Ampicillin, répond aux spécifications des tests USP

Code: a1593-25g D2-231

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Used to select for ampicillin resistance in mutated and transformed cells.

Biochem/physiol Actions

A β-lactam antibiotic with an...


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Votre prix
£206.00 25G

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Used to select for ampicillin resistance in mutated and transformed cells.

Biochem/physiol Actions

A β-lactam antibiotic with an amino group side chain attached to the penicillin structure. Penicillin derivative that inhibits bacterial cell-wall synthesis (peptidoglycan cross-linking) by inactivating transpeptidases on the inner surface of the bacterial cell membrane. Bactericidal only to growing Escherichia coli . Mode of resistance: Cleavage of β-lactam ring of ampicillin by β-lactamase. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.

General description

Chemical structure: ß-lactam

Other Notes

Keep container tightly closed in a dry and well-ventilated place.

Packaging

25g

agencymeets USP testing specifications, USP/NF
antibiotic activity spectrumGram-positive bacteria, Gram-negative bacteria
application(s)pharmaceutical (small molecule)
colorwhite
formsolid
InChI keyRXDALBZNGVATNY-CWLIKTDRSA-N
InChI1S/C16H19N3O4S.3H2O/c1-16(2)11(15(22)23)19-13(21)10(14(19)24-16)18-12(20)9(17)8-6-4-3-5-7-8;;;/h3-7,9-11,14H,17H2,1-2H3,(H,18,20)(H,22,23);3*1H2/t9-,10-,11+,14-;;;/m1.../s1
mode of actioncell wall synthesis | interferes
mp198-200 °C (dec.) (lit.)
Quality Level200
SMILES stringO.O.O.CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(O)=O
solubilityH2O: soluble 10 g/L
storage temp.2-8°C
Cas Number7177-48-2
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