| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA3740337
Max Phase: Preclinical
Molecular Formula: C16H14O5S
Molecular Weight: 318.35
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: COc1cc2oc(-c3cccs3)cc(=O)c2c(OC)c1OC
Standard InChI: InChI=1S/C16H14O5S/c1-18-12-8-11-14(16(20-3)15(12)19-2)9(17)7-10(21-11)13-5-4-6-22-13/h4-8H,1-3H3
Standard InChI Key: UPLALYBOWHMIMA-UHFFFAOYSA-N
Associated Targets(Human)
Receptor-type tyrosine-protein phosphatase S 105 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: 318.35 | Molecular Weight (Monoisotopic): 318.0562 | AlogP: 3.55 | #Rotatable Bonds: 4 |
| Polar Surface Area: 57.90 | Molecular Species: NEUTRAL | HBA: 6 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: | CX LogP: 2.41 | CX LogD: 2.41 |
| Aromatic Rings: 3 | Heavy Atoms: 22 | QED Weighted: 0.74 | Np Likeness Score: 0.22 |
References
| 1. Lee HS, Ku B, Park TH, Park H, Choi JK, Chang KT, Kim CH, Ryu SE, Kim SJ.. (2016) Identification of novel protein tyrosine phosphatase sigma inhibitors promoting neurite extension., 26 (1): [PMID:26602279] [10.1016/j.bmcl.2015.11.026] |
Source
Source(1):