ID: ALA5189518

Max Phase: Preclinical

Molecular Formula: C26H18F3N5S

Molecular Weight: 489.53

Associated Items:

Representations

Canonical SMILES:  FC(F)(F)c1cccc(Nc2nc(Nc3ccc(-c4ccsc4)cn3)ncc2-c2ccccc2)c1

Standard InChI:  InChI=1S/C26H18F3N5S/c27-26(28,29)20-7-4-8-21(13-20)32-24-22(17-5-2-1-3-6-17)15-31-25(34-24)33-23-10-9-18(14-30-23)19-11-12-35-16-19/h1-16H,(H2,30,31,32,33,34)

Standard InChI Key:  QMKNNEGMFCGQTO-UHFFFAOYSA-N

Associated Targets(Human)

Dipeptidyl peptidase I 1385 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 489.53Molecular Weight (Monoisotopic): 489.1235AlogP: 7.77#Rotatable Bonds: 6
Polar Surface Area: 62.73Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 10.22CX Basic pKa: 3.07CX LogP: 7.53CX LogD: 7.53
Aromatic Rings: 5Heavy Atoms: 35QED Weighted: 0.26Np Likeness Score: -1.66

References

1. Chen X, Yan Y, Du J, Shen X, He C, Pan H, Zhu J, Liu X..  (2022)  Non-peptidyl non-covalent cathepsin C inhibitoEEr bearing a unique thiophene-substituted pyridine: Design, structure-activity relationship and anti-inflammatory activity in vivo.,  236  [PMID:35429909] [10.1016/j.ejmech.2022.114368]

Source