Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA5271303
Max Phase: Preclinical
Molecular Formula: C23H34N4O2
Molecular Weight: 398.55
Associated Items:
ID: ALA5271303
Max Phase: Preclinical
Molecular Formula: C23H34N4O2
Molecular Weight: 398.55
Associated Items:
Canonical SMILES: CC(C)n1nc(C(=O)NCC2CCN(CC3CCOCC3)CC2)c2ccccc21
Standard InChI: InChI=1S/C23H34N4O2/c1-17(2)27-21-6-4-3-5-20(21)22(25-27)23(28)24-15-18-7-11-26(12-8-18)16-19-9-13-29-14-10-19/h3-6,17-19H,7-16H2,1-2H3,(H,24,28)
Standard InChI Key: YXMFEPSJTSPYKD-UHFFFAOYSA-N
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: 398.55 | Molecular Weight (Monoisotopic): 398.2682 | AlogP: 3.49 | #Rotatable Bonds: 6 |
Polar Surface Area: 59.39 | Molecular Species: BASE | HBA: 5 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: 10.04 | CX LogP: 2.56 | CX LogD: -0.02 |
Aromatic Rings: 2 | Heavy Atoms: 29 | QED Weighted: 0.81 | Np Likeness Score: -1.39 |
1. Nirogi R, Mohammed AR, Shinde AK, Gagginapally SR, Kancharla DM, Ravella SR, Bogaraju N, Middekadi VR, Subramanian R, Palacharla RC, Benade V, Muddana N, Abraham R, Medapati RB, Thentu JB, Mekala VR, Petlu S, Lingavarapu BB, Yarra S, Kagita N, Goyal VK, Pandey SK, Jasti V.. (2021) Discovery and Preclinical Characterization of Usmarapride (SUVN-D4010): A Potent, Selective 5-HT4 Receptor Partial Agonist for the Treatment of Cognitive Deficits Associated with Alzheimer's Disease., 64 (15.0): [PMID:34251799] [10.1021/acs.jmedchem.1c00703] |
Source(1):