Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4855758
Max Phase: Preclinical
Molecular Formula: C20H22N4O
Molecular Weight: 334.42
Molecule Type: Unknown
Associated Items:
ID: ALA4855758
Max Phase: Preclinical
Molecular Formula: C20H22N4O
Molecular Weight: 334.42
Molecule Type: Unknown
Associated Items:
Canonical SMILES: O=C(NCC1CCNCC1)c1cc2ccc(-c3ccncc3)cc2[nH]1
Standard InChI: InChI=1S/C20H22N4O/c25-20(23-13-14-3-7-21-8-4-14)19-12-17-2-1-16(11-18(17)24-19)15-5-9-22-10-6-15/h1-2,5-6,9-12,14,21,24H,3-4,7-8,13H2,(H,23,25)
Standard InChI Key: CFJAZYHCODKCAA-UHFFFAOYSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
Molecule Type: Unknown | 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: 334.42 | Molecular Weight (Monoisotopic): 334.1794 | AlogP: 2.96 | #Rotatable Bonds: 4 |
Polar Surface Area: 69.81 | Molecular Species: BASE | HBA: 3 | HBD: 3 |
#RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: 10.05 | CX LogP: 1.60 | CX LogD: -0.95 |
Aromatic Rings: 3 | Heavy Atoms: 25 | QED Weighted: 0.69 | Np Likeness Score: -0.77 |
1. Nie S, Zhao J, Wu X, Yao Y, Wu F, Lin YL, Li X, Kneubehl AR, Vogt MB, Rico-Hesse R, Song Y.. (2021) Synthesis, structure-activity relationship and antiviral activity of indole-containing inhibitors of Flavivirus NS2B-NS3 protease., 225 [PMID:34450494] [10.1016/j.ejmech.2021.113767] |
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