| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA265683
Max Phase: Preclinical
Molecular Formula: C14H17NO4
Molecular Weight: 263.29
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CCOc1ccc(CC(=O)N[C@H]2CCOC2=O)cc1
Standard InChI: InChI=1S/C14H17NO4/c1-2-18-11-5-3-10(4-6-11)9-13(16)15-12-7-8-19-14(12)17/h3-6,12H,2,7-9H2,1H3,(H,15,16)/t12-/m0/s1
Standard InChI Key: UCACBDCCNSRYHV-LBPRGKRZSA-N
Associated Targets(non-human)
PhzR 76 Activities
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 |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Properties
| Molecular Weight: 263.29 | Molecular Weight (Monoisotopic): 263.1158 | AlogP: 1.06 | #Rotatable Bonds: 5 |
| Polar Surface Area: 64.63 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 12.15 | CX Basic pKa: | CX LogP: 0.95 | CX LogD: 0.95 |
| Aromatic Rings: 1 | Heavy Atoms: 19 | QED Weighted: 0.81 | Np Likeness Score: -0.76 |
References
| 1. Mattmann ME, Geske GD, Worzalla GA, Chandler JR, Sappington KJ, Greenberg EP, Blackwell HE.. (2008) Synthetic ligands that activate and inhibit a quorum-sensing regulator in Pseudomonas aeruginosa., 18 (10): [PMID:18083553] [10.1016/j.bmcl.2007.11.095] |
Source
Source(1):