ID: ALA349364
Chembl Id: CHEMBL349364
PubChem CID: 44375511
Max Phase: Preclinical
Molecular Formula: C22H35NO3
Molecular Weight: 361.53
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CCCCCC(C)OC(=O)CC(=O)Nc1c(C(C)C)cccc1C(C)C
Standard InChI: InChI=1S/C22H35NO3/c1-7-8-9-11-17(6)26-21(25)14-20(24)23-22-18(15(2)3)12-10-13-19(22)16(4)5/h10,12-13,15-17H,7-9,11,14H2,1-6H3,(H,23,24)
Standard InChI Key: SAZVVYBGNVECIB-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: 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 |
|---|
| Molecular Weight: 361.53 | Molecular Weight (Monoisotopic): 361.2617 | AlogP: 5.77 | #Rotatable Bonds: 10 |
| Polar Surface Area: 55.40 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 1 |
| #RO5 Violations: 1 | HBA (Lipinski): 4 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: 12.71 | CX Basic pKa: ┄ | CX LogP: 6.37 | CX LogD: 6.37 |
| Aromatic Rings: 1 | Heavy Atoms: 26 | QED Weighted: 0.33 | Np Likeness Score: -0.18 |
| 1. Sliskovic D, Picard J, Roark W, Essenburg A, Krause B, Minton L, Reindel J, Stanfield R. (1996) Inhibitors of acyl-CoA: cholesterol O-acyl transferase (ACAT) as hypocholesterolemic agents. The synthesis and biological activity of a series of malonester amides, 6 (6): [10.1016/0960-894X(96)00098-4] |
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