Responsive image

Common name


Nilutamide

IUPAC name


5,5-dimethyl-3-[4-nitro-3-(trifluoromethyl)phenyl]imidazolidine-2,4-dione

SMILES


CC1(C)NC(=O)N(C1=O)C1=CC(=C(C=C1)[N+]([O-])=O)C(F)(F)F

Compound class


Antineoplastic Agents; Androgen Antagonists; Antineoplastic and Immunomodulating Agents; Endocrine Therapy; Hormone Antagonists and Related Agents; Anti-Androgens; Cytochrome P-450 CYP2C9 Inhibitors; Cytochrome P-450 CYP2C8 Inhibitors; Cytochrome P-450 CYP2C9 Inducers; Cytochrome P-450 CYP2C19 Inducers; Cytochrome P-450 CYP2C8 Inducers;

Therapeutic area


For use in combination with surgical castration for the treatment of metastatic prostate cancer involving distant lymph nodes, bone, or visceral organs (Stage D2).

Common name


Nilutamide

IUPAC name


5,5-dimethyl-3-[4-nitro-3-(trifluoromethyl)phenyl]imidazolidine-2,4-dione

SMILES


CC1(C)NC(=O)N(C1=O)C1=CC(=C(C=C1)[N+]([O-])=O)C(F)(F)F

INCHI


InChI=1S/C12H10F3N3O4/c1-11(2)9(19)17(10(20)16-11)6-3-4-8(18(21)22)7(5-6)12(13,14)15/h3-5H,1-2H3,(H,16,20)

FORMULA


C12H10F3N3O4

Responsive image

Common name


Nilutamide

IUPAC name


5,5-dimethyl-3-[4-nitro-3-(trifluoromethyl)phenyl]imidazolidine-2,4-dione

Molecular weight


317.221

clogP


1.255

clogS


-3.577

HBond Acceptor


4

HBond Donor


1

Total Polar
Surface Area


101.22

Number of Rings


2

Rotatable Bond


3

Drug ID Common name Structure CAS SMILE Frequency
FDBF00177 fluoroform Responsive image FC(F)F 0.0704
FDBF00779 nitrobenzene Responsive image O=N(=O)c1ccccc1 0.0134
FDBF01107 1-nitro-2-(trifluoromethyl)benzene Responsive image FC(F)(F)c1ccccc1N(=O)=O 0.0007
FDBF01538 5,5-dimethylimidazolidine-2,4-dione Responsive image O=C1NC(=O)NC1(C)C 0.0003
4 , 1