Amoxicillin trihydrate
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Delivery time: 3- 8 working days
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Shipment: not cooled. Store at -20°C. For laboratory usage only!
Amoxicillin is an inhibitor of bacterial cell wall synthesis. It inhibits the crosslinking of peptidoglycan by binding and inactivating transpeptidases. High acitivity against gram-negative bacteria like Agrobacterium species. Sensitive to lactamase. Amoxicillin is also effective against gram positive. In opposite to Ampicillin less harmful against normal gut flora.
Synonyms: (2S,5R,6R)-6-[[(2R)-2-Amino-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; AMPC; Amoxillat.
Specifications:
Assay: 95% - 102% (anhydrous basis)
Appearance: White to almost white
pH-value: 3.5 - 5.5 (0.1g/50mL)
C16H19N3O5S x 3H2O
MW = 365.40 g/mol (anhydrous)
Soluble in water
Sicherheits Hinweise / Safety
H-Sätze: H314, H317GHS-Symbole: GHS07, GHS08
Klassifizierungen / Classification
EC-Nr: 243-003-8CAS-Nr: 61336-70-7
eclass-Nr: 32-19-90-90
Documents:
Safety Data SheetCertificate
Category List
Source: NCBI PubMed
Klebsiella oxytoca enterotoxins tilimycin and tilivalline have distinct host DNA-damaging and microtubule-stabilizing activities
Katrin Unterhauser, Lisa Pöltl, Georg Schneditz, Sabine Kienesberger, Ronald A. Glabonjat, Maksym Kitsera, Jakob Pletz, Fernando Josa-Prado, Elisabeth Dornisch, Christian Lembacher-Fadum, Sandro Roier, Gregor Gorkiewicz, Daniel Lucena, Isabel Barasoain, Wolfgang Kroutil, Marc Wiedner, Joanna I. Loizou, Rolf Breinbauer, José Fernando Díaz, Stefan Schild, Christoph Högenauer, Ellen L. Zechner
Proc Natl Acad Sci U S A. 2019 Feb 26; 116(9): 3774–3783.
doi: 10.1073/pnas.1819154116
PMCID: PMC6397511