2-((3-(3-chlorobenzyl)piperidin-3-yl)methoxy)-9H-carbazole

ID: ALA4450187

PubChem CID: 155520946

Max Phase: Preclinical

Molecular Formula: C25H25ClN2O

Molecular Weight: 404.94

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  Clc1cccc(CC2(COc3ccc4c(c3)[nH]c3ccccc34)CCCNC2)c1

Standard InChI:  InChI=1S/C25H25ClN2O/c26-19-6-3-5-18(13-19)15-25(11-4-12-27-16-25)17-29-20-9-10-22-21-7-1-2-8-23(21)28-24(22)14-20/h1-3,5-10,13-14,27-28H,4,11-12,15-17H2

Standard InChI Key:  BUMABZFDIYXNFN-UHFFFAOYSA-N

Molfile:  

 
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   36.4791   -4.9006    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

Alternative Forms

  1. Parent:

    ALA4450187

    ---

Associated Targets(non-human)

Acetylcholine-binding protein (240 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

Calculated Properties

Molecular Weight: 404.94Molecular Weight (Monoisotopic): 404.1655AlogP: 5.97#Rotatable Bonds: 5
Polar Surface Area: 37.05Molecular Species: BASEHBA: 2HBD: 2
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 9.69CX LogP: 5.75CX LogD: 3.51
Aromatic Rings: 4Heavy Atoms: 29QED Weighted: 0.43Np Likeness Score: -0.06

References

1. Yang X, Shen J, Jiang L, Li W, Yu M, Pan G, Yan Y, Zhang C, Jia W, Xiao L, Yu H, Chen H, Zheng Y, Yu L, Xie Q, Zhou L, Shao L..  (2018)  Discovery, cocrystallization and biological evaluation of novel piperidine derivatives as high affinity Ls-AChBP ligands possessing α7 nAChR activities.,  160  [PMID:30317024] [10.1016/j.ejmech.2018.09.073]

Source