Imuracetam

Imuracetam
Names
	Preferred IUPAC name N,N′-Bis[(2-oxopyrrolidin-1-yl)methyl]urea
	Other names UCB-G218
Identifiers
CAS Number	67542-41-0 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL2106342;
ChemSpider	143327 ;
PubChem CID	163319;
UNII	972FNV35ZM ;
CompTox Dashboard (EPA)	DTXSID20217875 ;
	InChI InChI=1S/C11H18N4O3/c16-9-3-1-5-14(9)7-12-11(18)13-8-15-6-2-4-10(15)17/h1-8H2,(H2,12,13,18) Key: WMKONRFEZGAHTE-UHFFFAOYSA-N ; InChI=1/C11H18N4O3/c16-9-3-1-5-14(9)7-12-11(18)13-8-15-6-2-4-10(15)17/h1-8H2,(H2,12,13,18) Key: WMKONRFEZGAHTE-UHFFFAOYAT;
	SMILES O=C(NCN1C(=O)CCC1)NCN2C(=O)CCC2;
Properties
Chemical formula	C11H18N4O3
Molar mass	254.290 g·mol−1
Melting point	184.5 °C (364.1 °F; 457.6 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Imuracetam (INNTooltip International Nonproprietary Name; developmental code name UCB-G218) is a drug of the racetam group described as a nootropic (cognitive enhancer).^[2]^[3] It was under development in the 1970s but was never marketed.^[1]

References

^ ^a ^b Ganellin CR, Triggle DJ (1996). Dictionary of Pharmacological Agents. Vol. 3. CRC Press.
^ Elks, J. (2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer US. p. 681. ISBN 978-1-4757-2085-3. Retrieved 1 October 2024.
^ Avetisyan SA, Kocharov SL, Azaryan LV, Dzhagatspanyan IA, Melikyan GG (February 1998). "Synthesis and psychotropic activity of new 2-pyrrolidone derivatives". Pharmaceutical Chemistry Journal. 32 (2): 55–58. doi:10.1007/BF02464161. S2CID 29810469.

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[GanellinTriggle1996-1] Ganellin CR, Triggle DJ (1996). Dictionary of Pharmacological Agents. Vol. 3. CRC Press.

[Elks2014-2] Elks, J. (2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer US. p. 681. ISBN 978-1-4757-2085-3. Retrieved 1 October 2024.

[AvetisyanKocharovAzaryan1998-3] Avetisyan SA, Kocharov SL, Azaryan LV, Dzhagatspanyan IA, Melikyan GG (February 1998). "Synthesis and psychotropic activity of new 2-pyrrolidone derivatives". Pharmaceutical Chemistry Journal. 32 (2): 55–58. doi:10.1007/BF02464161. S2CID 29810469.

[1]

v t e Racetams
Racetams	Nootropics: Aniracetam Coluracetam Dimiracetam Doliracetam Dupracetam Fasoracetam Imuracetam Nebracetam Nefiracetam Nicoracetam Oxiracetam Piperacetam Piracetam Pramiracetam Rolipram Rolziracetam Anticonvulsants: Brivaracetam Etiracetam Levetiracetam Seletracetam
Phenylpiracetams	Nootropics and/or stimulants: Cebaracetam Methylphenylpiracetam E1R ((4R,5S)-methylphenylpiracetam) Phenylpiracetam (phenotropil; fonturacetam) MRZ-9547 ((R)-phenylpiracetam) (S)-Phenylpiracetam RGPU-95 (chlorophenylpiracetam) Anticonvulsants: Phenylpiracetam hydrazide
Racetam-like	Nootropics: Aloracetam Molracetam Omberacetam (Noopept) Tenilsetam Traneurocin (cycloprolylglycine; NA-831) Anticonvulsants: Padsevonil