Sel de déodium Carbenicillin, base anhydre, base anhydre, 89,0-100,5% base anhydre

Code: c1389-5g D2-231

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

Analysis Note

Stable at 37 °C for 3 days

Application

Used for selection of ampr transformed cells and to study the role of penicillin-sensit...

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$664.10 5G

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

Analysis Note

Stable at 37 °C for 3 days

Application

Used for selection of ampr transformed cells and to study the role of penicillin-sensitive transpeptidases in cell wall biosynthesis.

Biochem/physiol Actions

Carboxypenicillin antibiotic that inhibits bacterial cell-wall synthesis (peptidoglycan cross-linking) by inactivating transpeptidases on the inner surface of the bacterial cell membrane. Analog to ampicillin. Antimicrobial spectrum: Gram-positive and Gram-negative bacteria, Pseudomonas.

General description

Chemical structure: peptide

Other Notes

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

antibiotic activity spectrum	Gram-positive bacteria, Gram-negative bacteria
assay	89.0-100.5% anhydrous basis
form	powder
InChI key	RTYJTGSCYUUYAL-YCAHSCEMSA-L
InChI	1S/C17H18N2O6S.2Na/c1-17(2)11(16(24)25)19-13(21)10(14(19)26-17)18-12(20)9(15(22)23)8-6-4-3-5-7-8;;/h3-7,9-11,14H,1-2H3,(H,18,20)(H,22,23)(H,24,25);;/q;2*+1/p-2/t9?,10-,11+,14-;;/m1../s1
mode of action	cell wall synthesis \| interferes
Quality Level	200
SMILES string	[Na+].[Na+].CC1(C)S[C@@H]2[C@H](NC(=O)C(C([O-])=O)c3ccccc3)C(=O)N2[C@H]1C([O-])=O
solubility	H₂O: 50 mg/mL
storage temp.	2-8°C