Amoxicillin sodiumProduct ingredient for Amoxicillin

Name
Amoxicillin sodium
Drug Entry
Amoxicillin

Amoxicillin, or BRL-2333, is a penicillin G derivative first described in the literature in 1972.6 Amoxicillin has similar activity to penicillin and ampicillin, but leads to higher serum concentrations than ampicillin.6

Amoxicillin was granted FDA approval on 18 January 1974.12

Accession Number
DBSALT000868
Structure
Synonyms
Amoxicillin natrium
UNII
544Y3D6MYH
CAS Number
34642-77-8
Weight
Average: 387.39
Monoisotopic: 387.08648615
Chemical Formula
C16H18N3NaO5S
InChI Key
BYHDFCISJXIVBV-YWUHCJSESA-M
InChI
InChI=1S/C16H19N3O5S.Na/c1-16(2)11(15(23)24)19-13(22)10(14(19)25-16)18-12(21)9(17)7-3-5-8(20)6-4-7;/h3-6,9-11,14,20H,17H2,1-2H3,(H,18,21)(H,23,24);/q;+1/p-1/t9-,10-,11+,14-;/m1./s1
IUPAC Name
sodium (2S,5R,6R)-6-[(2R)-2-amino-2-(4-hydroxyphenyl)acetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
SMILES
[Na+].[H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@H]2NC(=O)[C@H](N)C1=CC=C(O)C=C1)C([O-])=O
PubChem Compound
23663126
ChemSpider
82723
ChEBI
51255
ChEMBL
CHEMBL2105950
Wikipedia
Amoxicillin
Predicted Properties
PropertyValueSource
Water Solubility1.99 mg/mLALOGPS
logP0.76ALOGPS
logP-2.3Chemaxon
logS-2.3ALOGPS
pKa (Strongest Acidic)3.23Chemaxon
pKa (Strongest Basic)7.22Chemaxon
Physiological Charge0Chemaxon
Hydrogen Acceptor Count6Chemaxon
Hydrogen Donor Count3Chemaxon
Polar Surface Area135.79 Å2Chemaxon
Rotatable Bond Count4Chemaxon
Refractivity100.34 m3·mol-1Chemaxon
Polarizability35.56 Å3Chemaxon
Number of Rings3Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon