Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA3343335
Max Phase: Preclinical
Molecular Formula: C17H26N2O
Molecular Weight: 274.41
Molecule Type: Small molecule
Associated Items:
ID: ALA3343335
Max Phase: Preclinical
Molecular Formula: C17H26N2O
Molecular Weight: 274.41
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CCCCCCCCn1nc2ccccc2c1OCC
Standard InChI: InChI=1S/C17H26N2O/c1-3-5-6-7-8-11-14-19-17(20-4-2)15-12-9-10-13-16(15)18-19/h9-10,12-13H,3-8,11,14H2,1-2H3
Standard InChI Key: JESAMYZHBQQFKU-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: 274.41 | Molecular Weight (Monoisotopic): 274.2045 | AlogP: 4.80 | #Rotatable Bonds: 9 |
Polar Surface Area: 27.05 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 0 |
#RO5 Violations: 0 | HBA (Lipinski): 3 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: 1.51 | CX LogP: 5.17 | CX LogD: 5.17 |
Aromatic Rings: 2 | Heavy Atoms: 20 | QED Weighted: 0.61 | Np Likeness Score: -0.83 |
1. Roth A, Ott S, Farber KM, Palazzo TA, Conrad WE, Haddadin MJ, Tantillo DJ, Cross CE, Eiserich JP, Kurth MJ.. (2014) Inhibition of myeloperoxidase: evaluation of 2H-indazoles and 1H-indazolones., 22 (22): [PMID:25438766] [10.1016/j.bmc.2014.09.044] |
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