| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA3125361
Max Phase: Preclinical
Molecular Formula: C23H25FN4O
Molecular Weight: 392.48
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CCN(CC)C(=O)Cc1c(-c2ccc(C#CCF)cc2)nn2c(C)cc(C)nc12
Standard InChI: InChI=1S/C23H25FN4O/c1-5-27(6-2)21(29)15-20-22(19-11-9-18(10-12-19)8-7-13-24)26-28-17(4)14-16(3)25-23(20)28/h9-12,14H,5-6,13,15H2,1-4H3
Standard InChI Key: DEJZWCOVFSCYDB-UHFFFAOYSA-N
Associated Targets(non-human)
Liver microsome 4459 Activities
Peripheral-type benzodiazepine receptor 1942 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: 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: 392.48 | Molecular Weight (Monoisotopic): 392.2012 | AlogP: 3.75 | #Rotatable Bonds: 5 |
| Polar Surface Area: 50.50 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 1.40 | CX LogP: 3.61 | CX LogD: 3.61 |
| Aromatic Rings: 3 | Heavy Atoms: 29 | QED Weighted: 0.62 | Np Likeness Score: -1.68 |
References
| 1. Médran-Navarrete V, Damont A, Peyronneau MA, Kuhnast B, Bernards N, Pottier G, Marguet F, Puech F, Boisgard R, Dollé F.. (2014) Preparation and evaluation of novel pyrazolo[1,5-a]pyrimidine acetamides, closely related to DPA-714, as potent ligands for imaging the TSPO 18kDa with PET., 24 (6): [PMID:24560538] [10.1016/j.bmcl.2014.01.080] |
Source
Source(1):