| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA155988
Max Phase: Preclinical
Molecular Formula: C14H23N3O4
Molecular Weight: 297.36
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CCCCNCC1OC(n2cc(C)c(=O)[nH]c2=O)CC1O
Standard InChI: InChI=1S/C14H23N3O4/c1-3-4-5-15-7-11-10(18)6-12(21-11)17-8-9(2)13(19)16-14(17)20/h8,10-12,15,18H,3-7H2,1-2H3,(H,16,19,20)
Standard InChI Key: NOKNOLDMIBWTAS-UHFFFAOYSA-N
Associated Targets(non-human)
Thymidine kinase 2 53 Activities
Thymidine kinase 94 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 |
|---|
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: 297.36 | Molecular Weight (Monoisotopic): 297.1689 | AlogP: -0.12 | #Rotatable Bonds: 6 |
| Polar Surface Area: 96.35 | Molecular Species: BASE | HBA: 6 | HBD: 3 |
| #RO5 Violations: 0 | HBA (Lipinski): 7 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 10.12 | CX Basic pKa: 9.46 | CX LogP: 0.06 | CX LogD: -1.65 |
| Aromatic Rings: 1 | Heavy Atoms: 21 | QED Weighted: 0.64 | Np Likeness Score: 0.57 |
References
| 1. Hampton A, Chawla RR, Kappler F.. (1982) Species- or isozyme-specific enzyme inhibitors. 5. Differential effects of thymidine substituents on affinity for rat thymidine kinase isozymes., 25 (6): [PMID:7097717] [10.1021/jm00348a007] |
Source
Source(1):