ID: ALA5207591

Max Phase: Preclinical

Molecular Formula: C22H25FN2O

Molecular Weight: 352.45

Associated Items:

Representations

Canonical SMILES:  C[C@]12Cc3cnn(-c4ccc(F)cc4)c3C=C1CCC[C@@H]2[C@@H](O)C1CC1

Standard InChI:  InChI=1S/C22H25FN2O/c1-22-12-15-13-24-25(18-9-7-17(23)8-10-18)20(15)11-16(22)3-2-4-19(22)21(26)14-5-6-14/h7-11,13-14,19,21,26H,2-6,12H2,1H3/t19-,21+,22+/m1/s1

Standard InChI Key:  KQBIQSVMSPEZDP-HJNYFJLDSA-N

Associated Targets(non-human)

Glucocorticoid receptor 1330 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: 352.45Molecular Weight (Monoisotopic): 352.1951AlogP: 4.53#Rotatable Bonds: 3
Polar Surface Area: 38.05Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 1.60CX LogP: 4.32CX LogD: 4.32
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.88Np Likeness Score: -0.01

References

1. Lato AM, Burke SJ, Ducote MP, Kennedy BJ, Collier JJ, Campagna SR..  (2022)  Stereoisomers of an Aryl Pyrazole Glucocorticoid Receptor Agonist Scaffold Elicit Differing Anti-inflammatory Responses.,  13  (9.0): [PMID:36105346] [10.1021/acsmedchemlett.2c00299]

Source