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ID: ALA2435808
Max Phase: Preclinical
Molecular Formula: C16H16N2O3
Molecular Weight: 284.31
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: COc1cc(NCc2ccc(C)o2)ccc1-c1cnco1
Standard InChI: InChI=1S/C16H16N2O3/c1-11-3-5-13(21-11)8-18-12-4-6-14(15(7-12)19-2)16-9-17-10-20-16/h3-7,9-10,18H,8H2,1-2H3
Standard InChI Key: SCVLCUJLVCQMNZ-UHFFFAOYSA-N
Associated Targets(non-human)
Coxsackievirus B6 58 Activities
Coxsackievirus B3 1096 Activities
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Vero 26788 Activities
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Hepatitis C virus 23859 Activities
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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 |
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Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Properties
| Molecular Weight: 284.31 | Molecular Weight (Monoisotopic): 284.1161 | AlogP: 3.86 | #Rotatable Bonds: 5 |
| Polar Surface Area: 60.43 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 1.86 | CX LogP: 1.78 | CX LogD: 1.78 |
| Aromatic Rings: 3 | Heavy Atoms: 21 | QED Weighted: 0.77 | Np Likeness Score: -1.21 |
References
| 1. Zhong ZJ, Zhang DJ, Peng ZG, Li YH, Shan GZ, Zuo LM, Wu LT, Li SY, Gao RM, Li ZR.. (2013) Synthesis and antiviral activity of a novel class of (5-oxazolyl)phenyl amines., 69 [PMID:23999140] [10.1016/j.ejmech.2013.07.053] |
Source
Source(1):