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Gemopatrilat

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Gemopatrilat
Clinical data
Other namesBMS-189921
ATC code
  • None
Identifiers
  • (6S)-Hexahydro-6-[(αS)-α-mercaptohydrocinnamido]-2,2-dimethyl-7-oxo-1H-azepine-1-acetic acid
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC19H26N2O4S
Molar mass378.49g·mol−1
3D model (JSmol)
  • CC1(CCC[C@@H](C(=O)N1CC(=O)O)NC(=O)[C@H](CC2=CC=CC=C2)S)C
  • InChI=1S/C19H26N2O4S/c1-19(2)10-6-9-14(18(25)21(19)12-16(22)23)20-17(24)15(26)11-13-7-4-3-5-8-13/h3-5,7-8,14-15,26H,6,9-12H2,1-2H3,(H,20,24)(H,22,23)/t14-,15-/m0/s1
  • Key:YRSVDSQRGBYVIY-GJZGRUSLSA-N

Gemopatrilat(INN)[1]is an experimentaldrugthat was never marketed.[2]It acts as a vasopeptidaseinhibitor.[3][4]It inhibits bothangiotensin-converting enzyme(ACE) and neutral endopeptidase (neprilysin).[5]

References

[edit]
  1. ^"International Nonproprietary Names for Pharmaceutical Substances (INN). Recommended International Nonproprietary Names: List 46"(PDF).World Health Organization. p. 200.Retrieved2 March2017.
  2. ^"Gemopatrilat".AdisInsight.Highest Development Phases: Discontinued
  3. ^Laverman GD, Van Goor H, Henning RH, De Jong PE, De Zeeuw D, Navis G (January 2003)."Renoprotective effects of VPI versus ACEI in normotensive nephrotic rats on different sodium intakes".Kidney International.63(1): 64–71.doi:10.1046/j.1523-1755.2003.00708.x.PMID12472769.
  4. ^Wait JC, Vaccharajani N, Mitroka J, Jemal M, Khan S, Bonacorsi SJ, et al. (June 2006). "Metabolism of [14C]gemopatrilat after oral administration to rats, dogs, and humans".Drug Metabolism and Disposition.34(6): 961–70.doi:10.1124/dmd.105.007500.PMID16540589.S2CID25629874.
  5. ^Hubner RA, Kubota E, Casley DJ, Johnston CI, Burrell LM (May 2001). "In-vitro and in-vivo inhibition of rat neutral endopeptidase and angiotensin converting enzyme with the vasopeptidase inhibitor gemopatrilat".Journal of Hypertension.19(5): 941–6.doi:10.1097/00004872-200105000-00015.PMID11393678.S2CID9162678.