ID: ALA5281474

Max Phase: Preclinical

Molecular Formula: C26H35N5O7

Molecular Weight: 439.56

Associated Items:

Representations

Canonical SMILES:  COC(=O)N1CCC(N2CC3C(CNC(=O)c4nn(C(C)C)c5ccccc45)C3C2)CC1.O=C(O)C(=O)O

Standard InChI:  InChI=1S/C24H33N5O3.C2H2O4/c1-15(2)29-21-7-5-4-6-17(21)22(26-29)23(30)25-12-18-19-13-28(14-20(18)19)16-8-10-27(11-9-16)24(31)32-3;3-1(4)2(5)6/h4-7,15-16,18-20H,8-14H2,1-3H3,(H,25,30);(H,3,4)(H,5,6)

Standard InChI Key:  MWHSDMXOILOCHX-UHFFFAOYSA-N

Associated Targets(Human)

Serotonin 4 (5-HT4) receptor 2068 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 439.56Molecular Weight (Monoisotopic): 439.2583AlogP: 2.76#Rotatable Bonds: 5
Polar Surface Area: 79.70Molecular Species: BASEHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 10.23CX LogP: 1.39CX LogD: -1.35
Aromatic Rings: 2Heavy Atoms: 32QED Weighted: 0.78Np Likeness Score: -0.92

References

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