| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA2270898
Max Phase: Preclinical
Molecular Formula: C19H14ClN5OS
Molecular Weight: 395.88
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Cc1cc(=O)c(-c2nnc(Nc3ccccc3)s2)nn1-c1ccccc1Cl
Standard InChI: InChI=1S/C19H14ClN5OS/c1-12-11-16(26)17(24-25(12)15-10-6-5-9-14(15)20)18-22-23-19(27-18)21-13-7-3-2-4-8-13/h2-11H,1H3,(H,21,23)
Standard InChI Key: GDVCZACLIRZWDA-UHFFFAOYSA-N
Associated Targets(non-human)
Puccinia recondita 281 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: 395.88 | Molecular Weight (Monoisotopic): 395.0608 | AlogP: 4.46 | #Rotatable Bonds: 4 |
| Polar Surface Area: 72.70 | Molecular Species: NEUTRAL | HBA: 7 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 9.81 | CX Basic pKa: | CX LogP: 5.13 | CX LogD: 5.13 |
| Aromatic Rings: 4 | Heavy Atoms: 27 | QED Weighted: 0.55 | Np Likeness Score: -2.09 |
References
| 1. Zou XJ, Jin GY, Zhang ZX.. (2002) Synthesis, fungicidal activity, and QSAR of pyridazinonethiadiazoles., 50 (6): [PMID:11879019] [10.1021/jf0109266] |
| 2. Zou XJ, Lai LH, Jin GY, Zhang ZX.. (2002) Synthesis, fungicidal activity, and 3D-QSAR of pyridazinone-substituted 1,3,4-oxadiazoles and 1,3,4-thiadiazoles., 50 (13): [PMID:12059155] [10.1021/jf0201677] |
Source
Source(1):