ID: ALA118949

Max Phase: Preclinical

Molecular Formula: C11H18N2O

Molecular Weight: 194.28

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C[C@@H]1CC(=O)N(CC#CCN(C)C)C1

Standard InChI:  InChI=1S/C11H18N2O/c1-10-8-11(14)13(9-10)7-5-4-6-12(2)3/h10H,6-9H2,1-3H3/t10-/m1/s1

Standard InChI Key:  XOOJWROJJGHQPD-SNVBAGLBSA-N

Associated Targets(non-human)

Muscarinic acetylcholine receptor M2 1011 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Muscarinic acetylcholine receptor M1 3437 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Muscarinic receptor M1 and M2 189 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: 194.28Molecular Weight (Monoisotopic): 194.1419AlogP: 0.42#Rotatable Bonds: 2
Polar Surface Area: 23.55Molecular Species: NEUTRALHBA: 2HBD: 0
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 7.98CX LogP: 0.50CX LogD: -0.18
Aromatic Rings: 0Heavy Atoms: 14QED Weighted: 0.59Np Likeness Score: -0.46

References

1. Trybulski EJ, Zhang J, Kramss RH, Mangano RM..  (1993)  The synthesis and biochemical pharmacology of enantiomerically pure methylated oxotremorine derivatives.,  36  (23): [PMID:8246221] [10.1021/jm00075a007]

Source