O-DSMT Rac
O-Desmethyl-cis-tramadol(also called O-DSMT Rac, O-Desmethyltramadol R) is an opioid analgesic, an active metabolite of tramdol, a racemic compound with similar effects.
This substance has a more active effect than its related compound O-Desmethyltramadol(O-DSMT).
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Pagoclone
$21.00
Pagoclone is an anxiolytic substance of the cyclopyrrolone family, which is closely related to a drug such as zopiclone, known as a sleeping pill. This substance was first synthesized by a team of scientists at Rhone-Poulenc & Rorer S.A. as a sedative with fewer side effects, safe for the liver. Due to possible abuse, it has never been used for medical purposes or marketed and is currently sold online as a research drug.
This substance is not bezodiazepine and has a different chemical structure, although the sedative effects of these substances are very similar.
Pagoclone is a partial agonist of GABA receptors (alpha2, alpha3 subtypes), which is the reason for its sedative effects. This drug can also be used as a sedative and antianxiety agent, as shown by studies on rats. In low doses pagoclone has only anxiolytic effect.
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Pagoclone 10 MG Pellets
$16.95 – $229.95Pagoclone properties
Synonym: Pagoclone CAS Number: 133737-32-3 Formula: 2-(7-chloro-1,8-naphthyridin-2-yl)-3-(5-methyl-2-oxohexyl)isoindolin-1-one Mole mass: 407.9 g/mol Purity: >99%
PRO-LAD 175 MCG Blotters
$14.00 – $470.23PRO-LAD
Synonym: 6-propyl- 6-nor- Lysergic acid diethylamide CAS Number: 65527-63-1 Formula: C22H29N3O Molmassa: 351.494 g·mol Purity: >97%
Propylnitazene
$27.00
Propylnitazene is an opioid drug, a derivative of benzimidazole, with a strong analgesic effect. Studies in mice have shown that Propylnitazene can cause a number of effects similar to strong analgesics such as fentanyl and etonitazene, including strong analgesic, hypnotic and sedative effects at a moderate dosage.
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Protodesnitazene
$28.00
Protodesnitazene is an opioid substance derived from benzimidazole, a derivative of etonitazene, with similar analgesic properties. This substance is a designer substance and is intended for scientific research and work to identify analgesic properties.
This substance is poorly studied and there is insufficient data on its toxicological and pharmacological properties and dosage.
According to studies and tests of this drug on rodents, it was revealed that it is an active agonist of the μ-opioid receptors and has a strong analgesic effect exceeding morphine many times. This drug also has sedative and hypnotic effects.
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| Weight | 5g | 10g | 25g | 50g | 100g | 250g | 500g | 1000g |
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Protonitazepyne
$24.50
N-Pyrrolidino Protonitazene (also called Protonitazepyne) is an opioid substance derived from benzimidazole, a strong analgesic, and a literal analog of etonitazene.
This drug actively affects μ-opioid receptors and has opioid potency about 180 times higher than morphine. Its effects are similar to those of many benzimidazole opioids, it produces a sedative effect, analgesia, an euphoric and peaceful effect. Protonitazepyne does not cause dissociative effects.
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Pyrazolam
$25.00
Pyrazolam (SH-I-04) is a sedative drug of the benzodiazepine class, first developed at Hoffman-La Roche in the 1970s. This drug affects benzodiazepine receptors (selective against subtypes of α2 and α3 receptors), the neurotransmitter gamma-aminobutyric acid (GABA), its effect as a consequence leads to a calming, sedative effect, euphoria and anticonvulsant properties and improved sleep.
The structure of pyrazolam is similar to alprazolam, etizolam with some minor differences, it contains a benzene ring fused with a diazepine ring with two nitrogen components at R1 and R4, a bromine molecule is bound to the structure at R7, and R6 is replaced by a 2-pyridine ring and contains a 1-methylated triazole ring connected to R1 and R2.
With regular use of this drug, tolerance and addiction can develop, and at high dosages, a number of side effects are possible, such as dizziness, loss of balance, respiratory depression. It is not recommended to take pyrazolam with other sedative preaprates and alcohol may enhance their effect. In some cases, an overdose of pyrazolam may cause uncontrolled aggression, irritability and suicidal behavior.
Pyrazolam in moderate dosages, has low toxicity and acts as an excellent sedative and anti-anxiety agent.
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Rilmazafone
Rilmazafone (Rhythmy, 450191-S, rilmazafone hydrochloride) is a drug that has sedative and hypnotic properties when the drug is metabolized, it is the metabolites of this substance that turn into benzodiazepine metabolites, that cause impaired motor function as well as hypnotic effects.
Structurally, rilmazafone has no diazepine ring and does not affect benzodiazepine receptors and does not cause psychoactive effects prior to metabolism. This substance is not classified as a benzodiazepine in many countries.
Rilmazafone is available in powder form and is perfectly soluble in water.
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Ro4-1539
Ro4-1539 (furethylnorlevorphanol) is an opioid substance belonging to the morphinan series, a powerful agonist of the m-opioid receptors, with excellent analgesic properties.
This drug was first developed in the 1950s by Hoffmann-La Roche and was tested on mice, but never entered the commercial market of medical drugs, although it had a good therapeutic index.
Ro4-1539 belongs to the morphinan series of drugs and is about 30-60 times more powerful than its related drug levorphanol.
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SGT-152
$12.00
CUMYL-NBMINACA or also called SGT-152 is a synthetic cannabinoid, a designer drug developed as a replacement for SGT-151. This substance has a high cannabinoid potency and is an active agonist of the CB1 and CB2 receptors.
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SL-164
$15.00
Dicloqualon (also called SL-164, DCQ) this is a sedative drug, categorized as a quinazolinone, an analogue of methaqualone, which has similar hypnotic, anticonvulsant, sedative properties. This substance has never been sold for medical, clinical purposes.
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Spirochlorphine
$27.00
R6890 (also called Spirochlorphine) is an opioid substance with strong analgesic and ephoritic properties. Spirochlorphine(R-6890) has a strong opioid potency, exceeding fentanyl by about 2 times. This drug was developed as a research tool for studying analgesic properties and opioid potency in a specially equipped laboratory in compliance with all standards.
Studies on rodents have shown that Spirochlorphine acts as a strong analgesic, causing relaxing and sensory effects.
Regular use of the drug can cause physical and psychological dependence, and high dosages can lead to respiratory depression.
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SR-17018
SR-17018 is an opioid substance with an analgesic effect, is an active agonist of the m-opioid receptors, activates the binding of GTPyS, demonstrating signal bias.
SR-17018 can be compared with morphine in terms of the strength of the effect and analgesic data, but it is slightly more effective when the drug is re-administered, and also significantly less depresses breathing.
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| Weight | 5g | 10g | 25g | 50g | 100g | 250g | 500g | 1000g |
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| Price | €20.00/Per gram | €14.00/Per gram | €10.00/Per gram | €7.00/Per gram | €5.30/Per gram | €4.80/Per gram | €4.50/Per gram | €4.20/Per gram |
T-EREX Homotadalafil 20 MG Pellets
$16.96 – $63.71T-EREX Homotadalafil pellets properties
Synonym: N-Ethyl tadalafil, Homotadalafil CAS Number: 1609405-34-6 Formula: C22H19N3O4 Mole mass: 403.4 g/mol Purity: ≥98%
Thiopropamine
$11.00
Thiopropamine is a stimulating substance structurally similar to amphetamine, with the difference in which the phenyl ring is replaced by thiophene and the properties and effects on the body are similar to amphetamine, but have a somewhat weak effect. Thiopropamine is an active inhibitor of norepinephrine and dopamine uptake like amphetamine, which explains the stimulating effect and euphoria.
This drug is a designer and in many countries is not prohibited for research purposes, but in Germany thiopropamine is sold only for authorized scientific use, under the control of the authorities.
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| Weight | 5g | 10g | 25g | 50g | 100g | 250g | 500g | 1000g |
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Tianeptine Sodium
Tianeptine (Coaxil, Salymbra, Stablon, Tatinol, Tianeurax, Tynept, Zinosal) is an atypical tricyclic antidepressant and anxiolytic that is an atypical μ-opioid receptor (MOR) and δ-opioid receptor (DOR) agonist and a selective serotonin reuptake inhibitor. The substance was developed in the 1960s by the French chemical research community.
Tianeptine, unlike most antidepressant medications, has fewer side effects and has been shown to be effective against severe depressive episodes, as well as for the treatment of anxiety disorders, and has a beneficial effect on cognitive performance in cognitive dysfunction caused by depression.
Tianeptine is effective for treating such ailments as Parkinson’s disease, asthma, attention deficit hyperactivity disorder, and is also used as an anticonvulsant and analgesic.
Due to μ-opioid receptor agonists, tianeptine can induce euphoria and has a high abuse potential in high dosages. With regular use of tianeptine, withdrawal, depression and insomnia can occur.
Tianeptine acts as an antidepressant through inhibition of glutamate receptor activity, NMDA and AMPA receptors.
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Tilmetamine
$17.00
Tilmetamine is a dissociative substance, an agonist of NMDA receptors, a ketamine derivative with similar effects. This substance is a designer drug for chemical studies of properties.
Tilmetamine is an analog of ketamine and has a related chemical structure.
Studies on rodents have shown that Tilmetamine acts as an anesthetic, has a beneficial and strengthening effect.
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Tramadol N-Oxide
$18.50
Tramadol N-Oxide(also called 2-((dimethylamino)methyl)-1-(3-methoxyphenyl)cyclohexanol hydrochloride, RWJ 38705) is an opioid analgesic, a metabolite of tramadol with similar effects.
According to studies on rats, this substance can act as an excellent analgesic, as a sedative. With regular use of the substance, psychological and physical dependence can develop. High dosages can cause dizziness, drowsiness, respiratory depression.
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