3-(3-Butoxy-pyrazin-2-yl)-1-aza-bicyclo[2.2.2]octane

ID: ALA323719

Chembl Id: CHEMBL323719

PubChem CID: 11777446

Max Phase: Preclinical

Molecular Formula: C15H23N3O

Molecular Weight: 261.37

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCCOc1nccnc1C1CN2CCC1CC2

Standard InChI:  InChI=1S/C15H23N3O/c1-2-3-10-19-15-14(16-6-7-17-15)13-11-18-8-4-12(13)5-9-18/h6-7,12-13H,2-5,8-11H2,1H3

Standard InChI Key:  PLPNZJVLQVYLAH-UHFFFAOYSA-N

Alternative Forms

Associated Targets(non-human)

Chrm1 Muscarinic acetylcholine receptor M1 (3437 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A9 (98 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 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

Calculated Properties

Molecular Weight: 261.37Molecular Weight (Monoisotopic): 261.1841AlogP: 2.46#Rotatable Bonds: 5
Polar Surface Area: 38.25Molecular Species: NEUTRALHBA: 4HBD:
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 7.85CX LogP: 1.89CX LogD: 1.30
Aromatic Rings: 1Heavy Atoms: 19QED Weighted: 0.76Np Likeness Score: -0.23

References

1. Ward JS, Merritt L, Calligaro DO, Bymaster FP, Shannon HE, Sawyer BD, Mitch CH, Deeter JB, Peters SC, Sheardown MJ, Olesen PH, Swedberg MD, Sauerberg P..  (1995)  Functionally selective M1 muscarinic agonists. 3. Side chains and azacycles contributing to functional muscarinic selectivity among pyrazinylazacycles.,  38  (18): [PMID:7658434] [10.1021/jm00018a007]

Source