| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA2414644
Max Phase: Preclinical
Molecular Formula: C8H11N4O4P
Molecular Weight: 258.17
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: O=c1[nH]cnc2c(CNCP(=O)(O)O)c[nH]c12
Standard InChI: InChI=1S/C8H11N4O4P/c13-8-7-6(11-3-12-8)5(2-10-7)1-9-4-17(14,15)16/h2-3,9-10H,1,4H2,(H,11,12,13)(H2,14,15,16)
Standard InChI Key: RRXLVNVSBULWTH-UHFFFAOYSA-N
Associated Targets(Human)
Hypoxanthine-guanine phosphoribosyltransferase 369 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: 258.17 | Molecular Weight (Monoisotopic): 258.0518 | AlogP: -0.52 | #Rotatable Bonds: 4 |
| Polar Surface Area: 131.10 | Molecular Species: ACID | HBA: 4 | HBD: 5 |
| #RO5 Violations: 0 | HBA (Lipinski): 8 | HBD (Lipinski): 5 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: -0.59 | CX Basic pKa: 6.16 | CX LogP: -3.40 | CX LogD: -4.35 |
| Aromatic Rings: 2 | Heavy Atoms: 17 | QED Weighted: 0.47 | Np Likeness Score: -0.16 |
References
| 1. Clinch K, Crump DR, Evans GB, Hazleton KZ, Mason JM, Schramm VL, Tyler PC.. (2013) Acyclic phosph(on)ate inhibitors of Plasmodium falciparum hypoxanthine-guanine-xanthine phosphoribosyltransferase., 21 (17): [PMID:23810424] [10.1016/j.bmc.2013.02.016] |
Source
Source(1):