ID: ALA5280897

Max Phase: Preclinical

Molecular Formula: C13H12FNO2S

Molecular Weight: 265.31

Associated Items:

Representations

Canonical SMILES:  CC(C)C(=O)c1sc(-c2cccc(F)c2)nc1O

Standard InChI:  InChI=1S/C13H12FNO2S/c1-7(2)10(16)11-12(17)15-13(18-11)8-4-3-5-9(14)6-8/h3-7,17H,1-2H3

Standard InChI Key:  JIOMSJAFXSIVFK-UHFFFAOYSA-N

Associated Targets(Human)

Transient receptor potential cation channel subfamily M member 8 1168 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: 265.31Molecular Weight (Monoisotopic): 265.0573AlogP: 3.49#Rotatable Bonds: 3
Polar Surface Area: 50.19Molecular Species: ACIDHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 5.75CX Basic pKa: CX LogP: 4.67CX LogD: 3.33
Aromatic Rings: 2Heavy Atoms: 18QED Weighted: 0.86Np Likeness Score: -1.35

References

1. Bianchini G, Tomassetti M, Lillini S, Sirico A, Bovolenta S, Za L, Liberati C, Novelli R, Aramini A..  (2021)  Discovery of Novel TRPM8 Blockers Suitable for the Treatment of Somatic and Ocular Painful Conditions: A Journey through pKa and LogD Modulation.,  64  (22): [PMID:34762442] [10.1021/acs.jmedchem.1c01647]

Source