6-[2-(Benzothiazol-2-ylsulfanyl)-ethoxy]-7-(2-naphthalen-1-yl-ethoxy)-1,2,3,4-tetrahydro-1,4-epiazano-naphthalene

ID: ALA4529998

PubChem CID: 85384269

Max Phase: Preclinical

Molecular Formula: C31H28N2O2S2

Molecular Weight: 524.71

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  c1ccc2c(CCOc3cc4c(cc3OCCSc3nc5ccccc5s3)C3CCC4N3)cccc2c1

Standard InChI:  InChI=1S/C31H28N2O2S2/c1-2-9-22-20(6-1)7-5-8-21(22)14-15-34-28-18-23-24(26-13-12-25(23)32-26)19-29(28)35-16-17-36-31-33-27-10-3-4-11-30(27)37-31/h1-11,18-19,25-26,32H,12-17H2

Standard InChI Key:  KUYOGFBOBRRTME-UHFFFAOYSA-N

Molfile:  

 
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M  END

Associated Targets(non-human)

PMII Plasmepsin 2 (774 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmepsin 4 (112 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

Calculated Properties

Molecular Weight: 524.71Molecular Weight (Monoisotopic): 524.1592AlogP: 7.72#Rotatable Bonds: 9
Polar Surface Area: 43.38Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 2HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 8.23CX LogP: 7.49CX LogD: 6.60
Aromatic Rings: 5Heavy Atoms: 37QED Weighted: 0.16Np Likeness Score: -0.80

References

1. Bobrovs R, Jaudzems K, Jirgensons A..  (2019)  Exploiting Structural Dynamics To Design Open-Flap Inhibitors of Malarial Aspartic Proteases.,  62  (20): [PMID:31062983] [10.1021/acs.jmedchem.9b00184]

Source