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ID: ALA2420244
Max Phase: Preclinical
Molecular Formula: C21H20N2O2
Molecular Weight: 332.40
Molecule Type: Small molecule
Associated Items:
ID: ALA2420244
Max Phase: Preclinical
Molecular Formula: C21H20N2O2
Molecular Weight: 332.40
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: COc1ccc(/N=C(\Nc2ccc(OC)cc2)c2ccccc2)cc1
Standard InChI: InChI=1S/C21H20N2O2/c1-24-19-12-8-17(9-13-19)22-21(16-6-4-3-5-7-16)23-18-10-14-20(25-2)15-11-18/h3-15H,1-2H3,(H,22,23)
Standard InChI Key: DJVHHMMPKWIKGZ-UHFFFAOYSA-N
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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 |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 332.40 | Molecular Weight (Monoisotopic): 332.1525 | AlogP: 4.89 | #Rotatable Bonds: 5 |
Polar Surface Area: 42.85 | 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: 7.82 | CX LogP: 4.81 | CX LogD: 4.27 |
Aromatic Rings: 3 | Heavy Atoms: 25 | QED Weighted: 0.53 | Np Likeness Score: -0.90 |
1. Rodrigues-Santos CE, Leon LL, Bortoluzzi AJ, Canto-Cavalheiro MM, Machado GC, Echevarria A.. (2013) Synthesis, antileishmanial activity and structure-activity relationship of 1-N-X-phenyl-3-N'-Y-phenyl-benzamidines., 67 [PMID:23851118] [10.1016/j.ejmech.2013.06.040] |
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