| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA3356386
Max Phase: Preclinical
Molecular Formula: C37H42ClN5
Molecular Weight: 555.77
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Cl.c1ccc(Nc2cc3nc4ccccc4n(-c4ccccc4)c-3c/c2=N/CCCCC23CCCCN2CCCC3)cc1
Standard InChI: InChI=1S/C37H41N5.ClH/c1-3-15-29(16-4-1)39-33-27-34-36(42(30-17-5-2-6-18-30)35-20-8-7-19-31(35)40-34)28-32(33)38-24-12-9-21-37-22-10-13-25-41(37)26-14-11-23-37;/h1-8,15-20,27-28,39H,9-14,21-26H2;1H/b38-32-;
Standard InChI Key: RWGQTOCUOHAFOJ-OSTYKXRUSA-N
Associated Targets(non-human)
Leishmania infantum 5912 Activities
Leishmania tropica 461 Activities
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Leishmania braziliensis 1091 Activities
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Plasmodium falciparum 966862 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: 555.77 | Molecular Weight (Monoisotopic): 555.3362 | AlogP: 8.35 | #Rotatable Bonds: 8 |
| Polar Surface Area: 45.45 | Molecular Species: BASE | HBA: 5 | HBD: 1 |
| #RO5 Violations: 2 | HBA (Lipinski): 5 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 2 |
| CX Acidic pKa: | CX Basic pKa: 9.28 | CX LogP: 8.05 | CX LogD: 5.66 |
| Aromatic Rings: 3 | Heavy Atoms: 42 | QED Weighted: 0.15 | Np Likeness Score: -0.57 |
References
| 1. Barteselli A, Casagrande M, Basilico N, Parapini S, Rusconi CM, Tonelli M, Boido V, Taramelli D, Sparatore F, Sparatore A.. (2015) Clofazimine analogs with antileishmanial and antiplasmodial activity., 23 (1): [PMID:25497962] [10.1016/j.bmc.2014.11.028] |
Source
Source(1):