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ID: ALA2230021
Max Phase: Preclinical
Molecular Formula: C10H6FNO2S
Molecular Weight: 223.23
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: O=[N+]([O-])c1cc(F)ccc1-c1ccsc1
Standard InChI: InChI=1S/C10H6FNO2S/c11-8-1-2-9(7-3-4-15-6-7)10(5-8)12(13)14/h1-6H
Standard InChI Key: XVSFXGJLKBIYQI-UHFFFAOYSA-N
Associated Targets(non-human)
Mycosphaerella arachidis 441 Activities
Fusarium oxysporum 3998 Activities
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Botryosphaeria berengeriana 484 Activities
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Fusarium graminearum 1554 Activities
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Alternaria solani 773 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: 223.23 | Molecular Weight (Monoisotopic): 223.0103 | AlogP: 3.46 | #Rotatable Bonds: 2 |
| Polar Surface Area: 43.14 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 3 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: | CX LogP: 3.48 | CX LogD: 3.48 |
| Aromatic Rings: 2 | Heavy Atoms: 15 | QED Weighted: 0.58 | Np Likeness Score: -2.54 |
References
| 1. Wang MZ, Xu H, Feng Q, Wang LZ, Wang SH, Li ZM.. (2009) Design, synthesis, and fungicidal activity of novel analogues of pyrrolnitrin., 57 (17): [PMID:19681615] [10.1021/jf902320e] |
Source
Source(1):