ID: ALA2391820

Max Phase: Preclinical

Molecular Formula: C31H32F6N4O5

Molecular Weight: 410.57

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C1=C\CNc2cc[n+](c3ccccc23)CCCCC[n+]2ccc(c3ccccc32)NC/1.O.O=C([O-])C(F)(F)F.O=C([O-])C(F)(F)F

Standard InChI:  InChI=1S/C27H28N4.2C2HF3O2.H2O/c1-8-18-30-20-14-24(22-10-2-4-12-26(22)30)28-16-6-7-17-29-25-15-21-31(19-9-1)27-13-5-3-11-23(25)27;2*3-2(4,5)1(6)7;/h2-7,10-15,20-21H,1,8-9,16-19H2;2*(H,6,7);1H2/b7-6-,28-24+,29-25+;;;

Standard InChI Key:  WLIWTBXOHBNAAN-ICRBSXOJSA-N

Associated Targets(non-human)

Small conductance calcium-activated potassium channel protein 3 210 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: 410.57Molecular Weight (Monoisotopic): 410.2459AlogP: 4.83#Rotatable Bonds: 0
Polar Surface Area: 31.82Molecular Species: NEUTRALHBA: 2HBD: 2
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: -4.19CX LogD: -4.19
Aromatic Rings: 4Heavy Atoms: 31QED Weighted: 0.32Np Likeness Score: 0.25

References

1. Yang D, Arifhodzic L, Ganellin CR, Jenkinson DH..  (2013)  Further studies on bis-charged tetraazacyclophanes as potent inhibitors of small conductance Ca(2+)-activated K+ channels.,  63  [PMID:23685886] [10.1016/j.ejmech.2013.02.029]

Source