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ID: ALA2253338
Max Phase: Preclinical
Molecular Formula: C15H13ClFN5O2
Molecular Weight: 349.75
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: C=CCOc1cc(-n2nnc3c(c(C)nn3C)c2=O)c(F)cc1Cl
Standard InChI: InChI=1S/C15H13ClFN5O2/c1-4-5-24-12-7-11(10(17)6-9(12)16)22-15(23)13-8(2)19-21(3)14(13)18-20-22/h4,6-7H,1,5H2,2-3H3
Standard InChI Key: WDHXQQYVMZJJTB-UHFFFAOYSA-N
Associated Targets(non-human)
Digitaria sanguinalis 1594 Activities
Echinochloa crus-galli 3685 Activities
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Amaranthus retroflexus 1838 Activities
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Brassica rapa subsp. oleifera 1696 Activities
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Protoporphyrinogen IX oxidase 35 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: 349.75 | Molecular Weight (Monoisotopic): 349.0742 | AlogP: 2.18 | #Rotatable Bonds: 4 |
| Polar Surface Area: 74.83 | Molecular Species: NEUTRAL | HBA: 7 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 7 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: | CX LogP: 3.64 | CX LogD: 3.64 |
| Aromatic Rings: 3 | Heavy Atoms: 24 | QED Weighted: 0.67 | Np Likeness Score: -2.00 |
References
| 1. Li HB, Zhu YQ, Song XW, Hu FZ, Liu B, Li YH, Niu ZX, Liu P, Wang ZH, Song HB, Zou XM, Yang HZ.. (2008) Novel protoporphyrinogen oxidase inhibitors: 3H-pyrazolo[3,4-d][1,2,3]triazin-4-one derivatives., 56 (20): [PMID:18808144] [10.1021/jf801774k] |
Source
Source(1):