4-Mercapto-6-methyl-1-((5-methylfuran-2-yl)methylene)furo[3,4-c]pyridin-3(1H)-one

ID: ALA519058

Max Phase: Preclinical

Molecular Formula: C14H11NO3S

Molecular Weight: 273.31

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cc2c(c(=S)[nH]1)C(=O)O/C2=C\c1ccc(C)o1

Standard InChI:  InChI=1S/C14H11NO3S/c1-7-5-10-11(6-9-4-3-8(2)17-9)18-14(16)12(10)13(19)15-7/h3-6H,1-2H3,(H,15,19)/b11-6-

Standard InChI Key:  UCKLIUAJVINKBS-WDZFZDKYSA-N

Associated Targets(Human)

PRF1 Tchem Perforin-1 (540 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TNFSF10 Tchem Tumor necrosis factor ligand superfamily member 10 (21 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FASLG Tbio Tumor necrosis factor ligand superfamily member 6 (2 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Salmonella typhimurium (15756 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ply Pneumolysin (3 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: 273.31Molecular Weight (Monoisotopic): 273.0460AlogP: 3.62#Rotatable Bonds: 1
Polar Surface Area: 55.23Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 10.23CX Basic pKa: CX LogP: 1.64CX LogD: 1.64
Aromatic Rings: 2Heavy Atoms: 19QED Weighted: 0.64Np Likeness Score: -0.53

References

1. Lena G, Trapani JA, Sutton VR, Ciccone A, Browne KA, Smyth MJ, Denny WA, Spicer JA..  (2008)  Dihydrofuro[3,4-c]pyridinones as inhibitors of the cytolytic effects of the pore-forming glycoprotein perforin.,  51  (23): [PMID:19007200] [10.1021/jm801063n]
2. Spicer JA, Huttunen KM, Jose J, Dimitrov I, Akhlaghi H, Sutton VR, Voskoboinik I, Trapani J..  (2022)  Small Molecule Inhibitors of Lymphocyte Perforin as Focused Immunosuppressants for Infection and Autoimmunity.,  65  (21.0): [PMID:36263926] [10.1021/acs.jmedchem.2c01338]

Source