| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA3357035
Max Phase: Preclinical
Molecular Formula: C24H27ClN2O2
Molecular Weight: 410.95
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CC(C)COC(=O)N1CCC(=C2c3ccc(Cl)cc3CCc3cccnc32)CC1
Standard InChI: InChI=1S/C24H27ClN2O2/c1-16(2)15-29-24(28)27-12-9-17(10-13-27)22-21-8-7-20(25)14-19(21)6-5-18-4-3-11-26-23(18)22/h3-4,7-8,11,14,16H,5-6,9-10,12-13,15H2,1-2H3
Standard InChI Key: AMBATUWSQRROKC-UHFFFAOYSA-N
Associated Targets(Human)
Histamine H1 receptor 7573 Activities
Sodium-dependent neutral amino acid transporter B(0)AT2 42 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 |
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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: 410.95 | Molecular Weight (Monoisotopic): 410.1761 | AlogP: 5.52 | #Rotatable Bonds: 2 |
| Polar Surface Area: 42.43 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 0 |
| #RO5 Violations: 1 | HBA (Lipinski): 4 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: | CX Basic pKa: 4.33 | CX LogP: 5.44 | CX LogD: 5.44 |
| Aromatic Rings: 2 | Heavy Atoms: 29 | QED Weighted: 0.65 | Np Likeness Score: -0.66 |
References
| 1. Cuboni S, Devigny C, Hoogeland B, Strasser A, Pomplun S, Hauger B, Höfner G, Wanner KT, Eder M, Buschauer A, Holsboer F, Hausch F.. (2014) Loratadine and analogues: discovery and preliminary structure-activity relationship of inhibitors of the amino acid transporter B(0)AT2., 57 (22): [PMID:25318072] [10.1021/jm501086v] |
Source
Source(1):