ID: ALA5197264
Chembl Id: CHEMBL5197264
PubChem CID: 168287239
Max Phase: Preclinical
Molecular Formula: C16H19NO2S
Molecular Weight: 289.40
Associated Items:
Canonical SMILES: CC(C)(c1ccccc1)c1cccc(NS(C)(=O)=O)c1
Standard InChI: InChI=1S/C16H19NO2S/c1-16(2,13-8-5-4-6-9-13)14-10-7-11-15(12-14)17-20(3,18)19/h4-12,17H,1-3H3
Standard InChI Key: CWPFSIZJHUVRGK-UHFFFAOYSA-N
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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| 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 |
| 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: 289.40 | Molecular Weight (Monoisotopic): 289.1136 | AlogP: 3.38 | #Rotatable Bonds: 4 |
| Polar Surface Area: 46.17 | Molecular Species: NEUTRAL | HBA: 2 | HBD: 1 |
| #RO5 Violations: ┄ | HBA (Lipinski): 3 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): ┄ |
| CX Acidic pKa: 9.89 | CX Basic pKa: ┄ | CX LogP: 3.03 | CX LogD: 3.02 |
| Aromatic Rings: 2 | Heavy Atoms: 20 | QED Weighted: 0.94 | Np Likeness Score: -1.16 |
| 1. Iijima T, Katoh M, Takedomi K, Yamamoto Y, Akatsuka H, Shirata N, Nishi A, Takakuwa M, Watanabe Y, Munakata H, Koyama N, Ikeda T, Iguchi T, Kato H, Kikkawa K, Kawaguchi T.. (2022) Discovery of Apararenone (MT-3995) as a Highly Selective, Potent, and Novel Nonsteroidal Mineralocorticoid Receptor Antagonist., 65 (12.0): [PMID:35652647] [10.1021/acs.jmedchem.2c00402] |
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