TheAcetildenafil, also known as Hongdenafil is defined as a structural analogue of Viagra. According to studies, it has been found out thatAcetildenafilacts as a PDE5 inhibitor, just like Viagra. The fact is, this compound is a great addition to people who are studying effects of Viagra. However, Acetildenafilis not yet licensed for any form of Vivo (inside of a living organism) research. Due to the fact it has a strong chemical resemblance to Viagra, it binds in similar ways to receptors in Vitro (outside of a living organism).
The analogue ofAcetildenafilwas first discovered as an extract of pre-mixed bulk powder. As the story goes, it was intended to be encapsulated and labeled as a dietary product. Its structure was analyzed by different analyses such as NMR, HR-ESI, MS, ESI-Msn and even FTIR Analyses. Owing to the inclusion of hydroxyl group in ace iDEN fil, the detected compound was called Hydroxyacetildenafi.
What is it used for?
TheAcetildenafilis strictly for research purposes at the moment. According to research, it has been found thatAcetildenafilcan be used in conjunction with other PDE5 inhibitors including Sildenafil as long as home office license is held for it. The competitive ligand binding assays can be performed using this compound to learn about its affinity.
The solutions that contain cGMP specific phosphodiesterase type 5 can be used for determination of efficacy and binding site profile ofAcetildenafil. The array of in vitro research opportunities exists for the novel inhibitor.
TheAcetildenafilis a new search chemical that is used by different chemical study libraries and sample reference for NMR, HPLC, FTIPR and GC analysis. The chemists can also use this compound as a reagent. Apart from its dietary and other benefits, it’s also beneficial for sex life. But how? Let’s shed some light over it.
Effects of Acetildenafil
TheAcetildenafilimproves libido as it increases blood flow to sexual organs. This helps to improve the sex drive. The problem is, it’s not very noticeable, but this compound doesn’t help to achieve and maintain harder erections. People who take this compound reported had erections time from time for 2 to 3 days with minimum vasodilation. Acetildenafilis also the analog sildenafil, better say Viagra. The effects of this compound are similar to one of Cialis. Men who take the methylene and MDMA experience temporary erectile dysfunction, and thus, they need to take an aphrodisiac to take part in any sexual activity.
The problem is, the dosage ofAcetildenafilis not established at this time. At this moment, it is available in only 5, 10, 20, and even 110 mg tablets. Taken orally, it’s advised to be taken an hour before engaging in any activity. Anything that is too high can lead to uncomfortable erections that often last for more than 24 hours. Keeping this in mind, the first time users are advised to start with a low dosage and build up their tolerance. It is easily available in the market, but you may need to consult with your physician first.
Nifoxipamis known as a long lasting psychoactive drug that belongs to the class of Benzodiazepine. This drug is known for its sedative, hypnotic, anxiolytic, anticonvulsant and muscle relaxant effects. It binds to sites on GABAA gamma-Amino Butyric acid receptor.
Classified as seven nitro benzodiazepine, it belongs to the same category as some other hypnotic Nitrobenzodiazepines. These can be Nitrazepam, Nimetazepam, Flurazepam and others. Moreover, this drug has potential use for short-term treatment of anxiety, acute seizures, and sedation of hospitalized patients. It is sold online by the research chemical vendors and is only allowed for psychoactive recreational purposes.
At this moment, Nifoxipamremains in a gray area compound in most parts of the world. Its legality in any county is not verified but people can be charged with its possession under different circumstances.
Belonging to Benzodiazepine class, theNifoxipamcontains a benzene ring fused to diazepine ring that is a seven-membered ring with two nitrogen constituents located right at R1 and R4. Moreover, Nifoxipamis the active metabolite of flunitrazepam. Benzyl ring ofNifoxipamis substituted at R7 with the nitro group of NO2 AR2 fluorine-substituted phenyl ring that is bound to the structure of R5. Adding up, Nifoxipamcontains an OH- group which is substituted R3. TheNifoxipamalso has an oxygen group that doubles which is bonded with R2 of the diazepine ring to make a ketone. The oxygen substation of R2 is shared with the Benzodiazepine drugs with Suffix azepam. As with Flunitrazepam, Nifoxipamis insoluble in water but adding hydroxyl can make it a bit soluble.
The Benzodiazepine produces a broad range of effects as it binds to the receptor site and magnifies efficiency with effects of neurotransmitter gamma amino butyric acid by acting on its receptors. This site is the most beneficial inhibitory receptor inside the brain, and therefore, modulation results in sedating ofNifoxipamon the nervous system.
The effects ofNifoxipamare stated as below; these are based on the subjective effects index and persona experiences of subjects. The listed effects rarely occurred and for once only. However heavy dosage can often lead to serious circumstances.
Control Loss of Motor
The cognitive effects ofNifoxipameasily break into different components that intensify proportional to dosage. The general head space of this compound is described as one of intense sedation and with decreased inhibition, it also has a lot of depressant cognitive effects.
Delusions of Sobriety
Information Processing Suppression
The Paradoxical reactions are increased seizures, aggression, increased anxiety, violent behavior, impulse control loss, irritability and even suicidal behavior. Such effects take place with great frequency in recreational abusers, people who are affected by some mental disorders or children and patients with high dosage regime. The lethal dose ofNifoxipamremains unestablished, but it has a large therapeutic index with a margin of safety.
Introduction to 3F-Phenmetrazine: Everything You Need to Know
3F-Phenmetrazineis better known as 2-3 fluorophenyl-3-methymorpholine and fluoro phenmetrazine analogue of Phenmetrazine. Phenmetrazine is itself a compound that consists of Phenethylamine backbone.
The 3-FPM is provided in solid powder and white crystalline form. It’s easily soluble in organic solvents such as DMF, DCM, DMSO, methanol, and ethanol. This can be executed with any inert gas. The ethanol solubility is 12 mg per ml while the DMF and DMSO are 16 mg per ML.
It’s a short-lived stimulant drug of Phenethylamine variety. It has no history of human usage before 2014. With its effects, it’s considered to be subtle when compared with other stimulants. It’s widely regarded for its ability to cause less nervousness, euphoria, and insomnia as compared to the amphetamine drugs.
It’s used as recreational drugs in many countries. 3F-Phenmetrazineis well received for its ability to induce euphoria with its potential for recurrent abuse. It’s prescribed for mental illness and obesity.
This is rooted from a well-known chemical agent. It possesses Phenethylamine skeleton. The major difference with3F-Phenmetrazineas it comes with 3 Fluoro group bonded to its parent molecule. Since the introduction, it always had an unpredictable lab behavior.
But as compared to other compounds sharing its structure, 3 FPM plays an important role in the regulation of neurotransmitter with a powerful affinity for serotonin and lower dopamine and noradrenaline value.
This compound is recognized under many names; it has the patent mark of PAL-593 while it possesses the molecular mass of 195 g/mol. It appears as a crystalline powder at room temperature that makes it quite ideal for shipping and testing in any lab. Right now it is simply described as a potent simulated which is aimed at central nervous.
It can release the chemical messengers in the brain. These messengers are classified as Norepinephrine and Dopamine. It is unknown how3F-Phenmetrazinecan inhibit center in the hypothalamus which can control the appetite. According to some old studies published helps to provide some evidence that3-FPMis effective for appetite suppression.
Yes, it promotes weight loss for everyone, especially children. Still, these are banned in some countries. 3F-Phenmetrazineis not often prescribed for its potential of abuse. Moreover, there was a study published that clearly states its user developed a resistance to its appetite suppressant effects and this the weight loss decreases after few weeks of not taking the drugs.
The early studies on3F-Phenmetrazineshows its ability to act as it releases a medium of dopamine and norepinephrine. This drug is considered to be bought by some countries for research reasons, but it’s mostly banned. As the core of 3FPM remains Phenethylamine, it is believed to be the cause some side effects.
1p-LSD, short for 1 Propionyl Lysergic Acid Diethylamide is the hallucinogenic, psychedelic drug that belongs to the family of lysergamide. This substance has almost no history of human use. This substance has never been reported in any formal scientific literature making it unknown to the public and the academics.
Surprisingly it is structurally similar to LSD and ALD 52 which suggest it has an identical effect profile as well. With the lack of research related to this substance, every argument related to the pharmacology of this drug is completely according to its structure and the subjective effect that are not different from other such lysergamides.
In the early months of 2015, 1p-LSDgot its legal alternative LSZ and LSD, and it was marketed through online chemical vendors who were selling it. This compound as mainly sold in blotter sheet tabs. It was marketed as a research chemical that made it easy to sell it legal, although it was sold for human consumption
According to its molecular structure, it belongs to lysergamide family. It is quite analogous to LSD, and it has been named for its propionyl group that is bound to the nitrogen of polycyclic indole group. The propionyl consists of carbonyl chain that is bound to an amino group. 1p-LSDcontains a polycyclic group that features the bicyclic Hexahydro indole bound to its quinolone bicyclic group. At carbon 9 of quinoline, the n-diethyl carboxamide becomes bound.
Right now it is in the grey market area that makes its purchase a bit unsafe.
It acts as the partial agonist of 5 HT2A. Psychedelic effects come from efficacy at 5HT2A receptors. The role of such interactions and how these result in psychedelic experience always remain elusive.
Moreover, it has been theorized that1p-LSDis a prodrug to LS. It shows only 35% potency of LDS in mice. The LSD is detected with the help of LC-MS when the1p-LSDis incubated in Human Serum. This means that1p-LSDdoesn’t only acts as a prodrug for LSD but also, it directly acts as serotonin receptor against its very own rights.
The subjective effects of1p-LSDare similar to those structurally related to it. The differences are minuscule that are negligible and virtually indistinguishable from each other. As comparing to other psychedelics which includes LS and Psilocin, the1p-LSDproves to be even more stimulating and fast paced when it comes to a specific type of its physical and cognitive effects. The effects are listed blow that are based on the subjective effects index and personal experience of some subjects. The listed effects rarely occur and only once. However if the dosage is heavy, it can lead to severe cases.
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