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Clobenpropit

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Clobenpropit
Clinical data
ATC code
  • None
Legal status
Legal status
Identifiers
  • N'-[(4-chlorophenyl)methyl]-1-[3-(3H-imidazol-4-yl)propylsulfanyl]formamidine
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC14H17ClN4S
Molar mass308.83 g·mol−1
3D model (JSmol)
  • C1=CC(=CC=C1CN=C(N)SCCCC2=CN=CN2)Cl

Clobenpropit is ahistamineH3 receptor antagonist.[1] It hasneuroprotective effects via stimulation ofGABA release in brain cellsin vitro.[2]

References

[edit]
  1. ^Sahlholm K, Nilsson J, Marcellino D, Fuxe K, Arhem P (2007). "The human histamine H3 receptor couples to GIRK channels inXenopus oocytes".European Journal of Pharmacology.567 (3):206–210.doi:10.1016/j.ejphar.2007.04.032.PMID 17537431.
  2. ^Dai H, Fu Q, Shen Y, Hu W, Zhang Z, Timmerman H, Leurs R, Chen Z (2007). "The histamine H3 receptor antagonist clobenpropit enhances GABA release to protect against NMDA-induced excitotoxicity through the cAMP/protein kinase A pathway in cultured cortical neurons".European Journal of Pharmacology.563 (1–3):117–123.doi:10.1016/j.ejphar.2007.01.069.PMID 17350613.
H1
Agonists
Antagonists
H2
Agonists
Antagonists
H3
Agonists
Antagonists
H4
Agonists
Antagonists


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