| Weight | 174.108 g/mol |
|---|---|
| Formula | C6H6O6 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
trans-Aconitic acid (499-12-7, 4023-65-8)
Aconitic Acid · Aconitate · Equisetic Acid
Score:
#1255 in Biochemistry
,
#3100 in Biology
,
#3875 in Chemistry
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- 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)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Aconitic Acid
- Aconitate
- Equisetic Acid
- Achilleic Acid
- Citridic Acid
- Citridinic Acid
- Acontic Acid
- Carboxyglutaconic Acid
- Pyrocitric Acid
- Adonic Acid
-
SMILESC(C(=CC(=O)O)C(=O)O)C(=O)O
-
InChIKeyGTZCVFVGUGFEME-UHFFFAOYSA-N
- Pubchem - trans-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.
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trans-Aconitic acid
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