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ID: ALA2401949
Max Phase: Preclinical
Molecular Formula: C21H21N3OS
Molecular Weight: 363.49
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Cc1ccc(/C=N/c2nc(-c3ccc(N4CCOCC4)cc3)cs2)cc1
Standard InChI: InChI=1S/C21H21N3OS/c1-16-2-4-17(5-3-16)14-22-21-23-20(15-26-21)18-6-8-19(9-7-18)24-10-12-25-13-11-24/h2-9,14-15H,10-13H2,1H3/b22-14+
Standard InChI Key: OKLSHMQIVOJKRE-HYARGMPZSA-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: 363.49 | Molecular Weight (Monoisotopic): 363.1405 | AlogP: 4.71 | #Rotatable Bonds: 4 |
| Polar Surface Area: 37.72 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 0.56 | CX LogP: 5.63 | CX LogD: 5.63 |
| Aromatic Rings: 3 | Heavy Atoms: 26 | QED Weighted: 0.63 | Np Likeness Score: -1.91 |
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):