ID: ALA2159690

Max Phase: Preclinical

Molecular Formula: C23H24ClF2NO6S

Molecular Weight: 515.96

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCNC(=O)OCC[C@@H]1OCC[C@@]2(S(=O)(=O)c3ccc(Cl)cc3)c3c(F)ccc(F)c3OC[C@@H]12

Standard InChI:  InChI=1S/C23H24ClF2NO6S/c1-2-27-22(28)32-11-9-19-16-13-33-21-18(26)8-7-17(25)20(21)23(16,10-12-31-19)34(29,30)15-5-3-14(24)4-6-15/h3-8,16,19H,2,9-13H2,1H3,(H,27,28)/t16-,19-,23-/m0/s1

Standard InChI Key:  CBBFOFOYZAQDFL-NVVBAYIOSA-N

Associated Targets(Human)

PSEN2 Tchem Presenilin 2 (10 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PSEN1 Tchem Presenilin 1 (302 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: 515.96Molecular Weight (Monoisotopic): 515.0981AlogP: 4.22#Rotatable Bonds: 6
Polar Surface Area: 90.93Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 1HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.78CX Basic pKa: CX LogP: 3.55CX LogD: 3.55
Aromatic Rings: 2Heavy Atoms: 34QED Weighted: 0.62Np Likeness Score: -0.35

References

1. Wu WL, Domalski M, Burnett DA, Josien H, Bara T, Rajagopalan M, Xu R, Clader J, Greenlee WJ, Brunskill A, Hyde LA, Del Vecchio RA, Cohen-Williams ME, Song L, Lee J, Terracina G, Zhang Q, Nomeir A, Parker EM, Zhang L..  (2012)  Discovery of SCH 900229, a Potent Presenilin 1 Selective γ-Secretase Inhibitor for the Treatment of Alzheimer's Disease.,  (11): [PMID:24900404] [10.1021/ml300044f]

Source