ID: ALA242990

Max Phase: Preclinical

Molecular Formula: C41H64N4O4

Molecular Weight: 676.99

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccccc1CNCCCCCC(=O)N1CCC(CCCC2CCN(C(=O)CCCCCNCc3ccccc3OC)CC2)CC1

Standard InChI:  InChI=1S/C41H64N4O4/c1-48-38-18-9-7-16-36(38)32-42-26-11-3-5-20-40(46)44-28-22-34(23-29-44)14-13-15-35-24-30-45(31-25-35)41(47)21-6-4-12-27-43-33-37-17-8-10-19-39(37)49-2/h7-10,16-19,34-35,42-43H,3-6,11-15,20-33H2,1-2H3

Standard InChI Key:  ZYVBLECRVSYZOD-UHFFFAOYSA-N

Associated Targets(Human)

Muscarinic acetylcholine receptor M2 10671 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Muscarinic acetylcholine receptor M4 6041 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Muscarinic acetylcholine receptor M3 1154 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: 676.99Molecular Weight (Monoisotopic): 676.4928AlogP: 7.35#Rotatable Bonds: 22
Polar Surface Area: 83.14Molecular Species: BASEHBA: 6HBD: 2
#RO5 Violations: 2HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 9.34CX LogP: 6.07CX LogD: 2.80
Aromatic Rings: 2Heavy Atoms: 49QED Weighted: 0.13Np Likeness Score: -0.35

References

1. Tumiatti V, Minarini A, Milelli A, Rosini M, Buccioni M, Marucci G, Ghelardini C, Bellucci C, Melchiorre C..  (2007)  Structure-activity relationships of methoctramine-related polyamines as muscarinic antagonist: effect of replacing the inner polymethylene chain with cyclic moieties.,  15  (6): [PMID:17276075] [10.1016/j.bmc.2007.01.022]

Source