| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA3120703
Max Phase: Preclinical
Molecular Formula: C21H34
Molecular Weight: 286.50
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: C=CCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC
Standard InChI: InChI=1S/C21H34/c1-3-5-7-9-11-13-15-17-19-21-20-18-16-14-12-10-8-6-4-2/h3,11-14,17-20H,1,4-10,15-16,21H2,2H3/b13-11-,14-12-,19-17-,20-18-
Standard InChI Key: WMMKRRHSYGLRHN-MAZCIEHSSA-N
Associated Targets(non-human)
LOX1.4 Seed linoleate 9S-lipoxygenase (11 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: 286.50 | Molecular Weight (Monoisotopic): 286.2661 | AlogP: 7.32 | #Rotatable Bonds: 14 |
| Polar Surface Area: 0.00 | Molecular Species: | HBA: 0 | HBD: 0 |
| #RO5 Violations: 1 | HBA (Lipinski): 0 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: | CX Basic pKa: | CX LogP: 8.05 | CX LogD: 8.05 |
| Aromatic Rings: 0 | Heavy Atoms: 21 | QED Weighted: 0.23 | Np Likeness Score: 1.10 |
References
| 1. Kurihara H, Kagawa Y, Konno R, Kim SM, Takahashi K.. (2014) Lipoxygenase inhibitors derived from marine macroalgae., 24 (5): [PMID:24495846] [10.1016/j.bmcl.2014.01.046] |
Source
Source(1):