Dimethylheptylpyran

Legal statusLegal status Pharmacokinetic dataElimination half-life20–39 hoursIdentifiersCAS NumberPubChem CIDChemSpiderUNIIKEGGChEMBLCompTox Dashboard (EPA)Chemical and physical dataFormulaC₂₅H₃₈O₂Molar mass370.577 g·mol⁻¹3D model (JSmol) ^NY (what is this?)  (verify)

Dimethylheptylpyran (DMHP, 3-(1,2-dimethylheptyl)-Δ^6a(10a)-THC, 1,2-dimethylheptyl-Δ³-THC, A-40824, or EA-2233) is a synthetic analog of THC, which was invented in 1949 during attempts to elucidate the structure of Δ⁹-THC, one of the active components of Cannabis.^[2] DMHP is a pale yellow, viscous oil which is insoluble in water but dissolves in alcohol or non-polar solvents.

Effects

DMHP is similar in structure to THC, differing only in the position of one double bond, and the replacement of the 3-pentyl chain with a 3-(1,2-dimethylheptyl) chain.^[3] It produces similar activity to THC, such as sedative effects, but is considerably more potent,^[4] especially having much stronger analgesic and anticonvulsant effects than THC, although comparatively weaker psychological effects. It is thought to act as a CB₁ agonist, in a similar manner to other cannabinoid derivatives.^[5][6] While DMHP itself has been subject to relatively little study since the characterization of the cannabinoid receptors, the structural isomer 1,2-dimethylheptyl-Δ⁸-THC has been shown to be a highly potent cannabinoid agonist, and the activity of its enantiomers has been studied separately.^[7]

Investigation as non-lethal incapacitating agent

DMHP and its O-acetate ester were extensively investigated by the US military chemical weapons program in the Edgewood Arsenal experiments, as possible non-lethal incapacitating agents.^[8]

DMHP has three stereocenters and consequently has eight possible stereoisomers, which differ considerably in potency. The mixture of all eight isomers of the O-acetyl ester was given the code number EA-2233, with the eight individual isomers numbered EA-2233-1 through EA-2233-8. The most potent isomer is EA-2233-2, with an active dose range in humans of 0.5–2.8 μg/kg (i.e. ~35–200 μg for a 70 kg adult). Active doses varied markedly between individuals, but when the dose of EA-2233 was taken up to 1–2 mg, all volunteers were considered to be incapable of performing military duties, with the effects lasting as long as 2–3 days.

DMHP is metabolized in a similar manner to THC, producing the active metabolite 11-hydroxy-DMHP, but the lipophilicity of DMHP is even higher than that of THC itself, giving it a long duration of action and an extended half-life in the body of between 20 and 39 hours, with the half-life of the 11-hydroxy-DMHP metabolite being longer than 48 hours.

DMHP and its esters produce sedation and mild hallucinogenic effects similar to large doses of THC. However, they also cause pronounced hypotension (low blood pressure), occurring at doses well below the hallucinogenic dose, which can lead to severe dizziness, fainting, ataxia and muscle weakness, sufficient to make it difficult to stand upright or carry out any kind of vigorous physical activity.^[9]

The acute toxicity of DMHP was found to be low in both human and animal studies, with the therapeutic index measured as a ratio of ED₅₀ to LD₅₀ in animals being around 2000 times. There have been no recorded deaths caused by any DMHP EA-2233 stereoisomers 1–8, only symptoms that are entirely consistent with the highest-known levels of THC intoxication.^[9] DMHP has an intravenous LD50 of 63 mg/kg in mice and an intravenous minimal lethal dose of 10 mg/kg in dogs. ^[10]

Unsuitability for military application

The combination of strong incapacitating effects and a favorable safety margin led the Edgewood Arsenal team to conclude that DMHP and its derivatives, especially the O-acetyl ester of the most active isomer, EA-2233-2, were among the more promising non-lethal incapacitating agents to come out of their research program.

However, DMHP had the disadvantage of sometimes producing severe hypotension at pre-incapacitating doses, which did not occur with the more widely studied and publicized belladonnoid anticholinergic agents, such as 3-Quinuclidinyl benzilate (BZ), which was discovered and subsequently weaponized.^[11] Military applications of synthetic cannabis were limited because the drug was both illegal and politically toxic to study via laboratory administration to enlisted servicemen. Both EA-2233-2 and the red-oil THC distillate predecessor (called EA-1476) received limited budget and resources compared to the study of other incapacitating agents of BZ derivatives and EA 1729 (LSD) (which was widely believed at the time to be a viable mind-control and truth serum useful in a variety of Cold War applications).^[9] Initially, the 8 stereoisomers of EA-2233 could not be separated; later, two of the individual isomers of EA 2233 were isolated and tested, but were found to cause both orthostatic hypotension and minimal effects on performance at the very low doses used. EA 2233 did not seem to have sufficient potency to be of military interest, since an oral dose of 60mcg/kg caused a maximum decline of only 40% (at most) in performance at language and number processing tasks. A study was later published^{[citation needed]} which showed that the oral effects of ordinary THC were only about one-third of that of THC smoked as marijuana. The study suggests that the effectiveness of EA 2233 in an aerosol might be much greater than by the oral route, but this has never been independently verified using DMHP EA 2233. EA 2233 has never been used outside of the Edgewood Arsenal where it caused zero deaths in healthy volunteers from the military, but it has been theorized to pose a risk to those either very young, very old or possibly to cause loss of motor skills in those with pre-existing hypotension. In all cases, it was reported that after 72 hours the subjects showed no detectable residual effects, flashbacks, etc.

Edgewood Arsenal and EA 2233

The fiscal budgeting and planning for Edgewood Arsenal (established in 1948) considered it to be primarily a defensive research facility. The US military, at the time, knew that the USSR was spending 10 times more than the USA on chemical weapons development. Edgewood initially enjoyed a mandate^{[clarification needed]} and lack of oversight. Edgewood Arsenal Chemical Corps was tasked with ensuring that America was prepared with adequate counter-tactics if needed and that it could mount its own psychochemical retaliatory strike against the USSR if necessary. Edgewood performed analysis and submitted data to military commanders who could then choose to incorporate that into their strategy. In practice, however, it was mostly to make the strategists aware of special weapons and tactics that the enemy could instead deploy.

The Edgewood Laboratory was originally founded in 1948. The original cannabinoid distillate (the precursor to EA 2233, called EA-1476 or "Red oil"), known today as THC Delta-9, was first created in 1949, and laboratory study of EA-1476 occurred in the mid-1950s. A single batch of EA 2233 was prepared by chemist Harry Pars of A.D. Little Labs in 1962 under a top-secret government contract. It was administered to groups of consenting & informed^{[citation needed]} enlisted servicemen by Dr. James Ketchum in 1962. The Edgewood laboratory was shut down in 1975. Government funding for continued military development of synthetic cannabis was lacking and the cannabinoid research program was indefinitely suspended along with the rest of the Edgewood Arsenal experiments in the late 1970s for a variety of reasons. There was growing public distrust of the military and government, and there was little useful purpose for the further development of chemical incapacitating agents during and after the Vietnam era.^[9]

Multiple newspapers criticized the EA 2233 experiments. Since the 1930s, cannabis and cannabinoids had consistently been seen by the public as dangerous and addictive drugs. DMHP was compared to BZ, a non-cannabis chemical that was cited to be useless among military planners, and was only tested once in a hastily constructed operation called "Project Dork" (part of Project 112).^[12]

Isomerism

7 double bond isomers of dimethylheptylpyran and their 120 stereoisomers
Dibenzopyran numbering			Monoterpenoid numbering		Additional chiral centers on side chain		Number of stereoisomers	Natural occurrence	Convention on Psychotropic Substances Schedule
Short name	Chiral centers in dibenzopyran backbone	Full name	Short name	Chiral centers in dibenzopyran backbone	1,2-dimethylheptyl numbering	3-methyloctan-2-yl numbering
Δ6a(7)-DMHP	9 and 10a	3-(1,2-dimethylheptyl)-8,9,10,10a-tetrahydro-6,6,9-trimethyl-6H-dibenzo[b,d]pyran-1-ol	Δ4-DMHP	1 and 3	1 and 2	2 and 3	16	No	unscheduled
Δ7-DMHP	6a, 9 and 10a	3-(1,2-dimethylheptyl)-6a,9,10,10a-tetrahydro-6,6,9-trimethyl-6H-dibenzo[b,d]pyran-1-ol	Δ5-DMHP	1, 3 and 4	1 and 2	2 and 3	32	No	unscheduled
Δ8-DMHP	6a and 10a	3-(1,2-dimethylheptyl)-6a,7,10,10a-tetrahydro-6,6,9-trimethyl-6H-dibenzo[b,d]pyran-1-ol	Δ6-DMHP	3 and 4	1 and 2	2 and 3	16	No	unscheduled
Δ9,11-DMHP	6a and 10a	3-(1,2-dimethylheptyl)-6a,7,8,9,10,10a-hexahydro-6,6-dimethyl-9-methylene-6H-dibenzo[b,d]pyran-1-ol	Δ1(7)-DMHP	3 and 4	1 and 2	2 and 3	16	No	unscheduled
Δ9-DMHP	6a and 10a	3-(1,2-dimethylheptyl)-6a,7,8,10a-tetrahydro-6,6,9-trimethyl-6H-dibenzo[b,d]pyran-1-ol	Δ1-DMHP	3 and 4	1 and 2	2 and 3	16	No	unscheduled
Δ10-DMHP	6a and 9	3-(1,2-dimethylheptyl)-6a,7,8,9-tetrahydro-6,6,9-trimethyl-6H-dibenzo[b,d]pyran-1-ol	Δ2-DMHP	1 and 4	1 and 2	2 and 3	16	No	unscheduled
Δ6a(10a)-DMHP	9	3-(1,2-dimethylheptyl)-7,8,9,10-tetrahydro-6,6,9-trimethyl-6H-dibenzo[b,d]pyran-1-ol	Δ3-DMHP	1	1 and 2	2 and 3	8	No	Schedule I

Note that 6H-dibenzo[b,d]pyran-1-ol is the same as 6H-benzo[c]chromen-1-ol.

See also

• Tinabinol
• Nabitan
• Menabitan
• A-40174
• A-41988
• Δ-3-Tetrahydrocannabinol
• Tetrahydrocannabinol
• Tetrahydrocannabiphorol
• THCP-O-acetate
• Synthetic cannabinoids
• Effects of cannabis

References