ID: ALA2391685

Max Phase: Preclinical

Molecular Formula: C30H30F6N4O5S

Molecular Weight: 446.62

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C([O-])C(F)(F)F.O=C([O-])C(F)(F)F.c1ccc2c(c1)c1cc[n+]2CCSCC[n+]2ccc(c3ccccc32)NCCOCCN1

Standard InChI:  InChI=1S/C26H28N4OS.2C2HF3O2/c1-3-7-25-21(5-1)23-9-13-29(25)15-19-32-20-16-30-14-10-24(22-6-2-4-8-26(22)30)28-12-18-31-17-11-27-23;2*3-2(4,5)1(6)7/h1-10,13-14H,11-12,15-20H2;2*(H,6,7)/b27-23+,28-24+;;

Standard InChI Key:  IZKYFGZAHFXSNN-UQHZGTLSSA-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: 446.62Molecular Weight (Monoisotopic): 446.2129AlogP: 3.86#Rotatable Bonds: 0
Polar Surface Area: 41.05Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: -5.25CX LogD: -5.25
Aromatic Rings: 4Heavy Atoms: 32QED Weighted: 0.40Np Likeness Score: -0.18

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