Therapeutic Targets Database
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TTD Drug ID: DAP000714

Drug Information
NameOseltamivir
SynonymsRo-64-0796; 1-Cyclohexene-1-carboxylic acid, 4-(acetylamino)-5-amino-3-(1-ethylpropoxy)-, ethyl ester, (3R-(3alpha,4beta,5alpha))-; C08092; ethyl (3R,4R,5S)-4-acetamido-5-amino-3-pentan-3-yloxycyclohexene-1-carboxylate; GS 4104; Oseltamivir (INN); (-)-oseltamivir; MolPort-005-933-026; GS-4104; D08306; BRD-K76011241-045-01-5; FT-0082384; ethyl (3R,4R,5S)-4-acetamido-5-amino-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate; BIDD:GT0426; (3R,4R,5S)-4-acetamido-5-amino-3-(pentan-3-yloxy)cyclohex-1-enecarboxylic acid; UNII-20O93L6F9H; DB00198; Agucort (TN); Ro-640796; HMS2090C11; 204255-11-8; Agucort; GS4104; CID65028; 4-Acetylamino-5-amino-3-(1-ethyl-propoxy)-cyclohex-1-enecarboxylic acid; Tamiflu-Free; oseltamivirum; oseltamivir; 196618-13-0; AC1L22FK; Tamvir; CHEMBL1229; AC1Q63H0; Oseltamivir [INN:BAN]; NCGC00178698-01; CHEBI:7798; Ethyl (5S,3R,4R)-4-(acetylamino)-5-amino-3-(ethylpropoxy)cyclohex-1-enecarboxylate; 1-Cyclohexene-1-carboxylic acid, 4-(acetylamino)-5-amino-3-(1-ethylpropoxy)-, ethyl ester, (3R,4R,5S)-; Ethyl (3R,4R,5S)-4-acetamido-5-amino-3-(1-ethylpropoxy)-1-cyclohexene-1-carboxylate; LS-57422; Tamiflu (*Phosphate salt 1:1*); (3R,4R,5S)-4-Acetylamino-5-amino-3-(1-ethyl-propoxy)-cyclohex-1-enecarboxylic acid; HSDB 7433
Trade NameTamiflu
CompanyHoffmann-La Roche pharmaceutical company
IndicationInfluenza virus infection
[ICD9: 487   ICD10: J10, J11]
Approved    [1]
Structure

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InChI1S/C16H28N2O4/c1-5-12(6-2)22-14-9-11(16(20)21-7-3)8-13(17)15(14)1
8-10(4)19/h9,12-15H,5-8,17H2,1-4H3,(H,18,19)/t13-,14+,15+/m0/s1
InChIKeyVSZGPKBBMSAYNT-RRFJBIMHSA-N
Canonical SMILESCCC(CC)OC1C=C(CC(C1NC(=O)C)N)C(=O)OCC    
Isomeric SMILESCCC(CC)O[C@@H]1C=C(C[C@@H]([C@H]1NC(=O)C)N)C(=O)OCC
Therapeutic ClassAntiviral Agents
CAS NumberCAS 204255-11-8
FormulaC16H28N2O4
PubChem Compound IDCID 65028.
PubChem Substance IDSID 10292.
ChEBI7799;
SuperDrug ATC IDJ05AH02
SuperDrug CAS ID196618130;
TargetNeuraminidaseInhibitor[2][3]
Ref 1Natural products as sources of new drugs over the last 25 years. J Nat Prod. 2007 Mar;70(3):461-77. Epub 2007 Feb 20. To Reference
Ref 2Current and future antiviral therapy of severe seasonal and avian influenza. Antiviral Res. 2008 Apr;78(1):91-102. Epub 2008 Feb 4. To Reference
Ref 3Antiviral agents for influenza, hepatitis C and herpesvirus, enterovirus and rhinovirus infections. Med J Aust. 2001 Jul 16;175(2):112-6. To Reference



 

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