ID: ALA4855956

Max Phase: Preclinical

Molecular Formula: C19H20N8

Molecular Weight: 360.43

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Nc1cc(Cc2ccn(Cc3ccc4c(c3)CCNC4)n2)c2nn[nH]c2n1

Standard InChI:  InChI=1S/C19H20N8/c20-17-9-15(18-19(22-17)24-26-23-18)8-16-4-6-27(25-16)11-12-1-2-14-10-21-5-3-13(14)7-12/h1-2,4,6-7,9,21H,3,5,8,10-11H2,(H3,20,22,23,24,26)

Standard InChI Key:  KCEPIJYYUSUAFH-UHFFFAOYSA-N

Associated Targets(Human)

Myeloperoxidase 1002 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Thyroid peroxidase 64 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cytochrome P450 3A4 53859 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: 360.43Molecular Weight (Monoisotopic): 360.1811AlogP: 1.42#Rotatable Bonds: 4
Polar Surface Area: 110.33Molecular Species: BASEHBA: 7HBD: 3
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.27CX Basic pKa: 9.13CX LogP: 0.95CX LogD: 0.28
Aromatic Rings: 4Heavy Atoms: 27QED Weighted: 0.51Np Likeness Score: -0.93

References

1. Hu CH, Neissel Valente MW, Halpern OS, Jusuf S, Khan JA, Locke GA, Duke GJ, Liu X, Duclos FJ, Wexler RR, Kick EK, Smallheer JM..  (2021)  Small molecule and macrocyclic pyrazole derived inhibitors of myeloperoxidase (MPO).,  42  [PMID:33811992] [10.1016/j.bmcl.2021.128010]

Source