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ID: ALA4793883
Max Phase: Preclinical
Molecular Formula: C37H20F3N7O6
Molecular Weight: 715.60
Molecule Type: Unknown
Associated Items:
ID: ALA4793883
Max Phase: Preclinical
Molecular Formula: C37H20F3N7O6
Molecular Weight: 715.60
Molecule Type: Unknown
Associated Items:
Canonical SMILES: O=[N+]([O-])c1cc(F)cc(-c2c3ccc([nH]3)c(-c3cc(F)ccc3[N+](=O)[O-])c3nc(c4ccc([nH]4)c(-c4cc(F)ccc4[N+](=O)[O-])c4ccc2[nH]4)C=C3)c1
Standard InChI: InChI=1S/C37H20F3N7O6/c38-19-1-11-33(46(50)51)23(16-19)36-29-5-3-25(41-29)26-4-6-30(42-26)37(24-17-20(39)2-12-34(24)47(52)53)32-10-8-28(44-32)35(27-7-9-31(36)43-27)18-13-21(40)15-22(14-18)45(48)49/h1-17,41,43-44H/b26-25-,35-27-,35-28-,36-29-,36-31-,37-30-,37-32-
Standard InChI Key: NRYKVBTZEBWLMR-GOTVHWMUSA-N
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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: 715.60 | Molecular Weight (Monoisotopic): 715.1427 | AlogP: 9.84 | #Rotatable Bonds: 6 |
Polar Surface Area: 189.68 | Molecular Species: NEUTRAL | HBA: 7 | HBD: 3 |
#RO5 Violations: 2 | HBA (Lipinski): 13 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 3 |
CX Acidic pKa: 13.25 | CX Basic pKa: 4.17 | CX LogP: 9.41 | CX LogD: 9.41 |
Aromatic Rings: 7 | Heavy Atoms: 53 | QED Weighted: 0.11 | Np Likeness Score: -0.46 |
1. Bucher, Leo, Kappler-Gratias, Sandrine, Desbois, Nicolas, Bystricky, Kerstin, Gallardo, Franck, Gros, Claude P.. (2020) A3- and A2B-nitrocorroles: synthesis and antiviral activity evaluation against human cytomegalovirus infection, 11 (7): [PMID:33479674] [10.1039/d0md00034e] |
Source(1):