ID: ALA5091477

Max Phase: Preclinical

Molecular Formula: C21H15F3N2O3

Molecular Weight: 400.36

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1ccc2c(c1)Oc1ccccc1C2NC(=O)c1ccc(C(F)(F)F)[nH]c1=O

Standard InChI:  InChI=1S/C21H15F3N2O3/c1-11-6-7-13-16(10-11)29-15-5-3-2-4-12(15)18(13)26-20(28)14-8-9-17(21(22,23)24)25-19(14)27/h2-10,18H,1H3,(H,25,27)(H,26,28)

Standard InChI Key:  FUPWKQSZHNEKIW-UHFFFAOYSA-N

Associated Targets(Human)

Estradiol 17-beta-dehydrogenase 1 2224 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Estradiol 17-beta-dehydrogenase 2 1671 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Peroxisomal multifunctional enzyme type 2 123 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Endoplasmic reticulum-associated amyloid beta-peptide-binding protein 20669 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 400.36Molecular Weight (Monoisotopic): 400.1035AlogP: 4.33#Rotatable Bonds: 2
Polar Surface Area: 71.19Molecular Species: NEUTRALHBA: 3HBD: 2
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.38CX Basic pKa: CX LogP: 3.37CX LogD: 3.37
Aromatic Rings: 3Heavy Atoms: 29QED Weighted: 0.67Np Likeness Score: -0.81

References

1.  (2021)  Modulators of hsd17b13 and methods of use thereof, 

Source