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Amoxicillin
SKU
HY-B0467A-1 g
Category Reference compound
Tags Anti-infection, Antibiotic;Bacterial, Infection; Cancer
$50 – $114
Products Details
Product Description
– Amoxicillin (Amoxycillin) is an antibiotic with good oral absorption and broad spectrum antimicrobial activity. Amoxicillin inhibits the biosynthesis of polypeptides in the cell wall, thereby inhibiting cell growth[1][2][3].
Web ID
– HY-B0467A
Storage Temperature
– 4°C (Powder, protect from light)
Shipping
– Room Temperature
Applications
– COVID-19-immunoregulation
Molecular Formula
– C16H19N3O5S
Citations
– Antimicrob Agents Chemother. 2021 Feb 17;65(3):e01921-20.|Biomed Res Int. 2018 Jul 2;2018:3579832. |Chemosphere. 2019 Jun;225:378-387. |Chemosphere. 2023 Oct 3:344:140353.|Environ Sci Pollut Res Int. 2017 Feb;24(6):5918-5932.|Genomics. 2022: 110527.|Institute of Chemistry, Federal University of Rio Grande do Sul (UFRGS). 2017 Nov.|Nat Commun. 2022 Mar 2;13(1):1116.|Drug Metab Pers Ther. 2020 Mar 5;35(1).|Interdisciplinary Graduate School, Nanyang Environment & Water Research Institute. 2020 Mar.|J Fluoresc. 2019 Jan;29(1):221-229. |SSRN. 2023 May 30.
References
– [1]Geddes AM, et al. Introduction: historical perspective and development of amoxicillin/clavulanate. Int J Antimicrob Agents. 2007 Dec;30 Suppl 2:S109-12.|[2]Handsfield HH,et al. Amoxicillin, a new penicillin antibiotic. Antimicrob Agents Chemother. 1973 Feb;3(2):262-5.|[3]Guo Y, et, al. Metabolic response of Lactobacillus acidophilus exposed to amoxicillin. J Antibiot (Tokyo). 2022 May;75(5):268-281.|[4]Andes D, et, al. In vivo activities of amoxicillin and amoxicillin-clavulanate against Streptococcus pneumoniae: application to breakpoint determinations. Antimicrob Agents Chemother. 1998 Sep;42(9):2375-9.|[5]Kramer MJ, et, al. Activity of oral amoxicillin, ampicillin, and oxytetracycline against infection with chlamydia trachomatis in mice. J Infect Dis. 1979 Jun;139(6):717-9.
CAS Number
– 26787-78-0
Molecular Weight
– 365.40
Compound Purity
– 98.0
SMILES
– OC([C@@H]1N(C2=O)[C@]([C@@H]2NC([C@@H](C3=CC=C(O)C=C3)N)=O)([H])SC1(C)C)=O
Clinical Information
– Launched
Research Area
– Infection; Cancer
Solubility
– DMSO : 83.33 mg/mL (ultrasonic)|H2O : 2 mg/mL (ultrasonic)
Target
– Antibiotic;Bacterial
Pathway
– Anti-infection
Product type
– Reference compound
Disclaimer: All products are for Research use only unless clearly stated otherwise on the product datasheet. Datasheets provided on the website are drafts for reference purpose only and you are requested to always refer to the hard copy included in the kit for your experimentation. Agdia Products are available for delivery only in Canada.