| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA5279164
Max Phase: Preclinical
Molecular Formula: C17H15Br2NO3
Molecular Weight: 441.12
Associated Items:
Representations
Canonical SMILES: COc1cc(Br)c(/C=C/C(=N/O)c2ccc(Br)cc2)cc1OC
Standard InChI: InChI=1S/C17H15Br2NO3/c1-22-16-9-12(14(19)10-17(16)23-2)5-8-15(20-21)11-3-6-13(18)7-4-11/h3-10,21H,1-2H3/b8-5+,20-15-
Standard InChI Key: SUKZUBWYMMGLIB-ZEUYVESBSA-N
Associated Targets(non-human)
LLC-PK1 2135 Activities
Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: | 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 |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Properties
| Molecular Weight: 441.12 | Molecular Weight (Monoisotopic): 438.9419 | AlogP: 5.12 | #Rotatable Bonds: 5 |
| Polar Surface Area: 51.05 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 1 |
| #RO5 Violations: 1 | HBA (Lipinski): 4 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: 6.72 | CX Basic pKa: 1.79 | CX LogP: 5.12 | CX LogD: 4.37 |
| Aromatic Rings: 2 | Heavy Atoms: 23 | QED Weighted: 0.40 | Np Likeness Score: -0.32 |
References
| 1. Lee D, Hyuk Lee S, Lee H, Choi YK, Sung Kang K, Wook Lee J.. (2023) Elucidation of protective effects of oxime derivatives against cisplatin-induced cytotoxicity in LLC-PK1 kidney cells., 80 [PMID:36574854] [10.1016/j.bmcl.2022.129114] |
Source
Source(1):