Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4213250
Max Phase: Preclinical
Molecular Formula: C12H6FN3O2
Molecular Weight: 243.20
Molecule Type: Small molecule
Associated Items:
ID: ALA4213250
Max Phase: Preclinical
Molecular Formula: C12H6FN3O2
Molecular Weight: 243.20
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: O=c1oc(-c2ccccc2F)nc2nccnc12
Standard InChI: InChI=1S/C12H6FN3O2/c13-8-4-2-1-3-7(8)11-16-10-9(12(17)18-11)14-5-6-15-10/h1-6H
Standard InChI Key: UDSVMNOFWJGGFJ-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: 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: 243.20 | Molecular Weight (Monoisotopic): 243.0444 | AlogP: 1.78 | #Rotatable Bonds: 1 |
Polar Surface Area: 68.88 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 0 |
#RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: | CX LogP: 2.04 | CX LogD: 2.04 |
Aromatic Rings: 3 | Heavy Atoms: 18 | QED Weighted: 0.65 | Np Likeness Score: -1.29 |
1. Xie Z, Tian Y, Lv X, Xiao X, Zhan M, Cheng K, Li S, Liao C.. (2018) The selectivity and bioavailability improvement of novel oral anticoagulants: An overview., 146 [PMID:29407959] [10.1016/j.ejmech.2018.01.067] |
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