Histamine glutarimide

Histamine glutarimide
Clinical data
Other names	XC-8
Legal status
Legal status	Investigational;
Identifiers
	IUPAC name 1-[2-(1H-imidazol-5-yl)ethyl]piperidine-2,6-dione;
CAS Number	1464897-15-1 ;
PubChem CID	24826317 ;
DrugBank	DB16016 ;
ChemSpider	48673501 ;
UNII	VOM9DP10M3 ;
Chemical and physical data
Formula	C10H13N3O2
Molar mass	207.233 g·mol−1
3D model (JSmol)	Interactive image ;
	SMILES C1CC(=O)N(C(=O)C1)CCC2=CN=CN2;
	InChI InChI=1S/C10H13N3O2/c14-9-2-1-3-10(15)13(9)5-4-8-6-11-7-12-8/h6-7H,1-5H2,(H,11,12); Key:DYKZYSKWOHKZMF-UHFFFAOYSA-N;

Last updated June 27, 2025

Histamine glutarimide is an investigational new drug that is being evaluated for the treatment of cough in acute respiratory infection.^[1]^[2] It is a glutaminyl cyclase inhibitor.^[3]

References

↑ "Histamine glutarimide - EURRUS Biotech". AdisInsight. Springer Nature Switzerland AG.
↑ Clinical trial number NCT05273619 for "Efficacy and Safety of XC8, Film-coated Tablets, 40 mg in Patients With Dry Non-productive Cough Against Acute Respiratory Viral Infection" at ClinicalTrials.gov
↑ Romanova J, Chikina E, Rydlovskaya A, Pohl W, Renner A, Zeifman A, et al. (December 2020). "New Anti-Chemokine Oral Drug XC8 in the Treatment of Asthma Patients with Poor Response to Corticosteroids: Results of a Phase 2A Randomized Controlled Clinical Trial". Pulmonary Therapy. 6 (2): 351–369. doi:10.1007/s41030-020-00134-5. PMC 7671956 . PMID 33095411.

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[1] "Histamine glutarimide - EURRUS Biotech". AdisInsight. Springer Nature Switzerland AG.

[2] Clinical trial number NCT05273619 for "Efficacy and Safety of XC8, Film-coated Tablets, 40 mg in Patients With Dry Non-productive Cough Against Acute Respiratory Viral Infection" at ClinicalTrials.gov

[Romanova_2020-3] Romanova J, Chikina E, Rydlovskaya A, Pohl W, Renner A, Zeifman A, et al. (December 2020). "New Anti-Chemokine Oral Drug XC8 in the Treatment of Asthma Patients with Poor Response to Corticosteroids: Results of a Phase 2A Randomized Controlled Clinical Trial". Pulmonary Therapy. 6 (2): 351–369. doi:10.1007/s41030-020-00134-5. PMC 7671956 . PMID 33095411.

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