ID: ALA4172142
Chembl Id: CHEMBL4172142
PubChem CID: 145950315
Max Phase: Preclinical
Molecular Formula: C17H19ClN2O4S
Molecular Weight: 382.87
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: COc1ccc(Cl)cc1C(C)NC(=O)N(C)S(=O)(=O)c1ccccc1
Standard InChI: InChI=1S/C17H19ClN2O4S/c1-12(15-11-13(18)9-10-16(15)24-3)19-17(21)20(2)25(22,23)14-7-5-4-6-8-14/h4-12H,1-3H3,(H,19,21)
Standard InChI Key: HPXVGGYLFAGRTK-UHFFFAOYSA-N
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| 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 |
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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| Molecular Weight: 382.87 | Molecular Weight (Monoisotopic): 382.0754 | AlogP: 3.44 | #Rotatable Bonds: 5 |
| Polar Surface Area: 75.71 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 1 |
| #RO5 Violations: ┄ | HBA (Lipinski): 6 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): ┄ |
| CX Acidic pKa: 12.95 | CX Basic pKa: ┄ | CX LogP: 3.27 | CX LogD: 3.27 |
| Aromatic Rings: 2 | Heavy Atoms: 25 | QED Weighted: 0.86 | Np Likeness Score: -1.61 |
| 1. Bouhedja M, Peres B, Fhayli W, Ghandour Z, Boumendjel A, Faury G, Khelili S.. (2018) Design, synthesis and biological evaluation of novel ring-opened cromakalim analogues with relaxant effects on vascular and respiratory smooth muscles and as stimulators of elastin synthesis., 144 [PMID:29291445] [10.1016/j.ejmech.2017.12.071] |
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