Citrulline

The organic compound citrulline is an α-amino acid. Its name is derived from citrullus, the Latin word for watermelon. Although named and described by gastroenterologists since the late 19th century, it was first isolated from watermelon in 1914 by Japanese researchers Yotaro Koga and Ryo Odake and further codified by Mitsunori Wada of Tokyo Imperial University in 1930. It has the formula H2NC(O)NH(CH2)3CH(NH2)CO2H. It is a key intermediate in the urea cycle, the pathway by which mammals excrete ammonia by converting it into urea. Citrulline is also produced as a byproduct of the enzymatic production of nitric oxide from the amino acid arginine, catalyzed by nitric oxide synthase.

Citrulline
Names
IUPAC name
2-Amino-5-(carbamoylamino)pentanoic acid
Identifiers
3D model (JSmol)
3DMet
1725417, 1725415 D, 1725416 L
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.006.145
EC Number
  • 211-012-2
774677 L
KEGG
MeSH Citrulline
PubChem CID
UNII
  • InChI=1S/C6H13N3O3/c7-4(5(10)11)2-1-3-9-6(8)12/h4H,1-3,7H2,(H,10,11)(H3,8,9,12) N
    Key: RHGKLRLOHDJJDR-UHFFFAOYSA-N N
SMILES
  • NC(CCCNC(N)=O)C(O)=O
Properties
C6H13N3O3
Molar mass 175.188 g·mol−1
Appearance White crystals
Odor Odourless
log P −1.373
Acidity (pKa) 2.508
Basicity (pKb) 11.489
Thermochemistry
232.80 J K−1 mol−1
Std molar
entropy (S298)
254.4 J K−1 mol−1
Related compounds
Related alkanoic acids
  • N-Acetylaspartic acid
  • Aceglutamide
  • N-Acetylglutamic acid
  • Pivagabine
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
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