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ID: ALA2401943
Max Phase: Preclinical
Molecular Formula: C15H19N5OS
Molecular Weight: 317.42
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: C/C(=N\NC1=NC(=N)CS1)c1ccc(N2CCOCC2)cc1
Standard InChI: InChI=1S/C15H19N5OS/c1-11(18-19-15-17-14(16)10-22-15)12-2-4-13(5-3-12)20-6-8-21-9-7-20/h2-5H,6-10H2,1H3,(H2,16,17,19)/b18-11+
Standard InChI Key: CUUYVLGRXQIXPP-WOJGMQOQSA-N
Associated Targets(non-human)
Serratia marcescens 3237 Activities
Proteus mirabilis 3894 Activities
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Bacillus cereus 7522 Activities
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Staphylococcus aureus 210822 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: 317.42 | Molecular Weight (Monoisotopic): 317.1310 | AlogP: 1.92 | #Rotatable Bonds: 3 |
| Polar Surface Area: 73.07 | Molecular Species: NEUTRAL | HBA: 6 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 10.49 | CX Basic pKa: 4.07 | CX LogP: 1.36 | CX LogD: 1.36 |
| Aromatic Rings: 1 | Heavy Atoms: 22 | QED Weighted: 0.66 | Np Likeness Score: -1.57 |
References
| 1. Helal MH, Salem MA, El-Gaby MS, Aljahdali M.. (2013) Synthesis and biological evaluation of some novel thiazole compounds as potential anti-inflammatory agents., 65 [PMID:23787438] [10.1016/j.ejmech.2013.04.005] |
Source
Source(1):