| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4249973
Max Phase: Preclinical
Molecular Formula: C24H40N2O3
Molecular Weight: 404.60
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CCCCCCCCCCCCCCCC(=O)N/N=C/c1ccc(O)c(OC)c1
Standard InChI: InChI=1S/C24H40N2O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-24(28)26-25-20-21-17-18-22(27)23(19-21)29-2/h17-20,27H,3-16H2,1-2H3,(H,26,28)/b25-20+
Standard InChI Key: ZWAVNZJXKSPVEF-LKUDQCMESA-N
Associated Targets(non-human)
Transient receptor potential cation channel subfamily V member 2 148 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: 404.60 | Molecular Weight (Monoisotopic): 404.3039 | AlogP: 6.33 | #Rotatable Bonds: 17 |
| Polar Surface Area: 70.92 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 2 |
| #RO5 Violations: 1 | HBA (Lipinski): 5 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: 9.59 | CX Basic pKa: 1.97 | CX LogP: 7.13 | CX LogD: 7.12 |
| Aromatic Rings: 1 | Heavy Atoms: 29 | QED Weighted: 0.18 | Np Likeness Score: -0.39 |
References
| 1. Schiano Moriello A, López Chinarro S, Novo Fernández O, Eras J, Amodeo P, Canela-Garayoa R, Vitale RM, Di Marzo V, De Petrocellis L.. (2018) Elongation of the Hydrophobic Chain as a Molecular Switch: Discovery of Capsaicin Derivatives and Endogenous Lipids as Potent Transient Receptor Potential Vanilloid Channel 2 Antagonists., 61 (18): [PMID:30176215] [10.1021/acs.jmedchem.8b00734] |
Source
Source(1):