Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA5183971
Max Phase: Preclinical
Molecular Formula: C21H19Cl2N3
Molecular Weight: 384.31
Associated Items:
ID: ALA5183971
Max Phase: Preclinical
Molecular Formula: C21H19Cl2N3
Molecular Weight: 384.31
Associated Items:
Canonical SMILES: Clc1ccc(-c2ccc3nc(Cl)nc(N[C@@H]4C[C@H]5CC[C@@H]4C5)c3c2)cc1
Standard InChI: InChI=1S/C21H19Cl2N3/c22-16-6-3-13(4-7-16)14-5-8-18-17(11-14)20(26-21(23)25-18)24-19-10-12-1-2-15(19)9-12/h3-8,11-12,15,19H,1-2,9-10H2,(H,24,25,26)/t12-,15+,19+/m0/s1
Standard InChI Key: HWUWNFWEFPZCPR-IOHHAYIISA-N
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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 |
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Molecular Weight: 384.31 | Molecular Weight (Monoisotopic): 383.0956 | AlogP: 6.20 | #Rotatable Bonds: 3 |
Polar Surface Area: 37.81 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 1 |
#RO5 Violations: 1 | HBA (Lipinski): 3 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: | CX Basic pKa: 2.34 | CX LogP: 6.20 | CX LogD: 6.20 |
Aromatic Rings: 3 | Heavy Atoms: 26 | QED Weighted: 0.55 | Np Likeness Score: -0.70 |
1. Huszár J, Petró JL, Hadady Z, Bobok AÁ, Sághy K, Halász AS, Hornyánszky G, Román V, Greiner I, Éles J.. (2022) 6-Aryl-quinazolines as novel GABAB receptor positive allosteric modulators., 67 [PMID:35367591] [10.1016/j.bmcl.2022.128714] |
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