1-Isopropyl-3-[5-(1-isopropyl-piperidin-4-yl)-[1,2,4]oxadiazol-3-yl]-1H-indazole

ID: ALA5283820

Chembl Id: CHEMBL5283820

Max Phase: Preclinical

Molecular Formula: C20H27N5O

Molecular Weight: 353.47

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(C)N1CCC(c2nc(-c3nn(C(C)C)c4ccccc34)no2)CC1

Standard InChI:  InChI=1S/C20H27N5O/c1-13(2)24-11-9-15(10-12-24)20-21-19(23-26-20)18-16-7-5-6-8-17(16)25(22-18)14(3)4/h5-8,13-15H,9-12H2,1-4H3

Standard InChI Key:  FXFLHCNFYIUXRP-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5283820

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Associated Targets(Human)

HTR4 Tclin 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

Calculated Properties

Molecular Weight: 353.47Molecular Weight (Monoisotopic): 353.2216AlogP: 4.26#Rotatable Bonds: 4
Polar Surface Area: 59.98Molecular Species: BASEHBA: 6HBD:
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 8.87CX LogP: 4.13CX LogD: 2.64
Aromatic Rings: 3Heavy Atoms: 26QED Weighted: 0.70Np Likeness Score: -1.65

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