Nopaline

Nopaline

Names
IUPAC name N-{1-Carboxy-4-[(diaminomethylene)amino]butyl}glutamic acid[1]
Other names N^2-(D-1,3-dicarboxypropyl)-L-arginine
Identifiers
3D model (Jmol)	Interactive image Interactive image
ChemSpider	19976727 (2R)-2-Amino 388639 2-{[(1R)-1-Carboxybutyl]amino} 19951243 2-{[(1S)-1-Carboxybutyl]amino}
PubChem	426 21118330 (2R)-2-Amino 57105058 (2S)-2-Amino 439546 2-{[(1R)-1-Carboxybutyl]amino} 440320 2-{[(1S)-1-Carboxybutyl]amino}
InChI InChI=1S/C11H20N4O6/c12-11(13)14-5-1-2-6(9(18)19)15-7(10(20)21)3-4-8(16)17/h6-7,15H,1-5H2,(H,16,17)(H,18,19)(H,20,21)(H4,12,13,14) Key: LMKYZBGVKHTLTN-UHFFFAOYSA-N
SMILES [nH]:c(:[nH2]):[nH]CCCC(NC(CCc(:[o]):[oH])c(:[o]):[oH])c(:[o]):[oH] NC(=N)NCCCC(NC(CCC(O)=O)C(O)=O)C(O)=O
Properties
Chemical formula	C11H20N4O6
Molar mass	304.30 g·mol^−1
Related compounds
Related alkanoic acids	Octopine
Related compounds	Bis-tris propane Pantetheine Spermine
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Nopaline is a chemical compound derived from the amino acids glutamic acid and arginine. It is classified as an opine. Ti plasmids are classified on the basis of the different types of opines they produce. These may be nopaline plasmids, octopine plasmids and agropine plasmids. These opines are condensation products of amino acids and keto acids or may be derived from sugars. The opines are used as carbon and nitrogen sources and metabolized by Agrobacterium.

References

1. PubChem: https://pubchem.ncbi.nlm.nih.gov/compound/108012