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  1. General Info
  2. Effects Info
  3. Reference
Drug Details
01. General Information
Name Flutamide
PubChem CID 3397
Molecular Weight 276.21g/mol
Synonyms

flutamide, 13311-84-7, Niftolide, Eulexin, Niftholide, niftolid, NFBA, 2-Methyl-N-[4-nitro-3-(trifluoromethyl)phenyl]propanamide, Sch 13521, Drogenil, Cebatrol, veterinary, Flutamidum, Flutamida, Flutamin, 4'-Nitro-3'-trifluoromethylisobutyranilide, Sch-13521, Ham's F-12 medium, N-(4-NITRO-3-(TRIFLUOROMETHYL)PHENYL)ISOBUTYRAMIDE, Flutamidum [INN-Latin], 2-Methyl-N-(4-nitro-3-[trifluoromethyl]phenyl)propanamide, Flutamida [INN-Spanish], SCH13521, Propanamide, 2-methyl-N-[4-nitro-3-(trifluoromethyl)phenyl]-, CCRIS 7246, NSC 215876, alpha,alpha,alpha-Trifluoro-2-methyl-4'-nitro-m-propionotoluidide, EINECS 236-341-9, MFCD00072009, NSC-215876, BRN 2157663, CHEBI:5132, Propanamide, 2-methyl-N-(4-nitro-3-(trifluoromethyl)phenyl)-, DTXSID7032004, UNII-76W6J0943E, CHEMBL806, 76W6J0943E, 4-Nitro-3-(trifluoromethyl)isobutyranilide, 2-Methyl-N-[4-nitro-3-(trifluoromethyl)phenyl]propionamide, DTXCID9011121, Flutamide [USAN:USP:INN:BAN], NCGC00015452-09, Eulexine, Chimax, 4'-Nitro-3'-trifluoromethylisobutyramilide, Flutamidum (INN-Latin), CAS-13311-84-7, m-Propionotoluidide, 2-methyl-4'-nitro-alpha,alpha,alpha-triflouro-, m-Propionotoluidide, alpha,alpha,alpha-trifluoro-2-methyl-4'-nitro-, Flutamida (INN-Spanish), FLUTAMIDE (MART.), FLUTAMIDE [MART.], FLUTAMIDE (USP-RS), FLUTAMIDE [USP-RS], Flutamide USP25, FLUTAMIDE (EP IMPURITY), FLUTAMIDE [EP IMPURITY], FLUTAMIDE (EP MONOGRAPH), FLUTAMIDE [EP MONOGRAPH], FLUTAMIDE (USP MONOGRAPH), FLUTAMIDE [USP MONOGRAPH], Flutamide (USAN:USP:INN:BAN), Prostandril, Odyne, .alpha.,.alpha.,.alpha.-Trifluoro-2-methyl-4'-nitro-m-propionotoluidide, SMR000058187, Eulexin (TN), m-Propionotoluidide,.alpha.,.alpha.-trifluoro-, SR-01000075888, N-[4-Nitro-3-(trifluoromethyl)phenyl]isobutyramide, 2-Methyl-N-(4-nitro-3-(trifluoromethyl)phenyl)propanamide, Flutamid, .alpha.,.alpha.-Trifluoro-2-methyl-4'-nitro-m-propionotoluidide, m-Propionotoluidide,.alpha.,.alpha.-trifluoro-2-methyl-4'-nitro-, 4'-Nitro-3'-(trifluoromethyl)isobutyranilide, Flutamide,(S), Prestwick_228, Flutamide (Eulexin), NK-601, Spectrum_001210, CPD000058187, FLUTAMIDE [INN], FLUTAMIDE [JAN], FLUTAMIDE [MI], FLUTAMIDE [USAN], Prestwick0_000180, Prestwick1_000180, Prestwick2_000180, Prestwick3_000180, Spectrum2_001201, Spectrum3_001421, Spectrum4_000829, Spectrum5_001450, Lopac-F-9397, F0663, Flutamide (pubertal study), F 9397, FLUTAMIDE [WHO-DD], SCHEMBL3934, Lopac0_000557, BSPBio_000079, BSPBio_003122, KBioGR_001377, KBioSS_001690, MLS000069634, MLS001065596, MLS002548892, DivK1c_000459, SPECTRUM1500995, SPBio_000982, SPBio_002000, Flutamide (JP17/USP/INN), BPBio1_000087, GTPL6943, FLUTAMIDE [ORANGE BOOK], CHEMBL4759307, SCHEMBL12932289, HMS501G21, KBio1_000459, KBio2_001690, KBio2_004258, KBio2_006826, KBio3_002342, L02BB01, NINDS_000459, HMS1568D21, HMS1921O16, HMS2090I18, HMS2092O14, HMS2095D21, HMS2230P19, HMS3259I03, HMS3261P15, HMS3373C12, HMS3655G22, HMS3712D21, Pharmakon1600-01500995, AMY32524, BCP23006, HY-B0022, Tox21_110154, Tox21_202169, Tox21_300536, Tox21_500557, BDBM50131270, CCG-39105, NSC147834, NSC215876, NSC757817, s1908, AKOS001025465, AKOS015994751, AKOS025243203, m-Propionotoluidide, .alpha.,.alpha.,.alpha.-trifluoro-2-methyl-4'-nitro-, Tox21_110154_1, AB02835, DB00499, KS-5091, LP00557, NC00451, NSC-147834, NSC-757817, SDCCGSBI-0050540.P004, IDI1_000459, NCGC00015452-01, NCGC00015452-02, NCGC00015452-03, NCGC00015452-04, NCGC00015452-05, NCGC00015452-06, NCGC00015452-07, NCGC00015452-08, NCGC00015452-10, NCGC00015452-11, NCGC00015452-12, NCGC00015452-13, NCGC00015452-14, NCGC00015452-15, NCGC00015452-16, NCGC00015452-19, NCGC00015452-20, NCGC00015452-32, NCGC00091460-01, NCGC00091460-02, NCGC00091460-03, NCGC00091460-04, NCGC00091460-05, NCGC00091460-06, NCGC00091460-07, NCGC00091460-08, NCGC00091460-09, NCGC00254495-01, NCGC00259718-01, NCGC00261242-01, AC-24192, BF166239, SY036411, SBI-0050540.P003, DB-042163, 3'-Trifluoromethyl-4'-Nitro-Isobutyranilide, AB00052188, EU-0100557, FT-0626493, FT-0668764, NS00002675, SW196536-4, 4''-nitro-3''-trifluoromethylisobutyranilide, C07653, D00586, EN300-119548, AB00052188-09, AB00052188_10, AB00052188_11, A806562, Q418669, Q-201131, SR-01000075888-1, SR-01000075888-6, SR-01000075888-7, SR-01000075888-9, BRD-K28307902-001-05-0, Flutamide, certified reference material, TraceCERT(R), Z56755651, Flutamide, European Pharmacopoeia (EP) Reference Standard, N1-[4-nitro-3-(trifluoromethyl)phenyl]-2-methylpropanamide, 2-Methyl-N-[4-nitro-3-(trifluoromethyl)phenyl]propanamide #, Flutamide, United States Pharmacopeia (USP) Reference Standard, 2-methyl-N-[4-nitro-3-(trifluoromethyl)phenyl]propanamide;Flutamide, alpha,alpha,alpha-trifluoro-2-methyl-4''-nitro-m-propionotoluidide, m-Propionotoluidide, 2-methyl-4'-nitro-.alpha.,.alpha.,.alpha.-trifluoro-, Flutamide for system suitability, European Pharmacopoeia (EP) Reference Standard, 37209-54-4

Drug Type Small molecule
Formula C₁₁H₁₁F₃N₂O₃
SMILES CC(C)C(=O)NC1=CC(=C(C=C1)[N+](=O)[O-])C(F)(F)F
InChI 1S/C11H11F3N2O3/c1-6(2)10(17)15-7-3-4-9(16(18)19)8(5-7)11(12,13)14/h3-6H,1-2H3,(H,15,17)
InChIKey MKXKFYHWDHIYRV-UHFFFAOYSA-N
CAS Number 13311-84-7
ChEMBL ID CHEMBL806
ChEBI ID CHEBI:5132
TTD ID D0Y0SW
Drug Bank ID DB00499
KEGG ID C07653
Toxicity Organism Test Type Route(Dose)
rat LD50 intraperitoneal(165 mg/kg)
mouse LD50 intraperitoneal(254 mg/kg)
rat LD50 oral(322 mg/kg)
Structure 2D-img
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2D MOL 3D MOL
02. Combinatorial Therapeutic Effect(s)
Synergistic Effect
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Enhancing Drug Efficacy
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Combination Pair ID: 809
Pair Name Resveratrol, Flutamide
Partner Name Resveratrol
Disease Info [ICD-11: 2C82] Prostate cancer Investigative
Gene Regulation Down-regulation Expression AR hsa367
In Vitro Model LNCaP Prostate carcinoma Homo sapiens (Human) CVCL_0395
PC-3 Prostate carcinoma Homo sapiens (Human) CVCL_0035
DU145 Prostate carcinoma Homo sapiens (Human) CVCL_0105
Result Resveratrol works in concert with antiandrogen flutamide to reduce the amount and activity of AR, suggesting new therapeutic strategies for the treatment of PCa.
03. Reference
No. Title Href
1 Combination of resveratrol and antiandrogen flutamide has synergistic effect on androgen receptor inhibition in prostate cancer cells. Anticancer Res. 2011;31(10):3323-3330. Click
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