| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4515732
Max Phase: Preclinical
Molecular Formula: C19H21F3N2OS
Molecular Weight: 382.45
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: CC(C)(Sc1ccc(C(F)(F)F)cn1)C(=O)NCCCc1ccccc1
Standard InChI: InChI=1S/C19H21F3N2OS/c1-18(2,26-16-11-10-15(13-24-16)19(20,21)22)17(25)23-12-6-9-14-7-4-3-5-8-14/h3-5,7-8,10-11,13H,6,9,12H2,1-2H3,(H,23,25)
Standard InChI Key: IQCKNMMYFVPQRZ-UHFFFAOYSA-N
Associated Targets(Human)
HEp-2 3859 Activities
Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: Unknown | 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: 382.45 | Molecular Weight (Monoisotopic): 382.1327 | AlogP: 4.72 | #Rotatable Bonds: 7 |
| Polar Surface Area: 41.99 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 3 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 2.18 | CX LogP: 4.90 | CX LogD: 4.90 |
| Aromatic Rings: 2 | Heavy Atoms: 26 | QED Weighted: 0.56 | Np Likeness Score: -1.17 |
References
| 1. Seleem MA, Rodrigues de Almeida N, Chhonker YS, Murry DJ, Guterres ZDR, Blocker AM, Kuwabara S, Fisher DJ, Leal ES, Martinefski MR, Bollini M, Monge ME, Ouellette SP, Conda-Sheridan M.. (2020) Synthesis and Antichlamydial Activity of Molecules Based on Dysregulators of Cylindrical Proteases., 63 (8): [PMID:32227948] [10.1021/acs.jmedchem.0c00371] |
Source
Source(1):