N-Methyl-4-((6-(5-methyl-1,2,4-oxadiazol-3-yl)naphthalen-2-yl)oxy)picolinamide

ID: ALA4213246

Chembl Id: CHEMBL4213246

PubChem CID: 138549837

Max Phase: Preclinical

Molecular Formula: C20H16N4O3

Molecular Weight: 360.37

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CNC(=O)c1cc(Oc2ccc3cc(-c4noc(C)n4)ccc3c2)ccn1

Standard InChI:  InChI=1S/C20H16N4O3/c1-12-23-19(24-27-12)15-4-3-14-10-16(6-5-13(14)9-15)26-17-7-8-22-18(11-17)20(25)21-2/h3-11H,1-2H3,(H,21,25)

Standard InChI Key:  RRRSAURDWVMSJV-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4213246

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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: 360.37Molecular Weight (Monoisotopic): 360.1222AlogP: 3.75#Rotatable Bonds: 4
Polar Surface Area: 90.14Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 14.00CX Basic pKa: 3.03CX LogP: 2.98CX LogD: 2.98
Aromatic Rings: 4Heavy Atoms: 27QED Weighted: 0.60Np Likeness Score: -1.29

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