| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA1160243
Max Phase: Preclinical
Molecular Formula: C14H23N6O8P
Molecular Weight: 434.35
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CC(O)[C@H](N)COP(=O)(O)OC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1O
Standard InChI: InChI=1S/C14H23N6O8P/c1-6(21)7(15)2-26-29(24,25)27-3-8-10(22)11(23)14(28-8)20-5-19-9-12(16)17-4-18-13(9)20/h4-8,10-11,14,21-23H,2-3,15H2,1H3,(H,24,25)(H2,16,17,18)/t6?,7-,8-,10-,11-,14-/m1/s1
Standard InChI Key: VPHDLKUTUSQRCE-PQVKCCMRSA-N
Associated Targets(Human)
Threonyl-tRNA synthetase 88 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: 434.35 | Molecular Weight (Monoisotopic): 434.1315 | AlogP: -2.13 | #Rotatable Bonds: 8 |
| Polar Surface Area: 221.32 | Molecular Species: ZWITTERION | HBA: 13 | HBD: 6 |
| #RO5 Violations: 2 | HBA (Lipinski): 14 | HBD (Lipinski): 8 | #RO5 Violations (Lipinski): 2 |
| CX Acidic pKa: 1.85 | CX Basic pKa: 9.74 | CX LogP: -3.86 | CX LogD: -3.86 |
| Aromatic Rings: 2 | Heavy Atoms: 29 | QED Weighted: 0.24 | Np Likeness Score: 1.32 |
References
| 1. Forrest AK, Jarvest RL, Mensah LM, O'Hanlon PJ, Pope AJ, Sheppard RJ.. (2000) Aminoalkyl adenylate and aminoacyl sulfamate intermediate analogues differing greatly in affinity for their cognate Staphylococcus aureus aminoacyl tRNA synthetases., 10 (16): [PMID:10969988] [10.1016/s0960-894x(00)00360-7] |
Source
Source(1):