Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4861741
Max Phase: Preclinical
Molecular Formula: C14H17N3O3
Molecular Weight: 275.31
Molecule Type: Unknown
Associated Items:
ID: ALA4861741
Max Phase: Preclinical
Molecular Formula: C14H17N3O3
Molecular Weight: 275.31
Molecule Type: Unknown
Associated Items:
Canonical SMILES: Cc1cccc(COCCn2c([N+](=O)[O-])cnc2C)c1
Standard InChI: InChI=1S/C14H17N3O3/c1-11-4-3-5-13(8-11)10-20-7-6-16-12(2)15-9-14(16)17(18)19/h3-5,8-9H,6-7,10H2,1-2H3
Standard InChI Key: RVMGWRGTKNFFEY-UHFFFAOYSA-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: 275.31 | Molecular Weight (Monoisotopic): 275.1270 | AlogP: 2.62 | #Rotatable Bonds: 6 |
Polar Surface Area: 70.19 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 0 |
#RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: 3.03 | CX LogP: 2.42 | CX LogD: 2.42 |
Aromatic Rings: 2 | Heavy Atoms: 20 | QED Weighted: 0.46 | Np Likeness Score: -1.88 |
1. Patel OPS, Jesumoroti OJ, Legoabe LJ, Beteck RM.. (2021) Metronidazole-conjugates: A comprehensive review of recent developments towards synthesis and medicinal perspective., 210 [PMID:33234343] [10.1016/j.ejmech.2020.112994] |
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