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About This Item
Empirical Formula (Hill Notation):
C7H12N2O5
CAS Number:
Molecular Weight:
204.18
EC Number:
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26
Recommended Products
Assay
≥98% (TLC)
form
powder
color
white
mp
155-158 °C
storage temp.
−20°C
SMILES string
NCC(=O)N[C@@H](CCC(O)=O)C(O)=O
InChI
1S/C7H12N2O5/c8-3-5(10)9-4(7(13)14)1-2-6(11)12/h4H,1-3,8H2,(H,9,10)(H,11,12)(H,13,14)/t4-/m0/s1
InChI key
IEFJWDNGDZAYNZ-BYPYZUCNSA-N
Related Categories
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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K Brand et al.
Metabolism: clinical and experimental, 38(8 Suppl 1), 29-33 (1989-08-01)
Pathways of glutamine metabolism in resting and proliferating rat thymocytes and established human T- and B-lymphoblastoid cell lines were evaluated by in vitro incubations of freshly prepared or cultured cells for one to two hours with [U14C]glutamine. Complete recovery of
C Winckler et al.
Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology, 169(7), 495-500 (1999-12-14)
Characteristics of dipeptide transport in pig jejunum were investigated in vitro by applying the Ussing-chamber technique and mucosal uptake studies. Addition of both glycyl-L-glutamine and glycyl-L-sarcosine (20 mmol.l-1) to the mucosal buffer solution significantly increased the short-circuit current by 2.60
Intravenous use of glutamine in peptide form: clinical applications of old and new observations.
S A Adibi
Metabolism: clinical and experimental, 38(8 Suppl 1), 89-92 (1989-08-01)
G B Koelle et al.
Proceedings of the National Academy of Sciences of the United States of America, 84(19), 6944-6947 (1987-10-01)
Intracarotid infusion of glycyl-L-glutamine (Gly-Gln) was shown previously to oppose the fall in the acetylcholinesterase and butyrylcholinesterase contents of the cat superior cervical ganglion (SCG) that otherwise follows preganglionic denervation. However, its effect was demonstrable only on the vascularly remote
Takayuki K Nemoto et al.
Analytical biochemistry, 548, 78-81 (2018-02-13)
Bacterial dipeptidyl-peptidase (DPP) 7 liberates a dipeptide with a preference for aliphatic and aromatic penultimate residues from the N-terminus. Although synthetic substrates are useful for activity measurements, those currently used are problematic, because they are more efficiently degraded by DPP5.
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