ID: ALA3561736

Max Phase: Preclinical

Molecular Formula: C29H25F6N3O2

Molecular Weight: 561.53

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COC(=O)C1=C(C)N(Cc2ccc(C(F)(F)F)cc2)C(NCc2ccccc2C(F)(F)F)=NC1c1ccccc1

Standard InChI:  InChI=1S/C29H25F6N3O2/c1-18-24(26(39)40-2)25(20-8-4-3-5-9-20)37-27(36-16-21-10-6-7-11-23(21)29(33,34)35)38(18)17-19-12-14-22(15-13-19)28(30,31)32/h3-15,25H,16-17H2,1-2H3,(H,36,37)

Standard InChI Key:  HTKUYDWXNWUZMO-UHFFFAOYSA-N

Associated Targets(non-human)

RNA-editing ligase 1, mitochondrial 130 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: 561.53Molecular Weight (Monoisotopic): 561.1851AlogP: 6.87#Rotatable Bonds: 6
Polar Surface Area: 53.93Molecular Species: BASEHBA: 5HBD: 1
#RO5 Violations: 2HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 9.88CX LogP: 6.81CX LogD: 4.66
Aromatic Rings: 3Heavy Atoms: 40QED Weighted: 0.26Np Likeness Score: -0.98

References

1. PubChem BioAssay data set, 

Source

Source(1):