4-((6-(5-Isopropyl-1,2,4-oxadiazol-3-yl)pyridin-3-yl)oxy)-N-methylpicolinamide

ID: ALA4215667

Chembl Id: CHEMBL4215667

PubChem CID: 138549861

Max Phase: Preclinical

Molecular Formula: C17H17N5O3

Molecular Weight: 339.36

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CNC(=O)c1cc(Oc2ccc(-c3noc(C(C)C)n3)nc2)ccn1

Standard InChI:  InChI=1S/C17H17N5O3/c1-10(2)17-21-15(22-25-17)13-5-4-12(9-20-13)24-11-6-7-19-14(8-11)16(23)18-3/h4-10H,1-3H3,(H,18,23)

Standard InChI Key:  QRIAFWUHEHZGTD-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4215667

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Associated Targets(Human)

H1-HeLa (123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

rhinovirus B14 (1052 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rhinovirus A21 (119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 339.36Molecular Weight (Monoisotopic): 339.1331AlogP: 2.80#Rotatable Bonds: 5
Polar Surface Area: 103.03Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.99CX Basic pKa: 2.99CX LogP: 2.32CX LogD: 2.32
Aromatic Rings: 3Heavy Atoms: 25QED Weighted: 0.76Np Likeness Score: -1.66

References

1. Kim J, Shin JS, Ahn S, Han SB, Jung YS..  (2018)  3-Aryl-1,2,4-oxadiazole Derivatives Active Against Human Rhinovirus.,  (7): [PMID:30034598] [10.1021/acsmedchemlett.8b00134]

Source