ID: ALA4857307

Max Phase: Preclinical

Molecular Formula: C20H21NO6

Molecular Weight: 371.39

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1cccc(-c2cnc(-c3ccc(OC)c(OC)c3OC)o2)c1OC

Standard InChI:  InChI=1S/C20H21NO6/c1-22-14-8-6-7-12(17(14)24-3)16-11-21-20(27-16)13-9-10-15(23-2)19(26-5)18(13)25-4/h6-11H,1-5H3

Standard InChI Key:  VSGXZFSFDLDIJY-UHFFFAOYSA-N

Associated Targets(non-human)

Trypanosoma brucei brucei 13300 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Trypanosoma brucei gambiense 523 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Trypanosoma brucei rhodesiense 7991 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Trypanosoma congolense 178 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Trypanosoma evansi 198 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: 371.39Molecular Weight (Monoisotopic): 371.1369AlogP: 4.05#Rotatable Bonds: 7
Polar Surface Area: 72.18Molecular Species: NEUTRALHBA: 7HBD: 0
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 0.16CX LogP: 2.72CX LogD: 2.72
Aromatic Rings: 3Heavy Atoms: 27QED Weighted: 0.62Np Likeness Score: -0.18

References

1. Narita K, Suganuma K, Murata T, Kondo R, Satoh H, Watanabe K, Sasaki K, Inoue N, Yoshimura Y..  (2021)  Synthesis and evaluation of trypanocidal activity of derivatives of naturally occurring 2,5-diphenyloxazoles.,  42  [PMID:34130218] [10.1016/j.bmc.2021.116253]

Source