cis-Aconitic acid (585-84-2, 499-12-7)

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  100 mg
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  250 mg
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  1 g
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Most-cited Publications

• The oxidation of citrate, isocitrate and cis-aconitate by isolated mitochondria (Biochemical Journal, 1964)
• Stimulating effect of citrate and cis-Aconitate on the transformation of Trypanosoma brucei bloodstream forms to procyclic forms in vitro. (Parasitology Research, 1981)
• The effect of citrate/cis-aconitate on oxidative metabolism during transformation of Trypanosoma brucei (FEBS Journal, 1986)
• Cloning and functional characterization of the cis-aconitic acid decarboxylase (CAD) gene from Aspergillus terreus (Applied Microbiology and Biotechnology, 2008)
• Trypanosoma brucei: cis-Aconitate and temperature reduction as triggers of synchronous transformation of bloodstream to procyclic trypomastigotes in vitro (Experimental Parasitology, 1986)
• Thermal behaviour of citric acid and isomeric aconitic acids (Journal of Thermal Analysis and Calorimetry, 2011)

Areas of Application

Safety

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Trends

Alternate Names

• Aconitic Acid
• Aconitate
• Equisetic Acid
• Achilleic Acid
• Citridic Acid
• Citridinic Acid
• Acontic Acid
• Carboxyglutaconic Acid
• Pyrocitric Acid
• Adonic Acid
• SMILES
  C(C(=CC(=O)O)C(=O)O)C(=O)O
• InChIKey
  GTZCVFVGUGFEME-UHFFFAOYSA-N

External Links

• Pubchem - cis-Aconitic acid
• Wikipedia - aconitic acid
  Aconitic acid is an organic acid. The two isomers are cis-aconitic acid and trans-aconitic acid. The conjugate base of cis-aconitic acid, cis-aconitate is an intermediate in the isomerization of citrate to isocitrate in the citric acid cycle.

Synthesis

Reactant  +  1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide (Nicolaou IBX dehydrogenation)

Synthesis of cis-Aconitic acid ›

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