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ID: ALA3415253
Max Phase: Preclinical
Molecular Formula: C15H16ClN3S2
Molecular Weight: 337.90
Molecule Type: Small molecule
Associated Items:
ID: ALA3415253
Max Phase: Preclinical
Molecular Formula: C15H16ClN3S2
Molecular Weight: 337.90
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: Clc1ccc2sc(SCCCCCn3ccnc3)nc2c1
Standard InChI: InChI=1S/C15H16ClN3S2/c16-12-4-5-14-13(10-12)18-15(21-14)20-9-3-1-2-7-19-8-6-17-11-19/h4-6,8,10-11H,1-3,7,9H2
Standard InChI Key: ISHOSZWXUJZMLH-UHFFFAOYSA-N
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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 |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 337.90 | Molecular Weight (Monoisotopic): 337.0474 | AlogP: 5.11 | #Rotatable Bonds: 7 |
Polar Surface Area: 30.71 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 0 |
#RO5 Violations: 1 | HBA (Lipinski): 3 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: | CX Basic pKa: 6.54 | CX LogP: 4.86 | CX LogD: 4.81 |
Aromatic Rings: 3 | Heavy Atoms: 21 | QED Weighted: 0.44 | Np Likeness Score: -2.50 |
1. Salerno L, Pittalà V, Romeo G, Modica MN, Marrazzo A, Siracusa MA, Sorrenti V, Di Giacomo C, Vanella L, Parayath NN, Greish K.. (2015) Novel imidazole derivatives as heme oxygenase-1 (HO-1) and heme oxygenase-2 (HO-2) inhibitors and their cytotoxic activity in human-derived cancer cell lines., 96 [PMID:25874340] [10.1016/j.ejmech.2015.04.003] |
2. Salerno L, Amata E, Romeo G, Marrazzo A, Prezzavento O, Floresta G, Sorrenti V, Barbagallo I, Rescifina A, Pittalà V.. (2018) Potholing of the hydrophobic heme oxygenase-1 western region for the search of potent and selective imidazole-based inhibitors., 148 [PMID:29454190] [10.1016/j.ejmech.2018.02.007] |
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