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ID: ALA4633352
Max Phase: Preclinical
Molecular Formula: C22H24FN5O4S
Molecular Weight: 473.53
Molecule Type: Unknown
Associated Items:
ID: ALA4633352
Max Phase: Preclinical
Molecular Formula: C22H24FN5O4S
Molecular Weight: 473.53
Molecule Type: Unknown
Associated Items:
Canonical SMILES: CCn1cc(C(=O)O)c(=O)c2cc(F)c(N3CCN(C/C(=N/OC)c4cccs4)CC3)nc21
Standard InChI: InChI=1S/C22H24FN5O4S/c1-3-27-12-15(22(30)31)19(29)14-11-16(23)21(24-20(14)27)28-8-6-26(7-9-28)13-17(25-32-2)18-5-4-10-33-18/h4-5,10-12H,3,6-9,13H2,1-2H3,(H,30,31)/b25-17-
Standard InChI Key: CLVCLLWAWQYJBW-UQQQWYQISA-N
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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: 473.53 | Molecular Weight (Monoisotopic): 473.1533 | AlogP: 2.49 | #Rotatable Bonds: 7 |
Polar Surface Area: 100.26 | Molecular Species: ACID | HBA: 9 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 9 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 5.44 | CX Basic pKa: 4.71 | CX LogP: 2.93 | CX LogD: 1.26 |
Aromatic Rings: 3 | Heavy Atoms: 33 | QED Weighted: 0.42 | Np Likeness Score: -1.49 |
1. Gao F, Zhang X, Wang T, Xiao J.. (2019) Quinolone hybrids and their anti-cancer activities: An overview., 165 [PMID:30660827] [10.1016/j.ejmech.2019.01.017] |
Source(1):