ID: ALA5204122
Chembl Id: CHEMBL5204122
PubChem CID: 168293904
Max Phase: Preclinical
Molecular Formula: C14H12BrClN6O
Molecular Weight: 395.65
Associated Items:
Canonical SMILES: Cc1cn(CCC#N)c(=O)c2cc(Cn3nc(Br)cc3Cl)nn12
Standard InChI: InChI=1S/C14H12BrClN6O/c1-9-7-20(4-2-3-17)14(23)11-5-10(18-22(9)11)8-21-13(16)6-12(15)19-21/h5-7H,2,4,8H2,1H3
Standard InChI Key: ALGOCFFJWFCMTN-UHFFFAOYSA-N
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: | Topical: No | First In Class: No | Black Box: No |
| Chirality: No | Availability: No | Prodrug: No |
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
| Molecular Weight: 395.65 | Molecular Weight (Monoisotopic): 393.9944 | AlogP: 2.38 | #Rotatable Bonds: 4 |
| Polar Surface Area: 80.91 | Molecular Species: NEUTRAL | HBA: 7 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 7 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 0.02 | CX LogP: 1.31 | CX LogD: 1.31 |
| Aromatic Rings: 3 | Heavy Atoms: 23 | QED Weighted: 0.68 | Np Likeness Score: -1.65 |
| 1. Sakurai F, Yukawa T, Kina A, Murakami M, Takami K, Morimoto S, Seto M, Kamata M, Yamashita T, Nakashima K, Narita N, Bettini E, Ugolini A, Corsi M, Hasui T.. (2022) Discovery of Pyrazolo[1,5-a]pyrazin-4-ones as Potent and Brain Penetrant GluN2A-Selective Positive Allosteric Modulators Reducing AMPA Receptor Binding Activity., 56 [PMID:35051811] [10.1016/j.bmc.2021.116576] |
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