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Cicloprolol

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
Cicloprolol
Clinical data
Other namesCycloprolol; SL-75177
Identifiers
  • 1-[4-[2-(cyclopropylmethoxy)ethoxy]phenoxy]-3-(propan-2-ylamino)propan-2-ol
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC18H29NO4
Molar mass323.433 g·mol−1
3D model (JSmol)
  • CC(C)NCC(COC1=CC=C(C=C1)OCCOCC2CC2)O
  • InChI=1S/C18H29NO4/c1-14(2)19-11-16(20)13-23-18-7-5-17(6-8-18)22-10-9-21-12-15-3-4-15/h5-8,14-16,19-20H,3-4,9-13H2,1-2H3
  • Key:JNDJPKHYZWRRIS-UHFFFAOYSA-N

Cicloprolol (INNTooltip International Nonproprietary Name; developmental code nameSL-75177), orcycloprolol (BANTooltip British Approved Name), is aβ-adrenergic receptor antagonist (beta blocker) described as anantihypertensive agent which was never marketed.[1][2][3][4][5] It has weakpartial agonist orintrinsic sympathomimetic activity (30%) at theβ-adrenergic receptors.[4][2] This is higher than that of many other beta blockers but is lower than that ofxamoterol (45%).[4] The drug isselective for theβ1-adrenergic receptor.[3] It has been studied in the treatment ofheart failure.[3]

Chemistry

[edit]

Thechemical structure of cicloprolol is very similar to that ofbetaxolol.

Synthesis

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Cicloprolol can be synthesized starting from 4-benzyloxyphenol.[6][7]

Cicloprolol synthesis

References

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  1. ^Elks J (2014).The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer US. p. 272.ISBN 978-1-4757-2085-3. Retrieved29 August 2024.
  2. ^abMorton IK, Hall JM (2012).Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Netherlands. p. 88.ISBN 978-94-011-4439-1. Retrieved2024-08-29.
  3. ^abcPersson H, Erhardt L (June 1991). "Beta receptor antagonists in the treatment of heart failure".Cardiovascular Drugs and Therapy.5 (3):589–604.doi:10.1007/BF03029728.PMID 1678962.
  4. ^abcWaller DG (August 1990)."Beta-adrenoceptor partial agonists: a renaissance in cardiovascular therapy?".British Journal of Clinical Pharmacology.30 (2):157–171.doi:10.1111/j.1365-2125.1990.tb03760.x.PMC 1368213.PMID 1976342.
  5. ^Cocco G, Alfiero R, Pouleur H (January 1992)."An evaluation of the safety of the beta-modulator cicloprolol in chronic heart failure".Clinical Cardiology.15 (1):38–42.doi:10.1002/clc.4960150109.PMID 1347258.
  6. ^DE 2649605, Manoury PM, Cavero IA, Majer H, Giudicelli DP, "Phenoläther, Verfahren zu ihrer Herstellung und sie enthaltende Arzneimttel [Phenol ethers, processes for their preparation and medicinal products containing them]", published 1977-05-18, assigned toSynthelabo S.A. 
  7. ^P. M. J. Manouri, I. A. G. Carero, H. Majer, and P. R. L. Giudicelli, (1977) Chem. Abstr., 87:134,543j (1977). eidemU.S. patent 4,311,708
α1
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α2
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Antagonists
β
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Antagonists
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