| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA5202672
Max Phase: Preclinical
Molecular Formula: C17H14N2O4S
Molecular Weight: 342.38
Associated Items:
Representations
Canonical SMILES: COc1ccc2sc(C(=O)NC(=O)c3cccc(OC)n3)cc2c1
Standard InChI: InChI=1S/C17H14N2O4S/c1-22-11-6-7-13-10(8-11)9-14(24-13)17(21)19-16(20)12-4-3-5-15(18-12)23-2/h3-9H,1-2H3,(H,19,20,21)
Standard InChI Key: PDJNPXMUVORVAS-UHFFFAOYSA-N
Associated Targets(Human)
Dual specificty protein kinase CLK1 2189 Activities
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 |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Properties
| Molecular Weight: 342.38 | Molecular Weight (Monoisotopic): 342.0674 | AlogP: 2.88 | #Rotatable Bonds: 4 |
| Polar Surface Area: 77.52 | Molecular Species: NEUTRAL | HBA: 6 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 8.87 | CX Basic pKa: 0.76 | CX LogP: 3.12 | CX LogD: 3.11 |
| Aromatic Rings: 3 | Heavy Atoms: 24 | QED Weighted: 0.74 | Np Likeness Score: -1.58 |
References
| 1. El-Gamil DS, ElHady AK, Chen PJ, Hwang TL, Abadi AH, Abdel-Halim M, Engel M.. (2022) Development of novel conformationally restricted selective Clk1/4 inhibitors through creating an intramolecular hydrogen bond involving an imide linker., 238 [PMID:35635953] [10.1016/j.ejmech.2022.114411] |
Source
Source(1):