ID: ALA4588998

Max Phase: Preclinical

Molecular Formula: C19H21NO4S2

Molecular Weight: 391.51

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(C(=O)CCCCS(=O)(=O)c2ccc(C3=NCCO3)cc2)s1

Standard InChI:  InChI=1S/C19H21NO4S2/c1-14-5-10-18(25-14)17(21)4-2-3-13-26(22,23)16-8-6-15(7-9-16)19-20-11-12-24-19/h5-10H,2-4,11-13H2,1H3

Standard InChI Key:  STIAGEXUHIBJMI-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: 391.51Molecular Weight (Monoisotopic): 391.0912AlogP: 3.66#Rotatable Bonds: 8
Polar Surface Area: 72.80Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 3.11CX LogP: 3.56CX LogD: 3.56
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.51Np Likeness Score: -1.29

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