wiktionary DMTDMT may refer to In chemical substances Dimethyltryptamine , a psychedelic tryptamine Dimethyl terephthalate , a polyester precursor Desoxymethyltestosterone , a designer anabolic steroid In other uses Digital Monetary Trust Discrete multitone modulation Discrete multi tone modulation , a form of orthogonal frequency division multiplexing OFDM D mt , a historical kingdom in what is now Eritrea and northern Ethiopia Diver Medic Technician, a certification offered by the National Board of Diving and Hyperbaric Medical Technology Dreamtime , a creation belief from the Australian Aborigines DSL Modem Tool See also disambig de DMT et DMT es DMT fr DMT hr DMT it DMT hu DMT egy rtelm s t lap ja DMT no Dmt pl DMT pt DMT fi DMT ... more details
chembox ImageFile 5,6 MDO DMT.png ImageSize 120px IUPACName OtherNames 5,6 methylenedioxy N,N dimethyltryptamine Section1 Chembox Identifiers CASNo PubChem SMILES Section2 Chembox Properties Formula C sub 13 sub H sub 16 sub N sub 2 sub O sub 2 sub MolarMass Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition 5,6 MDO DMT , or 5,6 methylene di oxy N,N di methyl tryptamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is the 5,6 methylene di oxy analog chemistry analog of Dimethyltryptamine DMT . 5,6 MDO DMT was first synthesized by Alexander Shulgin . In his book TiHKAL Tryptamines I Have Known and Loved , 5,6 MDO DMT produces no noticeable psychoactive effects, although it was only tested up to a dose of 5mg. Very little data exists about the pharmacological properties, metabolism, and toxicity of 5,6 MDO DMT. See also Tryptamine Dimethyltryptamine 5,6 MDO MiPT Psychedelics, dissociatives and deliriants External links http www.erowid.org library books online tihkal tihkal31.shtml 5,6 MDO DMT Entry in TIHKAL http tihkal.info read.php?domain tk&id 31 5,6 MDO DMT Entry in TiHKAL info Categorization TiHKAL Category Psychedelic tryptamines Psychoactive stub ... more details
chembox ImageFile 4,5 MDO DMT.svg ImageSize 200px IUPACName OtherNames 4,5 methylenedioxy N,N dimethyltryptamine Section1 Chembox Identifiers CASNo PubChem SMILES Section2 Chembox Properties Formula C sub 14 sub H sub 16 sub N sub 2 sub O sub 2 sub MolarMass Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition 4,5 MDO DMT , or 4,5 methylene di oxy N,N di methyl tryptamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is the 4,5 methylene di oxy analog chemistry analog of dimethyltryptamine DMT . 4,5 MDO DMT was first synthesized by Alexander Shulgin . In his book TiHKAL Tryptamines I Have Known and Loved , 4,5 MDO DMT produces few to no noticeable psychoactive effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of 4,5 MDO DMT. External links http www.erowid.org library books online tihkal tihkal30.shtml 4,5 MDO DMT Entry in TIHKAL http tihkal.info read.php?domain tk&id 30 4,5 MDO DMT Entry in TiHKAL info Categorization TiHKAL Category Psychedelic tryptamines Psychoactive stub ... more details
chembox verifiedrevid 411946414 ImageFile 5 MeS DMT.png ImageSize 120px IUPACName 5 methylthio N,N dimethyltryptamine OtherNames Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 19917 InChI 1 C13H18N2S c1 15 2 7 6 10 9 14 13 5 4 11 16 3 8 12 10 13 h4 5,8 9,14H,6 7H2,1 3H3 InChIKey YOGJZQGRTVMCPY UHFFFAOYAL ChEMBL Ref ebicite correct EBI ChEMBL 31783 StdInChI Ref stdinchicite correct chemspider StdInChI 1S C13H18N2S c1 15 2 7 6 10 9 14 13 5 4 11 16 3 8 12 10 13 h4 5,8 9,14H,6 7H2,1 3H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey YOGJZQGRTVMCPY UHFFFAOYSA N CASNo PubChem 21180 SMILES S c1cc2c cc1 ncc2CCN C C C Section2 Chembox Properties Formula C sub 13 sub H sub 18 sub N sub 2 sub S MolarMass 234.36 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition 5 MeS DMT , or 5 methyl thio N,N di methyl tryptamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is the 5 methyl thio analog chemistry analog of Dimethyltryptamine DMT . 5 MeS DMT was first synthesized by Alexander Shulgin . In his book TiHKAL Tryptamines I Have Known and Loved , the minimum dosage is listed as 15 30 Milligram mg . The duration listed as very short less than one hour , just like its analog, DMT. 5 MeS DMT produces similar effects to DMT, but weaker. Shulgin describes his feelings while on a low dose of this drug as pointlessly stoned , although at a higher dose of 20 mg he says it is quite intense and suggests that a higher dose still might have full activity. Very little data exists about the pharmacological properties, metabolism, and toxicity of 5 MeS DMT. See also Tryptamine Dimethyltryptamine Psychedelics, dissociatives and deliriants External links http www.erowid.org library books online tihkal tihkal46.shtml 5 MeS DMT Entry in TIHKAL http tihkal.info read.php?domain tk&id 46 5 MeS DMT Entry in TiHKAL info Categorization TiHKAL Ca ... more details
dimethylethanamine image 5 MeO DMT.svg image2 5 MeO DMT 3d sticks.png width 160 width2 180 KEGG Ref ... Smoked, Insufflated 5 MeO DMT 5 methoxy dimethyltryptamine is a powerful psychedelic drug psychedelic ... its close relatives Dimethyltryptamine DMT and bufotenin 5 OH DMT , it has been used as an entheogen .... Chemistry 5 MeO DMT was first synthesized in 1936, and in 1959 it was isolated as one of the psychoactive ... that contain bufotenin e 5 hydroxy DMT , and is the O methyl Analog chemistry analogue of that compound. History Traditionally 5 MeO DMT has been used in psychedelic snuff made from virola bark resin ... as an admixture. 5 MeO DMT is also found in the venom of the Colorado River toad Bufo alvarius , although ... 5 MeO DMT is a sacrament of the Church of the Tree of Life . From approximately 1971 to the late 1980s 5 MeO DMT was discreetly available to members of the Church of the Tree of Life from Inner Center ... 5 Meo DMT Timeline cite web url http www.erowid.org chemicals 5meo dmt 5meo dmt timeline.php title Erowid 5 Meo DMT Timeline author Erowid ref Between 1970 and 1990 smoking of 5 MeO DMT on parsley was probably ... DMT Timeline A member of the Church of the Tree of Life estimates there were less than 6000 active ... alvarius1.jpg thumb 300px right Colorado River Toad Bufo alvarius , which has 5 MeO DMT in its venom and skin. When used as a psychoactive drug drug in its purified form, 5 MeO DMT is smoked, insufflated, or injected and is active at a dose of as little as 2 mg. 5 MeO DMT is also active orally ... Ott , 5 MeO DMT is active orally with doses over 30 mg without aid of an MAOI. The onset of effects ... DMT and bufotenin 5 OH DMT , the effects are typically not as visual. Some users report ... chemicals 5meo dmt 5meo dmt effects.shtml title Effects author Erowid ref br Some report ... ref Erowid lists the following effects for smoked 5 MeO DMT ref name Erowid Positive immersive ... Law Denmark As of December 1, 2004, 5 MeO DMT is legally restricted to medical or scientific ... more details
chembox verifiedrevid 413275757 Name 5 Bromo DMT ImageFile 5 Bromo DMT.svg ImageSize 200px ImageName IUPACName 2 5 bromo 1H indol 3 yl ethyl dimethylamine Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 319812 InChI 1 C12H15BrN2 c1 15 2 6 5 9 8 14 12 4 3 10 13 7 11 9 12 h3 4,7 8,14H,5 6H2,1 2H3 InChIKey ATEYZYQLBQUZJE UHFFFAOYAL SMILES1 CN C CCc2cnc1ccc Br cc12 ChEMBL Ref ebicite correct EBI ChEMBL 403031 StdInChI Ref stdinchicite correct chemspider StdInChI 1S C12H15BrN2 c1 15 2 6 5 9 8 14 12 4 3 10 13 7 11 9 12 h3 4,7 8,14H,5 6H2,1 2H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey ATEYZYQLBQUZJE UHFFFAOYSA N CASNo 17274 65 6 PubChem 360252 SMILES CN C CCC1 CNC2 C1C C Br C C2 Section2 Chembox Properties Formula C sub 12 sub H sub 15 sub N sub 2 sub Br MolarMass Density MeltingPt 98 99 C BoilingPt 5 Bromo DMT 5 bromo N,N dimethyltryptamine is a bromide brominated indole alkaloid found in certain marine invertebrate s. It is the 5 bromo analog chemistry analogue of dimethyltryptamine DMT , a hallucinogen found in many plants and animals. ref cite journal author Djura, Peter et al. year 1980 title Some Metabolites of the Marine Sponges Smenospongia aurea and Smenospongia Polyfibrospongia echina journal Journal of Organic Chemistry volume 45 issue 8 pages 1435 1441 doi 10.1021 jo01296a019 ref Other naturally occurring 5 substituted analogues of DMT include bufotenin and 5 MeO DMT , both of which, like DMT, are psychoactive and found in plants and animals. Animal studies on 5 bromo DMT showed it to produce effects suggestive of sedative and antidepressant activity. ref cite journal author Kochanowska AJ, Rao KV, Childress S, El Alfy A, Matsumoto RR, Kelly M, Stewart GS, Sufka KJ, Hamann MT title Secondary metabolites ... 5,6 diBr DMT 0.35 dry wt. was found as well as seven other alkaloids. 5 Br DMT caused significant ... References reflist Tryptamines DEFAULTSORT Bromo DMT, 5 Category Natural tryptamine alkaloids Category ... more details
Drugbox verifiedrevid 399060016 IUPAC name 1 2 methyl 1H indol 3 yl propan 2 amine image 2,a DMT.svg width 200 image2 2,alpha DMT 3d structure.png width 200 CASNo Ref cascite 1 ?? CAS number ATC prefix ATC suffix PubChem ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 23511903 smiles Cc1c c2ccccc2 nH 1 CC C N InChI 1S C12H16N2 c1 8 13 7 11 9 2 14 12 6 4 3 5 10 11 12 h3 6,8,14H,7,13H2,1 2H3 DrugBank chemical formula C 12 H 16 N 2 molecular weight bioavailability protein bound metabolism elimination half life excretion pregnancy AU A B1 B2 B3 C D X pregnancy US A B C D X pregnancy category legal AU Unscheduled S2 S3 S4 S5 S6 S7 S8 S9 legal CA Schedule I, II, III, IV, V, VI, VII, VIII legal UK GSL P POM CD Class A, B, C legal US OTC Rx only Schedule I, II, III, IV, V legal status routes of administration 2,alpha DMT , or 2, dimethyltryptamine , is a tryptamine and a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is the 2,a di methyl analog chemistry analog of dimethyltryptamine DMT . 2, DMT was first synthesized by Alexander Shulgin . In his book TiHKAL Tryptamines I Have Known and Loved , Shulgin lists the dosage as 300 500 milligram mg , and the duration as 7 10 hours. ref CiteTiHKAL pages 422 ref 2, DMT causes mydriasis and paresthesia . It also produces a calm, drunk like feeling. Very little data exists about the pharmacological properties, metabolism, and toxicity of 2, DMT. References reflist External links http www.erowid.org library books online tihkal tihkal07.shtml 2,a DMT Entry in TIHKAL http tihkal.info read.php?domain tk&id 7 2, DMT Entry in TiHKAL info TiHKAL Category Psychedelic tryptamines Psychoactive stub ... more details
1 2 pages 29 37 year 2002 pmid 11900766 ref See also 5 F AMT 5 fluoro AMT 6 fluoro DMT 4 fluoro 5 methoxy DMT http www.erowid.org library books online tihkal tihkal03.shtml 6 Fluoro DET References Reflist 2 Hallucinogens Tryptamines Use dmy dates date September 2010 DEFAULTSORT 5 Fluoro Dmt Category ... more details
drugbox IUPAC name 2 5 ethoxy 1H indol 3 yl N,N dimethylethanamine image 5 EtO DMT structure.png CAS number ATC prefix ATC suffix PubChem IUPHAR ligand ChemSpiderID Ref ChemSpiderID smiles CCOc cc12 ccc1ncc2CCN C C C 14 H 20 N 2 O 1 molecular weight 232.321 g mol bioavailability metabolism elimination half life excretion pregnancy category legal status routes of administration 5 Ethoxy N , N dimethyltryptamine 5 EtO DMT , O Ethylbufotenine is a tryptamine chemical derivative derivative , which has been previously synthesised as a chemical intermediate, but has not been studied to determine its pharmacology. ref http www.erowid.org library books online tihkal tihkal19.shtml TIHKAL 19 ref Some closely related compounds have been studied and found to act as agonist s at the 5 HT1A receptor 5 HT sub 1A sub and 5 HT1D receptor 5 HT sub 1D sub serotonin Receptor biochemistry receptors , with increasing selectivity for 5 HT sub 1D sub as the 5 alkoxy chain is lengthened, but generally reduced affinity with N,N dialkylation. ref name pmid8568822 cite journal author Glennon RA, Hong SS, Bondarev M, Law H, Dukat M, Rakhi S, Power P, Fan E, Kinneau D, Kamboj R, Teitler M, Herrick Davis K, Smith C title Binding of O alkyl derivatives of serotonin at human 5 HT1D beta receptors journal Journal of Medicinal Chemistry volume 39 issue 1 pages 314 22 year 1996 month January pmid 8568822 doi 10.1021 jm950498t url ref The affinity of larger 5 position substituted N,N dialkyltryptamines at the 5 HT2 receptor 5 HT sub 2 sub receptor subtypes has in most cases not been studied, but the widespread recreational use of N,N dialkylated 5 methoxytryptamine derivatives including 5 MeO DMT , 5 MeO MiPT and 5 MeO DiPT has led to concern that the 5 ethoxy homologues of these drugs could emerge as novel designer drug s, and consequently not only 5 EtO DMT but also other derivatives including 5 EtO DET .... ref Cite doi 10.1002 dta.223 ref See also 5 Benzyloxytryptamine 5 Ethyl DMT 5 Nonyloxy ... more details
drugbox verifiedrevid 387558813 IUPAC name 4 Fluoro 5 Methoxy N , N dimethyltryptamine image 4 Fluoro 5 methoxy N,N dimethyltryptamine.svg width CAS number 312314 18 4 ATC prefix ATC suffix PubChem C 13 H 17 F 1 N 2 O 1 molecular weight 236,13 g mol smiles bioavailability protein bound metabolism elimination half life excretion pregnancy category legal status routes of administration 4 Fluoro 5 Methoxy N , N dimethyltryptamine 4 F 5 MeO DMT was first described by David E. Nichols team in 2000. It is a potent 5 HT sub 1A sub agonist. Substitution with the 4 fluorine markedly increased 5 HT sub 1A sub selectivity over 5 HT sub 2A 2C sub receptors with potency greater than that of the 5 HT sub 1A sub agonist 8 OH DPAT . ref cite journal author Joseph B. Blair, Deborah Kurrasch Orbaugh, Danuta Marona Lewicka, Medhane G. Cumbay, Val J. Watts, Eric L. Barker, and David E. Nichols title Effect of Ring Fluorination on the Pharmacology of Hallucinogenic Tryptamines journal Journal of Medicinal Chemistry year 2000 volume 43 issue 24 pmid 11101361 pages 4701 4710 doi 10.1021 jm000339w ref The analog compound with the N , N dialkyl substituents constrained into a pyrrolidine ring, is a slightly stronger agonist for the 5 HT sub 1A sub receptor and retains the selectivity over the 5 HT sub 2A 2C sub receptors. ref cite journal doi 10.1016 S0960 894X 01 00062 2 author Uros Laban, Deborah Kurrasch Orbaugh, Danuta Marona Lewicka and David E. Nichols title A Novel Fluorinated Tryptamine with Highly Potent Serotonin 5 HT1A Receptor Agonist Properties journal Bioorganic & Medicinal Chemistry Letters year 2001 volume 11 issue 6 pages 793 795 pmid 11277522 ref See also 5 F AMT 5 fluoro AMT 6 fluoro DMT References Reflist 2 Hallucinogens Tryptamines DEFAULTSORT Fluoro 5 methoxy DMT, 4 Category Psychedelic tryptamines Category Tryptamines hallucinogen stub ... more details
drugbox IUPAC name 2 5 ethyl 1H indol 3 yl N,N dimethylethanamine image 5 Ethyl DMT structure.png CAS number ATC prefix ATC suffix PubChem 10775128 IUPHAR ligand ChemSpiderID Ref ChemSpiderID smiles CN C CCc1cnc ccc2CC c1c2 C 14 H 20 N 2 molecular weight 216.321 g mol bioavailability metabolism elimination half life excretion pregnancy category legal status routes of administration 5 Ethyl N , N dimethyltryptamine is a tryptamine chemical derivative derivative which acts as an agonist at the 5 HT1A receptor 5 HT sub 1A sub and 5 HT1D receptor 5 HT sub 1D sub serotonin Receptor biochemistry receptors , with around 3x selectivity for 5 HT sub 1D sub . ref name pmid8568822 cite journal author Glennon RA, Hong SS, Bondarev M, Law H, Dukat M, Rakhi S, Power P, Fan E, Kinneau D, Kamboj R, Teitler M, Herrick Davis K, Smith C title Binding of O alkyl derivatives of serotonin at human 5 HT1D beta receptors journal Journal of Medicinal Chemistry volume 39 issue 1 pages 314 22 year 1996 month January pmid 8568822 doi 10.1021 jm950498t url ref See also 5 Benzyloxytryptamine 5 Carboxamidotryptamine 5 Ethoxy DMT 5 Methyl DMT Sumatriptan References Reflist Serotonergics Tryptamines Category Serotonin receptor agonists Category Tryptamines pharmacology stub ... more details
Drugbox IUPAC name 2 6 fluoro 1H indol 3 yl N , N dimethyl ethanamine image 6 Fluoro DMT skeletal.svg CAS number ATC prefix none ATC suffix PubChem 2762738 ChemSpiderID C 12 H 15 F 1 N 2 molecular weight 206.26 g mol smiles CN C CCC1 CNC2 C1C C C C2 F bioavailability protein bound metabolism elimination half life excretion pregnancy category legal status routes of administration 6 Fluoro N , N dimethyltryptamine 6 Fluoro DMT is a chemical synthesis synthetic drug of the tryptamine chemical class . Pharmacology Binding profile 6 Fluoro DMT possess affinity pharmacology affinity for the 5 HT1A 5 HT sub 1A sub 392.6 nM , 5 HT1B 5 HT sub 1B sub 217.7 nM , 5 HT1D 5 HT sub 1D sub 55.4 nM , 5 HT1E 5 HT sub 1E sub 460.8 nM , 5 HT2A 5 HT sub 2A sub 866 nM , 5 HT2B 5 HT sub 2B sub 29.8 nM , 5 HT2C 5 HT sub 2C sub 674.2 nM , 5 HT5A 5 HT sub 5A sub 960.5 nM , 5 HT6 5 HT sub 6 sub 25.6 nM , 5 HT7 5 HT sub 7 sub 40.8 nM , D1 receptor D sub 1 sub 547.3 nM , D2 receptor D sub 2 sub 610.4 nM , D3 receptor D sub 3 sub 866.8 nM , D4 receptor D sub 4 sub 1,454 nM , D5 receptor D sub 5 sub 6,291 nM , 1A adrenergic sub 1A sub adrenergic 173.3 nM , 2B adrenergic sub 2B sub adrenergic 295.5 nM , 2C adrenergic sub 2C sub adrenergic 148.8 nM , H1 receptor H sub 1 sub 46.6 nM , H2 receptor H sub 2 sub 925.4 nM , Imidazoline 1 receptor I sub 1 sub 898.4 nM , Sigma 1 receptor sub 1 sub 6,892 nM , and Sigma 2 receptor sub 2 sub 7,128 nM receptor biochemistry receptor s, as well as the serotonin transporter SERT 144.6 nM . ref name pmid20126400 cite journal author Ray TS title Psychedelics and the human receptorome journal Plos One volume 5 issue 2 pages e9019 year 2010 pmid 20126400 doi 10.1371 journal.pone.0009019 url pmc 2814854 ref It has low negligible 10,000 nM affinity for the 5 HT3 5 HT sub 3 sub , 1B adrenergic sub 1B sub adrenergic , 2A adrenergic sub 2A sub adrenergic , 1 ... 5 Fluoro DMT 5 Fluoro MT 5 Bromo DMT References Reflist External links http www.erowid.org library ... more details
Drugbox IUPAC name image a,N DMT.png width 120 CAS number 61 50 7 ATC prefix ATC suffix PubChem DrugBank chemical formula C 12 H 16 N 2 molecular weight bioavailability protein bound metabolism elimination half life excretion pregnancy AU A B1 B2 B3 C D X pregnancy US A B C D X pregnancy category legal AU Unscheduled S2 S3 S4 S5 S6 S7 S8 S9 legal CA Schedule I, II, III, IV, V, VI, VII, VIII legal UK GSL P POM CD Class A, B, C legal US OTC Rx only Schedule I, II, III, IV, V legal status routes of administration Alpha,N DMT , or ,N di methyl tryptamine , is a lesser known Psychedelics, dissociatives and deliriants psychedelic drug . It is the ,N di methyl analog chemistry analog of dimethyltryptamine DMT . ,N DMT was first synthesized by Alexander Shulgin . In his book TiHKAL Tryptamines I Have Known and Loved , Shulgin lists the dosage as 50 100 milligram mg , and the duration as 6 8 hours. ref CiteTiHKAL pages 425 ref ,N DMT causes an unpleasant body load. Very little data exists about the pharmacological properties, metabolism, and toxicity of ,N DMT. References reflist External links http www.erowid.org library books online tihkal tihkal08.shtml ,N DMT Entry in TIHKAL http tihkal.info read.php?domain tk&id 8 , N DMT Entry in TiHKAL info TiHKAL Category Psychedelic tryptamines Psychoactive stub ... more details
Summary Non free use rationale Description Sample of psytrance track 1200 Micrograms DMT Source CD Article Psychedelic trance Portion 29 second Low resolution 1 ogg Purpose to explain genre and artist Replaceability copyrighted example, cannot be made with free sources other information Licensing Non free audio sample ... more details
Description Chemical structure of w Dimethyltryptamine Dimethyltryptamine Author, date of creation w User talk Cacycle Cacycle , 2005 UTC Source selfmade Copyright w GNU Free Documentation License GNU Free Documentation License GFDL Comments ChemOffice IrfanView GFDL self with disclaimers migration relicense ... more details
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