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Home > Products >  Imipenem-Cilastatin 92309-29-0

Imipenem-Cilastatin 92309-29-0 CAS NO.92309-29-0

  • Min.Order: 1 Kilogram
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  • Product Details

Keywords

  • Imipenem-Cilastatin sodium hydrate
  • Primaxin
  • 1-Azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid,6-[(1R)-1-hydroxyethyl]-3-[[2-[(iminomethyl) amino]ethyl]thio]-7-oxo-,(5R,6S)-,mixt. with (2Z)-7-[[(2R)-2-amino-2-carboxyethyl] thio]-2-[[[(1S)-2,2-dime

Quick Details

  • ProName: Imipenem-Cilastatin
  • CasNo: 92309-29-0
  • Molecular Formula: C28H43N5O9S2
  • Appearance: White crystallization
  • Application: antithrombotic drug
  • DeliveryTime: in two weeks
  • PackAge: 25kg/drum
  • Port: SHANGHAI BEIJING
  • ProductionCapacity: 10 Metric Ton/Day
  • Purity: USP/EP/BP
  • Storage: room temperature
  • Transportation: AIR SEA TRAIN
  • LimitNum: 1 Kilogram

Superiority

Product Name: Imipenem-Cilastatin sodium hydrate
Synonyms: Primaxin;Thienam;Tienam 500;IMipeneM and Cilastatin SodiuM with SodiuM Bicarbonate;7-[(2S)-2-amino-2-carboxy-ethyl]sulfanyl-2-[[(1S)-2,2-dimethylcyclopro panecarbonyl]amino]hept-2-enoic acid: (5R)-3-[2-(aminomethylideneamino )ethylsulfanyl]-6-(1-hydroxyethyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene -2-carboxylic acid;Imipenem-Cilastatin sodium hydrate;Sodium (Z)-7-[(2R)-2-amino-3-hydroxy-3-oxopropyl]sulfanyl-2-[[(1S)-2,2-dimethylcyclopropanecarbonyl]amino]hept-2-enoate (5R,6S)-3-[2-(aminomethylideneamino)ethylsulfanyl]-6-(1-hydroxyethyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid hydrate;1-Azabicyclo(3.2.0)hept-2-ene-2-carboxylic acid, 6-((1R)-1-hydroxyethyl)-3-((2-((iminomethyl)amino)ethyl)thio)-7-oxo-, (5R,6S)-, mixt. with (2Z)-7-(((2R)-2-amino-2-carboxyethyl)thio)-2-((((1S)-2,2-dimethylcyclopropyl)carbonyl)amino)-2-heptenoic acid
CAS: 92309-29-0
MF: C28H43N5O9S2
MW: 657.8
EINECS: 1592732-453-0
Product Categories:  
Mol File: 92309-29-0.mol
Imipenem-Cilastatin sodium hydrate Structure
Imipenem-Cilastatin sodium hydrate Usage And Synthesis
Clinical Use Antibacterial agent
Drug interactions Potentially hazardous interactions with other drugs
Antiepileptics: reduced valproate concentration - avoid.
Antivirals: convulsions reported with concomitant administration of ganciclovir and valganciclovir.
Ciclosporin: variable reports of increase / no change in ciclosporin levels, and of neurotoxicity.
Metabolism When administered alone, imipenem is metabolised in the kidneys by dehydropeptidase-I, an enzyme in the brush border of the renal tubules, to inactive, nephrotoxic metabolites, with only about 5 to 40 or 45% of a dose excreted in the urine as unchanged active drug. Cilastin inhibits the metabolism of imipenem. When given with cilastatin about 70% of an intravenous dose of imipenem is recovered unchanged in the urine within 10 hours. Cilastatin is also excreted mainly in the urine, the majority as unchanged drug and about 12% as N-acetyl cilastatin. Less than 1% of imipenem is excreted via the bile in the faeces.

 

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