| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA3361248
Max Phase: Preclinical
Molecular Formula: C20H20O5
Molecular Weight: 340.38
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: COCCCc1cc(OC)c2oc(-c3ccc4c(c3)OCO4)cc2c1
Standard InChI: InChI=1S/C20H20O5/c1-21-7-3-4-13-8-15-11-17(25-20(15)19(9-13)22-2)14-5-6-16-18(10-14)24-12-23-16/h5-6,8-11H,3-4,7,12H2,1-2H3
Standard InChI Key: BNNSZVXJKPLGHT-UHFFFAOYSA-N
Associated Targets(Human)
A2058 690 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: 340.38 | Molecular Weight (Monoisotopic): 340.1311 | AlogP: 4.42 | #Rotatable Bonds: 6 |
| Polar Surface Area: 50.06 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: | CX LogP: 3.77 | CX LogD: 3.77 |
| Aromatic Rings: 3 | Heavy Atoms: 25 | QED Weighted: 0.62 | Np Likeness Score: 0.37 |
References
| 1. Hajdu Z, Haskó J, Krizbai IA, Wilhelm I, Jedlinszki N, Fazakas C, Molnár J, Forgo P, Hohmann J, Csupor D.. (2014) Evaluation of lignans from Heliopsis helianthoides var. scabra for their potential antimetastatic effects in the brain., 77 (12): [PMID:25479041] [10.1021/np500508y] |
Source
Source(1):