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ID: ALA2442676
Max Phase: Preclinical
Molecular Formula: C11H9BrN2O3
Molecular Weight: 297.11
Molecule Type: Small molecule
Associated Items:
ID: ALA2442676
Max Phase: Preclinical
Molecular Formula: C11H9BrN2O3
Molecular Weight: 297.11
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: O=C(O)CCc1nc(-c2ccc(Br)cc2)no1
Standard InChI: InChI=1S/C11H9BrN2O3/c12-8-3-1-7(2-4-8)11-13-9(17-14-11)5-6-10(15)16/h1-4H,5-6H2,(H,15,16)
Standard InChI Key: LBFLFJKKZLTGOV-UHFFFAOYSA-N
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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: 297.11 | Molecular Weight (Monoisotopic): 295.9797 | AlogP: 2.52 | #Rotatable Bonds: 4 |
Polar Surface Area: 76.22 | Molecular Species: ACID | HBA: 4 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 4.25 | CX Basic pKa: | CX LogP: 2.93 | CX LogD: -0.09 |
Aromatic Rings: 2 | Heavy Atoms: 17 | QED Weighted: 0.94 | Np Likeness Score: -1.73 |
1. Neves Filho RA, da Silva CA, da Silva CS, Brustein VP, do Amaral Ferraz Navarro DM, dos Santos FA, Alves LC, dos Santos Cavalcanti MG, Srivastava RM, das Graças Carneiro-Da-Cunha M.. (2009) Improved microwave-mediated synthesis of 3-(3-aryl-1,2,4-oxadiazol-5-yl)propionic acids and their larvicidal and fungal growth inhibitory properties., 57 (8): [PMID:19652406] [10.1248/cpb.57.819] |
2. Oliveira VS, Pimenteira C, da Silva-Alves DC, Leal LL, Neves-Filho RA, Navarro DM, Santos GK, Dutra KA, dos Anjos JV, Soares TA.. (2013) The enzyme 3-hydroxykynurenine transaminase as potential target for 1,2,4-oxadiazoles with larvicide activity against the dengue vector Aedes aegypti., 21 (22): [PMID:24095017] [10.1016/j.bmc.2013.09.020] |
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