| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4293829
Max Phase: Preclinical
Molecular Formula: C16H24N2O4S
Molecular Weight: 340.45
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CN(C)CC[C@@H]1CCCCN1S(=O)(=O)c1ccc2c(c1)OCO2
Standard InChI: InChI=1S/C16H24N2O4S/c1-17(2)10-8-13-5-3-4-9-18(13)23(19,20)14-6-7-15-16(11-14)22-12-21-15/h6-7,11,13H,3-5,8-10,12H2,1-2H3/t13-/m0/s1
Standard InChI Key: AMGHKOBOERSKPP-ZDUSSCGKSA-N
Associated Targets(Human)
Glycine receptor alpha-3/beta 286 Activities
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 |
|---|
Properties
| Molecular Weight: 340.45 | Molecular Weight (Monoisotopic): 340.1457 | AlogP: 1.91 | #Rotatable Bonds: 5 |
| Polar Surface Area: 59.08 | Molecular Species: BASE | HBA: 5 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 9.26 | CX LogP: 1.64 | CX LogD: -0.22 |
| Aromatic Rings: 1 | Heavy Atoms: 23 | QED Weighted: 0.82 | Np Likeness Score: -1.30 |
References
| 1. Chakka N, Andrews KL, Berry LM, Bregman H, Gunaydin H, Huang L, Guzman-Perez A, Plant MH, Simard JR, Gingras J, DiMauro EF.. (2017) Applications of parallel synthetic lead hopping and pharmacophore-based virtual screening in the discovery of efficient glycine receptor potentiators., 137 [PMID:28575722] [10.1016/j.ejmech.2017.05.036] |
Source
Source(1):