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ID: ALA5083882
Max Phase: Preclinical
Molecular Formula: C14H12Cl2N2O4
Molecular Weight: 343.17
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: N[C@H](CNC(=O)c1ccc(-c2ccc(Cl)c(Cl)c2)o1)C(=O)O
Standard InChI: InChI=1S/C14H12Cl2N2O4/c15-8-2-1-7(5-9(8)16)11-3-4-12(22-11)13(19)18-6-10(17)14(20)21/h1-5,10H,6,17H2,(H,18,19)(H,20,21)/t10-/m1/s1
Standard InChI Key: PKDXPHTYXBJISW-SNVBAGLBSA-N
Associated Targets(non-human)
Glutamate NMDA receptor; Grin1/Grin2a 798 Activities
Glutamate NMDA receptor; Grin1/Grin2c 1127 Activities
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Ionotropic glutamate receptor NMDA 1/2D 870 Activities
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Glutamate NMDA receptor; Grin1/Grin2b 1028 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 |
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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: 343.17 | Molecular Weight (Monoisotopic): 342.0174 | AlogP: 2.40 | #Rotatable Bonds: 5 |
| Polar Surface Area: 105.56 | Molecular Species: ZWITTERION | HBA: 4 | HBD: 3 |
| #RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 4 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 2.06 | CX Basic pKa: 8.50 | CX LogP: -0.48 | CX LogD: -0.52 |
| Aromatic Rings: 2 | Heavy Atoms: 22 | QED Weighted: 0.77 | Np Likeness Score: -0.82 |
References
| 1. Zhao F, Atxabal U, Mariottini S, Yi F, Lotti JS, Rouzbeh N, Liu N, Bunch L, Hansen KB, Clausen RP.. (2022) Derivatives of (R)-3-(5-Furanyl)carboxamido-2-aminopropanoic Acid as Potent NMDA Receptor Glycine Site Agonists with GluN2 Subunit-Specific Activity., 65 (1.0): [PMID:34918931] [10.1021/acs.jmedchem.1c01810] |
Source
Source(1):