| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA2253359
Max Phase: Preclinical
Molecular Formula: C10H13N5S2
Molecular Weight: 267.38
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CSc1nn(C)c(NCCCN=C=S)c1C#N
Standard InChI: InChI=1S/C10H13N5S2/c1-15-9(13-5-3-4-12-7-16)8(6-11)10(14-15)17-2/h13H,3-5H2,1-2H3
Standard InChI Key: AWLDLZJWXSXGOM-UHFFFAOYSA-N
Associated Targets(non-human)
Trifolium repens 19 Activities
Dactylis glomerata 15 Activities
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Cyperus iria 145 Activities
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Echinochloa crus-galli 3685 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: 267.38 | Molecular Weight (Monoisotopic): 267.0612 | AlogP: 1.92 | #Rotatable Bonds: 6 |
| Polar Surface Area: 66.00 | Molecular Species: NEUTRAL | HBA: 7 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 2.07 | CX LogP: 2.00 | CX LogD: 2.00 |
| Aromatic Rings: 1 | Heavy Atoms: 17 | QED Weighted: 0.37 | Np Likeness Score: -1.28 |
References
| 1. Wu H, Feng JT, Lin KC, Zhang X.. (2012) Synthesis and herbicidal activity of substituted pyrazole isothiocyanates., 17 (10): [PMID:23075815] [10.3390/molecules171012187] |
Source
Source(1):