ID: ALA5192869

Max Phase: Preclinical

Molecular Formula: C18H15FN2O4

Molecular Weight: 342.33

Associated Items:

Representations

Canonical SMILES:  O=C1[C@@H]2Cc3cc(O)c(O)cc3CN2C(=O)N1Cc1ccc(F)cc1

Standard InChI:  InChI=1S/C18H15FN2O4/c19-13-3-1-10(2-4-13)8-21-17(24)14-5-11-6-15(22)16(23)7-12(11)9-20(14)18(21)25/h1-4,6-7,14,22-23H,5,8-9H2/t14-/m0/s1

Standard InChI Key:  DZUDZYVCTGFCTG-AWEZNQCLSA-N

Associated Targets(Human)

Vanilloid receptor 8273 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Transient receptor potential cation channel subfamily M member 8 889 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: 342.33Molecular Weight (Monoisotopic): 342.1016AlogP: 2.13#Rotatable Bonds: 2
Polar Surface Area: 81.08Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.20CX Basic pKa: CX LogP: 2.23CX LogD: 2.23
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.65Np Likeness Score: -0.52

References

1. Di Sarno V, Giovannelli P, Medina-Peris A, Ciaglia T, Di Donato M, Musella S, Lauro G, Vestuto V, Smaldone G, Di Matteo F, Bifulco G, Castoria G, Migliaccio A, Fernandez-Carvajal A, Campiglia P, Gomez-Monterrey I, Ostacolo C, Bertamino A..  (2022)  New TRPM8 blockers exert anticancer activity over castration-resistant prostate cancer models.,  238  [PMID:35598411] [10.1016/j.ejmech.2022.114435]

Source