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gamma-Glutamyl-1-amino-D-proline

Base Information Edit
  • Chemical Name:gamma-Glutamyl-1-amino-D-proline
  • CAS No.:10139-06-7
  • Molecular Formula:C10H17N3O5
  • Molecular Weight:259.262
  • Hs Code.:2933990090
  • Mol file:10139-06-7.mol
gamma-Glutamyl-1-amino-D-proline

Synonyms:SCHEMBL298422;1-[n-(g-l-glutamyl)amino]-d-proline;AKOS040747096;GAMMA-GLUTAMYL-1-AMINO-D-PROLINE;NN-[(2R)-2-carboxypyrrolidin-1-yl]-L-glutamine;1-((4-Amino-4-carboxy-1-oxobutyl)amino)-(S)-D-Proline

Suppliers and Price of gamma-Glutamyl-1-amino-D-proline
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 2 raw suppliers
Chemical Property of gamma-Glutamyl-1-amino-D-proline Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:132.96000 
  • Density:1.43g/cm3 
  • LogP:-0.21220 
  • XLogP3:-5.1
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:6
  • Exact Mass:259.11682065
  • Heavy Atom Count:18
  • Complexity:346
Purity/Quality:

98%,99%, *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CC(N(C1)NC(=O)CCC(C(=O)O)N)C(=O)O
  • Uses Linatine, found in flaxseed, is the only pyridoxine antagonist known and seems to function by the formation of a stable complex. Linatine is an anti-pyridoxine compound with antibacterial properties. A Bacterial inhibitor.
Technology Process of gamma-Glutamyl-1-amino-D-proline

There total 2 articles about gamma-Glutamyl-1-amino-D-proline 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:
Guidance literature:
Z-Glu-NHNH2, Z-Pro-CH2C6H5;
DOI:10.1021/bi00853a028
Guidance literature:
Z-Glu-NHNH2, Z-D-Pro-CH2C6H5;
DOI:10.1021/bi00853a028
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