Drug

D0056 | Fenoprofen

Molecular Formula C15H14O3
Molecular Weight 242.27
Structure
State solid
Protein binding 99% to albumin.
Half life Plasma half-life is approximately 3 hours.
Absorption Rapidly absorbed under fasting conditions, and peak plasma levels of 50 µg/mL are achieved within 2 hours after oral administration of 600 mg doses.
Trade names Nalfon
Description nonsteroidal anti-inflammatory drug (NSAID); anti-inflammatory analgesic and antipyretic

M

M01AE04 Fenoprofen


[M01AE] Propionic acid derivatives


[M01A] ANTIINFLAMMATORY AND ANTIRHEUMATIC PRODUCTS, NON-STEROIDS


[M01] ANTIINFLAMMATORY AND ANTIRHEUMATIC PRODUCTS


[M] Musculoskeletal system


Pictogram Signal Statements Precautionary Statement Codes
Warning

Aggregated GHS information provided by 40 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.


H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]


H312 (97.5%): Harmful in contact with skin [Warning Acute toxicity, dermal]


H332 (97.5%): Harmful if inhaled [Warning Acute toxicity, inhalation]


Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown.


P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, and P501; (The corresponding statement to each P-code can be found at the GHS Classification page.)
Warning

The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.


H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]


P264, P270, P301+P312, P330, and P501; (The corresponding statement to each P-code can be found at the GHS Classification page.)

Organism Test type Route Dose (normalized dose) Effect Source
rat LD oral > 200mg/kg (200mg/kg) gastrointestinal: ulceration or bleeding from stomach Toxicology and Applied Pharmacology. Vol. 52, Pg. 454, 1980.
rat LD50 oral 415mg/kg (415mg/kg) Kiso to Rinsho. Clinical Report. Vol. 14, Pg. 4385, 1980.
human TDLo oral 4286ug/kg (4.286mg/kg) endocrine: evidence of thyroid hyperfunction British Medical Journal. Vol. 292, Pg. 1560, 1986.
women TDLo oral 720mg/kg/30D- (720mg/kg) kidney, ureter, and bladder: "changes in tubules (including acute renal failure, acute tubular necrosis)" JAMA, Journal of the American Medical Association. Vol. 242, Pg. 1896, 1979.
man TDLo oral 521mg/kg/17W- (521mg/kg) Annals of Internal Medicine. Vol. 93, Pg. 508, 1980.
women TDLo oral 1898mg/kg/12W (1898mg/kg) Annals of Internal Medicine. Vol. 92, Pg. 72, 1980.
rat LD50 intravenous 526mg/kg (526mg/kg) Yakkyoku. Pharmacy. Vol. 34, Pg. 363, 1983.
rat LD50 intraperitoneal 234mg/kg (234mg/kg) Yakkyoku. Pharmacy. Vol. 34, Pg. 363, 1983.
mouse LD50 oral 439mg/kg (439mg/kg) Yaoxue Tongbao. Bulletin of Pharmacology. Vol. 21, Pg. 36, 1986.
mouse LD50 oral 1400mg/kg (1400mg/kg) United States Patent Document. Vol. #3985779,
mouse LD50 subcutaneous 463mg/kg (463mg/kg) Yakkyoku. Pharmacy. Vol. 34, Pg. 363, 1983.
rat LD50 subcutaneous 366mg/kg (366mg/kg) Iyakuhin Kenkyu. Study of Medical Supplies. Vol. 13, Pg. 1128, 1982.
women TDLo oral 9386mg/kg/1Y- (9386mg/kg) kidney, ureter, and bladder: interstitial nephritis New England Journal of Medicine. Vol. 301, Pg. 1271, 1979.
mouse LD50 intravenous 471mg/kg (471mg/kg) Yakkyoku. Pharmacy. Vol. 34, Pg. 363, 1983.
women LDLo oral 8748mg/kg/35W (8748mg/kg) American Journal of Medicine. Vol. 72, Pg. 81, 1982.
women TDLo oral 5832mg/kg/35W (5832mg/kg) American Journal of Medicine. Vol. 72, Pg. 81, 1982.
women TDLo oral 1092mg/kg/13W (1092mg/kg) Mayo Clinic Proceedings. Vol. 55, Pg. 103, 1980.
mouse LD50 intraperitoneal 286mg/kg (286mg/kg) Yakkyoku. Pharmacy. Vol. 34, Pg. 363, 1983.

  • Arthritis

  • Osteoarthritis

  • Pain

  • Rheumatoid arthritis

  • (+-)-2-(3-Phenoxyphenyl)propionic acid (+-)-m-Phenoxyhydratropic acid (+/-)-Fenoprofen
    (+/-)-m-phenoxyhydratropic acid (.+/-.)-m-Phenoxyhydratropic acid 2-(3-Phenoxy-phenyl)-propionic acid
    2-(3-Phenoxyphenyl)propanoic acid 2-(3-Phenoxyphenyl)propanoic acid # 2-(3-Phenoxyphenyl)propionic acid
    2-(3-phenoxyphenyl)-propionic acid 2-(m-phenoxyphenyl)propionic acid 2-[3-(phenyloxy)phenyl]propanoic acid
    29679-58-1 3-Phenoxyhydratropic acid 3-phenoxy-hydratropic acid
    31879-05-7 4CH-007316 53746-45-5
    879F057 AB00052197 AB00052197-04
    AB00052197_05 AB00052197_06 AB0065019
    AK116448 AKOS005256238 AS-30559
    BBL100921 BDBM54705 BPBio1_000846
    BRN 2118687 BSPBio_000768 Benzeneacetic acid, .alpha.-methyl-3-phenoxy-, (.+/-.)-
    Benzeneacetic acid, a-methyl-3-phenoxy-, (as)- Benzeneacetic acid, alpha-methyl-3-phenoxy- Benzeneacetic acid, alpha-methyl-3-phenoxy-, (+-)-
    Benzeneacetic acid, |A-methyl-3-phenoxy- C06997 CCG-39009
    CHEBI:5004 CHEMBL1297 CTK4G3649
    D02350 DB00573 DL-2-(3-phenoxyphenyl)propionic acid
    DS-017185 DTXSID9023045 Di-benzeneacetate, .alpha.-methyl-3-phenoxy-, calcium salt, dihydrate
    DivK1c_000848 EINECS 249-770-1 EINECS 250-850-3
    Epitope ID:139975 Feneprofen calcium salt dihydrate Fenoprofen (USAN/INN)
    Fenoprofen Dihydrate, Calcium Salt Fenoprofen [USAN:BAN:INN] Fenoprofen [USAN:INN:BAN]
    Fenoprofen calcium Fenoprofen calcium hydrate FenoprofenCa
    Fenoprofene Fenoprofene [INN-French] Fenoprofeno
    Fenoprofeno [INN-Spanish] Fenoprofenum Fenoprofenum [INN-Latin]
    GTPL4820 HMS1921B19 HMS2090G18
    HMS2092B07 HMS502K10 HSDB 3328
    Hydratropic acid, m-phenoxy-, (+-)- Hydratropic acid, m-phenoxy-, (.+/-.)- IDI1_000848
    J-018559 KBio1_000848 KBio2_001732
    KBio2_004300 KBio2_006868 KBio3_001860
    KBioGR_001477 KBioSS_001732 LS-76362
    Lilly 53838 Lilly 53858 Lilly-53858
    M-8808 MCULE-2686503876 N6-[2-[[4-(Diethylamino)-1-methylbu-tyl]amino]-6-methyl-4-pyrimidinyl]-2-methyl-4,6-qu-inolinediamine trihydrochloride
    NCGC00094887-01 NCGC00094887-02 NCGC00094887-03
    NINDS_000848 NSC-757813 NSC757813
    Nalfon Pharmakon1600-01501011 Prestwick0_000754
    Prestwick1_000754 Prestwick2_000754 Prestwick3_000754
    Q2555245 RDJGLLICXDHJDY-UHFFFAOYSA-N SBI-0051632.P002
    SCHEMBL3797 SPBio_001402 SPBio_002707
    SPECTRUM1501011 SR-05000001767 SR-05000001767-1
    ST24027516 STL554715 Spectrum2_001391
    Spectrum3_000910 Spectrum4_001009 Spectrum5_001311
    Spectrum_001252 UNM-0000306101 Z4588
    alpha-(m-phenoxyphenyl)-propionic acid alpha-(m-phenoxyphenyl)propionic acid alpha-Methyl-3-phenoxybenzeneacetic acid
    calcium;2-(3-phenoxyphenyl)propanoic acid;hydrate calcium;2-(3-phenoxyphenyl)propionic acid;hydrate cid_16219353
    fenoprofen

    DrugBank Name Fenoprofen
    DrugBank DB00573
    CAS Number 1177865-17-6, 29679-58-1, 31879-05-7, 34597-40-5, 53746-45-5, 71720-56-4, 95907-05-4
    PubChem Compound 3342
    KEGG Compound ID C06997
    KEGG Drug D00968
    PubChem.Substance 46504597
    ChEBI 5004
    PharmGKB PA449597
    ChemSpider 3225
    BindingDB 54705.0
    TTD DAP000619
    Wikipedia Fenoprofen
    DPD 11356

    1. Dykens et al. (2007)
    2. Chan et al. (2005)