| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA19205
Max Phase: Preclinical
Molecular Formula: C3H3N3OS
Molecular Weight: 129.14
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: O/N=C\c1cnsn1
Standard InChI: InChI=1S/C3H3N3OS/c7-4-1-3-2-5-8-6-3/h1-2,7H/b4-1-
Standard InChI Key: RQUWGXXOEYMUCZ-RJRFIUFISA-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: 129.14 | Molecular Weight (Monoisotopic): 128.9997 | AlogP: 0.35 | #Rotatable Bonds: 1 |
| Polar Surface Area: 58.37 | Molecular Species: ACID | HBA: 5 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 5.59 | CX Basic pKa: | CX LogP: 0.75 | CX LogD: -0.96 |
| Aromatic Rings: 1 | Heavy Atoms: 8 | QED Weighted: 0.34 | Np Likeness Score: -1.32 |
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):