| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA2253185
Max Phase: Preclinical
Molecular Formula: C15H8BrCl2FN4O
Molecular Weight: 430.06
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: O=C(Nc1ccc(F)c(Cl)c1)c1cc(Br)nn1-c1ncccc1Cl
Standard InChI: InChI=1S/C15H8BrCl2FN4O/c16-13-7-12(23(22-13)14-9(17)2-1-5-20-14)15(24)21-8-3-4-11(19)10(18)6-8/h1-7H,(H,21,24)
Standard InChI Key: USJCERQPSHYCTO-UHFFFAOYSA-N
Associated Targets(non-human)
Culex pipiens pallens 759 Activities
Mythimna separata 3306 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: 430.06 | Molecular Weight (Monoisotopic): 427.9243 | AlogP: 4.73 | #Rotatable Bonds: 3 |
| Polar Surface Area: 59.81 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 13.84 | CX Basic pKa: | CX LogP: 4.77 | CX LogD: 4.77 |
| Aromatic Rings: 3 | Heavy Atoms: 24 | QED Weighted: 0.65 | Np Likeness Score: -2.18 |
References
| 1. Dong WL, Xu JY, Xiong LX, Li ZM.. (2012) Synthesis, structure and insecticidal activities of some novel amides containing N-pyridylpyrazole moeities., 17 (9): [PMID:22941222] [10.3390/molecules170910414] |
Source
Source(1):