| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA2288510
Max Phase: Preclinical
Molecular Formula: C20H20N6O6S
Molecular Weight: 472.48
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2ncccc2C(=O)N(C)c2ccccc2)n1
Standard InChI: InChI=1S/C20H20N6O6S/c1-26(13-8-5-4-6-9-13)18(27)14-10-7-11-21-17(14)33(29,30)25-20(28)24-19-22-15(31-2)12-16(23-19)32-3/h4-12H,1-3H3,(H2,22,23,24,25,28)
Standard InChI Key: VOWKWOJGMBNACE-UHFFFAOYSA-N
Associated Targets(non-human)
Zea mays 820 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: 472.48 | Molecular Weight (Monoisotopic): 472.1165 | AlogP: 1.68 | #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: 2.68 | CX LogP: 2.44 | CX LogD: 1.51 |
| Aromatic Rings: 3 | Heavy Atoms: 33 | QED Weighted: 0.52 | Np Likeness Score: -1.54 |
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):