Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA3706590
Max Phase: Preclinical
Molecular Formula: C30H26FN3O3
Molecular Weight: 495.55
Molecule Type: Small molecule
Associated Items:
ID: ALA3706590
Max Phase: Preclinical
Molecular Formula: C30H26FN3O3
Molecular Weight: 495.55
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CN(CCOc1ccc(NC(=O)c2cccc3c(=O)c4ccccc4[nH]c23)cc1)Cc1ccc(F)cc1
Standard InChI: InChI=1S/C30H26FN3O3/c1-34(19-20-9-11-21(31)12-10-20)17-18-37-23-15-13-22(14-16-23)32-30(36)26-7-4-6-25-28(26)33-27-8-3-2-5-24(27)29(25)35/h2-16H,17-19H2,1H3,(H,32,36)(H,33,35)
Standard InChI Key: FAXSWSFSYAJEAT-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: 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: 495.55 | Molecular Weight (Monoisotopic): 495.1958 | AlogP: 5.58 | #Rotatable Bonds: 8 |
Polar Surface Area: 74.43 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 2 |
#RO5 Violations: 1 | HBA (Lipinski): 6 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: | CX Basic pKa: 8.36 | CX LogP: 7.02 | CX LogD: 6.02 |
Aromatic Rings: 5 | Heavy Atoms: 37 | QED Weighted: 0.28 | Np Likeness Score: -1.25 |
1. Dodic N, Dumaitre B, Daugan A, Pianetti P.. (1995) Synthesis and activity against multidrug resistance in Chinese hamster ovary cells of new acridone-4-carboxamides., 38 (13): [PMID:7608906] [10.1021/jm00013a017] |
Source(1):