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ID: ALA3764819
Max Phase: Preclinical
Molecular Formula: C27H29N3O6
Molecular Weight: 491.54
Molecule Type: Small molecule
Associated Items:
ID: ALA3764819
Max Phase: Preclinical
Molecular Formula: C27H29N3O6
Molecular Weight: 491.54
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CCCCOC(=O)c1c2nc3ccc(N(C)C)cc3oc-2c(O)c(=O)c1NCc1ccc(OC)cc1
Standard InChI: InChI=1S/C27H29N3O6/c1-5-6-13-35-27(33)21-22(28-15-16-7-10-18(34-4)11-8-16)24(31)25(32)26-23(21)29-19-12-9-17(30(2)3)14-20(19)36-26/h7-12,14,28,32H,5-6,13,15H2,1-4H3
Standard InChI Key: NZTDWHFUCHYGAK-UHFFFAOYSA-N
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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: 491.54 | Molecular Weight (Monoisotopic): 491.2056 | AlogP: 4.64 | #Rotatable Bonds: 9 |
Polar Surface Area: 114.13 | Molecular Species: NEUTRAL | HBA: 9 | HBD: 2 |
#RO5 Violations: 0 | HBA (Lipinski): 9 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 8.35 | CX Basic pKa: 3.01 | CX LogP: 4.34 | CX LogD: 4.30 |
Aromatic Rings: 2 | Heavy Atoms: 36 | QED Weighted: 0.20 | Np Likeness Score: -0.52 |
1. Thysiadis S, Mpousis S, Avramidis N, Katsamakas S, Balomenos A, Remelli R, Efthimiopoulos S, Sarli V.. (2016) Discovery of novel phenoxazinone derivatives as DKK1/LRP6 interaction inhibitors: Synthesis, biological evaluation and structure-activity relationships., 24 (5): [PMID:26819000] [10.1016/j.bmc.2016.01.025] |
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