ID: ALA4288640

Max Phase: Preclinical

Molecular Formula: C14H19F3N4OS

Molecular Weight: 348.39

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCN(CCCC)c1nn2c(=O)cc(C(F)(F)F)nc2s1

Standard InChI:  InChI=1S/C14H19F3N4OS/c1-3-5-7-20(8-6-4-2)13-19-21-11(22)9-10(14(15,16)17)18-12(21)23-13/h9H,3-8H2,1-2H3

Standard InChI Key:  GHQCRNROGYLFHB-UHFFFAOYSA-N

Associated Targets(Human)

Alkaline phosphatase, tissue-nonspecific isozyme 1551 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Intestinal alkaline phosphatase 724 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: 348.39Molecular Weight (Monoisotopic): 348.1232AlogP: 3.58#Rotatable Bonds: 7
Polar Surface Area: 50.50Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 1.11CX LogP: 4.48CX LogD: 4.48
Aromatic Rings: 2Heavy Atoms: 23QED Weighted: 0.77Np Likeness Score: -1.86

References

1. Jafari B, Ospanov M, Ejaz SA, Yelibayeva N, Khan SU, Amjad ST, Safarov S, Abilov ZA, Turmukhanova MZ, Kalugin SN, Ehlers P, Lecka J, Sévigny J, Iqbal J, Langer P..  (2018)  2-Substituted 7-trifluoromethyl-thiadiazolopyrimidones as alkaline phosphatase inhibitors. Synthesis, structure activity relationship and molecular docking study.,  144  [PMID:29268128] [10.1016/j.ejmech.2017.11.068]

Source