ID: ALA4164239

Max Phase: Preclinical

Molecular Formula: C23H16FNO3

Molecular Weight: 373.38

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cc(-c2ccc3ccc(C(=O)c4ccc(F)c(O)c4)nc3c2)ccc1O

Standard InChI:  InChI=1S/C23H16FNO3/c1-13-10-15(6-9-21(13)26)16-3-2-14-5-8-19(25-20(14)11-16)23(28)17-4-7-18(24)22(27)12-17/h2-12,26-27H,1H3

Standard InChI Key:  WIUVWFXHLWMQRJ-UHFFFAOYSA-N

Associated Targets(Human)

HSD17B2 Tchem Estradiol 17-beta-dehydrogenase 2 (1671 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSD17B14 Tchem 17-beta-hydroxysteroid dehydrogenase 14 (155 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSD17B1 Tchem Estradiol 17-beta-dehydrogenase 1 (2224 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: 373.38Molecular Weight (Monoisotopic): 373.1114AlogP: 4.99#Rotatable Bonds: 3
Polar Surface Area: 70.42Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.76CX Basic pKa: 1.69CX LogP: 5.67CX LogD: 5.52
Aromatic Rings: 4Heavy Atoms: 28QED Weighted: 0.50Np Likeness Score: -0.41

References

1. Braun F, Bertoletti N, Möller G, Adamski J, Frotscher M, Guragossian N, Madeira Gírio PA, Le Borgne M, Ettouati L, Falson P, Müller S, Vollmer G, Heine A, Klebe G, Marchais-Oberwinkler S..  (2018)  Structure-based design and profiling of novel 17β-HSD14 inhibitors.,  155  [PMID:29859505] [10.1016/j.ejmech.2018.05.029]

Source