Details
Stereochemistry | ACHIRAL |
Molecular Formula | C23H32N6O5S |
Molecular Weight | 504.602 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCC1=NN(C)C2=C1N=C(NC2=O)C3=CC(=CC=C3OCC)S(=O)(=O)N4CCN(CCO)CC4
InChI
InChIKey=NEYKRKVLEWKOBI-UHFFFAOYSA-N
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)
Lodenafil carbonate, a novel phosphodiesterase 5 inhibitor developed in Brazil. Lodenafil carbonate is a prodrug that is metabolized with formation of the active compound, lodenafil. Lodenafil carbonate participated in phase III clinical trial for erectile dysfunction and showed a satisfactory efficacy-safety profile.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: O76074 Gene ID: 8654.0 Gene Symbol: PDE5A Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/18593576 |
PubMed
Title | Date | PubMed |
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Pharmacological characterization of a novel phosphodiesterase type 5 (PDE5) inhibitor lodenafil carbonate on human and rabbit corpus cavernosum. | 2008 Sep 4 |
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Cardiovascular repercussion of lodenafil carbonate, a new PDE5 inhibitor, with and without alcohol consumption. | 2010 Feb |
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Efficacy and tolerability of lodenafil carbonate for oral therapy of erectile dysfunction: a phase III clinical trial. | 2010 May |
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Lodenafil treatment in the monocrotaline model of pulmonary hypertension in rats. | 2014 Jul-Aug |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20214718
lodenafil carbonate (LC) 40 mg or LC 80 mg and followed for 4 weeks
Route of Administration:
Oral
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WIKIPEDIA |
Designer-drugs-Lodenafil
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DTXSID60161161
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139755-85-4
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LODENAFIL
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80X7B1F6NW
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135452901
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ACTIVE MOIETY
PRODRUG (METABOLITE ACTIVE)