| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA2348588
Max Phase: Preclinical
Molecular Formula: C24H28Cl2N2O6S
Molecular Weight: 543.47
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: COc1ccc(OCCN2CCC3CCCC(C2=O)N3S(=O)(=O)c2cc(Cl)cc(Cl)c2)cc1OC
Standard InChI: InChI=1S/C24H28Cl2N2O6S/c1-32-22-7-6-19(15-23(22)33-2)34-11-10-27-9-8-18-4-3-5-21(24(27)29)28(18)35(30,31)20-13-16(25)12-17(26)14-20/h6-7,12-15,18,21H,3-5,8-11H2,1-2H3
Standard InChI Key: CQULSFOXJMUYFL-UHFFFAOYSA-N
Associated Targets(Human)
Peptidyl-prolyl cis-trans isomerase FKBP5 259 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: 543.47 | Molecular Weight (Monoisotopic): 542.1045 | AlogP: 4.23 | #Rotatable Bonds: 8 |
| Polar Surface Area: 85.38 | Molecular Species: NEUTRAL | HBA: 6 | HBD: 0 |
| #RO5 Violations: 1 | HBA (Lipinski): 8 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: | CX Basic pKa: | CX LogP: 3.69 | CX LogD: 3.69 |
| Aromatic Rings: 2 | Heavy Atoms: 35 | QED Weighted: 0.50 | Np Likeness Score: -0.90 |
References
| 1. Wang Y, Kirschner A, Fabian AK, Gopalakrishnan R, Kress C, Hoogeland B, Koch U, Kozany C, Bracher A, Hausch F.. (2013) Increasing the efficiency of ligands for FK506-binding protein 51 by conformational control., 56 (10): [PMID:23647266] [10.1021/jm400087k] |
Source
Source(1):