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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)
K Brand et al.
Journal of cellular physiology, 132(3), 559-564 (1987-09-01)
Pathways of glutamine metabolism in resting and proliferating rat thymocytes were evaluated by in vitro incubations of freshly prepared or 60-h cultured cells for 1-2 h with [U14C]glutamine. Complete recovery of glutamine carbons utilized in products allowed quantification of the
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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