| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA2322549
Max Phase: Preclinical
Molecular Formula: C28H29NO6
Molecular Weight: 475.54
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Cc1c(CCC(=O)NC(Cc2ccccc2)C(=O)O)c(=O)oc2cc3occ(C(C)(C)C)c3cc12
Standard InChI: InChI=1S/C28H29NO6/c1-16-18(10-11-25(30)29-22(26(31)32)12-17-8-6-5-7-9-17)27(33)35-24-14-23-20(13-19(16)24)21(15-34-23)28(2,3)4/h5-9,13-15,22H,10-12H2,1-4H3,(H,29,30)(H,31,32)
Standard InChI Key: ZBFPZTIBQSFXMD-UHFFFAOYSA-N
Associated Targets(Human)
Nuclear factor NF-kappa-B p105 subunit 1459 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: 475.54 | Molecular Weight (Monoisotopic): 475.1995 | AlogP: 4.89 | #Rotatable Bonds: 7 |
| Polar Surface Area: 109.75 | Molecular Species: ACID | HBA: 5 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 7 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 3.56 | CX Basic pKa: | CX LogP: 4.87 | CX LogD: 1.51 |
| Aromatic Rings: 4 | Heavy Atoms: 35 | QED Weighted: 0.37 | Np Likeness Score: -0.19 |
References
| 1. Marzaro G, Guiotto A, Borgatti M, Finotti A, Gambari R, Breveglieri G, Chilin A.. (2013) Psoralen derivatives as inhibitors of NF-κB/DNA interaction: synthesis, molecular modeling, 3D-QSAR, and biological evaluation., 56 (5): [PMID:23414143] [10.1021/jm3009647] |
Source
Source(1):