| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA2304276
Max Phase: Preclinical
Molecular Formula: C16H23N5Na2O14P2
Molecular Weight: 573.35
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: C[C@@H]1O[C@H](OP(=O)([O-])OP(=O)([O-])OC[C@H]2O[C@@H](n3cnc4c(N)ncnc43)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@H]1O.[Na+].[Na+]
Standard InChI: InChI=1S/C16H25N5O14P2.2Na/c1-5-8(22)10(24)12(26)16(32-5)34-37(29,30)35-36(27,28)31-2-6-9(23)11(25)15(33-6)21-4-20-7-13(17)18-3-19-14(7)21;;/h3-6,8-12,15-16,22-26H,2H2,1H3,(H,27,28)(H,29,30)(H2,17,18,19);;/q;2*+1/p-2/t5-,6+,8-,9+,10-,11+,12-,15+,16+;;/m0../s1
Standard InChI Key: MAIWPEAVJNGCPB-CBXQLZMWSA-L
Associated Targets(Human)
Galactoside 3(4)-L-fucosyltransferase 5 Activities
Fucosyltransferase 6 19 Activities
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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 |
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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: 573.35 | Molecular Weight (Monoisotopic): 573.0873 | AlogP: -2.89 | #Rotatable Bonds: 8 |
| Polar Surface Area: 291.52 | Molecular Species: ACID | HBA: 17 | HBD: 8 |
| #RO5 Violations: 3 | HBA (Lipinski): 19 | HBD (Lipinski): 9 | #RO5 Violations (Lipinski): 3 |
| CX Acidic pKa: 1.73 | CX Basic pKa: 4.92 | CX LogP: -5.85 | CX LogD: -8.37 |
| Aromatic Rings: 2 | Heavy Atoms: 37 | QED Weighted: 0.15 | Np Likeness Score: 1.49 |
References
| 1. Baisch G, Ohrlein R, Katopodis A. (1996) Enzymatic fucosylations with purine-diphosphate-fucoses (PDP-Fucoses), 6 (24): [10.1016/S0960-894X(96)00543-4] |
Source
Source(1):