| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA308139
Max Phase: Preclinical
Molecular Formula: C9H16N2O5
Molecular Weight: 232.24
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: O=C1NCCCN1C1OC[C@@H](O)[C@H](O)[C@@H]1O
Standard InChI: InChI=1S/C9H16N2O5/c12-5-4-16-8(7(14)6(5)13)11-3-1-2-10-9(11)15/h5-8,12-14H,1-4H2,(H,10,15)/t5-,6+,7+,8?/m1/s1
Standard InChI Key: NVRYHNNOILWLET-JXMHAVLCSA-N
Associated Targets(non-human)
Cytidine deaminase 37 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: 232.24 | Molecular Weight (Monoisotopic): 232.1059 | AlogP: -2.16 | #Rotatable Bonds: 1 |
| Polar Surface Area: 102.26 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 4 |
| #RO5 Violations: 0 | HBA (Lipinski): 7 | HBD (Lipinski): 4 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 12.47 | CX Basic pKa: | CX LogP: -2.59 | CX LogD: -2.59 |
| Aromatic Rings: 0 | Heavy Atoms: 16 | QED Weighted: 0.41 | Np Likeness Score: 1.22 |
References
| 1. Kelley JA, Driscoll JS, McCormack JJ, Roth JS, Marquez VE.. (1986) Furanose-pyranose isomerization of reduced pyrimidine and cyclic urea ribosides., 29 (11): [PMID:3783592] [10.1021/jm00161a034] |
Source
Source(1):