| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA165499
Max Phase: Preclinical
Molecular Formula: C13H17NO3S
Molecular Weight: 267.35
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: C[C@H](C(=O)O)C(=O)N[C@H](CS)Cc1ccccc1
Standard InChI: InChI=1S/C13H17NO3S/c1-9(13(16)17)12(15)14-11(8-18)7-10-5-3-2-4-6-10/h2-6,9,11,18H,7-8H2,1H3,(H,14,15)(H,16,17)/t9-,11-/m0/s1
Standard InChI Key: KNPYRNCCTABBPX-ONGXEEELSA-N
Associated Targets(non-human)
Neprilysin 537 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: 267.35 | Molecular Weight (Monoisotopic): 267.0929 | AlogP: 1.36 | #Rotatable Bonds: 6 |
| Polar Surface Area: 66.40 | Molecular Species: ACID | HBA: 3 | HBD: 3 |
| #RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 4.13 | CX Basic pKa: | CX LogP: 2.11 | CX LogD: -0.97 |
| Aromatic Rings: 1 | Heavy Atoms: 18 | QED Weighted: 0.54 | Np Likeness Score: 0.09 |
References
| 1. Fournié-Zaluski MC, Lucas-Soroca E, Devin J, Roques BP.. (1986) 1H NMR configurational correlation for retro-inverso dipeptides: application to the determination of the absolute configuration of "enkephalinase" inhibitors. Relationships between stereochemistry and enzyme recognition., 29 (5): [PMID:3517331] [10.1021/jm00155a027] |
Source
Source(1):