Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
ID: ALA3961462
Max Phase: Preclinical
Molecular Formula: C12H22N2O4
Molecular Weight: 258.32
Molecule Type: Small molecule
Associated Items:
ID: ALA3961462
Max Phase: Preclinical
Molecular Formula: C12H22N2O4
Molecular Weight: 258.32
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CN(C)C1=N[C@@H]2[C@@H](O)[C@H](O)[C@@H](C(C)(C)O)C[C@@H]2O1
Standard InChI: InChI=1S/C12H22N2O4/c1-12(2,17)6-5-7-8(10(16)9(6)15)13-11(18-7)14(3)4/h6-10,15-17H,5H2,1-4H3/t6-,7-,8-,9+,10+/m0/s1
Standard InChI Key: XJKJBDQRTHNGHG-RXKWGBCNSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
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 |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
---|
Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
---|
Molecular Weight: 258.32 | Molecular Weight (Monoisotopic): 258.1580 | AlogP: -0.82 | #Rotatable Bonds: 1 |
Polar Surface Area: 85.52 | Molecular Species: NEUTRAL | HBA: 6 | HBD: 3 |
#RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 13.14 | CX Basic pKa: 6.83 | CX LogP: -0.85 | CX LogD: -0.95 |
Aromatic Rings: 0 | Heavy Atoms: 18 | QED Weighted: 0.57 | Np Likeness Score: 0.98 |
1. (2015) Selective glycosidase inhibitors and uses thereof, |
Source(1):