| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4783596
Max Phase: Preclinical
Molecular Formula: C17H13NO6
Molecular Weight: 327.29
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: O=C(O)Cn1c(=O)oc2c(/C=C/c3ccc(O)c(O)c3)cccc21
Standard InChI: InChI=1S/C17H13NO6/c19-13-7-5-10(8-14(13)20)4-6-11-2-1-3-12-16(11)24-17(23)18(12)9-15(21)22/h1-8,19-20H,9H2,(H,21,22)/b6-4+
Standard InChI Key: HIRNDDYBLQTIQW-GQCTYLIASA-N
Associated Targets(non-human)
Aldose reductase 4007 Activities
Molecule Features
| 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 |
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: 327.29 | Molecular Weight (Monoisotopic): 327.0743 | AlogP: 2.26 | #Rotatable Bonds: 4 |
| Polar Surface Area: 112.90 | Molecular Species: ACID | HBA: 6 | HBD: 3 |
| #RO5 Violations: 0 | HBA (Lipinski): 7 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 3.36 | CX Basic pKa: | CX LogP: 2.41 | CX LogD: -1.02 |
| Aromatic Rings: 3 | Heavy Atoms: 24 | QED Weighted: 0.50 | Np Likeness Score: 0.00 |
References
| 1. Zhang X,Chen H,Lei Y,Zhang X,Xu L,Liu W,Fan Z,Ma Z,Yin Z,Li L,Zhu C,Ma B. (2021) Multifunctional agents based on benzoxazolone as promising therapeutic drugs for diabetic nephropathy., 215 [PMID:33588177] [10.1016/j.ejmech.2021.113269] |
Source
Source(1):