LogP: 3.24 | CX LogD: 1.81 |
| Aromatic Rings: 2 | Heavy Atoms: 22 | QED Weighted: 0.63 | Np Likeness Score: -1.47 |
References
| 1. Gregory TF, Wright JL, Wise LD, Meltzer LT, Serpa KA, Konkoy CS, Whittemore ER, Woodward RM.. (2000) Parallel synthesis of a series of subtype-selective NMDA receptor antagonists., 10 (6): [PMID:10741546] [10.1016/s0960-894x(00)00035-4] |
Source
Source(1):