| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4761252
Max Phase: Preclinical
Molecular Formula: C25H26N2O2
Molecular Weight: 386.50
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: Cn1c(COc2ccccc2)nc2ccc(Oc3cccc(C(C)(C)C)c3)cc21
Standard InChI: InChI=1S/C25H26N2O2/c1-25(2,3)18-9-8-12-20(15-18)29-21-13-14-22-23(16-21)27(4)24(26-22)17-28-19-10-6-5-7-11-19/h5-16H,17H2,1-4H3
Standard InChI Key: YFZDWNPGURLUKR-UHFFFAOYSA-N
Associated Targets(Human)
Estrogen-related receptor alpha 573 Activities
Peroxisome proliferator-activated receptor gamma 15191 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: Unknown | 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: 386.50 | Molecular Weight (Monoisotopic): 386.1994 | AlogP: 6.24 | #Rotatable Bonds: 5 |
| Polar Surface Area: 36.28 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 0 |
| #RO5 Violations: 1 | HBA (Lipinski): 4 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: | CX Basic pKa: 4.57 | CX LogP: 6.17 | CX LogD: 6.17 |
| Aromatic Rings: 4 | Heavy Atoms: 29 | QED Weighted: 0.41 | Np Likeness Score: -1.23 |
References
| 1. Shinozuka T,Ito S,Kimura T,Izumi M,Wakabayashi K. (2021) Discovery of a Novel Class of ERRα Agonists., 12 (5.0): [PMID:34055231] [10.1021/acsmedchemlett.1c00100] |
Source
Source(1):