ID: ALA5200995

Max Phase: Preclinical

Molecular Formula: C21H25FN2O

Molecular Weight: 340.44

Associated Items:

Representations

Canonical SMILES:  CC[C@@H](O)[C@H]1CCCC2=Cc3c(cnn3-c3ccc(F)cc3)C[C@@]21C

Standard InChI:  InChI=1S/C21H25FN2O/c1-3-20(25)18-6-4-5-15-11-19-14(12-21(15,18)2)13-23-24(19)17-9-7-16(22)8-10-17/h7-11,13,18,20,25H,3-6,12H2,1-2H3/t18-,20-,21+/m1/s1

Standard InChI Key:  FVTPBHZOUZEZIV-NRSPTQNISA-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: 340.44Molecular Weight (Monoisotopic): 340.1951AlogP: 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: 4.42CX LogD: 4.42
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.89Np Likeness Score: 0.04

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