1.0 2016-05-25 03:28:01 UTC 2026-08-19 17:36:35 UTC Oseltamivir SmallMolecule Oseltamivir is an organic compound with the chemical formula C16H28N2O4 and an average molecular weight of 312.40 g/mol. Oseltamivir belongs to the amino acids, peptides, and analogues, a subclass of carboxylic acids and derivatives within the organic compounds. This compound is recorded as being found in or released from six distinct sources. These include healthcare, pharmaceuticals, and veterinary products in the form of antivirals, as well as household cleaning and consumer products such as other smoking requisites and non-electric simulated smoking devices. Additionally, it is associated with electrical and electronic equipment, specifically video games, television systems, and radio transmission systems. The recorded route of exposure for this substance is oral. At the molecular level, oseltamivir acts on three recorded protein targets. It functions as an inhibitor of neuraminidase (NA), sialidase-1 (NEU1), and sialidase-2 (NEU2). Human Neurotoxin C16H28N2O4 312.4045 312.204907394 ethyl (3R,4R,5S)-5-amino-4-acetamido-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate oseltamivir 196618-13-0 CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1 InChI=1S/C16H28N2O4/c1-5-12(6-2)22-14-9-11(16(20)21-7-3)8-13(17)15(14)18-10(4)19/h9,12-15H,5-8,17H2,1-4H3,(H,18,19)/t13-,14+,15+/m0/s1 VSZGPKBBMSAYNT-RRFJBIMHSA-N Organic compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues Gamma amino acids and derivatives Acetamides Carbonyl compounds Dialkyl ethers Enoate esters Hydrocarbon derivatives Monoalkylamines Monocarboxylic acids and derivatives Organic oxides Organopnictogen compounds Secondary carboxylic acid amides Acetamide Aliphatic homomonocyclic compound Alpha,beta-unsaturated carboxylic ester Amine Carbonyl group Carboxamide group Carboxylic acid ester Dialkyl ether Enoate ester Ether Gamma amino acid or derivatives Hydrocarbon derivative Monocarboxylic acid or derivatives Organic nitrogen compound Organic oxide Organic oxygen compound Organonitrogen compound Organooxygen compound Organopnictogen compound Primary aliphatic amine Primary amine Secondary carboxylic acid amide Aliphatic homomonocyclic compounds acetamides amino acid ester cyclohexenecarboxylate ester diester primary amino compound Detected and Not Quantified Oseltamivir Action Pathway SMP0125983 Oseltamivir Drug Metabolism Action Pathway SMP0142661 logp 1.16 logp 1.30 ALOGPS logs -2.66 ALOGPS solubility 6.86e-01 g/l ALOGPS logp 1.16 ChemAxon pka_strongest_acidic 14.03 ChemAxon pka_strongest_basic 9.31 ChemAxon iupac ethyl (3R,4R,5S)-5-amino-4-acetamido-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate ChemAxon average_mass 312.4045 ChemAxon mono_mass 312.204907394 ChemAxon smiles CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1 ChemAxon formula C16H28N2O4 ChemAxon inchi InChI=1S/C16H28N2O4/c1-5-12(6-2)22-14-9-11(16(20)21-7-3)8-13(17)15(14)18-10(4)19/h9,12-15H,5-8,17H2,1-4H3,(H,18,19)/t13-,14+,15+/m0/s1 ChemAxon inchikey VSZGPKBBMSAYNT-RRFJBIMHSA-N ChemAxon polar_surface_area 90.65 ChemAxon refractivity 84.2 ChemAxon polarizability 34.65 ChemAxon rotatable_bond_count 8 ChemAxon acceptor_count 4 ChemAxon donor_count 2 ChemAxon physiological_charge 1 ChemAxon formal_charge 0 ChemAxon #<HealthEffect::ActiveRecord_Associations_CollectionProxy:0x00007f3bae5fbf40> DB00198 65028 4442 BE0000584 BE0000914 BE0003200