ID: ALA4570550

Max Phase: Preclinical

Molecular Formula: C16H22O3

Molecular Weight: 262.35

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCCC1OC(=O)C1CCCc1ccc(OC)cc1

Standard InChI:  InChI=1S/C16H22O3/c1-3-5-15-14(16(17)19-15)7-4-6-12-8-10-13(18-2)11-9-12/h8-11,14-15H,3-7H2,1-2H3

Standard InChI Key:  GVNPMTJLKYPTPE-UHFFFAOYSA-N

Associated Targets(Human)

Cytosolic phospholipase A2 785 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Calcium-independent phospholipase A2 359 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: 262.35Molecular Weight (Monoisotopic): 262.1569AlogP: 3.36#Rotatable Bonds: 7
Polar Surface Area: 35.53Molecular Species: NEUTRALHBA: 3HBD: 0
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.10CX LogD: 4.10
Aromatic Rings: 1Heavy Atoms: 19QED Weighted: 0.71Np Likeness Score: 1.04

References

1. Dedaki C, Kokotou MG, Mouchlis VD, Limnios D, Lei X, Mu CT, Ramanadham S, Magrioti V, Dennis EA, Kokotos G..  (2019)  β-Lactones: A Novel Class of Ca2+-Independent Phospholipase A2 (Group VIA iPLA2) Inhibitors with the Ability To Inhibit β-Cell Apoptosis.,  62  (6): [PMID:30798607] [10.1021/acs.jmedchem.8b01216]

Source