| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA143127
Max Phase: Preclinical
Molecular Formula: C9H5ClFNO
Molecular Weight: 197.60
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Oc1c(F)cc(Cl)c2cccnc12
Standard InChI: InChI=1S/C9H5ClFNO/c10-6-4-7(11)9(13)8-5(6)2-1-3-12-8/h1-4,13H
Standard InChI Key: NJRFGEVCJFLFSV-UHFFFAOYSA-N
Associated Targets(non-human)
Aspergillus niger (16508 Activities)
Aspergillus oryzae (433 Activities)
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Trichoderma viride (1263 Activities)
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Trichophyton benhamiae (1686 Activities)
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Albifimbria verrucaria (26 Activities)
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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 |
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Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Properties
| Molecular Weight: 197.60 | Molecular Weight (Monoisotopic): 197.0044 | AlogP: 2.73 | #Rotatable Bonds: 0 |
| Polar Surface Area: 33.12 | Molecular Species: NEUTRAL | HBA: 2 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 2 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 7.39 | CX Basic pKa: 3.65 | CX LogP: 2.57 | CX LogD: 2.27 |
| Aromatic Rings: 2 | Heavy Atoms: 13 | QED Weighted: 0.70 | Np Likeness Score: -1.34 |
References
| 1. Lukovits I, Lopata A.. (1980) Decomposition of pharmacological activity indices into mutually independent components using principal component analysis., 23 (4): [PMID:7381845] [10.1021/jm00178a018] |
| 2. Liang SH, Southon AG, Fraser BH, Krause-Heuer AM, Zhang B, Shoup TM, Lewis R, Volitakis I, Han Y, Greguric I, Bush AI, Vasdev N.. (2015) Novel Fluorinated 8-Hydroxyquinoline Based Metal Ionophores for Exploring the Metal Hypothesis of Alzheimer's Disease., 6 (9): [PMID:26396692] [10.1021/acsmedchemlett.5b00281] |
Source
Source(1):