ID: ALA4445082

Max Phase: Preclinical

Molecular Formula: C17H22F2N6O2

Molecular Weight: 380.40

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C[C@@H](Nc1nc2c(cnn2C2CCCC2)c(=O)[nH]1)C(=O)N1CCC(F)(F)C1

Standard InChI:  InChI=1S/C17H22F2N6O2/c1-10(15(27)24-7-6-17(18,19)9-24)21-16-22-13-12(14(26)23-16)8-20-25(13)11-4-2-3-5-11/h8,10-11H,2-7,9H2,1H3,(H2,21,22,23,26)/t10-/m1/s1

Standard InChI Key:  NYOJJFMXAQIOSI-SNVBAGLBSA-N

Associated Targets(Human)

Phosphodiesterase 1B 178 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Phosphodiesterase 9A 1131 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: 380.40Molecular Weight (Monoisotopic): 380.1772AlogP: 1.90#Rotatable Bonds: 4
Polar Surface Area: 95.91Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 10.56CX Basic pKa: 1.57CX LogP: 1.13CX LogD: 1.13
Aromatic Rings: 2Heavy Atoms: 27QED Weighted: 0.84Np Likeness Score: -1.34

References

1. Wu Y, Zhou Q, Zhang T, Li Z, Chen YP, Zhang P, Yu YF, Geng H, Tian YJ, Zhang C, Wang Y, Chen JW, Chen Y, Luo HB..  (2019)  Discovery of Potent, Selective, and Orally Bioavailable Inhibitors against Phosphodiesterase-9, a Novel Target for the Treatment of Vascular Dementia.,  62  (8): [PMID:30916555] [10.1021/acs.jmedchem.8b01041]

Source