| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA2272242
Max Phase: Preclinical
Molecular Formula: C13H15NO3
Molecular Weight: 233.27
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CCCC(C)ON1C(=O)c2ccccc2C1=O
Standard InChI: InChI=1S/C13H15NO3/c1-3-6-9(2)17-14-12(15)10-7-4-5-8-11(10)13(14)16/h4-5,7-9H,3,6H2,1-2H3
Standard InChI Key: POHLWGOIFCAEMN-UHFFFAOYSA-N
Associated Targets(non-human)
Lepidium sativum 398 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: 233.27 | Molecular Weight (Monoisotopic): 233.1052 | AlogP: 2.40 | #Rotatable Bonds: 4 |
| Polar Surface Area: 46.61 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: | CX LogP: 2.81 | CX LogD: 2.81 |
| Aromatic Rings: 1 | Heavy Atoms: 17 | QED Weighted: 0.75 | Np Likeness Score: -0.05 |
References
| 1. Takekida Y, Okazaki M, Shuto Y.. (1999) Effect of Optically Active Ethyl 2-Phthalimidooxypropionate on the Growth of Cress, Lepidium sativum., 63 (10): [PMID:26300175] [10.1271/bbb.63.1831] |
Source
Source(1):