Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA1740643
Max Phase: Preclinical
Molecular Formula: C16H22N2
Molecular Weight: 242.37
Molecule Type: Small molecule
Associated Items:
ID: ALA1740643
Max Phase: Preclinical
Molecular Formula: C16H22N2
Molecular Weight: 242.37
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: c1cc(CNC23CC4CC(CC(C4)C2)C3)ccn1
Standard InChI: InChI=1S/C16H22N2/c1-3-17-4-2-12(1)11-18-16-8-13-5-14(9-16)7-15(6-13)10-16/h1-4,13-15,18H,5-11H2
Standard InChI Key: APISUIZGJDXZDM-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: 242.37 | Molecular Weight (Monoisotopic): 242.1783 | AlogP: 3.14 | #Rotatable Bonds: 3 |
Polar Surface Area: 24.92 | Molecular Species: BASE | HBA: 2 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 2 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: 9.70 | CX LogP: 2.41 | CX LogD: 0.15 |
Aromatic Rings: 1 | Heavy Atoms: 18 | QED Weighted: 0.88 | Np Likeness Score: -0.74 |
1. Wang J, Ma C, Wang J, Jo H, Canturk B, Fiorin G, Pinto LH, Lamb RA, Klein ML, DeGrado WF.. (2013) Discovery of novel dual inhibitors of the wild-type and the most prevalent drug-resistant mutant, S31N, of the M2 proton channel from influenza A virus., 56 (7): [PMID:23437766] [10.1021/jm301538e] |
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