Metampicillin

Metampicillin

Gene therapy
Clinical data
ATC code	J01CA14 (WHO)
Physiological data
Legal status
Pharmacokinetic data
Identifiers
IUPAC name 3,3-Dimethyl-6-[[2-(methylideneamino)-2-phenylacetyl]amino]-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
CAS Number	6489-97-0 Y
PubChem Template:Abbreviation	4084
UNII	G0H6U7VSTK
ChEMBL	ChEMBL1908324 N
Chemical and physical data
Formula	C17H19N3O4S
Molar mass	361.415 g/mol
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WikiDoc Resources for Metampicillin
Articles
Most recent articles on Metampicillin Most cited articles on Metampicillin Review articles on Metampicillin Articles on Metampicillin in N Eng J Med, Lancet, BMJ
Media
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Evidence Based Medicine
Cochrane Collaboration on Metampicillin Bandolier on Metampicillin TRIP on Metampicillin
Clinical Trials
Ongoing Trials on Metampicillin at Clinical Trials.gov Trial results on Metampicillin Clinical Trials on Metampicillin at Google
Guidelines / Policies / Govt
US National Guidelines Clearinghouse on Metampicillin NICE Guidance on Metampicillin NHS PRODIGY Guidance FDA on Metampicillin CDC on Metampicillin
Books
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News
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Commentary
Blogs on Metampicillin
Definitions
Definitions of Metampicillin
Patient Resources / Community
Patient resources on Metampicillin Discussion groups on Metampicillin Patient Handouts on Metampicillin Directions to Hospitals Treating Metampicillin Risk calculators and risk factors for Metampicillin
Healthcare Provider Resources
Symptoms of Metampicillin Causes & Risk Factors for Metampicillin Diagnostic studies for Metampicillin Treatment of Metampicillin
Continuing Medical Education (CME)
CME Programs on Metampicillin
International
Metampicillin en Espanol Metampicillin en Francais
Business
Metampicillin in the Marketplace Patents on Metampicillin
Experimental / Informatics
List of terms related to Metampicillin

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Metampicillin (INN) is a penicillin antibiotic. It is prepared by the reaction of ampicillin with formaldehyde, and is hydrolysed in aqueous solution with the formation of ampicillin. Hydrolysis is rapid under acid conditions, e.g., in the stomach, less rapid in neutral media, and incomplete in solutions such as human serum.

External links

• ChEBI ID

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