| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4100171
Max Phase: Preclinical
Molecular Formula: C20H12FNO4S
Molecular Weight: 381.38
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: O=C1C=Cc2c(c(-c3ccccc3)cn2S(=O)(=O)c2ccc(F)cc2)C1=O
Standard InChI: InChI=1S/C20H12FNO4S/c21-14-6-8-15(9-7-14)27(25,26)22-12-16(13-4-2-1-3-5-13)19-17(22)10-11-18(23)20(19)24/h1-12H
Standard InChI Key: LWLWVYIFUNGOIE-UHFFFAOYSA-N
Associated Targets(Human)
ELAV-like protein 1 119 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: 381.38 | Molecular Weight (Monoisotopic): 381.0471 | AlogP: 3.31 | #Rotatable Bonds: 3 |
| Polar Surface Area: 73.21 | Molecular Species: | 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: 3.93 | CX LogD: 3.93 |
| Aromatic Rings: 3 | Heavy Atoms: 27 | QED Weighted: 0.65 | Np Likeness Score: -0.58 |
References
| 1. Manzoni L, Zucal C, Maio DD, D'Agostino VG, Thongon N, Bonomo I, Lal P, Miceli M, Baj V, Brambilla M, Cerofolini L, Elezgarai S, Biasini E, Luchinat C, Novellino E, Fragai M, Marinelli L, Provenzani A, Seneci P.. (2018) Interfering with HuR-RNA Interaction: Design, Synthesis and Biological Characterization of Tanshinone Mimics as Novel, Effective HuR Inhibitors., 61 (4): [PMID:29313684] [10.1021/acs.jmedchem.7b01176] |
Source
Source(1):