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ID: ALA5205246
Max Phase: Preclinical
Molecular Formula: C14H19NO5
Molecular Weight: 281.31
Associated Items:
Representations
Canonical SMILES: Cc1ccc(C(=O)N[C@H]2O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]2O)cc1
Standard InChI: InChI=1S/C14H19NO5/c1-7-3-5-9(6-4-7)13(19)15-14-12(18)11(17)10(16)8(2)20-14/h3-6,8,10-12,14,16-18H,1-2H3,(H,15,19)/t8-,10+,11+,12-,14-/m0/s1
Standard InChI Key: SSQUOLDSQCHBDN-OOQSSMQOSA-N
Associated Targets(Human)
HepG2 196354 Activities
A549 127892 Activities
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Associated Targets(non-human)
Fucose-binding lectin PA-IIL 188 Activities
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CHO 4503 Activities
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Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: | 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 |
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Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Properties
| Molecular Weight: 281.31 | Molecular Weight (Monoisotopic): 281.1263 | AlogP: -0.45 | #Rotatable Bonds: 2 |
| Polar Surface Area: 99.02 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 4 |
| #RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 4 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 12.47 | CX Basic pKa: | CX LogP: 0.19 | CX LogD: 0.19 |
| Aromatic Rings: 1 | Heavy Atoms: 20 | QED Weighted: 0.59 | Np Likeness Score: 0.43 |
References
| 1. Mała P, Siebs E, Meiers J, Rox K, Varrot A, Imberty A, Titz A.. (2022) Discovery of N-β-l-Fucosyl Amides as High-Affinity Ligands for the Pseudomonas aeruginosa Lectin LecB., 65 (20.0): [PMID:36256875] [10.1021/acs.jmedchem.2c01373] |
Source
Source(1):