ID: ALA3659163

Max Phase: Preclinical

Molecular Formula: C25H25FN8O2

Molecular Weight: 488.53

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  [C-]#[N+]c1ccc([C@H]2CN3CCN(C(=O)C4CCc5cc(-n6cnnn6)ncc54)C[C@H]3CO2)c(C)c1F

Standard InChI:  InChI=1S/C25H25FN8O2/c1-15-18(5-6-21(27-2)24(15)26)22-12-32-7-8-33(11-17(32)13-36-22)25(35)19-4-3-16-9-23(28-10-20(16)19)34-14-29-30-31-34/h5-6,9-10,14,17,19,22H,3-4,7-8,11-13H2,1H3/t17-,19?,22+/m0/s1

Standard InChI Key:  FLDUIMICEOVVQD-JJKBQAIRSA-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: 488.53Molecular Weight (Monoisotopic): 488.2085AlogP: 2.37#Rotatable Bonds: 3
Polar Surface Area: 93.63Molecular Species: NEUTRALHBA: 8HBD: 0
#RO5 Violations: 0HBA (Lipinski): 10HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 4.05CX LogP: 0.11CX LogD: 0.11
Aromatic Rings: 3Heavy Atoms: 36QED Weighted: 0.52Np Likeness Score: -1.27

References

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

Source

Source(1):