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ID: ALA3753644
Max Phase: Preclinical
Molecular Formula: C26H19N5O3
Molecular Weight: 449.47
Molecule Type: Small molecule
Associated Items:
ID: ALA3753644
Max Phase: Preclinical
Molecular Formula: C26H19N5O3
Molecular Weight: 449.47
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: O=C(Nc1ccc(Nc2c3ccccc3nc3ccccc23)cc1)Nc1ccc([N+](=O)[O-])cc1
Standard InChI: InChI=1S/C26H19N5O3/c32-26(29-19-13-15-20(16-14-19)31(33)34)28-18-11-9-17(10-12-18)27-25-21-5-1-3-7-23(21)30-24-8-4-2-6-22(24)25/h1-16H,(H,27,30)(H2,28,29,32)
Standard InChI Key: FRBICWAQKKWVMX-UHFFFAOYSA-N
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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: 449.47 | Molecular Weight (Monoisotopic): 449.1488 | AlogP: 6.68 | #Rotatable Bonds: 5 |
Polar Surface Area: 109.19 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 3 |
#RO5 Violations: 1 | HBA (Lipinski): 8 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: 11.06 | CX Basic pKa: 8.50 | CX LogP: 6.03 | CX LogD: 5.00 |
Aromatic Rings: 5 | Heavy Atoms: 34 | QED Weighted: 0.16 | Np Likeness Score: -1.06 |
1. Medapi B, Meda N, Kulkarni P, Yogeeswari P, Sriram D.. (2016) Development of acridine derivatives as selective Mycobacterium tuberculosis DNA gyrase inhibitors., 24 (4): [PMID:26787274] [10.1016/j.bmc.2016.01.011] |
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