| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA282271
Max Phase: Preclinical
Molecular Formula: C9H16N4OS2
Molecular Weight: 260.39
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CCN(CC)CCS/C(=N/O)c1cnsn1
Standard InChI: InChI=1S/C9H16N4OS2/c1-3-13(4-2)5-6-15-9(11-14)8-7-10-16-12-8/h7,14H,3-6H2,1-2H3/b11-9+
Standard InChI Key: JFZPQVLNVGVBDZ-PKNBQFBNSA-N
Associated Targets(non-human)
Acetylcholinesterase 12221 Activities
Anguilliformes 23 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: 260.39 | Molecular Weight (Monoisotopic): 260.0766 | AlogP: 1.75 | #Rotatable Bonds: 6 |
| Polar Surface Area: 61.61 | Molecular Species: ZWITTERION | HBA: 7 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 6.09 | CX Basic pKa: 9.97 | CX LogP: 0.30 | CX LogD: 0.29 |
| Aromatic Rings: 1 | Heavy Atoms: 16 | QED Weighted: 0.37 | Np Likeness Score: -1.44 |
References
| 1. Kenley RA, Bedford CD, Dailey OD, Howd RA, Miller A.. (1984) Nonquaternary cholinesterase reactivators. 2. Alpha-heteroaromatic aldoximes and thiohydroximates as reactivators of ethyl methylphosphonyl-acetylcholinesterase in vitro., 27 (9): [PMID:6471073] [10.1021/jm00375a021] |
Source
Source(1):