| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4530287
Max Phase: Preclinical
Molecular Formula: C12H12N4O4
Molecular Weight: 276.25
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: Nc1[nH]c(=O)n(O)c(=O)c1C(=O)NCc1ccccc1
Standard InChI: InChI=1S/C12H12N4O4/c13-9-8(11(18)16(20)12(19)15-9)10(17)14-6-7-4-2-1-3-5-7/h1-5,20H,6,13H2,(H,14,17)(H,15,19)
Standard InChI Key: KTWJPYVRYQJIGD-UHFFFAOYSA-N
Associated Targets(Human)
CEM-SS 2428 Activities
Associated Targets(non-human)
Human immunodeficiency virus 1 70413 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Human immunodeficiency virus type 1 integrase 9041 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: Unknown | 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: 276.25 | Molecular Weight (Monoisotopic): 276.0859 | AlogP: -0.71 | #Rotatable Bonds: 3 |
| Polar Surface Area: 130.21 | Molecular Species: ACID | HBA: 6 | HBD: 4 |
| #RO5 Violations: 0 | HBA (Lipinski): 8 | HBD (Lipinski): 5 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 5.38 | CX Basic pKa: | CX LogP: -0.63 | CX LogD: -2.50 |
| Aromatic Rings: 2 | Heavy Atoms: 20 | QED Weighted: 0.55 | Np Likeness Score: -0.73 |
References
| 1. Wu B, Tang J, Wilson DJ, Huber AD, Casey MC, Ji J, Kankanala J, Xie J, Sarafianos SG, Wang Z.. (2016) 3-Hydroxypyrimidine-2,4-dione-5-N-benzylcarboxamides Potently Inhibit HIV-1 Integrase and RNase H., 59 (13): [PMID:27283261] [10.1021/acs.jmedchem.6b00040] |
Source
Source(1):