Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4871724
Max Phase: Preclinical
Molecular Formula: C25H35BrN2O2
Molecular Weight: 395.57
Molecule Type: Unknown
Associated Items:
ID: ALA4871724
Max Phase: Preclinical
Molecular Formula: C25H35BrN2O2
Molecular Weight: 395.57
Molecule Type: Unknown
Associated Items:
Canonical SMILES: CCCCCCCCn1c2c([n+](CCCCC)c1C)C(=O)c1ccccc1C2=O.[Br-]
Standard InChI: InChI=1S/C25H35N2O2.BrH/c1-4-6-8-9-10-14-18-27-19(3)26(17-13-7-5-2)22-23(27)25(29)21-16-12-11-15-20(21)24(22)28;/h11-12,15-16H,4-10,13-14,17-18H2,1-3H3;1H/q+1;/p-1
Standard InChI Key: VRESXBJACKRYCE-UHFFFAOYSA-M
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: Unknown | 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: 395.57 | Molecular Weight (Monoisotopic): 395.2693 | AlogP: 5.41 | #Rotatable Bonds: 11 |
Polar Surface Area: 42.95 | Molecular Species: | HBA: 3 | HBD: 0 |
#RO5 Violations: 1 | HBA (Lipinski): 4 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: | CX Basic pKa: | CX LogP: 1.83 | CX LogD: 1.83 |
Aromatic Rings: 2 | Heavy Atoms: 29 | QED Weighted: 0.32 | Np Likeness Score: -0.03 |
1. Fridianto KT, Li M, Hards K, Negatu DA, Cook GM, Dick T, Lam Y, Go ML.. (2021) Functionalized Dioxonaphthoimidazoliums: A Redox Cycling Chemotype with Potent Bactericidal Activities against Mycobacterium tuberculosis., 64 (21.0): [PMID:34706190] [10.1021/acs.jmedchem.1c01383] |
Source(1):