Fantofarone

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Fantofarone
Fantofarone.png
Names
Preferred IUPAC name
N-[2-(3,4-Dimethoxyphenyl)ethyl]-N-methyl-3-{4-[2-(propan-2-yl)indolizine-1-sulfonyl]phenoxy}propan-1-amine
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
UNII
  • InChI=1S/C31H38N2O5S/c1-23(2)27-22-33-18-7-6-9-28(33)31(27)39(34,35)26-13-11-25(12-14-26)38-20-8-17-32(3)19-16-24-10-15-29(36-4)30(21-24)37-5/h6-7,9-15,18,21-23H,8,16-17,19-20H2,1-5H3 ☒N
    Key: ITAMRBIZWGDOHW-UHFFFAOYSA-N ☒N
  • InChI=1/C31H38N2O5S/c1-23(2)27-22-33-18-7-6-9-28(33)31(27)39(34,35)26-13-11-25(12-14-26)38-20-8-17-32(3)19-16-24-10-15-29(36-4)30(21-24)37-5/h6-7,9-15,18,21-23H,8,16-17,19-20H2,1-5H3
    Key: ITAMRBIZWGDOHW-UHFFFAOYAL
  • CC(C)C1=CN2C=CC=CC2=C1S(=O)(=O)C3=CC=C(C=C3)OCCCN(C)CCC4=CC(=C(C=C4)OC)OC
Properties
C31H38N2O5S
Molar mass 550.70882
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Fantofarone is a calcium channel blocker.[1]

Fantofarone vs Verapamil[edit]

There are many different calcium channel blockers that show different results in use. Fantofarone and Verapamil are both calcium channel blockers that behave differently in different applications.

Fantofarone was shown in use for treatment of angioplasty-induced vasospasm in an atherosclerotic rabbits.[2] There are many different observations that show a potential cause of vasospasm, such as local injury on the body, but overall mechanism of it is still not fully understood.[2] In order to observe the efficiency of Fantofarone in the treatment of AIV ( Angioplasty-Induced Vasospasm), it was compared to the treatment of verapamil (which is also a calcium channel blocker). Fantofarone showed more effectiveness against a severity of vasospasm than verapamil. [2]

Fantofarone and Verapamil was also tested as an attempt of reversing of chloroquine resistance[3](Chloroquine is a medication that is used to treat malaria). In the treatment of reversing the chloroquine resistance it was observed that verapamil was more potent and more efficient than Fantofarone.[3]

References[edit]

  1. ^ Rosseels, Gilbert; Houben, Christian; Kerckx, Patricia (1995). "Synthesis of a metabolite of fantofarone". Advances in Organobromine Chemistry II. Industrial Chemistry Library. 7. pp. 152–159. doi:10.1016/S0926-9614(05)80016-4. ISBN 9780444821058.
  2. ^ a b c "Effect of Fantofarone, a New Ca2 Channel Antagonist, on Angioplasty-Induced Vasospasm in an Atherosclerotic Rabbit Model". Biochemical Pharmacology. 55 (12): 2047–2050. 1998-06-15. doi:10.1016/S0006-2952(98)00026-4. ISSN 0006-2952.
  3. ^ a b "Synergy between two calcium channel blockers, verapamil and fantofarone (SR33557), in reversing chloroquine resistance in Plasmodium falciparum". Biochemical Pharmacology. 55 (4): 433–440. 1998-02-15. doi:10.1016/S0006-2952(97)00482-6. ISSN 0006-2952.