| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA5286635
Max Phase: Preclinical
Molecular Formula: C17H28N2O2
Molecular Weight: 292.42
Associated Items:
Representations
Canonical SMILES: CCCCCCCCOCCc1ccc(N/C=N/O)cc1
Standard InChI: InChI=1S/C17H28N2O2/c1-2-3-4-5-6-7-13-21-14-12-16-8-10-17(11-9-16)18-15-19-20/h8-11,15,20H,2-7,12-14H2,1H3,(H,18,19)
Standard InChI Key: JYALKGVAYJUOLE-UHFFFAOYSA-N
Associated Targets(Human)
Cytochrome P450 4Z1 127 Activities
Molecule Features
| 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 |
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: 292.42 | Molecular Weight (Monoisotopic): 292.2151 | AlogP: 4.44 | #Rotatable Bonds: 12 |
| Polar Surface Area: 53.85 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 11.55 | CX Basic pKa: 2.36 | CX LogP: 4.44 | CX LogD: 4.44 |
| Aromatic Rings: 1 | Heavy Atoms: 21 | QED Weighted: 0.20 | Np Likeness Score: -0.38 |
References
| 1. Yuan Y, Yao H, Zhou M, Ma X, Zhou Y, Xu J, Niu M, Yin J, Zheng L, Xu S.. (2022) Identification of a Novel Potent CYP4Z1 Inhibitor Attenuating the Stemness of Breast Cancer Cells through Lead Optimization., 65 (23.0): [PMID:36414390] [10.1021/acs.jmedchem.2c01320] |
Source
Source(1):