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2-Amino-6-(diaminomethylideneamino)hexanoic acid

HCID 3626
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Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
156-86-5
Standard SMILES
NC(N)=NCCCCC(N)C(=O)O
InChIKey
QUOGESRFPZDMMT-UHFFFAOYSA-N
Molecular formula
C7H16N4O2
Average molar mass
188.23 g/mol
Monoisotopic mass
188.12732577

Overview

See also: L-Homoarginine (annotation moved to).

Names & identifiers

Preferred name
2-Amino-6-(diaminomethylideneamino)hexanoic acid
IUPAC
2-amino-6-(diaminomethylideneamino)hexanoic acid
English name
Homoarginine
Molecular formula
C7H16N4O2
Molecular weight
188.23

Names & synonyms

2-Amino-6-guanidinohexanoic acid143896-43-9(S)-2-Amino-6-guanidinohexanoic acidhomoarginin2-amino-6-guanidino-hexanoic acid2-amino-6-(diaminomethylideneamino)hexanoic acidSCHEMBL43288SCHEMBL8807282-Amino-6-guanidinohexanoicacidNSC27429NSC88868s6109
Show more names
l-lysinL-HOMOARGININEH-HOMOARG-OHHomo-L-arginineH-HAR-OHH-HOARG-OHC01924(3βH-HArg-OHHOMOARGININE
NS00044214

Database identifiers

CAS
156-86-5
PubChem CID
3626
Nikkaji
J238.616J

Properties

Computed structural properties

XLogP
-3.7
Topological polar surface area
128 Ų
Hydrogen bond donors
4
Hydrogen bond acceptors
4
Rotatable bonds
6
Heavy atoms
13
Formal charge
0
Complexity
189

Physicochemical properties

Melting point
207 · 207-209 °C
Boiling point
376.3 · 376.3±52.0 °C(Predicted)
Density
1.39 · 1.39±0.1 g/cm3(Predicted)
storage temp.
2 · Keep in dark place,Inert atmosphere,2-8°C
solubility
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form
Powder
pka
2.52 · 2.52±0.24(Predicted)
color
White to off-white
CAS DataBase Reference
156 · 156-86-5(CAS DataBase Reference)
FDA UNII
751 CK38I · JF751CK38I
Symbol(GHS)
7 · GHS07
Signal word
Warning
Hazard statements
302 · H302-H312-H332
Precautionary statements
261 · P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Safety data

Signal word
Warning
Symbol(GHS)
GHS07
Hazard statements
H302-H312-H332
Precautionary statements
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501

Chemistry & industry

Applications · 3 items

DescriptionHomoarginine and 1-hydroxyhomoarginine were originally detected in significant concentration in the seeds of many Lathyrus species (Bell, 1962a,b; 1963). Homoarginine was isolated from the seeds of L. cicera (Bell, 1962b) and L. sativus (Rao et al., 1963). The hydroxy compound was obtained from the seeds of L. tingitanus (Bell, 1964). The comparative distribution of guanidino compounds in the seeds of two genus of the Papilionoideae, Lathyrus and Vicia, exhibits interesting features (Bell and Tirimanna, 1964). For example, the genus Lathyrus stores predominantly the C7 amino acids homoarginine, y-hydroxyhomoarginine and the related compound lathyrine, while the genus Vicia stores relatively high concentrations of canavanine and of the C6 amino acids arginine and y-hydroxyarginine. Apart from plants, homoarginine was found in small amounts in human body fluids ,. urine (Armstrong, 1967), serum (Matsumoto et al., 1976a) and cerebrospinal fluid (Mori et al., 1981b) and in mammalian brain (Mori et al., 1978, 1979 ). Increased urinary excretion was reported in hyperlysinemia (Armstrong and Robinow, 1967) and citrullinemia (Scott-Emuakpor et al., 19(2). Homoarginine may be formed in mammals from lysine, by a homologous urea cycle in which arginine is replaced by lysine (Ryan and Wells, 1964; Scott-Emuakpor et al., 19(2). The excretion of homocitrulline and homoarginine in urine following administration of lysine to children supports this theory (Buergi et al., 1966). The biosynthesis of homoarginine has not been examined in plants, but y-hydroxyhomoarginine is synthesized from homoarginine in Lathyrus seeds (Bell, 1964). Subsequently both compounds have been identified as the precursors of the cyclic guanidino derivative, lathyrine, also present in Lathyrus seeds (Bell and Przybylska, 1965). Homoarginine and y-hydroxyhomoarginine probably serve as nitrogen reserves in Lathyrus seeds. Inhibition of growth by homoarginine has been reported In various microorganisms (Walker, 1955; Rao et al., 1963). gama-Hydroxyhomoarginine lactone isolated from the seeds of L. tingitanus (Bell, 1964) probably results from the cyclization of the open chain compound under acidic conditions.

UsesHomoarginine is an inhibitor of human arginase activity.

UsesHomoarginine as marker for exogenous protein Absorption and secretion of free homoarginine in the intestine: when 9 mmol homoarginine were infused into the proximal part of the jejunum, there was a 99.9% disappearance of the free amino acid homoarginine up to the ileum. In addition, following the infusion of 9 mmol homoarginine into the vena jugularis less than 0.2% of the infused homoarginine appeared in the intestine. We concluded from these data that with the homoarginine method endogenous protein in the chyme of the intestine can be distinguished from the food protein as homoarginine is not incorporated into endogenous secreta and free homo arginine is completely absorbed.

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Compound notes

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Additional notes

DefinitionChEBI: An L-lysine derivative that is the L-enantiomer of homoarginine.