2-(((3,5-Dimethylisoxazol-4-yl)methyl)thio)-1-(4-(2-fluorophenyl)piperazin-1-yl)ethan-1-one

ID: ALA4513309

PubChem CID: 18106212

Max Phase: Preclinical

Molecular Formula: C18H22FN3O2S

Molecular Weight: 363.46

Molecule Type: Unknown

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  Cc1noc(C)c1CSCC(=O)N1CCN(c2ccccc2F)CC1

Standard InChI:  InChI=1S/C18H22FN3O2S/c1-13-15(14(2)24-20-13)11-25-12-18(23)22-9-7-21(8-10-22)17-6-4-3-5-16(17)19/h3-6H,7-12H2,1-2H3

Standard InChI Key:  JSXBFJSTDXQCOA-UHFFFAOYSA-N

Molfile:  

 
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M  END

Associated Targets(Human)

AR Tclin Androgen Receptor (11781 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

Calculated Properties

Molecular Weight: 363.46Molecular Weight (Monoisotopic): 363.1417AlogP: 3.01#Rotatable Bonds: 5
Polar Surface Area: 49.58Molecular Species: NEUTRALHBA: 5HBD:
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 1.54CX LogP: 2.23CX LogD: 2.23
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.82Np Likeness Score: -2.52

References

1. Johnson JK, Skoda EM, Zhou J, Parrinello E, Wang D, O'Malley K, Eyer BR, Kazancioglu M, Eisermann K, Johnston PA, Nelson JB, Wang Z, Wipf P..  (2016)  Small Molecule Antagonists of the Nuclear Androgen Receptor for the Treatment of Castration-Resistant Prostate Cancer.,  (8): [PMID:27563404] [10.1021/acsmedchemlett.6b00186]

Source