| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4764169
Max Phase: Preclinical
Molecular Formula: C15H24KNO8
Molecular Weight: 347.36
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: CCCCO[C@@]1(C(=O)[O-])C=C[C@@H](NC(C)=O)[C@H]([C@H](O)[C@H](O)CO)O1.[K+]
Standard InChI: InChI=1S/C15H25NO8.K/c1-3-4-7-23-15(14(21)22)6-5-10(16-9(2)18)13(24-15)12(20)11(19)8-17;/h5-6,10-13,17,19-20H,3-4,7-8H2,1-2H3,(H,16,18)(H,21,22);/q;+1/p-1/t10-,11-,12-,13-,15+;/m1./s1
Standard InChI Key: VHROESOJXNDUPU-ZANLMATLSA-M
Associated Targets(Human)
Sialidase 3 398 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: 347.36 | Molecular Weight (Monoisotopic): 347.1580 | AlogP: -1.24 | #Rotatable Bonds: 9 |
| Polar Surface Area: 145.55 | Molecular Species: ACID | HBA: 7 | HBD: 5 |
| #RO5 Violations: 0 | HBA (Lipinski): 9 | HBD (Lipinski): 5 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 3.23 | CX Basic pKa: | CX LogP: -0.71 | CX LogD: -4.15 |
| Aromatic Rings: 0 | Heavy Atoms: 24 | QED Weighted: 0.26 | Np Likeness Score: 1.23 |
References
| 1. La Rocca P,Rota P,Piccoli M,Cirillo F,Ghiroldi A,Franco V,Allevi P,Anastasia L. (2020) 2β-3,4-Unsaturated sialic acid derivatives: Synthesis optimization, and biological evaluation as Newcastle disease virus hemagglutinin-neuraminidase inhibitors., 28 (14): [PMID:32616179] [10.1016/j.bmc.2020.115563] |
Source
Source(1):