Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Lodenafil

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Lodenafil
Clinical data
Trade namesHelleva
Pregnancy
category
  • Not for use in women
Routes of
administration
By mouth
Legal status
Legal status
  • In general: unscheduled
Identifiers
  • 5-(2-Ethoxy-5-{[4-(2-hydroxyethyl)-1-piperazinyl]sulfonyl}phenyl)-1-methyl-3-propyl-1,4-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC23H32N6O5S
Molar mass504.61 g·mol−1
3D model (JSmol)
  • CCCc1c2c(c(=O)nc([nH]2)c3cc(ccc3OCC)S(=O)(=O)N4CCN(CC4)CCO)n(n1)C
  • InChI=1S/C23H32N6O5S/c1-4-6-18-20-21(27(3)26-18)23(31)25-22(24-20)17-15-16(7-8-19(17)34-5-2)35(32,33)29-11-9-28(10-12-29)13-14-30/h7-8,15,30H,4-6,9-14H2,1-3H3,(H,24,25,31) ☒N
  • Key:NEYKRKVLEWKOBI-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)
Lodenafil carbonate

Lodenafil (also known ashydroxyhomosildenafil, trade nameHelleva) is a drug belonging to a class of drugs calledPDE5 inhibitor, which many other erectile dysfunction drugs such assildenafil,tadalafil, andvardenafil also belong to. Likeudenafil andavanafil it belongs to a new generation of PDE5 inhibitors.

Lodenafil is formulated as aprodrug in the form of thecarbonate esterdimer,lodenafil carbonate, which breaks down in the body to form two molecules of the active drug lodenafil. This formulation has higher oralbioavailability than the parent drug.[1]

It is manufactured byCristália Produtos Químicos e Farmacêuticos inBrazil and sold there under the brand-name Helleva.[2]

It has undergone Phase III clinical trials,[3][4] but is not yet approved for use in theUnited States by theU.S. Food and Drug Administration.

See also

[edit]

References

[edit]
  1. ^Toque HA, Teixeira CE, Lorenzetti R, Okuyama CE, Antunes E, De Nucci G (September 2008). "Pharmacological characterization of a novel phosphodiesterase type 5 (PDE5) inhibitor lodenafil carbonate on human and rabbit corpus cavernosum".European Journal of Pharmacology.591 (1–3):189–95.doi:10.1016/j.ejphar.2008.06.055.PMID 18593576.S2CID 29575687.
  2. ^CristáliaArchived 2015-03-15 at theWayback Machine Product page. Retrieved on September 16, 2009.
  3. ^Glina S, Toscano I, Gomatzky C, de Góes PM, Júnior AN, Claro JF, Pagani E (February 2009). "Efficacy and tolerability of lodenafil carbonate for oral therapy in erectile dysfunction: a phase II clinical trial".The Journal of Sexual Medicine.6 (2):553–7.doi:10.1111/j.1743-6109.2008.01079.x.PMID 19040623.
  4. ^Glina S, Fonseca GN, Bertero EB, Damião R, Rocha LC, Jardim CR, Cairoli CE, Teloken C, Torres LO, Faria GE, da Silva MB, Pagani E (February 2010). "Efficacy and Tolerability of Lodenafil Carbonate for Oral Therapy of Erectile Dysfunction: A Phase III Clinical Trial".The Journal of Sexual Medicine.7 (5):1928–1936.doi:10.1111/j.1743-6109.2010.01711.x.PMID 20214718.
Dopamine agonists
Melanocortin agonists
PDE5 inhibitors
Sex steroids
Others
PDE1
PDE2
PDE3
PDE4
PDE5
PDE7
PDE9
PDE10
PDE11
Non-selective
Unsorted
Simple piperazines
(no additional rings)
Phenylpiperazines
Benzylpiperazines
Diphenylalkylpiperazines
(benzhydrylalkylpiperazines)
Pyrimidinylpiperazines
Pyridinylpiperazines
Benzo(iso)thiazolylpiperazines
Tricyclics
(piperazine attached via side chain)
Others/Uncategorized
Stub icon

Thisdrug article relating to thegenito-urinary system is astub. You can help Wikipedia byexpanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Lodenafil&oldid=1147982746"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp