From Wikipedia, the free encyclopedia
Rolziracetam
Clinical data
Other names2,6,7,8-tetrahydro-1H-pyrrolizine-3,5-dione
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
  • AU: S4 (Prescription only)
  • US: Unscheduled
Identifiers
  • dihydro-1H-pyrrolizine-3,5(2H,6H)-dione
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard ( EPA)
Chemical and physical data
FormulaC7H9N2O2
Molar mass153.161 g·mol−1
3D model ( JSmol)
  • O=C2N1C(=O)CCC1CC2
  • InChI=1S/C7H9NO2/c9-6-3-1-5-2-4-7(10)8(5)6/h5H,1-4H2 checkY
  • Key:IEZDOKQWPWZVQF-UHFFFAOYSA-N checkY
 ☒NcheckY  (what is this?)   (verify)

Rolziracetam is a nootropic drug of the racetam family.

Rolziracetam was found to improve performance on a delayed-response task in aged rhesus monkeys. It has a wide margin of safety in animals and has been evaluated for use in cognitively impaired human subjects. [1]

See also

References

  1. ^ Butler DE, Leonard JD, Caprathe BW, L'Italien YJ, Pavia MR, Hershenson FM, Poschel PH, Marriott JG (March 1987). "Amnesia-reversal activity of a series of cyclic imides". Journal of Medicinal Chemistry. 30 (3): 498–503. doi: 10.1021/jm00386a010. PMID  3820221.


From Wikipedia, the free encyclopedia
Rolziracetam
Clinical data
Other names2,6,7,8-tetrahydro-1H-pyrrolizine-3,5-dione
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
  • AU: S4 (Prescription only)
  • US: Unscheduled
Identifiers
  • dihydro-1H-pyrrolizine-3,5(2H,6H)-dione
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard ( EPA)
Chemical and physical data
FormulaC7H9N2O2
Molar mass153.161 g·mol−1
3D model ( JSmol)
  • O=C2N1C(=O)CCC1CC2
  • InChI=1S/C7H9NO2/c9-6-3-1-5-2-4-7(10)8(5)6/h5H,1-4H2 checkY
  • Key:IEZDOKQWPWZVQF-UHFFFAOYSA-N checkY
 ☒NcheckY  (what is this?)   (verify)

Rolziracetam is a nootropic drug of the racetam family.

Rolziracetam was found to improve performance on a delayed-response task in aged rhesus monkeys. It has a wide margin of safety in animals and has been evaluated for use in cognitively impaired human subjects. [1]

See also

References

  1. ^ Butler DE, Leonard JD, Caprathe BW, L'Italien YJ, Pavia MR, Hershenson FM, Poschel PH, Marriott JG (March 1987). "Amnesia-reversal activity of a series of cyclic imides". Journal of Medicinal Chemistry. 30 (3): 498–503. doi: 10.1021/jm00386a010. PMID  3820221.



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