ID: ALA5081631

Max Phase: Preclinical

Molecular Formula: C15H10O2

Molecular Weight: 222.24

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=c1cc1-c1ccc(Oc2ccccc2)cc1

Standard InChI:  InChI=1S/C15H10O2/c16-15-10-14(15)11-6-8-13(9-7-11)17-12-4-2-1-3-5-12/h1-10H

Standard InChI Key:  DGVHLEMKWLRISG-UHFFFAOYSA-N

Associated Targets(Human)

Glutathione S-transferase Pi 449 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: 222.24Molecular Weight (Monoisotopic): 222.0681AlogP: 3.38#Rotatable Bonds: 3
Polar Surface Area: 26.30Molecular Species: NEUTRALHBA: 2HBD: 0
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.68CX LogD: 3.68
Aromatic Rings: 3Heavy Atoms: 17QED Weighted: 0.68Np Likeness Score: -0.28

References

1. Fan Y, Si H, Zhang Z, Zhong L, Sun H, Zhu C, Yin Z, Li H, Tang G, Yao SQ, Sun P, Zhang ZM, Ding K, Li Z..  (2021)  Novel Electrophilic Warhead Targeting a Triple-Negative Breast Cancer Driver in Live Cells Revealed by "Inverse Drug Discovery".,  64  (21.0): [PMID:34623802] [10.1021/acs.jmedchem.0c02024]

Source