| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA1794797
Max Phase: Preclinical
Molecular Formula: C6H13NO3
Molecular Weight: 147.17
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: C[C@@H](O)[C@H]1NC[C@@H](O)[C@H]1O
Standard InChI: InChI=1S/C6H13NO3/c1-3(8)5-6(10)4(9)2-7-5/h3-10H,2H2,1H3/t3-,4-,5-,6-/m1/s1
Standard InChI Key: HVRWFMCLXNLOCH-KVTDHHQDSA-N
Associated Targets(non-human)
Alpha-mannosidase 2C1 19 Activities
Molecule Features
| Natural Product: Yes | 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: 147.17 | Molecular Weight (Monoisotopic): 147.0895 | AlogP: -1.94 | #Rotatable Bonds: 1 |
| Polar Surface Area: 72.72 | Molecular Species: BASE | HBA: 4 | HBD: 4 |
| #RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 4 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 13.31 | CX Basic pKa: 9.52 | CX LogP: -1.84 | CX LogD: -3.93 |
| Aromatic Rings: 0 | Heavy Atoms: 10 | QED Weighted: 0.35 | Np Likeness Score: 2.37 |
References
| 1. Winkler DA, Holan G.. (1989) Design of potential anti-HIV agents. 1. Mannosidase inhibitors., 32 (9): [PMID:2504921] [10.1021/jm00129a011] |
Source
Source(1):