ID: ALA4453626

Max Phase: Preclinical

Molecular Formula: C20H19FN6O2

Molecular Weight: 394.41

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=C(NCc1ncccc1F)c1cnc(CCNCc2nc3ccccc3[nH]2)o1

Standard InChI:  InChI=1S/C20H19FN6O2/c21-13-4-3-8-23-16(13)10-25-20(28)17-11-24-19(29-17)7-9-22-12-18-26-14-5-1-2-6-15(14)27-18/h1-6,8,11,22H,7,9-10,12H2,(H,25,28)(H,26,27)

Standard InChI Key:  LQZZWBRMBZQXRE-UHFFFAOYSA-N

Associated Targets(Human)

SLC40A1 Tchem Solute carrier family 40 member 1 (725 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Slc40a1 Solute carrier family 40 member 1 (216 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 394.41Molecular Weight (Monoisotopic): 394.1554AlogP: 2.35#Rotatable Bonds: 8
Polar Surface Area: 108.73Molecular Species: NEUTRALHBA: 6HBD: 3
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.23CX Basic pKa: 7.86CX LogP: 0.59CX LogD: 0.01
Aromatic Rings: 4Heavy Atoms: 29QED Weighted: 0.40Np Likeness Score: -1.78

References

1.  (2018)  Novel Ferroportin Inhibitors, 

Source