ID: ALA2420365

Max Phase: Preclinical

Molecular Formula: C14H12F8O

Molecular Weight: 348.23

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(CCCCc1ccc(C(F)(F)F)cc1)C(F)(F)C(F)(F)F

Standard InChI:  InChI=1S/C14H12F8O/c15-12(16,14(20,21)22)11(23)4-2-1-3-9-5-7-10(8-6-9)13(17,18)19/h5-8H,1-4H2

Standard InChI Key:  IQKCXJURTJXIFN-UHFFFAOYSA-N

Associated Targets(Human)

Phospholipase A2 group V 238 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

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: Small moleculeTopical: 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: 348.23Molecular Weight (Monoisotopic): 348.0760AlogP: 5.18#Rotatable Bonds: 6
Polar Surface Area: 17.07Molecular Species: NEUTRALHBA: 1HBD: 0
#RO5 Violations: 1HBA (Lipinski): 1HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 5.99CX LogD: 5.99
Aromatic Rings: 1Heavy Atoms: 23QED Weighted: 0.51Np Likeness Score: -0.43

References

1. Magrioti V, Nikolaou A, Smyrniotou A, Shah I, Constantinou-Kokotou V, Dennis EA, Kokotos G..  (2013)  New potent and selective polyfluoroalkyl ketone inhibitors of GVIA calcium-independent phospholipase A2.,  21  (18): [PMID:23916152] [10.1016/j.bmc.2013.07.010]

Source