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Ampicillin Trihydrate

Ampicillin Trihydrate is a β-lactam antibiotic, which inhibits bacterial cell-wall synthesis (peptidoglycan cross-linking) by inactivating transpeptidases on the inner surface of the bacterial cell membrane. (In Vitro) :Ampicillin trihydrate (D- (-) -α-Aminobenzylpenicillin trihydrate) inhibits the growth of E. coli of swine origin in a dose-dependent manner. The effective inhibitory concentration of Ampicillin trihydrate is 2.5 uG/mL. (In Vivo) :Ampicillin trihydrate (D- (-) -α-Aminobenzylpenicillin trihydrate) is very effective in alleviating the symptoms of hemorrhagic enteritis in a 11-week old pig.Ampicillin trihydrate produces maximum concentrations in bile twice as high as in serum. The peak concentration of ampicillin after an oral dose is as twice as high in portal blood as in peripheral blood.Ampicillin trihydrate provides neuroprotection against ischemia-reperfusion brain injury. Ampicillin trihydrate reduces the activities of MMPs and increases the expression level of GLT-1. Pretreatment with Ampicillin trihydrate significantly reduces medial hippocampal cell death following global forebrain ischemia.

Product Specifications

CAS Number

7177-48-2

Product Name Alternative

Amcill | Aminobenzyl Penicillin | KS-R1 | KS R1 | KSR1 | Omnipen | Pentrexyl | Polycillin | Ukapen

Field of Research

Pharmacology & Drug Discovery

Purity

>98% (HPLC)

Solubility

Water: 2 mg/mL (4.95 mM) ; DMSO: 81 mg/mL (200.76 mM)

Smiles

O=C ([C@@H] (C (C) (C) S[C@]1 ([H]) [C@@H]2NC ([C@H] (N) C3=CC=CC=C3) =O) N1C2=O) O.[H]O[H].[H]O[H].[H]O[H]

Molecular Formula

C16H19N3O4S·3H2O

Molecular Weight

403.45

Storage Conditions

Storage temperature: -20°C. Stability: ≥ 2 years

Notes

For research use only.

Other Product Names

(2S,5R,6R) -6- ((R) -2-amino-2-phenylacetamido) -3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid trihydrate

Available Sizes

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