ID: ALA4530638

Max Phase: Preclinical

Molecular Formula: C20H23NO2S2

Molecular Weight: 373.54

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(C(=O)CCCCSc2ccc(C3=N[C@H](C)CO3)cc2)s1

Standard InChI:  InChI=1S/C20H23NO2S2/c1-14-13-23-20(21-14)16-7-9-17(10-8-16)24-12-4-3-5-18(22)19-11-6-15(2)25-19/h6-11,14H,3-5,12-13H2,1-2H3/t14-/m1/s1

Standard InChI Key:  BFXYHZOJWADZSG-CQSZACIVSA-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: 373.54Molecular Weight (Monoisotopic): 373.1170AlogP: 5.37#Rotatable Bonds: 8
Polar Surface Area: 38.66Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 3.75CX LogP: 5.51CX LogD: 5.51
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.35Np Likeness Score: -0.95

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