ID: ALA4640748

Max Phase: Preclinical

Molecular Formula: C22H28ClN3O2S

Molecular Weight: 434.01

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1c(C(=O)NN2C(=O)CSC23CCC(C(C)(C)C)CC3)[nH]c2ccc(Cl)cc12

Standard InChI:  InChI=1S/C22H28ClN3O2S/c1-13-16-11-15(23)5-6-17(16)24-19(13)20(28)25-26-18(27)12-29-22(26)9-7-14(8-10-22)21(2,3)4/h5-6,11,14,24H,7-10,12H2,1-4H3,(H,25,28)

Standard InChI Key:  QNQSSWFHQWKUGI-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: 434.01Molecular Weight (Monoisotopic): 433.1591AlogP: 5.28#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: 4.89CX LogD: 4.89
Aromatic Rings: 2Heavy Atoms: 29QED Weighted: 0.68Np Likeness Score: -0.76

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