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N-Ethyl Tadalafil is a designer analog of tadalafil, the long-acting PDE5 inhibitor behind Cialis, built by modifying the original molecule. It is presumed to share tadalafil's ability to relax blood vessels and support erections, and it turns up most often as an undeclared ingredient in sexual-enhancement supplements. Because the analog itself has not been formally tested, it is best understood through the well-established pharmacology of its parent drug rather than through direct evidence.
- Designer cousin of the long acting Cialis molecule
- Aimed at the PDE5 pathway behind erections
- Relaxes vessels for stronger blood flow
- Long duration expected from the tadalafil scaffold
- Orally active, no injection needed
- Never mix with nitrates; blood pressure can crash
- Headache and flushing
- Nasal congestion or back pain
Overview
N-Ethyl Tadalafil, also written N-ethylnortadalafil, is a synthetic analog of tadalafil, the long-acting phosphodiesterase type 5 (PDE5) inhibitor marketed as Cialis. It is created by making small structural changes to the tadalafil molecule, and it belongs to a large group of so-called designer PDE5 inhibitor analogs that are not approved as drugs anywhere [2].
The context in which these compounds appear is important. Around the world, dietary supplements and herbal products marketed for sexual performance have repeatedly been found adulterated with prescription PDE5 inhibitors and their unapproved analogs; one review counted more than 50 such analogs identified as hidden adulterants [2]. Analogs of this type, including close relatives such as aminotadalafil and other modified nortadalafils, are typically discovered by analytical chemists using techniques like liquid chromatography, mass spectrometry, and nuclear magnetic resonance rather than through any program of medical development [1][3][4].
The reason manufacturers use analogs rather than the approved drug is largely to evade detection by standard screening methods, since a novel structure may slip past routine tests [2]. The consequence for the consumer is a substance whose potency, purity, and safety have never been established, and which may be present at an unknown amount without appearing on the label [1].
N-Ethyl Tadalafil is therefore not a legitimate medicine but a research-grade and gray-market chemical. Its presumed activity is inferred from tadalafil, yet it carries the added hazards of unpredictable content and the same serious contraindication as its parent, namely a dangerous interaction with nitrate medications [2][5].
- N-Ethyl Tadalafil is one of more than fifty tadalafil analogs that regulators and analytical chemists have catalogued, most often as hidden ingredients in supplements.
- The analog has never been formally studied, so everything assumed about it is read across from its parent drug, tadalafil.
- Its parent, tadalafil, is nicknamed the weekend pill because a single dose can support the erectile response for more than twenty-four hours.
Mechanism
Because N-Ethyl Tadalafil has not been studied in its own right, its mechanism is understood by analogy to tadalafil, the approved drug it is derived from [1][5]. Tadalafil is a potent, highly selective inhibitor of phosphodiesterase type 5 (PDE5), the enzyme that breaks down cyclic guanosine monophosphate (cGMP) in the smooth muscle of the penis and blood vessels [5]. During sexual arousal, nerve signals release , which raises cGMP; cGMP relaxes the smooth muscle of the corpus cavernosum, allowing blood to flow in and produce an erection. By blocking PDE5, tadalafil prevents cGMP breakdown, so the erectile response to arousal is stronger and better sustained, without changing the underlying nitric oxide trigger [5].
A hallmark of tadalafil specifically is its long duration: its effect on the erectile response is relatively rapid in onset and lasts for at least 24 hours, far longer than the earlier PDE5 inhibitors, which is why it earned the nickname the weekend pill [5]. An N-ethyl modification to the molecule would be expected to retain PDE5 inhibition while potentially altering potency or how long the compound lasts, though none of this has actually been measured for the analog itself [1].
The practical implications, and the risks, follow from this shared mechanism. Like tadalafil, N-Ethyl Tadalafil is a vasodilator, so it must never be combined with nitrate medications, a combination that can cause a dangerous drop in blood pressure, and it can be expected to share side effects such as headache, flushing, and nasal congestion [5]. The distinctive danger of an analog, however, is uncertainty: when it appears hidden in a supplement, the amount present is unknown and unregulated, so the dose cannot be judged and the interaction risk cannot be managed, which is exactly why more than 50 such analogs have drawn the concern of regulators and analytical chemists [1][2].
receptor fingerprint
PDE5 enzymeinhibits
cGMP / pathwayraises signaling
PDE11 enzymeweakly inhibits
Dosingtypical ranges, not medical advice
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Safetyrisks and cautions, not medical advice
No human trials, no approval, and it is often present without being on the label. The hazards mirror the PDE5 class: severe low blood pressure when mixed with nitrates or alpha-blockers, headaches, flushing, nasal congestion, back pain, and rare but serious priapism or sudden vision or hearing loss. Because the amount in any given product is unknown and inconsistent, the effect is impossible to control, which is especially risky for anyone with heart disease or on cardiac medications. Not for human use.
History
N-Ethyl Tadalafil has no conventional discovery narrative of its own; it exists as a designer analog of tadalafil, the long-acting PDE5 inhibitor developed by ICOS Corporation in partnership with Eli Lilly and approved as Cialis in 2003. Rather than being created through a formal drug-development program, this analog is produced by making a small structural modification to the parent molecule, replacing a methyl group with an ethyl group, a change that yields a substance close enough to keep the presumed pharmacology while falling outside the exact patented structure.
Its appearances in the scientific record come almost entirely from analytical chemists and regulatory laboratories, who have repeatedly detected it as an undeclared ingredient hidden inside sexual-enhancement supplements. Because it has never undergone dedicated pharmacological or clinical study, essentially nothing about its potency, dosing or safety has been directly measured; its properties are inferred wholly from tadalafil. It is best understood as one member of a large and growing catalog of more than fifty tadalafil analogs that regulators track as adulterants rather than as an independently developed medicine.
Reputation
N-Ethyl Tadalafil draws its entire reputation from its distinguished parent; tadalafil is a genuinely landmark medication, a potent and highly selective PDE5 inhibitor famous for a duration of action exceeding twenty-four hours that earned it the nickname the weekend pill. By close structural analogy, N-Ethyl Tadalafil is presumed to share that ability to relax vascular smooth muscle and support erections in response to arousal.
What makes it interesting to chemists is precisely what makes it worth treating with caution; because the analog itself has never been formally tested, its exact strength and behavior remain genuinely unknown, and when it turns up undeclared in a supplement the amount present is unregulated and unmeasured. It is fairest to describe it as a compound whose plausible benefits are borrowed from tadalafil while its own profile stays uncharacterized, which is exactly why analytical and regulatory scientists keep a close eye on it.
Subjective profileweighing the evidence above
Not something to take deliberately. It is an untested analog that mostly turns up undeclared in sexual-enhancement supplements at amounts that vary batch to batch, which is precisely what makes it dangerous with nitrates or in anyone with heart disease. Prescribed tadalafil is measured; this is not.
Where to buy
Suppliers
Vendors carrying N-Ethyl Tadalafil, with live product details and codes. Links are affiliate links that support the wiki at no cost to you.
Kimera Chems
N-Ethyl Tadalafil
Research
- 2003first citedEfficacy and tolerability of tadalafil, a novel phosphodiesterase 5 inhibitor, in treatment of…
- 2015most recentDetection of a tadalafil analogue as an adulterant in a dietary supplement for erectile dysfunc…
- 1.Detection of a tadalafil analogue as an adulterant in a dietary supplement for erectile dysfunction.
- 2.Screening of synthetic PDE-5 inhibitors and their analogues as adulterants: analytical techniques and challenges.
- 3.Identification of sildenafil, tadalafil and vardenafil by gas chromatography-mass spectrometry on short capillary column.
- 4.Analysis of illicit dietary supplements sold in the Italian market: identification of a sildenafil thioderivative as adulterant using UPLC-TOF/MS and GC/MS.
- 5.Efficacy and tolerability of tadalafil, a novel phosphodiesterase 5 inhibitor, in treatment of erectile dysfunction.
5 listed here; entry last updated August 2026
Reviews
My notesprivate to this device
FAQ
What is N-Ethyl Tadalafil?
An unapproved analogue of tadalafil (Cialis) with an ethyl group swapped onto the molecule. It appears as a hidden ingredient in some erectile-dysfunction supplements.
Is it basically Cialis?
It targets the same PDE5 enzyme, so the intended effect is similar, but it was never tested in people so its true potency and safety are unknown.
Why does it end up in supplements?
It makes a "natural" product actually work while the structural tweak tries to sidestep regulators. The downside is it skipped every safety study a real drug goes through.
What are the main risks?
Dangerous blood-pressure drops with nitrate medications, plus the usual PDE5 side effects, all made worse by not knowing the dose.
Is it approved?
No. It is an illegal adulterant and is sold only as a research chemical, not for human consumption.
Adverse effects
- Never mix with nitrates; blood pressure can crash
- Headache and flushing
- Nasal congestion or back pain
Notes and cautions
- Dose and purity are uncertain and unregulated