ID: ALA3659159

Max Phase: Preclinical

Molecular Formula: C27H28FN7O4

Molecular Weight: 533.56

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C[C@@H]1Cc2c(ccc([C@@H]3CN4CCN(C(=O)C5CCc6nc(-n7cnnn7)ccc65)C[C@@H]4CO3)c2F)C(=O)O1

Standard InChI:  InChI=1S/C27H28FN7O4/c1-15-10-21-19(27(37)39-15)2-3-20(25(21)28)23-12-33-8-9-34(11-16(33)13-38-23)26(36)18-4-6-22-17(18)5-7-24(30-22)35-14-29-31-32-35/h2-3,5,7,14-16,18,23H,4,6,8-13H2,1H3/t15-,16-,18?,23+/m1/s1

Standard InChI Key:  SOSQLHPGHQRBCR-DQSLTDSHSA-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: 533.56Molecular Weight (Monoisotopic): 533.2187AlogP: 1.61#Rotatable Bonds: 3
Polar Surface Area: 115.57Molecular Species: NEUTRALHBA: 10HBD: 0
#RO5 Violations: 1HBA (Lipinski): 11HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 4.23CX LogP: 2.01CX LogD: 2.01
Aromatic Rings: 3Heavy Atoms: 39QED Weighted: 0.46Np Likeness Score: -1.05

References

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

Source

Source(1):