Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4577334
Max Phase: Preclinical
Molecular Formula: C15H14F3N3O2S
Molecular Weight: 357.36
Molecule Type: Unknown
Associated Items:
ID: ALA4577334
Max Phase: Preclinical
Molecular Formula: C15H14F3N3O2S
Molecular Weight: 357.36
Molecule Type: Unknown
Associated Items:
Canonical SMILES: CCOC(=O)c1sc(N/N=C/c2ccccc2C(F)(F)F)nc1C
Standard InChI: InChI=1S/C15H14F3N3O2S/c1-3-23-13(22)12-9(2)20-14(24-12)21-19-8-10-6-4-5-7-11(10)15(16,17)18/h4-8H,3H2,1-2H3,(H,20,21)/b19-8+
Standard InChI Key: YUYNBUQKSOBZFT-UFWORHAWSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
Molecule Type: Unknown | 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: 357.36 | Molecular Weight (Monoisotopic): 357.0759 | AlogP: 4.09 | #Rotatable Bonds: 5 |
Polar Surface Area: 63.58 | Molecular Species: NEUTRAL | HBA: 6 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 10.25 | CX Basic pKa: 3.97 | CX LogP: 4.65 | CX LogD: 4.64 |
Aromatic Rings: 2 | Heavy Atoms: 24 | QED Weighted: 0.50 | Np Likeness Score: -2.18 |
1. Kovalenko OP, Volynets GP, Rybak MY, Starosyla SA, Gudzera OI, Lukashov SS, Bdzhola VG, Yarmoluk SM, Boshoff HI, Tukalo MA.. (2019) Dual-target inhibitors of mycobacterial aminoacyl-tRNA synthetases among N-benzylidene-N'-thiazol-2-yl-hydrazines., 10 (12): [PMID:32206244] [10.1039/C9MD00347A] |
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