ID: ALA3659169

Max Phase: Preclinical

Molecular Formula: C25H26FN9O

Molecular Weight: 487.54

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  [C-]#[N+]c1c(F)ccc([C@@H]2CN3CCN(C(=O)C4CCc5cc(-n6cnnn6)cnc54)C[C@H]3CN2)c1C

Standard InChI:  InChI=1S/C25H26FN9O/c1-15-19(5-6-21(26)23(15)27-2)22-13-33-7-8-34(12-18(33)11-28-22)25(36)20-4-3-16-9-17(10-29-24(16)20)35-14-30-31-32-35/h5-6,9-10,14,18,20,22,28H,3-4,7-8,11-13H2,1H3/t18-,20?,22+/m1/s1

Standard InChI Key:  ZIBROJNRLAFASA-PJDJYQKSSA-N

Associated Targets(non-human)

ATP-sensitive inward rectifier potassium channel 1 313 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: 487.54Molecular Weight (Monoisotopic): 487.2244AlogP: 1.94#Rotatable Bonds: 3
Polar Surface Area: 96.43Molecular Species: NEUTRALHBA: 8HBD: 1
#RO5 Violations: 0HBA (Lipinski): 10HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 7.48CX LogP: -0.41CX LogD: -0.49
Aromatic Rings: 3Heavy Atoms: 36QED Weighted: 0.56Np Likeness Score: -1.18

References

1.  (2015)  Inhibitors of the renal outer medullary potassium channel, 

Source

Source(1):