Aceglutamide

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Aceglutamide
Stereo, skeletal formula of aceglutamide (S)
Names
Preferred IUPAC name
2-Acetamido-5-amino-5-oxopentanoic acid
Other names
2-(Acetylamino)-glutaramidic acid
α-N-Acetylglutamine;[1]
N-Acetylglutamine
N-Acetyl-L-glutamine
Identifiers
3D model (
JSmol
)
ChemSpider
DrugBank
ECHA InfoCard
 100.017.862 Edit this at Wikidata
EC Number
  • 219-647-7
KEGG
MeSH aceglutamide
UNII
  • InChI=1S/C7H12N2O4/c1-4(10)9-5(7(12)13)2-3-6(8)11/h5H,2-3H2,1H3,(H2,8,11)(H,9,10)(H,12,13) checkY
    Key: KSMRODHGGIIXDV-UHFFFAOYSA-N checkY
  • CC(=O)NC(CCC(N)=O)C(O)=O
Properties
C7H12N2O4
Molar mass 188.183 g·mol−1
Appearance White crystals
Melting point 197 °C (387 °F; 470 K)
Related compounds
Related alkanoic acids
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Aceglutamide (brand name Neuramina), or aceglutamide aluminium (brand name Glumal), also known as acetylglutamine, is a

stability.[5]

Aceglutamide is used as a psychostimulant and nootropic, while aceglutamide aluminium is used in the treatment of ulcers.

cerebral ischemia.[5]

See also

References

  1. ^
    ISBN 978-1-4757-2085-3
    .
  2. ISBN 978-3-88763-075-1
    .
  3. ISBN 978-0-8155-1856-3
    .
  4. ISBN 978-94-011-4439-1
    .
  5. ^
    PMID 26444640
    .
  6. PMID 7095654
    .
  7. ^ Harada M, Yano S (1974). "Inhibitory effect of N-acetyl-L-glutamine aluminium complex (KW-110) and related compounds on gastric erosion and motility in stressed animals". Oyo Yakuri. 8 (1): 1–6.
  8. PMID 1790087
    .
  9. PMID 7098147
    .
  10. S2CID 37484555
    .
  11. ^ JP H10101576, Sasaki, Kazuyuki & Hayakawa, Toru, "Treating medicine for digestive organ disease", published 1998-04-21, assigned to Nisshin Flour Milling Co Ltd. 
  12. ^ US application 2003099722, Baxter, Jeffrey, "Methods and compositions for providing glutamine", published 2003-05-29, assigned to Abbott Laboratories , abandoned during patent examination