Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA2058732
Max Phase: Preclinical
Molecular Formula: C17H27NO3
Molecular Weight: 293.41
Molecule Type: Small molecule
Associated Items:
ID: ALA2058732
Max Phase: Preclinical
Molecular Formula: C17H27NO3
Molecular Weight: 293.41
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CC(=O)OCCCCCCCCCCOc1ccccn1
Standard InChI: InChI=1S/C17H27NO3/c1-16(19)20-14-10-6-4-2-3-5-7-11-15-21-17-12-8-9-13-18-17/h8-9,12-13H,2-7,10-11,14-15H2,1H3
Standard InChI Key: HIJGWQMBHZQCIR-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: 293.41 | Molecular Weight (Monoisotopic): 293.1991 | AlogP: 4.14 | #Rotatable Bonds: 12 |
Polar Surface Area: 48.42 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 0 |
#RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: 2.92 | CX LogP: 4.19 | CX LogD: 4.19 |
Aromatic Rings: 1 | Heavy Atoms: 21 | QED Weighted: 0.43 | Np Likeness Score: -0.53 |
1. García Liñares G, Parraud G, Labriola C, Baldessari A.. (2012) Chemoenzymatic synthesis and biological evaluation of 2- and 3-hydroxypyridine derivatives against Leishmania mexicana., 20 (15): [PMID:22781310] [10.1016/j.bmc.2012.06.028] |
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