Glu-lys

Base Information

• Chemical Name: Glu-lys
• CAS No.: 5891-53-2
• Molecular Formula: C11H21N3O5
• Molecular Weight: 275.3
• Hs Code.: 2924199090
• Nikkaji Number: J662.650E
• Wikidata: Q27140603
• Metabolomics Workbench ID: 78787
• ChEMBL ID: CHEMBL190361
• Mol file: 5891-53-2.mol

Synonyms:H-Glu-Lys-OH;GLU-LYS;5891-53-2;glutamyl-lysine;L-alpha-glutamyl-L-Lysine;CHEMBL190361;CHEBI:73521;(2S)-6-amino-2-[[(2S)-2-amino-4-carboxybutanoyl]amino]hexanoic acid;Glutamyllysine;L-Glu-L-Lys;L-Glutamyl-L-Lysine;N2-a-glutamyl-lysine;L-Glu-L-Lys-OH;N2-L-a-Glutamyllysine;N2-L-a-glutamyl-Lysine;N2-alpha-glutamyl-lysine;N2-L-alpha-Glutamyllysine;N2-L-alpha-glutamyl-Lysine;SCHEMBL170727;EK;BDBM50169173;HY-N11140;MFCD00056129;CS-0638981;Q27140603;(S)-6-Amino-2-((S)-2-amino-4-carboxy-butyrylamino)-hexanoic acid;E-K

Chemical Property of Glu-lys

Chemical Property:

• Vapor Pressure: 1.51E-16mmHg at 25°C
• Melting Point: >150 °C (decomp)(Solv: methanol (67-56-1))
• Refractive Index: 1.538
• Boiling Point: 611.9 °C at 760 mmHg
• PKA: 3.04±0.10(Predicted)
• Flash Point: 323.9 °C
• PSA: 155.74000
• Density: 1.29 g/cm³
• LogP: 0.66840
• Storage Temp.: -15°C
• Solubility.: Aqueous Acid (Slightly), Water (Sparingly, Sonicated)
• XLogP3: -6.3
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 10
• Exact Mass: 275.14812078
• Heavy Atom Count: 19
• Complexity: 322

Purity/Quality:

98% or more ^*data from raw suppliers

H-GLU-LYS-OH 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(CCN)CC(C(=O)O)NC(=O)C(CCC(=O)O)N
• Isomeric SMILES: C(CCN)C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)O)N
• Uses: H-Glu-Lys-Oh can be used for sustained-release external pharmaceutical composition.

Technology Process of Glu-lys

There total 3 articles about Glu-lys which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

L-glutamic acid (56-86-0,21675-62-7,23009-64-5,25104-13-6,84960-48-5,25513-46-6) + L-Lysine hydrochloride (657-27-2,10098-89-2,26124-78-7) → LysGluGlu (157535-07-4) + lysine tetrapeptide (997-20-6) + poly(L-lysine), 5-mer (19431-21-1) + Lys-Glu (45234-02-4) + L-glutamyl-L-glutamic acid (3929-61-1) + Lys-Lys-Lys (13184-14-0) + C11H19N3O4 (473452-81-2) + C16H24N4O6 + C22H36N6O7 + C27H41N7O9 + C28H48N8O8 + C32H46N8O11 + C33H53N9O10 + C34H60N10O9 + C33H55N9O11 + C38H58N10O12 + C38H58N10O12 + C39H65N11O11 + C44H70N12O13 + C49H75N13O15 + C55H87N15O16 + C50H82N14O14 + C49H75N13O15 + C44H70N12O13 + C39H65N11O11 + C38H58N10O12 + C38H58N10O12 + C33H53N9O10 + C32H46N8O11 + C27H41N7O9 + C21H29N5O8 + C16H24N4O6 + C11H19N3O4 + C55H87N15O16 + C54H80N14O17 + C49H75N13O15 + C44H70N12O13 + C39H65N11O11 + C38H58N10O12 + C38H58N10O12 + C35H67N11O8 + C33H53N9O10 + C33H55N9O11 + C28H48N8O8 + C32H46N8O11 + C27H41N7O9 + C22H36N6O7 + C17H31N5O5 + C50H82N14O14 + C40H72N12O10 + C44H70N12O13 + C39H65N11O11 + C34H60N10O9 + C29H55N9O7 + C23H43N7O6 + C36H44N8O14 + C31H39N7O12 + C26H34N6O10 + C21H29N5O8 + C20H24N4O10 + C15H19N3O8 + C10H14N2O6 (757898-70-7) + C39H69N11O13 + C33H57N9O12 + C32H50N8O13 + C32H48N8O12 + C27H45N7O11 + C28H50N8O9 + C27H43N7O10 + C22H38N6O8 + C17H33N5O6 (175175-64-1) + C17H33N5O6 (175176-04-2) + C34H62N10O10 + C39H67N11O12 + C40H74N12O11 + C45H79N13O13 + C46H86N14O12 + C45H81N13O14 + C33H57N9O12 + C38H62N10O14 + C43H67N11O16 + C44H74N12O15 + EKKK + EKKE (92172-18-4) + EKEE + KEKKK + EKKEK + EKEEK + KEKKKK (532436-32-1) + EKKEKK (927893-91-2) + EKEEKE (927894-29-9) + glu-Lys (5891-52-1,5891-53-2,130004-26-1)

Guidance literature:

With sulfuric acid; at 140 ℃; for 300h; Time; Temperature;

DOI:10.1007/s11172-012-0060-3

Reference yield:

L-lysine (56-87-1,3506-25-0) + L-glutamic acid (56-86-0,21675-62-7,23009-64-5,25104-13-6,84960-48-5,25513-46-6) → glu-Lys (5891-52-1,5891-53-2,130004-26-1)

Guidance literature:

Multistep reaction;

Reference yield:

→ glu-Lys (5891-52-1,5891-53-2,130004-26-1)

Guidance literature:

aus VIII;

upstream raw materials:

L-lysine

L-glutamic acid

L-Lysine hydrochloride

Downstream raw materials:

L-lysine

L-glutamic acid

Refernces

• 1、 Tamura, Masahiro,Nakatsuka, Tohru,Tada, Makoto,Kawasaki, Yoshihiro,Kikuchi, Eiichi,Okai, Hideo. "The Relationship between Taste and Primary Structure of "Delicious Peptide" (Lys-Gly-Asp-Glu-Glu-Ser-Leu-Ala) from Beef Soup". . p. 319 - 326. Retrieved 2007/10/02.