| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA611601
Max Phase: Preclinical
Molecular Formula: C18H29N4O8P
Molecular Weight: 460.42
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CCCCCCCCc1nc(O)c2ncn(C3O[C@@H](COP(=O)(O)O)[C@H](O)[C@@H]3O)c2n1
Standard InChI: InChI=1S/C18H29N4O8P/c1-2-3-4-5-6-7-8-12-20-16-13(17(25)21-12)19-10-22(16)18-15(24)14(23)11(30-18)9-29-31(26,27)28/h10-11,14-15,18,23-24H,2-9H2,1H3,(H,20,21,25)(H2,26,27,28)/t11-,14-,15-,18?/m0/s1
Standard InChI Key: ULHLQZBLXBEFDP-FWYGCHORSA-N
Associated Targets(non-human)
Inosine-5'-monophosphate dehydrogenase 49 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: 460.42 | Molecular Weight (Monoisotopic): 460.1723 | AlogP: 1.16 | #Rotatable Bonds: 11 |
| Polar Surface Area: 180.28 | Molecular Species: ACID | HBA: 10 | HBD: 5 |
| #RO5 Violations: 0 | HBA (Lipinski): 12 | HBD (Lipinski): 5 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: 1.22 | CX Basic pKa: 0.01 | CX LogP: 1.67 | CX LogD: -1.54 |
| Aromatic Rings: 2 | Heavy Atoms: 31 | QED Weighted: 0.24 | Np Likeness Score: 0.65 |
References
| 1. Wong CG, Meyer RB.. (1984) Inhibitors of inosinic acid dehydrogenase. 2-Substituted inosinic acids., 27 (4): [PMID:6142953] [10.1021/jm00370a003] |
Source
Source(1):