ID: ALA3792444

Max Phase: Preclinical

Molecular Formula: C27H21N3OS

Molecular Weight: 435.55

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cccc(NC(=O)CSc2nc(-c3ccccc3)cc(-c3ccccc3)c2C#N)c1

Standard InChI:  InChI=1S/C27H21N3OS/c1-19-9-8-14-22(15-19)29-26(31)18-32-27-24(17-28)23(20-10-4-2-5-11-20)16-25(30-27)21-12-6-3-7-13-21/h2-16H,18H2,1H3,(H,29,31)

Standard InChI Key:  FVYFDMIJOXJRSQ-UHFFFAOYSA-N

Associated Targets(Human)

HEK-293T (167025 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

MDCK (10148 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Influenza A virus (11224 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PA PA/PB1 (167 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

Properties

Molecular Weight: 435.55Molecular Weight (Monoisotopic): 435.1405AlogP: 6.33#Rotatable Bonds: 6
Polar Surface Area: 65.78Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.66CX Basic pKa: CX LogP: 6.63CX LogD: 6.63
Aromatic Rings: 4Heavy Atoms: 32QED Weighted: 0.36Np Likeness Score: -1.86

References

1. Trist IM, Nannetti G, Tintori C, Fallacara AL, Deodato D, Mercorelli B, Palù G, Wijtmans M, Gospodova T, Edink E, Verheij M, de Esch I, Viteva L, Loregian A, Botta M..  (2016)  4,6-Diphenylpyridines as Promising Novel Anti-Influenza Agents Targeting the PA-PB1 Protein-Protein Interaction: Structure-Activity Relationships Exploration with the Aid of Molecular Modeling.,  59  (6): [PMID:26924568] [10.1021/acs.jmedchem.5b01935]
2. D'Agostino I, Giacchello I, Nannetti G, Fallacara AL, Deodato D, Musumeci F, Grossi G, Palù G, Cau Y, Trist IM, Loregian A, Schenone S, Botta M..  (2018)  Synthesis and biological evaluation of a library of hybrid derivatives as inhibitors of influenza virus PA-PB1 interaction.,  157  [PMID:30142611] [10.1016/j.ejmech.2018.08.032]

Source