Ayahuasca Chemical Composition

The main active biochemicals of Banisteriopsis caapi , Banisteriopsis of inebrians and other species of Banisteriopsis are: ß – Carboline alkaloids arminici , harmaline , tetrahydroharmine , Harmol , armico acid , amide Methylesterarmico , Acetyl Norharmine , harmine N-oxide , acid and armalinico Ketotetra – idronorarmina .

The Banisteriopsis caapi has a higher percentage of tetrahydroharmine than the Peganum harmala ( Syrian Rue ) and some species of Passiflora sp. ( passion flower ), which also contain alkaloids . It may be for this reason that the therapeutic effects of the most complete and prolonged you feel with the authentic recipe of Ayahuasca preparations and not with ” similar ” to the original.

•   Banisteriopsis caapi

The Banisteriopsis caapi contains Armina , harmaline , tetrahydroharmine , Armol and 6 – Metoxitriptamina . The main active compounds of Banisteriopsis caapi alkaloids are Armina , harmaline and tetrahydroharmine . Both the Armina that the harmaline MAO inhibitors are highly reversible , while the tetrahydroharmine is a weak inhibitor , dedicated to the reuptake of serotonin ( 5 – hydroxytryptamine ) . In a first time . when it was discovered, Armina was called ” Telephatina ,” name rejected by scientists soon discovered that the same alkaloid was already obtained from Peganum harmala . MAO inhibitors , such as Armina , prevent the breakdown of monoamine neurotransmitters inhibiting activated by MAO enzymes , which normally are capable of degrading the DMT and prevent it from crossing the blood brain barrier.

ArminaLa crystalline substance called Armala is the alkaloid Armina , an inhibitor of monoamine oxidase A (MAO -A) reversible , but has no effect on MAO-B . When it was discovered was baptized with the name of ” Telephatina ” , but later was discarded , because scientists discovered that the same alkaloid had previously been obtained from Peganum harmala . The Armina is an alkaloid family of beta – carbolines able to prevent the breakdown of monoamine neurotransmitters inhibiting activated by MAO enzymes that normally degrade the DMT preventing it from crossing the blood brain barrier.

ArmalinaLa harmaline is a reduced form and hydrogenated dell’Armina and is a reversible inhibitor of MAO-A . The harmaline is a beta – carboline alkaloid family that acts as a stimulant of the central nervous system.

TatraidroarminaLa tetrahydroharmine is a derivative of beta – carbolines , a weak inhibitor of serotonin reuptake , but it is not able to inhibit the monoamine oxidase A.

ArmolL’Armol is a beta – carboline alkaloid indoleamino toxic (also present in Peganum harmala , Tribulus , Kallstroemia spp. , Elaeagnus angustifolia and Passiflora incarnata) .

DimetiltriptaminaLa dimethyltryptamine ( DMT with initials , traces were found in Mimosa tenuiflora and Diplopterys cabrerana ) is an endogenous chemical substance produced by the body during REM sleep , or in situations where it is subjected to pressures of extreme stress (such example in experiences in which you run the risk of losing their lives ) . The DMT has a chemical structure similar to Bufotenine , to Serotonin , to psilocin and psilocybin , the latter are the active chemical compounds of many magic mushrooms . This is a powerful hallucinogen , LSD even stronger . DMT is inactive when taken orally and moderate doses , but with an inhibitor of monoamine oxidase ( MAO) has the ability to get into the bloodstream into the digestive system and cross the blood-brain barrier . The DMT was synthesized in 1931 by the Canadian chemist Richard Manske Helmuth Fredrick 

MonometiltriptaminaLa Monometiltriptamina triptaminico is an alkaloid that was found in the leaves, bark and buds of many plants , but was also found in the urine of autistic patients , with problems of mental retardation and epilepsy.

2 -methyl-1 ,2,3,4- tetrahydro- ß – carbolineLa 2 -methyl-1 ,2,3,4- tetrahydro- ß – carboline is a fairly common substance contained in many plants with entheogenic tryptamines , among which we find Mimosa hostilis and Phalaris spp.

The Diplopterys cabrerana contains an indole alkaloid – ethylamine N, N- dimethyltryptamine , an alkaloid with a chemical structure similar to Serotonin . It binds to 5-HT2 receptors and only partially to the 5-HT2A receptors . The DMT itself, when taken orally, does not show any effect , because the enzyme monoamine oxidase synthesizes aldehydes inactive. The beta – carbolines in liana Banisteriopsis caapi inhibit , temporally , the production of this monoamine oxidase , thus allowing the DMT to achieve the perceptual parts of the brain , such as the prefrontal , parietal cortex somatonseriale and olfactory tubercle . The Diplopterys cabrerana also contains N- methyltryptamine , 5 – MeO -DMT (5- Metoxy – dimethyltryptamine ) , and N- Bufotenine Metiltetraidro – ß – carboline alkaloids that are rarely found in Psychotria viridis ( we were able to find only traces ) .

N- N- MetiltriptaminaLa methyltryptamine ( abbreviated as NMT) is an alkaloid triptaminico found on the leaves, bark and buds of many plants , such as Virola , the Acacia, Mimosa and Desmanthus ; traces were found in the natural components contained in human urine ( he is also endogenous ) . The human body synthesizes it as a final product of the metabilismo the type of amino acid L- tryptophan. The NMT seems to be inactive if taken orally and has no psychoactive effect , almost certainly due to the complex metabolic synthesis in which it is initially submitted .

5 – MeO- DMTLa 5 – MeO -DMT is part of the class and is a tryptamine – white crystalline substance . Exactly how the N- methyltryptamine , the human organism is able to synthesize it , reducing it to a final product metabolic acid L-tryptophan . The 5 – MeO -DMT is a natural substance in certain plants ; was found in the resin of Virola , in the seeds of Mucuna pruriens , in Yopo and in secretions of certain types of toads , such as the Colorado River toad TOAD , the toad of Rods . The 5 – MeO -DMT is smoked , but can also be consumed nasally or intravenously.

BufoteninaLa Bufotenine ( name derived from the toad Bufo ) is a hallucinogenic alkaloid triptaminico . Bufotenine is closely related to the neurotransmitter serotonin and is structurally similar to Psilocin , the 5 – MeO -DMT and DMT . Bufotenine was detected for the first time in the skin secretions of toads , but mainly in the secretions of the toad Colorado River Toad (Bufo alvarius ) . It was also found in Anadenanthera colubrina and Anadenanthera peregrina . For more information, you can check and visit shrooms online Canada. This will give you more insights about shrooms and other related topics. All information can be found online.