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Talk:2-Methyl-AP-237

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Literature

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2-Methyl-AP-237
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Chemical Nomenclature
Common names 2-Methyl-AP-237, Apex, 2-MAP
Substitutive name 2-Methyl-AP-237
Systematic name [[systematic name::1-[2-methyl-4-(3-phenyl-2-propen-1-yl)-1-piperazinyl]-1-butanone, 1-(4-cinnamyl-2-methylpiperazin-1-yl)butan-1-one]]
Class Membership
Psychoactive class Opioid
Chemical class Piperazines
Routes of Administration

WARNING: Always start with lower doses due to differences between individual body weight, tolerance, metabolism, and personal sensitivity. See responsible use section.



Oral
Dosage
Threshold < 10 mg
Light 10 - 15 mg
Common 15 - 20 mg
Strong 20 - 25 mg
Heavy 25 mg +
Duration
Total 4 - 6 hours
Onset 5 - 15 minutes
Come up 10 - 40 minutes
Peak 15 - 20 minutes
Offset 5 - 60 minutes
After effects 4 - 6 hours









DISCLAIMER: PW's dosage information is gathered from users and resources for educational purposes only. It is not a recommendation and should be verified with other sources for accuracy.

Interactions



Fatal overdose may occur when opiates are combined with other depressants such as benzodiazepines, barbiturates, gabapentinoids, thienodiazepines, alcohol or other GABAergic substances.[1]

It is strongly discouraged to combine these substances, particularly in common to heavy doses.

Summary sheet: 2-Methyl-AP-237


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History and culture

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2-methyl AP 237 is a research chemical opioid, Little is known about this chemical as was first identified by a police forensic laboratory in Slovenia in March 2019. Page text.[2] Studies have shown bucinnazine and similar acyl piperazines, substances close to 2 MAP to be potent and selective agonists of μ-opioid receptor and they are thought to raise tolerance quickly

Chemistry

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Pharmacology

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2-Methyl AP 237 is an agonist of Mu opioid receptor with potency about equal to morphine

2-Methyl AP-237 was found to bind to MOR with appreciable affinity (Ki = 12.9 nM) and high selectivity over the δ (Ki = 2910 nM) and κ subtypes (Ki = 5259 nM)

Janowsky A. 2-Methyl AP-237. 1-[2-Methyl-4-(3-phenyl-2-propen-1-yl)-1-piperazinyl]-1-butanone, HCl. Binding and functional activity at delta, kappa and mu opioid receptors. DEA-VA interagency agreement title: “In vitro receptor and transporter assays for abuse liability testing for the DEA by the VA”. Portland (OR): Department of Veterans Affairs Medical Center; 2019.

Caption text
   |NameCommon=2-Methyl-AP-237, Apex, 2-MAP
   Chemical Abstracts Service index name:
   1-Butanone, 1-[2-methyl-4-(3-phenyl-2-propen-1-yl)-1-piperazinyl]-

   |NameSubstitution=2-Methyl-AP-237
   |NameSystematic=1-[2-methyl-4-(3-phenyl-2-propen-1-yl)-1-piperazinyl]-1-butanone, 1-(4-cinnamyl-2-methylpiperazin-1-yl)butan-1-one

--GabaBGuy (talk) 18:30, 9 December 2023 (UTC)

===

Subjective effects

This subjective effects section is a stub.

As such, it is still in progress and may contain incomplete or wrong information.

You can help by expanding or correcting it.

Disclaimer: The effects listed below cite the Subjective Effect Index (SEI), an open research literature based on anecdotal user reports and the personal analyses of PsychonautWiki contributors. As a result, they should be viewed with a healthy degree of skepticism.

It is also worth noting that these effects will not necessarily occur in a predictable or reliable manner, although higher doses are more liable to induce the full spectrum of effects. Likewise, adverse effects become increasingly likely with higher doses and may include addiction, severe injury, or death ☠.

Physical effects

Cognitive effects

Visual effects

Tolerance and addiction

The short-term non-chronic use of opioids is not associated with any physical or neurological toxicity. 

The long-term use of opioids causes hormonal imbalance in both men and women. In men, this opioid-induced androgen deficiency results in abnormally low levels of sex hormones, particularly testosterone.

This negative change in endocrine function in males can lead to: reduced libido, erectile dysfunction, fatigue, depression, reduced facial and body hair, decreased muscle mass, and weight gain.

Another often observed long-term effect is hyperalgesia, an increase in the pain sensitivity of the person. This is specially seen in chronic pain patients on high dose opioid regimes. There is some evidence that NMDA antagonists like ketamine and opoids that are also weak NMDA antagonist such as methadone, levorphanol and tramadol may help delay the onset of hyperalgesia or even revert it. Nitric synthase inhibitor, COx2 antagonist and alpha 2 agonist can also help.

It is strongly recommended that one use harm reduction practices when using this class of substances.

Due to the highly euphoric nature of these substances, the recreational use and abuse of opioids has an extremely high rate of addiction and dependence. This is combined with a tolerance which builds up quickly, necessitates that the user take increasingly high dosages in order to get the same effects.

}}

Experience reports

There are currently 0 experience reports which describe the effects of this substance in our experience index.

Additional experience reports can be found here:


It is strongly recommended that one use harm reduction practices when using this substance. It is believed that 2-methyl AP237 is highly caustic.

Dangerous interactions

This dangerous interactions section is a stub.

As such, it may contain incomplete or invalid information. You can help by expanding upon or correcting it.

Any depressants is going to raise the risk of possibly life-endind events.

This legality section is a stub.

As such, it may contain incomplete or wrong information. You can help by expanding it.

See also

(List along order below)

Literature

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References

  1. Risks of Combining Depressants - TripSit 
  2. "Analytical Report 2-Methyl-AP-237" (PDF). Ljubljana, Slovenia: National Forensic Laboratory. 19 March 2019. 
2-Methyl-AP-237
[[ File: | frameless | center | 245px ]]
Chemical Nomenclature
Common names 2-Methyl-AP-237, Apex, 2-MAP
Substitutive name 2-Methyl-AP-237
Systematic name [[systematic name::1-[2-methyl-4-(3-phenyl-2-propen-1-yl)-1-piperazinyl]-1-butanone, 1-(4-cinnamyl-2-methylpiperazin-1-yl)butan-1-one]]
Class Membership
Psychoactive class Opioid
Chemical class Piperazines
Routes of Administration

WARNING: Always start with lower doses due to differences between individual body weight, tolerance, metabolism, and personal sensitivity. See responsible use section.



Oral
Dosage
Threshold < 10 mg
Light 10 - 15 mg
Common 15 - 20 mg
Strong 20 - 25 mg
Heavy 25 mg +
Duration
Total 4 - 6 hours
Onset 5 - 15 minutes
Come up 10 - 40 minutes
Peak 15 - 20 minutes
Offset 5 - 60 minutes
After effects 4 - 6 hours









DISCLAIMER: PW's dosage information is gathered from users and resources for educational purposes only. It is not a recommendation and should be verified with other sources for accuracy.

Interactions