ID: ALA511686

Max Phase: Preclinical

Molecular Formula: C17H22F2O3

Molecular Weight: 312.36

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)CC(=O)c1ccc(OC(F)F)c(OC2CCCC2)c1

Standard InChI:  InChI=1S/C17H22F2O3/c1-11(2)9-14(20)12-7-8-15(22-17(18)19)16(10-12)21-13-5-3-4-6-13/h7-8,10-11,13,17H,3-6,9H2,1-2H3

Standard InChI Key:  WSHHEXFRSSGSLG-UHFFFAOYSA-N

Associated Targets(Human)

Phosphodiesterase 4D 3546 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

PBMC 10003 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Phosphodiesterase 4 3344 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Cyclic nucleotide specific phosphodiesterase 69 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Trypanosoma cruzi 99888 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: 312.36Molecular Weight (Monoisotopic): 312.1537AlogP: 4.84#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: 4.93CX LogD: 4.93
Aromatic Rings: 1Heavy Atoms: 22QED Weighted: 0.68Np Likeness Score: -0.38

References

1. Zheng S, Kaur G, Wang H, Li M, Macnaughtan M, Yang X, Reid S, Prestegard J, Wang B, Ke H..  (2008)  Design, synthesis, and structure-activity relationship, molecular modeling, and NMR studies of a series of phenyl alkyl ketones as highly potent and selective phosphodiesterase-4 inhibitors.,  51  (24): [PMID:19049349] [10.1021/jm701635j]
2. King-Keller S, Li M, Smith A, Zheng S, Kaur G, Yang X, Wang B, Docampo R..  (2010)  Chemical validation of phosphodiesterase C as a chemotherapeutic target in Trypanosoma cruzi, the etiological agent of Chagas' disease.,  54  (9): [PMID:20625148] [10.1128/aac.00313-10]

Source