ID: ALA4514035

Max Phase: Preclinical

Molecular Formula: C22H19NO3S

Molecular Weight: 377.47

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(C(=O)c2cccc(COc3ccc(C4=NCCO4)cc3)c2)s1

Standard InChI:  InChI=1S/C22H19NO3S/c1-15-5-10-20(27-15)21(24)18-4-2-3-16(13-18)14-26-19-8-6-17(7-9-19)22-23-11-12-25-22/h2-10,13H,11-12,14H2,1H3

Standard InChI Key:  HMNFDCHLDMZALB-UHFFFAOYSA-N

Associated Targets(non-human)

Poliovirus 3 200 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Poliovirus 2 222 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Poliovirus 1 1274 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 377.47Molecular Weight (Monoisotopic): 377.1086AlogP: 4.64#Rotatable Bonds: 6
Polar Surface Area: 47.89Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 3.73CX LogP: 5.39CX LogD: 5.39
Aromatic Rings: 3Heavy Atoms: 27QED Weighted: 0.59Np Likeness Score: -0.99

References

1. Madia VN, Messore A, Pescatori L, Saccoliti F, Tudino V, De Leo A, Scipione L, Fiore L, Rhoden E, Manetti F, Oberste MS, Di Santo R, Costi R..  (2019)  In Vitro Antiviral Activity of New Oxazoline Derivatives as Potent Poliovirus Inhibitors.,  62  (2): [PMID:30512950] [10.1021/acs.jmedchem.8b01482]

Source