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ID: ALA4170062
Max Phase: Preclinical
Molecular Formula: C20H16F4N2O2S
Molecular Weight: 424.42
Molecule Type: Small molecule
Associated Items:
ID: ALA4170062
Max Phase: Preclinical
Molecular Formula: C20H16F4N2O2S
Molecular Weight: 424.42
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: O=S(=O)(NCCc1cccc(F)c1)c1cc(-c2cccnc2)cc(C(F)(F)F)c1
Standard InChI: InChI=1S/C20H16F4N2O2S/c21-18-5-1-3-14(9-18)6-8-26-29(27,28)19-11-16(15-4-2-7-25-13-15)10-17(12-19)20(22,23)24/h1-5,7,9-13,26H,6,8H2
Standard InChI Key: ZHOXZUVULSGHLN-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: 424.42 | Molecular Weight (Monoisotopic): 424.0869 | AlogP: 4.43 | #Rotatable Bonds: 6 |
Polar Surface Area: 59.06 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 9.89 | CX Basic pKa: 4.70 | CX LogP: 4.27 | CX LogD: 4.26 |
Aromatic Rings: 3 | Heavy Atoms: 29 | QED Weighted: 0.60 | Np Likeness Score: -1.82 |
1. Giordano A, Forte G, Massimo L, Riccio R, Bifulco G, Di Micco S.. (2018) Discovery of new erbB4 inhibitors: Repositioning an orphan chemical library by inverse virtual screening., 152 [PMID:29730188] [10.1016/j.ejmech.2018.04.018] |
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