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ID: ALA5282708
Max Phase: Preclinical
Molecular Formula: C23H24F3N5
Molecular Weight: 427.47
Associated Items:
Representations
Canonical SMILES: Cc1ccc(-c2ccnc(Nc3ccc(N4CCN(C)CC4)c(C(F)(F)F)c3)n2)cc1
Standard InChI: InChI=1S/C23H24F3N5/c1-16-3-5-17(6-4-16)20-9-10-27-22(29-20)28-18-7-8-21(19(15-18)23(24,25)26)31-13-11-30(2)12-14-31/h3-10,15H,11-14H2,1-2H3,(H,27,28,29)
Standard InChI Key: JGQOMJGZCRMYPO-UHFFFAOYSA-N
Associated Targets(Human)
CDK2 Tchem Cyclin-dependent kinase 2/cyclin A (2220 Activities)
THP-1 (11052 Activities)
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Associated Targets(non-human)
pknB Serine/threonine-protein kinase pknB (356 Activities)
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Mycobacterium tuberculosis (203094 Activities)
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Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: | Topical: No | First In Class: No | Black Box: No |
| Chirality: No | Availability: No | Prodrug: No |
Drug Indications
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Properties
| Molecular Weight: 427.47 | Molecular Weight (Monoisotopic): 427.1984 | AlogP: 4.97 | #Rotatable Bonds: 4 |
| Polar Surface Area: 44.29 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 7.66 | CX LogP: 5.55 | CX LogD: 5.10 |
| Aromatic Rings: 3 | Heavy Atoms: 31 | QED Weighted: 0.64 | Np Likeness Score: -1.58 |
References
| 1. Wlodarchak N, Feltenberger JB, Ye Z, Beczkiewicz J, Procknow R, Yan G, King TM, Golden JE, Striker R.. (2021) Engineering Selectivity for Reduced Toxicity of Bacterial Kinase Inhibitors Using Structure-Guided Medicinal Chemistry., 12 (2.0): [PMID:35035774] [10.1021/acsmedchemlett.0c00580] |
Source
Source(1):