Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
ID: ALA2047520
Max Phase: Preclinical
Molecular Formula: C11H7ClFN3O
Molecular Weight: 251.65
Molecule Type: Small molecule
Associated Items:
ID: ALA2047520
Max Phase: Preclinical
Molecular Formula: C11H7ClFN3O
Molecular Weight: 251.65
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: O=C(Nc1cnc(Cl)nc1)c1cccc(F)c1
Standard InChI: InChI=1S/C11H7ClFN3O/c12-11-14-5-9(6-15-11)16-10(17)7-2-1-3-8(13)4-7/h1-6H,(H,16,17)
Standard InChI Key: PVBHPXFLJOWZKI-UHFFFAOYSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
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 |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
---|
Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
---|
Molecular Weight: 251.65 | Molecular Weight (Monoisotopic): 251.0262 | AlogP: 2.52 | #Rotatable Bonds: 2 |
Polar Surface Area: 54.88 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: | CX LogP: 2.19 | CX LogD: 2.19 |
Aromatic Rings: 2 | Heavy Atoms: 17 | QED Weighted: 0.83 | Np Likeness Score: -2.16 |
1. Amato G, Roeloffs R, Rigdon GC, Antonio B, Mersch T, McNaughton-Smith G, Wickenden AD, Fritch P, Suto MJ.. (2011) N-Pyridyl and Pyrimidine Benzamides as KCNQ2/Q3 Potassium Channel Openers for the Treatment of Epilepsy., 2 (6): [PMID:24900334] [10.1021/ml200053x] |
Source(1):