| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA610712
Max Phase: Preclinical
Molecular Formula: C17H27N5O14P2
Molecular Weight: 587.37
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CC1OC(CP(=O)(O)OP(=O)(O)OC[C@H]2OC(n3cnc4c(O)nc(N)nc43)[C@H](O)[C@@H]2O)C(O)C(O)C1O
Standard InChI: InChI=1S/C17H27N5O14P2/c1-5-9(23)12(26)11(25)7(34-5)3-37(29,30)36-38(31,32)33-2-6-10(24)13(27)16(35-6)22-4-19-8-14(22)20-17(18)21-15(8)28/h4-7,9-13,16,23-27H,2-3H2,1H3,(H,29,30)(H,31,32)(H3,18,20,21,28)/t5?,6-,7?,9?,10-,11?,12?,13-,16?/m1/s1
Standard InChI Key: SSSKPLCIWDJGKO-KWFMURQUSA-N
Associated Targets(Human)
Fucosyltransferase 5 13 Activities
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 |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Properties
| Molecular Weight: 587.37 | Molecular Weight (Monoisotopic): 587.1030 | AlogP: -3.08 | #Rotatable Bonds: 8 |
| Polar Surface Area: 302.52 | Molecular Species: ACID | HBA: 17 | HBD: 9 |
| #RO5 Violations: 3 | HBA (Lipinski): 19 | HBD (Lipinski): 10 | #RO5 Violations (Lipinski): 3 |
| CX Acidic pKa: 1.93 | CX Basic pKa: 0.90 | CX LogP: -4.26 | CX LogD: -8.56 |
| Aromatic Rings: 2 | Heavy Atoms: 38 | QED Weighted: 0.14 | Np Likeness Score: 1.09 |
References
| 1. Norris AJ, Whitelegge JP, Strouse MJ, Faull KF, Toyokuni T.. (2004) Inhibition kinetics of carba- and C-fucosyl analogues of GDP-fucose against fucosyltransferase V: implication for the reaction mechanism., 14 (3): [PMID:14741245] [10.1016/j.bmcl.2003.12.003] |
Source
Source(1):