| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA3427496
Max Phase: Preclinical
Molecular Formula: C27H40N6O4
Molecular Weight: 512.66
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: COc1ccc(-c2nnn(CC(=O)N(C3CCCCC3)C(C(=O)NC3CCCC3)C(C)C)n2)cc1OC
Standard InChI: InChI=1S/C27H40N6O4/c1-18(2)25(27(35)28-20-10-8-9-11-20)33(21-12-6-5-7-13-21)24(34)17-32-30-26(29-31-32)19-14-15-22(36-3)23(16-19)37-4/h14-16,18,20-21,25H,5-13,17H2,1-4H3,(H,28,35)
Standard InChI Key: FLVINNJBZVGJBI-UHFFFAOYSA-N
Associated Targets(non-human)
Scavenger receptor class B member 1 349 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: 512.66 | Molecular Weight (Monoisotopic): 512.3111 | AlogP: 3.60 | #Rotatable Bonds: 10 |
| Polar Surface Area: 111.47 | Molecular Species: NEUTRAL | HBA: 8 | HBD: 1 |
| #RO5 Violations: 1 | HBA (Lipinski): 10 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: | CX Basic pKa: | CX LogP: 4.34 | CX LogD: 4.34 |
| Aromatic Rings: 2 | Heavy Atoms: 37 | QED Weighted: 0.52 | Np Likeness Score: -1.40 |
References
| 1. Dockendorff C, Faloon PW, Germain A, Yu M, Youngsaye W, Nag PP, Bennion M, Penman M, Nieland TJ, Dandapani S, Perez JR, Munoz B, Palmer MA, Schreiber SL, Krieger M.. (2015) Discovery of bisamide-heterocycles as inhibitors of scavenger receptor BI (SR-BI)-mediated lipid uptake., 25 (12): [PMID:25958245] [10.1016/j.bmcl.2015.03.074] |
Source
Source(1):