This page is a W.I.P and most likely will always be one. This most likely will not have the common psychedelics you are used to, but if you ever want to learn more about the "other" side of psychedelics, this could potentially be a starting point. There also may (There is as of this edit) doubles, as this started as a project between two people, and mashed together.
PSYCHEDELICS
- 4, 5 MDO-xxT - MDMA Tryptamine
- 5, 6 MDO-xxT - MDMA Tryptamine
- 7-MeO/HO/Fl/Cl/Br/I/MeS-xxT - 4 position in phens
- 4,5-DHP-xxT - Phenyl Ringed Tryptamine
- RU-28306 - HT1 & 2 agonistA substance that initiates a physiological response when combined with a receptor., binding affinity similar to DMT
- 4,5-DHP-xxT - Phenyl Ringed Tryptamine
- 5-Benzyloxytryptamine - 5-HT1D,2,6 agonistA substance that initiates a physiological response when combined with a receptor..
xxT ───────────────┐
- 4-Propioniyl-xxT ▼
- 4-HO-xxT - Halogens: FT, CT, BT, IT, TT (Thiosulphate), DFT, DCT, DBRT, DIT, DTHT
- 4-HO-xxT - IB (ethyl-dimethyl --<) : DIBT, MIBT, EIBT, PIBT, iPIBT, BIBT, IBMT, IBET, IBPT, IBiPT, IBBT, ALIBT, IBALT
- 4-HO-MPMI - alpha-pyrrole n, methylT,
- 5-Fluoro-xxT - Fluoro T
- 6-Fluoro-xxT - Fluoro T
- 4-Fluoro-xxt??
- 4,5/5,6-Dihydroxy/Dimethyl/Dimethoxy/Difluoro-DMT
- 4/5-Me-xxT: 4-Me-DMT is antidepressive, 5-Me-DMT is psychedelic but high dose than MeO.
- 4-HO-5-MeO-DMT - Explored by Marc Julia, never tested.
- 5-MeO-2,N,N-TMT (Indapex) - 50-100mg: Empathogeic, antidepressive, 100mg+: depressive with body load (ORAL)
- 10-30mg: Psychedelic, OEV, CEV. Visual 5-MeO. 5hrs (INSUFFLATED)
- 4-HO,5-MeO-DMT-5-HemiFLY: furan ring from 5-Meo to 6 position
- 4/5 benzofuran-xxT - like 4,5 MDO but ABPish. 4=potent, 5=psychedelic
- 6-HO-xxT - Metabolised from 4-HO-xxT
- 4, 7 DiMeO 5-Fl/Cl/Pr/etc xxT **
- 4,5,6 - Halogen - xxT - Halogenated T
- 7-TMT - 7 position could be 'magical' position along with 5
- MMDA - Brain Movies
- N-Methyl DOM - potentiated 5mg Psilocin. Possible Irreversible MAOMonoamine Oxidase, an enzyme that catalyses the metabolism of many drugs (e.g., DMT, dopamine and serotonin).-A inhibitor??
- dextro-DOM - inactive however managed to potentiate 'poor' hash the following day??
- Beta-Methyl PhenethylaminePhenethylamine (PEA) is a natural monoamine alkaloid, trace amine, and psychoactive drug with stimulant effects. In the mammalian central nervous system, phenethylamine is believed to function as a neuromodulator or neurotransmitter. analogues -> halfway between 2C-x's and DOx
- MMDPEA - Entactogen. A-demethylated homologue of MMDA. Closely related to Mescaline. Active in 150-250mg, 300+ seemed to resemble standard doses of mescaline.
- 2C-YN - ethynyl
- 2C-PYN - propynyl
- 2C-CN - cyanide
- 2C-BZ - benzyl
- 2C-SE - selenium
- 2C-IV - ethenyl
- 2C-PIV - propenyl
- 2C-TFE - trifluoroethyl
- 2C-TE - tellerium
- 2C-NH - amine group!
- 2C-IB - 4-ethyl-dimethyl --<
- 2C-AL - allyl
- 2C-MAL - methallyl
- 2C-COOH - carboxyl
- 2C-xM/E - Bromomethyl
- 2C-MY - methylene
Plants and shit!
- Sinicuichi - plant that gives golden tinted vision and euphoria
- RDS-127 - HT1a agonistA substance that initiates a physiological response when combined with a receptor., looks like frog!
- AL-37350A - potent selective HT2a agonistA substance that initiates a physiological response when combined with a receptor.
- AL-38022A - potent, selctive HT2 agonistA substance that initiates a physiological response when combined with a receptor., affinity for 2c
- 5-Benzyloxytryptamine
xxT ───────────────┐
- 4-Propioniyl-xxT ▼
- 4-HO-xxT - Halogens: FT, CT, BT, IT, TT (Thiosulphate), DFT, DCT, DBRT, DIT, DTHT
- 4-HO-xxT - IB (ethyl-dimethyl --<) : DIBT, MIBT, EIBT, PIBT, iPIBT, BIBT, IBMT, IBET, IBPT, IBiPT, IBBT, ALIBT, IBALT
- 4-HO-MPMI - alpha-pyrrole n, methylT,
- 5-Fluoro-xxT - Fluoro T
- 6-Fluoro-xxT - Fluoro T - Probably inactive but that silly Neurosoup girl said it was incredible (prob. means the 5).
- 4-Fluoro-xxt??
- 4,5/5,6-Dihydroxy/Dimethyl/Dimethoxy/Difluoro-DMT
- 4/5-Me-xxT: 4-Me-DMT is antidepressive, 5-Me-DMT is psychedelic but high dose than MeO.
- 4-HO-5-MeO-DMT - Explored by Marc Julia, never tested.
- 5-MeO-2,N,N-TMT (Indapex) - 50-100mg: Empathogeic, antidepressive, 100mg+: depressive with body load (ORAL)
- 10-30mg: Psychedelic, OEV, CEV. Visual 5-MeO. 5hrs (INSUFFLATED)
- 4-HO,5-MeO-DMT-5-HemiFLY: furan ring from 5-Meo to 6 position
- 4/5 benzofuran-xxT - like 4,5 MDO but ABPish. 4=potent, 5=psychedelic
- 6-HO-xxT - Metabolised from 4-HO-xxT
- 4, 7 DiMeO 5-Fl/Cl/Pr/etc xxT **
- 4,5,6 - Halogen - xxT - Halogenated T
- 7-TMT - 7 position could be 'magical' position along with 5
- ALEPH-x - Thio Psych Amps:
- MMA - 3-MeO, 4-Me Amp. - SRISerotonin Reuptake Inhibitor, S releaserA releasing agent (RA), or simply releaser, is a drug that induces the release of a neurotransmitter from the presynaptic neuron into the synapse, leading to an increase in the extracellular concentrations of the neurotransmitter., HT agonistA substance that initiates a physiological response when combined with a receptor.
- Ergometrine - LSA
- 2C-T-x (13, 17, 21)
- Di/tri-fluoromescaline - Di ~40-60mg, Tri ~<40mg
- MEM - MDMA type drug, useful for therapy. More of a potentiator but effects last several days afterwards. Possible NMDAN-methyl-D-aspartate receptor. NMDA antagonists are often dissociatives. antagonism?
- FLEA
- G-x - Very long duration Amp. psychedelics related to 2C-G
- 5-TOET
- 2-TOM
- 5-TOM
- HOT-x - Hydroxy Thiosulph
- CPM - Introspection oriented Mescaline analogue
- 2C-G-x - Long 2C. 4 substitutions: 2,5-dmo 4,3 dm pea
- 2C-T - Glowing reports at 80-130mg. 'Gem of Gems' - MGS
- MMMDA-2
- Methyl/MeO/HO/E/EO/AL-MDA-x(2,5,6) - MDA analogues
- MDOH - Degrades into MDA, 100-150~mg dose. 3-6 hour length. Comes up within 45 minutes.
- 2,5,6-Fluoro-MDA - Halogenated MDA (C,B,I,TFM?)
- x-LAD - LSD analogues
- 2-Me-xxT - weak tryptamines
- Mexamine (5-MeO-T) - Full agonistA substance that initiates a physiological response when combined with a receptor. at HT 1,2,4,6 & 7. Drug that causes dreams.
- ALD-52 - LSD acetate
- 2C-TFM - Trifluoro
- 2C-B-FLY - Phenyl rings
- BromoxxxxFLY - Phenyl rings +2C-B
- TCB-2 - potent nichols psych
- TFMFly - DRAGONfly analogue
- 5-CT - non-selective HT AgonistA substance that initiates a physiological response when combined with a receptor. - Tryptamine
- LSZ - Cyclo-butyl (dLSD analogue)
- LSB - Butyl
- 25x-Nxxxx - T(2,4,7,21) + novel 4-pos. (WILL BE AROUND SHORTLY WITH MORE 25*-NBOHN-Benzyl-HydrOxy derivatives of psychedelic phenethylamines./25*-NBFN-Benzyl-Fluoro derivatives of psychedelic phenethylamines.)
- 4MeO-2,5-DMePEA-NBOMeN-Benzyl-Ortho-Methoxy derivatives of psychedelic phenethylamines. (2C-O-4)
- 2,4 DMA- NBOMeN-Benzyl-Ortho-Methoxy derivatives of psychedelic phenethylamines.
- C30-NBOMeN-Benzyl-Ortho-Methoxy derivatives of psychedelic phenethylamines. - 25C-NBOMeN-Benzyl-Ortho-Methoxy derivatives of psychedelic phenethylamines. with Methylamine Mesc. attached to the Amine
- RH-34 - ketanserin nbome/nick
- PNU-22394 - HT2A, B & C agonistA substance that initiates a physiological response when combined with a receptor. - strange structure
- Dimemebfe - 5-MeO-DMT analogue
- Ro60-0175 - Selective HT2 agonistA substance that initiates a physiological response when combined with a receptor. - indole
- Meta-Escaline
- MAL - Very visual mescaline analogue
- IsoProscaline - Mescaline analogue at 40-80mg. Euphoric, MDMA type. XC@cianchong.com 10g's for 120
- 2CB-Ind
- LSP
- Methylisopropyllysergamide
- Lorcaserin - Selective, Hallucinogenic HT2C agonistA substance that initiates a physiological response when combined with a receptor.
- MK-212 - ??serotoninA monoamine neurotransmitter, biochemically derived from tryptophan, that is primarily found in the gastrointestinal (GI) tract, platelets, and central nervous system (CNS) of humans and animals. It is a well-known contributor to feelings of well-being. agonistA substance that initiates a physiological response when combined with a receptor.?? Weird ass substance.
- Jimscaline - indane mescaline analogue some 3-5x as potent
- MDPR - unresearched psychedelic drug potentiator
- Quipazine - selective HT2a & 3 agonistA substance that initiates a physiological response when combined with a receptor., piperazine
- G-5 **
- PSI-2C-x
- PSI-DOx - PSI-DOM found.
- PSI-25x-NBOMeN-Benzyl-Ortho-Methoxy derivatives of psychedelic phenethylamines.
- IM-Isomescaline - Iso in this nonmeculture is ISO, and not PSI. Which adds more to the benzyne ring.
- AEM - Ethyl
- APM - Propyl
- ABM - Butyl
- AAM - Amyl
- AHM - Hexyl
- ASM* - Heptyl
- AOM - Octyl
- ANM - Nonyl
- AUM - Undecyl
- = S is for Septyl, to distinguish heptyl from hexyl.
- AL - Allyl mesc.
- 2C-AL - Allyl
- 3C-AL - Allyl
- ASB - Asymbescaline.200-300:10-15 hours.
- SB - Symbescaline.
- Aleph-x - Thio psych amps.
- Ariadne - 4C-DOM, Not much here.
- ASB - Asymbescaline.200-300:10-15 hours.
- SB - Symbescaline.
- Buscaline
Note: The 3C-*'s listed below that the toxic symptom might be present at the higher dosages that are needed to achieve full psych.
- 3C-B - Three-carbon chain analogue of Buscaline.
- 3C-A - Three-carbon chain analogue of Amyloxy.
- 3C-H - Three-carbon chain analogue of Hexyloxy.
- 3C-S - Three-carbon chain analogue of Heptyloxy.
- 2C-AL - Allyl
- 3C-AL - Allyl
- N-Methyl-DOM - Some 25x less active than DOM.
- Methyl-DOB - Very hard on the body. Much less potent than DOB. Seems to potentiate non PEA's.
- 2-TOM - 60-100mg: 8-10 hours. CEV heavy.
- 5-TOM - 30-50mg: 6-10 hours.
- Beta-Methoxy-2C-X - 10-20mg: 10-20 hours. Most potent of the BOX series. Might be some dangers to physical concern.
B,D,H,HD,Mescaline.
- 4-BR-3,5-DMA - Acts as a depessant in humans. 3-10mg.
- 2-BR-MDA - Supposed to act like an amp.
- 2CB-2ETO
- 3C-FBZ - Flurobenzyloxy - Amphetamine like compound most likely. Tested up to 4mg's no activity noted.
- 3C-BZ - Very finnicky dosing. Seems to resemble TMA at high enough dosages.
- 3C-E - 4-sub was very important to potency and quality of action. 40-60mg dose.
- CPM - Sad looking compound. 60-80mg:12-18 hours. Mescaline with a methyl removed and a cyclopropylmethyl added.
- 3C-CPM - Amphetamine analogue of CPM.
- 4-D/Beta-D - The deuterium sub /has/ to be done with TMA.
- Desoxy (4-Desoxymescaline) - 40-120mg:6-8 hours.
Note: Mescaline analogue with bromo in place of the 4-methoxyl group must be done. MUST.
DIMETHYLAMPHETAMINES
- 2,4-DMA Tested up to 60mg's. Not fully active. Theory about it being harmful at higher levels.
- 2,5-DMA 80-200mg:6-8 hours. Fully stimulant.
- 3,4-DMA Was tested at 70mg IV'd and 700mg IV'd. Full stimulant that... well no.
- 2,3-DMA
- 2,6-DMA
- 3,5-DMA
- DMCPA - 15-20mg:4-8 hours. Most likely works as a MAOIMonoamine oxidase inhibitor are drugs that inhibit the action of monoamine oxidase in the brain and so allow monoamines to accumulate.. Like Tranylcypromine.
- DME - Inactive.
- DMMDA - 30-75mg:6-8 hours. Apiole from the Oil of Parsley.
- Methyl-MMDA-2
Ergolamide stuff!
- LSD - Golden staple of this class.
- AL-LAD - 40ug threshold, equipotent to LSD. 6-Allyl-6-Nor-LSD Slightly shorter lasting.
- LSZ - Only substance that I can think of that has a diethylamide constrained into an azetidine. Slightly more potent than LSD. (S,S)-(+) isomerEach of two or more compounds with the same formula but a different arrangement of atoms in the molecule and different properties. most active.
- ALD-52 - N-Acetyl-LSD. Dose is 50-175ug. "LSD-lite" Less anxiety, yet increased blood pressure in a few.
- LA-111 - LSA
- OML-632 - L-Oxymethyl D-Lysersergic Acid Diethylamide (wot, just an added chain?) Seems to be a bit more potent.
- LAE-32 - D-Lysergic acid ethylamide. Rerivative of Ergine. Some LSD-like effects, shorter lasting. 500-1500ug
- BOL-148 - 2-bromo found by Hofmann, inactive as a psychedelic, acts as a neutal antagonistA substance that interferes with or inhibits the physiological action of another., which makes it "useful" in cluster headaches and a bit more. (E.G useful in medicine, not in my hands)
- MLA-74 -
- ALA-10
- LPD-824
- DAM-57
- LME
- LAMP
- LEP
- MLD-41 - 1-methyl homologue of LSD. More Somatic than sensory. 100-300ug. Cardiovasculat responses are increased.
- LSM-775 - Somewhere between 75ug-700ug. Fewer signs of stimulation and peripheral toxicity.
- DAM-57
- LPD-821
- LAE-32
- UML-491 - Synthetic homologue of MLD-41
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