ID: ALA4863873

Max Phase: Preclinical

Molecular Formula: C18H19ClF3N

Molecular Weight: 341.80

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C[C@H](CCc1ccc(Cl)cc1)NCc1ccc(C(F)(F)F)cc1

Standard InChI:  InChI=1S/C18H19ClF3N/c1-13(2-3-14-6-10-17(19)11-7-14)23-12-15-4-8-16(9-5-15)18(20,21)22/h4-11,13,23H,2-3,12H2,1H3/t13-/m1/s1

Standard InChI Key:  SNSIQWWUXFSTGO-CYBMUJFWSA-N

Associated Targets(Human)

Sigma intracellular receptor 2 973 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HERG 29587 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

N2a 708 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: 341.80Molecular Weight (Monoisotopic): 341.1158AlogP: 5.47#Rotatable Bonds: 6
Polar Surface Area: 12.03Molecular Species: BASEHBA: 1HBD: 1
#RO5 Violations: 1HBA (Lipinski): 1HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 9.61CX LogP: 5.89CX LogD: 3.72
Aromatic Rings: 2Heavy Atoms: 23QED Weighted: 0.73Np Likeness Score: -1.11

References

1. Rishton GM, Look GC, Ni ZJ, Zhang J, Wang Y, Huang Y, Wu X, Izzo NJ, LaBarbera KM, Limegrover CS, Rehak C, Yurko R, Catalano SM..  (2021)  Discovery of Investigational Drug CT1812, an Antagonist of the Sigma-2 Receptor Complex for Alzheimer's Disease.,  12  (9.0): [PMID:34531947] [10.1021/acsmedchemlett.1c00048]

Source