ID: ALA4636638

Max Phase: Preclinical

Molecular Formula: C23H30ClN3O2S

Molecular Weight: 448.03

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1c(C(=O)NN2C(=O)C(C)SC23CCC(C(C)(C)C)CC3)[nH]c2ccc(Cl)cc12

Standard InChI:  InChI=1S/C23H30ClN3O2S/c1-13-17-12-16(24)6-7-18(17)25-19(13)20(28)26-27-21(29)14(2)30-23(27)10-8-15(9-11-23)22(3,4)5/h6-7,12,14-15,25H,8-11H2,1-5H3,(H,26,28)

Standard InChI Key:  IDNWQFMWQBAHNN-UHFFFAOYSA-N

Associated Targets(non-human)

Influenza A virus H3N2 588 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MDCK 10148 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: 448.03Molecular Weight (Monoisotopic): 447.1747AlogP: 5.67#Rotatable Bonds: 2
Polar Surface Area: 65.20Molecular Species: NEUTRALHBA: 3HBD: 2
#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 11.39CX Basic pKa: CX LogP: 5.45CX LogD: 5.45
Aromatic Rings: 2Heavy Atoms: 30QED Weighted: 0.62Np Likeness Score: -0.63

References

1. Cihan-Üstündağ G, Zopun M, Vanderlinden E, Ozkirimli E, Persoons L, Çapan G, Naesens L..  (2020)  Superior inhibition of influenza virus hemagglutinin-mediated fusion by indole-substituted spirothiazolidinones.,  28  (1): [PMID:31753804] [10.1016/j.bmc.2019.115130]

Source