Lorglumide

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Lorglumide
Lorglumide.png
Clinical data
Synonyms 4-[(3,4-dichlorobenzoyl)amino]-5-(dipentylamino)-5-oxopentanoic acid
ATC code
  • none
Identifiers
CAS Number
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
ChEBI
ChEMBL
Chemical and physical data
Formula C22H32Cl2N2O4
Molar mass 459.406 g/mol
3D model (JSmol)
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Lorglumide (CR-1409) is a drug which inhibits gastrointestinal motility and reduces gastric secretions, acting as a cholecystokinin antagonist,[1] with fairly high selectivity for the CCKA subtype.[2] It has been suggested as a potential treatment for a variety of gastrointestinal problems including stomach ulcers, irritable bowel syndrome, dyspepsia, constipation and pancreatitis, as well as some forms of cancer, but animal and human testing has produced inconsistent results and no clear therapeutic role has been established, although it is widely used in scientific research.[3][4][5][6]

References[edit]

  1. ^ Makovec, F; Bani, M; Cereda, R; Chisté, R; Pacini, M. A.; Revel, L; Rovati, L. A.; Rovati, L. C.; Setnikar, I (1987). "Pharmacological properties of lorglumide as a member of a new class of cholecystokinin antagonists". Arzneimittel-Forschung. 37 (11): 1265–8. PMID 3440035. 
  2. ^ González-Puga, C; García-Navarro, A; Escames, G; León, J; López-Cantarero, M; Ros, E; Acuña-Castroviejo, D (2005). "Selective CCK-A but not CCK-B receptor antagonists inhibit HT-29 cell proliferation: Synergism with pharmacological levels of melatonin". Journal of Pineal Research. 39 (3): 243–50. doi:10.1111/j.1600-079X.2005.00239.x. PMID 16150104. 
  3. ^ De Tullio, P; Delarge, J; Pirotte, B (1999). "Recent advances in the chemistry of cholecystokinin receptor ligands (agonists and antagonists)". Current medicinal chemistry. 6 (6): 433–55. PMID 10213792. 
  4. ^ De Tullio, P; Delarge, J; Pirotte, B (2000). "Therapeutic and chemical developments of cholecystokinin receptor ligands". Expert Opinion on Investigational Drugs. 9 (1): 129–46. doi:10.1517/13543784.9.1.129. PMID 11060666. 
  5. ^ Herranz, R (2003). "Cholecystokinin antagonists: Pharmacological and therapeutic potential". Medicinal Research Reviews. 23 (5): 559–605. doi:10.1002/med.10042. PMID 12789687. 
  6. ^ Berna, M. J.; Tapia, J. A.; Sancho, V; Jensen, R. T. (2007). "Progress in developing cholecystokinin (CCK)/gastrin receptor ligands that have therapeutic potential". Current Opinion in Pharmacology. 7 (6): 583–92. doi:10.1016/j.coph.2007.09.011. PMC 2186776Freely accessible. PMID 17997137.