Therapeutic Targets Database
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TTD Drug ID: DAP000778

Drug Information
NameEtodolac    
Synonyms1,8-Diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid; E 0516; 1,3,4,9-Tetrahydro-1,8-diethylpyrano(3,4-b)indole-1-acetic acid; Edolan; KBioGR_000680; MLS000028474; Spectrum4_000410; SPECTRUM1501005; CID3308; 1,8-Diethyl-1,3,4,9-tetrahydropyrano(3,4-b)indole-1-acetic acid; BPBio1_000333; Etodolac, (+-)-Isomer; D00315; Etodolac, Monosodium Salt, (S)-Isomer; Lodine SR; Prestwick1_000231; 41340-25-4; NSC 282126; Etodolac, Monosodium Salt, (+-) Isomer; Osteluc; AC1L1FN2; Etodolic acid; Prestwick_209; SPBio_002222; HMS2092O20; NCGC00015399-04; LS-7393; E0516_SIGMA; SPBio_001374; D017308; CCRIS 3923; DivK1c_000147; HMS500H09; AC-4231; etodolac; Hypen; Spectrum_001244; Prestwick2_000231; Etodolac (JP15/USP/INN); AB00052194; Prestwick0_000231; MLS001077315; BSPBio_000301; NINDS_000147; Etodolac [USAN:INN:BAN]; KBio2_001724; SBB067257; AY24236; KBioSS_001724; 2-(1,8-diethyl-4,9-dihydro-3H-pyrano[3,4-b]indol-1-yl)acetic acid; Ramodar; NCGC00089769-05; (+-)-1,8-Diethyl-1,3,4,9-tetrahydropyrano(3,4-b)indole-1-acetic acid; IDI1_000147; Acid, Etodolic; CHEBI:4909; Lodine; CPD000058443; NCGC00089769-04; Pyrano[3,4-b]indole-1-acetic acid, 1,8-diethyl-1,3,4,9-tetrahydro-; (1,8-Diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indol-1-yl)acetic acid; (1,8-Diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indol-1-yl)acetic acid; 1,8-Diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid; Pyrano[3,4-b]indole-1-acetic acid, 1,8-diethyl-1,3,4,9-tetrahydro-; AY 24,236; RAK-591; AY24,236; Etodolacetodolic acid; Lodine XL; AY-24236; AY 24236; Etodolaco; Prestwick3_000231; Pyrano(3,4-b)indole-1-acetic acid, 1,8-diethyl-1,3,4,9-tetrahydro-(+-)-; Etodolacum [INN-Latin]; CHEMBL622; Etodolac [USAN:BAN:INN]; BRD-A74667430-001-05-3; Ultradol; Lodine (TN); Spectrum2_001387; KBio2_004292; Lopac0_000479; Spectrum3_001429; KBio1_000147; Etodolaco [INN-Spanish]; NCGC00089769-07; NCGC00089769-03; MolPort-001-759-084; [1,8-diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indol-1-yl]acetic acid; HMS1921B09; NCGC00015399-11; KBio2_006860; KBio3_002358; SMR000058443; DB00749; 110781-63-0 (mono-hydrochloride salt); SAM002589968; AY-24,236; Etodolacum; NCGC00089769-06; NSC282126; Etodolac, Monosodium Salt; NCGC00089769-02; 1,8-diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indol-1-ylacetic acid; Spectrum5_001347; HMS1568P03; CHEBI:126431; EU-0100479; UNII-2M36281008; Pyrano(3,4-b)indole-1-acetic acid, 1,3,4,9-tetrahydro-1,8-diethyl-; Pyrano(3,4-b)indole-1-acetic acid, 1,8-diethyl-1,3,4,9-tetrahydro-; BSPBio_003138    
Trade NameLodine SR; Eccoxolac    
CompanyMeda Pharmaceuticals    
IndicationPainApproved    [1]
Structure

Click to save drug structure in 3D MOL format

Click to save drug structure in 2D MOL format
   
Therapeutic ClassAnalgesics    
CAS NumberCAS 41340-25-4
FormularC17H21NO3    
PubChem Compound IDCID 3308.    
PubChem Substance IDSID 143623.    
SuperDrug ATC IDM01AB08;    
SuperDrug CAS ID041340254;    
TargetProstaglandin G/H synthase 2Inhibitor[2][3]
Ref 1FDA Approved Drug Products from FDA Official Website. 2009. Application Number: (ANDA) 074819 To Reference
Ref 2Membranous nephropathy associated with the relatively selective cyclooxygenase-2 inhibitor, etodolac, in a patient with early rheumatoid arthritis. Intern Med. 2007;46(13):1055-8. Epub 2007 Jul 2. To Reference
Ref 3Induction of apoptosis by cyclooxygenase-2 inhibitors in prostate cancer cell lines. Int J Urol. 2001 Jul;8(7):S35-9. To Reference



 

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