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ID: ALA496354
Max Phase: Preclinical
Molecular Formula: C22H23FN6
Molecular Weight: 390.47
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CCC(c1ccn2c(-c3ccnc(N)n3)c(-c3ccc(F)cc3)nc2c1)N(C)C
Standard InChI: InChI=1S/C22H23FN6/c1-4-18(28(2)3)15-10-12-29-19(13-15)27-20(14-5-7-16(23)8-6-14)21(29)17-9-11-25-22(24)26-17/h5-13,18H,4H2,1-3H3,(H2,24,25,26)
Standard InChI Key: PKWNHRGUHZKXHZ-UHFFFAOYSA-N
Associated Targets(non-human)
Eimeria acervulina 464 Activities
Eimeria maxima 199 Activities
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Eimeria tenella 990 Activities
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Eimeria mitis 216 Activities
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cGMP-dependent protein kinase 275 Activities
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Molecule Features
| 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 |
Drug Indications
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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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: 390.47 | Molecular Weight (Monoisotopic): 390.1968 | AlogP: 4.19 | #Rotatable Bonds: 5 |
| Polar Surface Area: 72.34 | Molecular Species: BASE | HBA: 6 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 8.95 | CX LogP: 3.70 | CX LogD: 2.14 |
| Aromatic Rings: 4 | Heavy Atoms: 29 | QED Weighted: 0.55 | Np Likeness Score: -1.24 |
References
| 1. Scribner A, Dennis R, Lee S, Ouvry G, Perrey D, Fisher M, Wyvratt M, Leavitt P, Liberator P, Gurnett A, Brown C, Mathew J, Thompson D, Schmatz D, Biftu T.. (2008) Synthesis and biological activity of imidazopyridine anticoccidial agents: Part II., 43 (6): [PMID:17981367] [10.1016/j.ejmech.2007.09.013] |
Source
Source(1):