Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4570434
Max Phase: Preclinical
Molecular Formula: C13H12N4O4S
Molecular Weight: 320.33
Molecule Type: Unknown
Associated Items:
ID: ALA4570434
Max Phase: Preclinical
Molecular Formula: C13H12N4O4S
Molecular Weight: 320.33
Molecule Type: Unknown
Associated Items:
Canonical SMILES: COC(=O)c1sc(N/N=C/c2ccc([N+](=O)[O-])cc2)nc1C
Standard InChI: InChI=1S/C13H12N4O4S/c1-8-11(12(18)21-2)22-13(15-8)16-14-7-9-3-5-10(6-4-9)17(19)20/h3-7H,1-2H3,(H,15,16)/b14-7+
Standard InChI Key: ILBAZZIATFVTLA-VGOFMYFVSA-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: 320.33 | Molecular Weight (Monoisotopic): 320.0579 | AlogP: 2.59 | #Rotatable Bonds: 5 |
Polar Surface Area: 106.72 | Molecular Species: NEUTRAL | HBA: 8 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 8 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 10.34 | CX Basic pKa: 4.13 | CX LogP: 3.35 | CX LogD: 3.35 |
Aromatic Rings: 2 | Heavy Atoms: 22 | QED Weighted: 0.39 | Np Likeness Score: -2.27 |
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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