| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA2288496
Max Phase: Preclinical
Molecular Formula: C16H20N6O6S
Molecular Weight: 424.44
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CCOc1cc(OC)nc(NC(=O)NS(=O)(=O)c2ncccc2C(=O)N(C)C)n1
Standard InChI: InChI=1S/C16H20N6O6S/c1-5-28-12-9-11(27-4)18-15(19-12)20-16(24)21-29(25,26)13-10(7-6-8-17-13)14(23)22(2)3/h6-9H,5H2,1-4H3,(H2,18,19,20,21,24)
Standard InChI Key: YKTCPPOEHRTVEF-UHFFFAOYSA-N
Associated Targets(non-human)
Amaranthus viridis 153 Activities
Zea mays 820 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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 |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Properties
| Molecular Weight: 424.44 | Molecular Weight (Monoisotopic): 424.1165 | AlogP: 0.49 | #Rotatable Bonds: 7 |
| Polar Surface Area: 152.71 | Molecular Species: ACID | HBA: 9 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 12 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: 4.98 | CX Basic pKa: 2.65 | CX LogP: 1.14 | CX LogD: 0.21 |
| Aromatic Rings: 2 | Heavy Atoms: 29 | QED Weighted: 0.65 | Np Likeness Score: -1.72 |
References
| 1. MURAI S, HAGA T, SAKASHITA N, NAKAMURA Y, HONDA C, HONZAWA S, KIMURA F, TSUJII Y, NISHIYAMA R. (1995) Synthesis and Herbicidal Activity of Sulfonylureas; SL-950 and Its Related Compounds, 20 (4): [10.1584/jpestics.20.453] |
Source
Source(1):