Squigs cannabinoid journal paper thread

Journal of Analytical Chemistry

Volume 1 - Volume 89 1929 - 2017

search term “cannabinoid”

Determination of Cannabinoids in Water and Human Saliva by Solid-Phase Microextraction and
Quadrupole Ion Trap Gas Chromatography/Mass Spectrometry

Determination of Cannabinoids in Water and Human Saliva.pdf (122.7 KB)

Capillary Electrochromatography of Cannabinoids

Capillary Electrochromatography of Cannabinoids.pdf (125.3 KB)

Mass Spectrometric Characterization of Cannabinoids in Raw Cannabis sativa L.
Samples

Mass Spectrometric Characterization of Cannabinoids in Raw Cannabis sativa L…pdf (324.6 KB)

Solid-Supported Reagents in the Determination of Cannabinoids in Plasma

Solid-Supported Reagents in the Determination of Cannabinoids.pdf (779.5 KB)

Analysis of Marijuana Samples from Different Origins by High-Resolution Gas-Liquid Chromatography for Forensic Application

Analysis of Marijuana Samples from Different Origins by High-Resolution Gas-Liquid Chromatography for Forensic Application.pdf (550.4 KB)

Forensic Science

“Cannabinoid Reference : Cannabinoids. Eight sensitive and specific spot tests for
the identification of cannabis materials have been described
(86)

Forensic Science.pdf (3.4 MB)

Forensic Science

“Cannabinoid Reference : Review Contents
Drugs and Poisons
Ethanol and Volatiles
Cannabinoids
Morphine and Related Narcotics
Cocaine
Amphetamines
Barbiturates
Miscellaneous Drugs and Poisons
General Procedures
Forensic Biochemistry
Trace Evidence
Petroleum Products
Explosives
Gunpowder and Primer Residue Detection
Paine and Glass
Hairs and Fibers
Fingerprints
Miscellaneous
Books

Forensic Science 2.pdf (3.5 MB)

Forensic Science 3

“Cannabinoid Reference : Cannabinoids. A preliminary study of the analysis of cannabis
by supercritical fluid chromatography (SFC) with atmospheric
pressure chemical ionization mass spectroscopy (APCIMS)
has been reported (51)

I have yet to chase the ref down in this but it looks interesting as SFC 
is normally used for low molecular weight compounds with higher dielectric 
constants than cannabinoids. 
I wonder how they have managed to get it to separate if they have 
the different cannabinoids update to that the reference is now posted

https://future4200.com/uploads/short-url/rdLGoxc5Rw5jfvbSLTPuPEsbRTi.pdf
and on the same line of thinking
https://future4200.com/uploads/short-url/nv1NuFVwLbe0jinTQXFIx90Wsw8.pdf

Forensic Science 3.pdf (162.0 KB)

Forensic Science 4

“Cannabinoid Reference : Cannabinoids. Analytical studies on marijuana have been
reviewed by Harvey et al. (60). Mass spectrometric differentiation
of cannabinoid-containing samples have been performed
by a direct-inlet probe mass spectrometry/multiple
regression procedure (61).

Forensic Science 4.pdf (3.4 MB)

Forensic Science 5

“Cannabinoid Reference : Cannabinoids. Several important events and early studies
on marijuana in Japan have been reviewed (67). Forensic
investigations of the A-%tetrahydrocannabinol (THC) contents of
Cannabis sativa plants raised from seeds originating from various
tropical and subtropical regions have been reported (68). The
stage of root development of C. sativa stem cuttings necessary to
produce viable plants has been studied (69). A spectrophotometric
method has been used for the determination of cannabidiol
in leaves from C. sativa (70).

Forensic Science 5.pdf (3.2 MB)

Determination of Cannabinoids by Circular Dichroism

Determination of Cannabinoids by Circular Dichroism.pdf (487.8 KB)

Forensic Science 6

“Cannabinoid Reference : An improved and altemative TLC method
has been developed for the detection and identification of
Cannabis involving prechromato aphic derivatization of the
cannabinoids present in Cannags (81). Distinctive aging
processes due to the physical and chemical pecularities of
sam les of different geogra hic origin have been observed b
GC-!IT3 (82). A simple mettod for the estimation of A9-TH6
in cannabis has been reported involving the oxidative coupling
of cannabinoids in cannabis with 3-methylbenzothiazolinone
2-h drazone (83)

here we find a thc testing compound :)

Forensic Science 6.pdf (3.5 MB)

Forensic Science 7

"Cannabinoid Reference : The
composition of the steam-distilled volatile oil of fresh and air-dried,
indoor-grown marijuana was studied by GC/FID and GC/MS

Forensic Science 7.pdf (212.8 KB)

Mass Fragmentographic Assay for Ag-Tetrahydrocannabinol in Plasma

Mass Fragmentographic Assay for Ag-Tetrahydrocannabinol in Plasma.pdf (321.6 KB)

Chromatography

“Cannabinoid Reference : silica gel
sheets treated with diethylamine for
cannabinoids (492)

Chromatography.pdf (6.0 MB)

Separation and Identification of Multicomponent Mixtures Using Centri-Chromatography/Mass Spectrometry

“Cannabinoid Reference : The method
has been applied successfully to the separation of steroid hormones
(a,li pids (7,8)a nd cannabinoids (9).

Separation and Identification of Multicomponent Mixtures Using.pdf (284.6 KB)

Determination of A 9-Tetrahydrocannabinol in Blood by Electron Capture Gas Chromatography

Determination of A 9-Tetrahydrocannabinol in Blood by Electron.pdf (480.0 KB)

Identification of Noncannabinoid Phenols in Marihuana Smoke Condensate Using Chemical Ionization Mass Spectrometry

Identification of Noncannabinoid Phenols in.pdf (418.2 KB)

3 Likes

:star_struck: me trying to read all the data hurts

4 Likes

it’s not ment to be all read at once.

it’s ment to be a source of information for when your looking.
ive read quite a bit of it otherwise the “Cannabinoid Reference …” would not be possible.

I have a lot to learn though I think I can get this all down in short order so as I can
be of more use in person with some people here.

its amazing what can be done with cannabinoid chemistry I am really enjoying my self and I
hope my work here brings others success and joy as well.

remember weed is and always has been a good thing.
it brings people together.
it helps people through hard times.
it works as a medication of many (though often less than whats stated) conditions.

what I am trying to do is find a place in this world what you guys/girls are doing is
pure love that flows through the entire communities around you.

be well and stay safe in these troubled times.

:heart: :heart: :heart:

10 Likes

But that’s not how we work! We’re all a bunch of data junkies here

6 Likes

cant post anymore in the separation thread so ill put it hear (ive run out of edits my work is done for today)

where to get RP media for cheap prices

https://purolite-life-sciences.myshopify.com/collections/chromatography-synthetic-resins

6 Likes

Thanks for you’re work @squig!!

3 Likes

Bumped you up a level, should allow a bit more editing freedom. Want me to make your second post a wiki for unlimited edits?

6 Likes

thanks I have much work to do :slight_smile:

4 Likes

Keep it up, we thank you! 2nd post now also a wiki.
Feel free to make a mess on draft:squigscannajournals [WikiJane.com]

8 Likes

interesting paper I found

The Total Synthesis of Cannabinoids
RAJ K. RAZDAN SISA Incorporated, Cambridge, Massachusetts

the-total-synthesis-of-cannabinoids.pdf (3.1 MB)

2 Likes

A post was split to a new topic: WikiJane structure and RSS

Journal of Analytical Chemistry

Volume 1 - Volume 89 1929 - 2017

Gas Chromatography

“Cannabinoid Reference : Chemical ionization GC-MS was used to identify noncannabinoid
phenols in marijuana smoke (256).

Gas Chromatography.pdf (3.8 MB)

Mass Spectrometry

“Cannabinoid Reference : The
chemistry of cannabis is being exhaustively explored and
reported, ranging from the contents of the plant and extracts
thereof (425, 426, 496, 501, 1510, 1511, 1549, 1550)
to the metabolism of cannabinoids (275, 1561). The CI
spectra of cannabinoids have been discussed (1394).

Mass Spectrometry.pdf (6.4 MB)

Fluorometric Analysis

“Cannabinoid Reference : The DANSYL derivatives
of nine different cannabinoids were separated by
TLC; the sensitivity of detection was less than a nanogram
(235)

Fluorometric Analysis.pdf (3.4 MB)

Essential Oils and Related Products

“Cannabinoid Reference : New constituents of oil of Cannabis sativa were identified
with mass, IR, and NMR spectra by Stahl and Kunde
(517). Malingre et al. (343) also characterized a number of
new substances including several cannabinoid components.

Essential Oils and Related Products.pdf (2.7 MB)

Gas Chromatography Mass Spectrometric and Nuclear Magnetic Resonance Spectrometric Studies of Carcinogenic Polynuclear Aromatic Hydrocarbons in Tobacco and Marijuana Smoke Condensates

Gas Chromatography Mass Spectrometric and Nuclear Magnetic Resonance Spectrometric Studies of Carcinogenic Polynuclear Aromatic Hydrocarbons in Tobacco and Marijuana Smoke Condensates.pdf (819.2 KB)

Mass Fragmentographic Assay for 11 -Hydroxy delta 9 tetrahydrocannabinol from Plasma

Mass Fragmentographic Assay for 1 I-Hydroxy-Agtetrahydrocannabinol from Plasma.pdf (463.9 KB)

Fluorometric and Phosphorometric Analysis

“Cannabinoid Reference : Metal ion and barbiturate additive effects on tetracycline
fluorescence (3370) and the fluorescence of cannabinoids
(1580) were discussed

Fluorometric and Phosphorometric Analysis.pdf (3.6 MB)

Journal of Analytical Chemistry

Volume 1 - Volume 89 1929 - 2017

Mass Spectrometry

“Cannabinoid Reference: The site of metabolic hydroxylation of cannabinoids can
be determined by GC/MS of trimethylsilyl derivatives (AA6),
and the determination of trazodone in rat plasma is described
by a GC/MS method using benperidol as an internal standard
(AA5)

Mass Spectrometry 2.pdf (6.1 MB)

Ion Exchange and Liquid Column Chromatography

"Cannabinoid Reference: Porous Polymers: Carbon Adsorbents. Nonionic
macroporous polymers, the XAD resins of Rohm and Haas
Co., are excellent general-purpose absorbents, but they are gefore they can 6e used in high-performance chromatography
(205, 356, 357). then states cannabinoid requirement for column in table looking up refs for you now

Ion Exchange and Liquid Column Chromatography.pdf (1.9 MB)

ref 2 HIGH-PRESSURE LIQUID CHROMATOGRAPHY OF CANNABIS

Journal of Chromatography A
HIGH-PRESSURE LIQUID CHROMATOGRAPHY OF CANNABIS.pdf (514.5 KB)

ref 3 CANNABINOID  ASSAYS IN  HUMANS

NIDA Research Monograph
CANNABINOID ASSAYSIN HUMANS.pdf (2.2 MB)

Paper and Thin Layer Chromatography

“Cannabinoid Reference: cannabinoids and their monooxygenated
derivatives by silica gel TLC (RF values for 33
compounds given) (128B); cannabinoids by sequential TLC
with one neutral and nonpolar, another basic, and a third
acidic solvent

Paper and Thin-Layer Chromatography.pdf (2.7 MB)

Journal of Analytical Chemistry

Volume 1 - Volume 89 1929 - 2017

Mass Spectrometry

“Cannabinoid Reference:Microbiological oxidation of cannabinoids has been investigated
by two groups. Christie et al. (ZI) demonstrated the
transformations of A9-THC by Chaetomium globosum into
a number of products, including the 3’-hydroxy, 1 I-hydroxy,
and 3’,11-dihydroxy derivatives, while Robertson and colleagues
(29) applied GC/EIMS and GC/CIMS techniques to
characterize alcoholic and acidic metabolites of cannabidiol
produced by Syncephalastrum racemossurn and Mycobacterium
rhodochrous.

this could be a new method of remediation. oxidation of the epoxy bridge 
vi bacteria back to CBD then UV light used to kill the bacteria.

MASS SPECTROMETRY 3.pdf (7.5 MB)

Characterization of the Basic Fraction of Marijuana Smoke by Capillary Gas Chromatography/Mass Spectrometry

Characterization of the Basic Fraction of Marijuana Smoke by.pdf (467.3 KB)

Analysis of Urine for 1 1-Nor-As-tetrahydrocannabinol-9-carboxylic Acid Using Sep-PAK
Cartridges for Sample Cleanup

Analysis of Urine for 1 1-Nor-As-tetrahydrocannabinol-9-carboxylic Acid Using Sep-PAK.pdf (420.0 KB)

Effect of Solvent on Solid-Supported Reactions on Styrene/Divinylbenzene Copolymeric Macroreticular Resin

“Cannabinoid Reference: Derivatization of Ag-THC was initiated as described above for
lipophilic acids by using preadsorption prior to the reaction (6,
9). Thus, Ag-THC was adsorbed onto 200 mg of resin from 4 mL
of aqueous solution at pH 3.5 containing 1.25 pg/mL of analyte.
In this instance, however, after adsorption of analyte, the resin
was isolated by aspiration and 4 mL of 0.1 M NaOH in H20/
CH,CN (4:1, v/v) was added followed by 10 pL of PFBBr in 90
pL of diluent (6,9)

Effect of Solvent on Solid-Supported Reactions on Styrene Divinylbenzene Copolymeric Macroreticular Resin.pdf (494.0 KB)

Drug of Abuse Confirmation in Human Urine Using Stepwise Solid-Phase Extraction and Micellar Electrokinetic Capillary Chromatography

“Cannabinoid Reference: It is important to add
that the confirmation of cannabinoids could not be achieved
without hydrolyzing the urine specimen prior to e~traction

Drug of Abuse Confirmation in Human Urine Using Stepwise.pdf (545.7 KB)

Quantitative Method for the Profiling of the Endocannabinoid Metabolome by LC-Atmospheric Pressure Chemical Ionization-MS

Quantitative Method for the Profiling of the Endocannabinoid Metabolome.pdf (249.7 KB)

Electrooxidation of New Synthetic Cannabinoids: Voltammetric Determination of Drugs in Seized Street Samples and Artificial Saliva

Electrooxidation of New Synthetic Cannabinoids Voltammetric.pdf (1.8 MB)

Qualitative Confirmation of 9 Synthetic Cannabinoids and 20 Metabolites in Human Urine Using LC−MS/MS and Library Search

Qualitative Confirmation of 9 Synthetic Cannabinoids and 20.pdf (1.1 MB)

Detection and Mapping of Cannabinoids in Single Hair Samples through Rapid Derivatization and Matrix-Assisted Laser Desorption Ionization Mass Spectrometry

Detection and Mapping of Cannabinoids in Single Hair Samples.pdf (2.4 MB)

Analysis of Synthetic Cannabinoids Using High-Resolution Mass Spectrometry and Mass Defect Filtering: Implications for Nontargeted Screening of Designer Drugs

Analysis of Synthetic Cannabinoids Using High-Resolution Mass.pdf (925.2 KB)

Targeted Metabolomic Approach for Assessing Human Synthetic Cannabinoid Exposure and Pharmacology

Targeted Metabolomic Approach for Assessing Human Synthetic.pdf (1.8 MB)

Screening of Several Drugs of Abuse in Italian Workplace Drug Testing: Performance Comparisons of On-Site Screening Tests and a Fluorescence Polarization Immunoassay-Based Device

Screening of Several Drugs of Abuse in Italian Workplace Drug.pdf (1.2 MB)

Detection and Activity Profiling of Synthetic Cannabinoids and Their Metabolites with a Newly Developed Bioassay

Detection and Activity Profiling of Synthetic Cannabinoids and Their.pdf (2.5 MB)

Analytical Differentiation of 1‑Alkyl-3-acylindoles and 1‑Acyl-3-alkylindoles: Isomeric Synthetic Cannabinoids

Analytical Differentiation of 1‑Alkyl-3-acylindoles and.pdf (1.5 MB)

Investigating a not-so-natural high Researchers identify synthetic cannabinoids in herbal incense.

Investigating a not-so-natural high.pdf (4.1 MB)

Fully Automated Determination in the Low Nanogram per Liter Level of Different Classes of Drugs of Abuse in Sewage Water by On-Line Solid-Phase Extraction-Liquid Chromatography-Electrospray-Tandem Mass Spectrometry

Fully Automated Determination in the Low Nanogram per Liter Level of Different Classes of Drugs of Abuse in Sewage.pdf (544.4 KB)

Quantitative Measurement of JWH-018 and JWH-073 Metabolites Excreted in Human Urine

Quantitative Measurement of JWH-018 and JWH-073 Metabolites.pdf (1.4 MB)

Forensic Science

“Cannabinoid Reference: Cannabinoids. It has been shown that DELTA9-THC (9-THC)
isomerized to DELTA8-THC (8-THC) during derivatization
(374). Liquid-liquid or solid-liquid extraction was used to
analyze for 9-THC commercial hemp products (375). Cannabinoid
contents in cannabis products were determined by GCFID
(376). A new method to determine 9-carboxy-11-nor-
DELTA9-THC (9-THC-COOH) and 11-hydroxy-DELTA9-THC
(11-OH-THC) using two-dimensional (2D) GC/MS was developed
to reduce interferences and carryover (377).

Forensic Science 8.pdf (169.3 KB)

Forensic Science

“Cannabinoid Reference: Cannabinoids. A comparison of Roche kinetic interaction of
microparticles in solution assay for cannabinoids and GC/MS
analysis for 11-nor-9-carboxy-¢-trahydrocannabionol (THCCOOH)
has been reported (256). The effects of oxidizing adulterants on
detection of 11-nor-¢-9 THC-carboxylic acid in urine specimens
has been studied (257).

Forensic Science 9.pdf (112.0 KB)

Screening and Selective Quantification of Illicit Drugs in Wastewater by Mixed-Mode Solid-Phase Extraction and Quadrupole-Time-of-Flight Liquid Chromatography−Mass Spectrometry

Screening and Selective Quantification of Illicit Drugs in Wastewater.pdf (1.6 MB)

Determination of Drugs of Abuse in Airborne Particles by Pressurized Liquid Extraction and
Liquid Chromatography-Electrospray-Tandem Mass Spectrometry

Determination of Drugs of Abuse in Airborne Particles.pdf (672.9 KB)

Solid-Phase Extraction and Quantitative Measurement of Omega and Omega-1 Metabolites of JWH-018 and JWH-073 in Human Urine Krishna C.

Solid-Phase Extraction and Quantitative Measurement of Omega and Omega-1 Metabolites of JWH-018 and JWH-073.pdf (1.3 MB)

Development and Validation of a Sensitive UPLC-ESI-MS/MS Method for the Simultaneous Quantification of 15 Endocannabinoids and Related Compounds in Milk and Other Biofluids

Development and Validation of a Sensitive UPLC-ESI-MS MS Method.pdf (1.8 MB)

Analysis of Cannabinoids and Their Metabolites in Human Urine

Analysis of Cannabinoids and Their Metabolites in Human Urine.pdf (1.1 MB)

2 Likes

Journal of Medicinal Chemistry

1951 - 2011

Characterization of a Region of Steric Interference at the Cannabinoid Receptor Using the Active Analog Approach1

Characterization of a Region of Steric Interference at the Cannabinoid Receptor.pdf (360.0 KB)

Aminoalkylindoles: Structure—Activity Relationships of Novel Cannabinoid Mimetics

Aminoalkylindoles Structure—Activity Relationships of Novel Cannabinoid.pdf (1.2 MB)

Derivation of a Pharmacophore Model for Anandamide Using Constrained Conformational Searching and Comparative Molecular Field Analysis

“Cannabinoid Reference: The proposed pharmacophore model was capable of discriminating between
structurally related compounds exhibiting different pharmacological potency for the CB1
cannabinoid receptor, i.e., anandamide and N-(2-hydroxyethyl)prostaglandinamide.

Derivation of a Pharmacophore Model for Anandamide Using Constrained.pdf (254.2 KB)

Three-Dimensional Quantitative Structure-Activity Relationship Study of the Cannabimimetic (Aminoalkyl)indoles Using Comparative Molecular Field Analysis

Three-Dimensional Quantitative Structure-Activity Relationship Study of the spice.pdf (244.0 KB)

Structure-Activity Analysis of Anandamide Analogs: Relationship to a Cannabinoid Pharmacophore

Structure-Activity Analysis of Anandamide Analogs Relationship to a Cannabinoid Pharmacophore.pdf (371.8 KB)

(Aminoalkyl)indole Isothiocyanates as Potential Electrophilic Affinity Ligands for the Brain Cannabinoid Receptor

(Aminoalkyl)indole Isothiocyanates as Potential Electrophilic Affinity Ligands for the Brain Cannabinoid Receptor.pdf (266.4 KB)

5-Azido-A8-THC: A Novel Photoaffinity Label for the Cannabinoid Receptor

5-Azido-A8-THC A Novel Photoaffinity Label for the Cannabinoid Receptor.pdf (185.1 KB)

Synthesis and Pharmacological Comparison of Dimethylheptyl and Pentyl Analogs of Anandamide

Synthesis and Pharmacological Comparison of Dimethylheptyl and Pentyl Analogs of Anandamide.pdf (133.0 KB)

Classical/Nonclassical Hybrid Cannabinoids: Southern Aliphatic Chain-Functionalized C-6â Methyl, Ethyl, and Propyl Analogues

Classical Nonclassical Hybrid Cannabinoids Southern Aliphatic Chain - Functionalized c-6b Methyl, Ethyl, and Propyl Analogues.pdf (290.4 KB)

Importance of the C-1 Substituent in Classical Cannabinoids to CB2 Receptor Selectivity Synthesis and Characterization of a Series of O,2-Propano delta 8 tetrahydrocannabinol Analogs

Importance of the C-1 Substituent in Classical Cannabinoids to CB2 Receptor Selectivity Synthesis and Characterization of a Series of O,2-Propano delta 8 tetrahydrocannabinol Analogs.pdf (172.3 KB)

Cannabinol Derivatives: Binding to Cannabinoid Receptors and Inhibition of Adenylylcyclase

Cannabinol Derivatives Binding to Cannabinoid Receptors and Inhibition of Adenylylcyclase.pdf (216.7 KB)

Use of a Potential Rabbit Model for Structure-Behavioral Activity Studies of Cannabinoids

Use of a Potential Rabbit Model for Structure-Behavioral Activity Studies of Cannabinoids.pdf (134.1 KB)

The Importance of the Orientation of the C9 Substituent to Cannabinoid Activity

The Importance of the Orientation of the C9 Substituent to Cannabinoid Activity.pdf (170.7 KB)

(-)-ll-Hydroxy-7’-isothiocyanato-l’,l’-dimethylheptyl-A8-THC: A Novel, High-Affinity Irreversible Probe for the Cannabinoid Receptor in the Brain

Close your eyes, give me your hand
Do you feel my heart beating
Do you understand?
Do you feel the same
Am I only dreaming
Or is this binding an eternal stone?

of course the body adjusts but cool idea ha :slight_smile:

(-)-ll-Hydroxy-7’-isothiocyanato-l’,l’-dimethylheptyl-A8-THC A Novel, High-Affinity Irreversible Probe for the Cannabinoid Receptor in the Brain.pdf (118.0 KB)

Design, Synthesis and Biological Evaluation of Novel Arachidonic Acid Derivatives as Highly Potent and Selective Endocannabinoid Transporter Inhibitors

Design, Synthesis and Biological Evaluation of Novel Arachidonic Acid Derivatives as Highly Potent and Selective Endocannabinoid Transporter Inhibitors.pdf (48.8 KB)

Conformational Analysis of the Prototype Nonclassical Cannabinoid CP-47,497, Using 2D NMR and Computer Molecular Modeling

Conformational Analysis of the Prototype Nonclassical Cannabinoid CP-47,497, Using 2D NMR and Computer Molecular Modeling.pdf (801.7 KB)

Molar Volume Relationships and the Specific Inhibition of a Synaptosomal Enzyme by Psychoactive Cannabinoids

Molar Volume Relationships and the Specific Inhibition of a Synaptosomal Enzyme by Psychoactive Cannabinoids.pdf (180.5 KB)

Synthesis and Pharmacological Evaluation of Ether and Related Analogues of Delta 8 -,Delta 9 -, and Delta 9/11 Tetrahydrocannabinol

pass me the bottle of methyl iodide please sir

Synthesis and Pharmacological Evaluation of Ether and Related Analogues of A8-,A9-, and A91 ^Tetrahydrocannabinol.pdf (228.1 KB)

Conformationally Restrained Analogues of Pravadoline: Nanomolar Potent, Enantioselective, (Aminoalkyl)indole Agonists of the Cannabinoid Receptor

Conformationally Restrained Analogues of Pravadoline Nanomolar Potent, Enantioselective, (Aminoalkyl)indole Agonists of the Cannabinoid Receptor.pdf (398.2 KB)

(R)-Methanandamide: A Chiral Novel Anandamide Possessing Higher Potency and Metabolic Stability

(R)-Methanandamide A Chiral Novel Anandamide Possessing Higher Potency and Metabolic Stability.pdf (159.1 KB)

A Novel Probe for the Cannabinoid Receptor

A Novel Probe for the Cannabinoid Receptor.pdf (196.0 KB)

Synthesis and Pharmacology of a Very Potent Cannabinoid Lacking a Phenolic Hydroxyl with High Affinity for the CB2 Receptor

Synthesis and Pharmacology of a Very Potent Cannabinoid Lacking a Phenolic Hydroxyl with High Affinity for the CB2 Receptor.pdf (105.9 KB)

Structural Requirements for Binding of Anandamide-Type Compounds to the Brain Cannabinoid Receptor

Structural Requirements for Binding of Anandamide-Type Compounds to the Brain Cannabinoid Receptor.pdf (220.6 KB)

Synthetic Nonpsychotropic Cannabinoids with Potent Antiinflammatory, Analgesic, and Leukocyte Antiadhesion Activities

Synthetic Nonpsychotropic Cannabinoids with Potent Antiinflammatory, Analgesic, and Leukocyte Antiadhesion Activities.pdf (246.0 KB)

Head Group Analogs of Arachidonylethanolamide, the Endogenous Cannabinoid Ligand

Head Group Analogs of Arachidonylethanolamide, the Endogenous Cannabinoid Ligand.pdf (143.2 KB)

Unsaturated Side Chain â-11-Hydroxyhexahydrocannabinol Analogs

Unsaturated Side Chain â-11-Hydroxyhexahydrocannabinol Analogs.pdf (178.1 KB)

Conformational Studies on a Diastereoisomeric Pair of Tricyclic Nonclassical Cannabinoids by NMR Spectroscopy and Computer Molecular Modeling

Conformational Studies on a Diastereoisomeric Pair of Tricyclic Nonclassical Cannabinoids by NMR Spectroscopy and Computer Molecular Modeling.pdf (408.1 KB)

Pharmacophoric Requirements for Cannabinoid Side Chains: Multiple Bond and C1¢-Substituted ¢8-Tetrahydrocannabinols

Pharmacophoric Requirements for Cannabinoid Side Chains Multiple Bond and C1-Substituted delta 8-Tetrahydrocannabinols.pdf (131.0 KB)

New Approaches to Antiglaucoma Therapy

"Cannabinoid Reference: Cannabinoid (CB) receptor ligands like WIN 55,512-2
and CP 55,940 reduce rabbit and monkey IOP when
given topically, showing enantiomeric selectivity.171,172
WIN 55,512-2 decreased aqueous humor production in
rabbits but had no effect on outflow in rabbits or
monkeys.173

New Approaches to Antiglaucoma Therapy.pdf (406.8 KB)

Synthesis and Pharmacological Evaluation of Amino, Azido, and Nitrogen Mustard Analogues of 10-Substituted Cannabidiol and 11- or 12-Substituted A8-Tetrahydrocannabinol

Synthesis and Pharmacological Evaluation of Amino, Azido, and Nitrogen Mustard Analogues of 10-Substituted Cannabidiol and 11- or 12-Substituted A8-Tetrahydrocannabinol.pdf (218.6 KB)

Cannabinoids. Structure-Activity Studies Related to 1,2-Dimethylheptyl Derivatives

Cannabinoids. Structure-Activity Studies Related to 1,2-Dimethylheptyl Derivatives.pdf (247.1 KB)

Potent Anandamide Analogs: The Effect of Changing the Length and Branching of the End Pentyl Chain

Potent Anandamide Analogs The Effect of Changing the Length and Branching of the End Pentyl Chain.pdf (199.5 KB)

Synthesis and Pharmacological Properties of ll-Hydroxy-3-(l’,l’-dimethylheptyl)hexahydrocannabinol: A High-Affinity Cannabinoid Agonist

Synthesis and Pharmacological Properties of ll-Hydroxy-3-(l’,l’-dimethylheptyl)hexahydrocannabinol A High-Affinity Cannabinoid Agonist.pdf (114.4 KB)

Activity of Novel Aminocannabinoids in Baboons

pass that boon a bong please

Activity of Novel Aminocannabinoids in Baboons.pdf (128.3 KB)

Cannabimimetic Activity of Novel Enantiomeric, Benzofuran Cannabinoids

Cannabimimetic Activity of Novel Enantiomeric, Benzofuran Cannabinoids.pdf (959.7 KB)

Some 9-Hydroxycannabinoid-like Compounds. Synthesis and Evaluation of Analgesic and Behavioral Properties

Some 9-Hydroxycannabinoid-like Compounds. Synthesis and Evaluation of Analgesic and Behavioral Properties.pdf (95.0 KB)

Two New Unsaturated Fatty Acid Ethanolamides in Brain That Bind to the Cannabinoid Receptor

Two New Unsaturated Fatty Acid Ethanolamides in Brain That Bind to the Cannabinoid Receptor.pdf (121.1 KB)

Stereochemical Requirements for Cannabinoid Activity

Stereochemical Requirements for Cannabinoid Activity.pdf (156.7 KB)

Potent Cyano and Carboxamido Side-Chain Analogues of 1’,1’-Dimethyl-delta 8-Tetrahydrocannabinol

Potent Cyano and Carboxamido Side-Chain Analogues of 1’,1’-Dimethyl-delta 8-Tetrahydrocannabinol.pdf (126.5 KB)

A Half Century in Medicinal Chemistry with Major Emphasis on Pain-Relieving Drugs and Their Antagonists

“Cannabinoid Reference: They developed a large series of bicyclic cannabinoids
(with retention of the alicyclic hydroxyl substituent)
far more potent as analgesics than morphine.

A Half Century in Medicinal Chemistry with Major Emphasis on Pain-Relieving Drugs and Their Antagonists.pdf (226.8 KB)

Synthesis of a Norcannabinoid

Synthesis of a Norcannabinoid part 1.pdf (112.7 KB)
Synthesis of a Norcannabinoid part 2.pdf (107.2 KB)

Benzoxocin and Benzoxonin Derivatives. Novel Groups of Terpenophenols with Central Nervous System Activity

“Cannabinoid Reference: Very few central nervous system (CNS) agents are
known which do not possess a nitrogen atom. The most
conspicuous ones among them are the active cannabinoids,
1 both natural and synthetic. The structure-activity
relationship in this series has been investigated in some
detail2,3 and it has been suggested2 that a tricyclic ring
system containing a benzopyran moiety is a requirement
for CNS activity.

THC is a Terpenophenol :slight_smile:

Benzoxocin and Benzoxonin Derivatives. Novel Groups of Terpenophenols with Central Nervous System Activity.pdf (228.8 KB)

9-Nor-A8-tetrahydrocannabinol, a Cannabinoid of Metabolic Interest

9-Nor-A8-tetrahydrocannabinol, a Cannabinoid of Metabolic Interest.pdf (108.6 KB)

Hashish.1 Importance of the Phenolic Hydroxyl Group in Tetrahydrocannabinols

Hashish.1 Importance of the Phenolic Hydroxyl Group in Tetrahydrocannabinols.pdf (100.4 KB)

Analgesic Properties of the Tetrahydrocannabinols, Their Metabolites, and Analogs

Analgesic Properties of the Tetrahydrocannabinols, Their Metabolites, and Analogs.pdf (153.5 KB)

Benzoxocin and Benzoxonin Derivatives. Novel Groups of Terpenophenols with Central Nervous System Activity. A Correction

Benzoxocin and Benzoxonin Derivatives. Novel Groups of Terpenophenols with Central Nervous System Activity. A Correction.pdf (62.6 KB)

Hashish.1 Unsaturated Side-Chain Analogues of A8-Tetrahydrocannabinol with Potent Biological Activity

Hashish.1 Unsaturated Side-Chain Analogues of A8-Tetrahydrocannabinol with Potent Biological Activity.pdf (98.3 KB)

Drugs Derived from Cannabinoids. 1. Nitrogen Analogs, Benzopyranopyridines and Benzopyranopyrroles

Drugs Derived from Cannabinoids. 1. Nitrogen Analogs, Benzopyranopyridines and Benzopyranopyrroles.pdf (251.2 KB)

Drugs Derived from Cannabinoids Basic Esters of Nitrogen and Carbocyclic Analogs

Drugs Derived from Cannabinoids Basic Esters of Nitrogen and Carbocyclic Analogs.pdf (222.4 KB)

Drugs Derived from Cannabinoids. 5. delta 6 delta 10-Tetrahydrocannabinol and Heterocyclic Analogs Containing Aromatic Side Chains

Drugs Derived from Cannabinoids. 5. A6al0a-Tetrahydrocannabinol and Heterocyclic Analogs Containing Aromatic Side Chains.pdf (294.9 KB)

Drugs Derived from Cannabinoids. and Thienobenzopyrans Sulfur Analogs, Thiopyranobenzopyrans

Drugs Derived from Cannabinoids. and Thienobenzopyrans Sulfur Analogs, Thiopyranobenzopyrans.pdf (103.6 KB)

Drugs Derived from Cannabinoids. Effect of Alkyl Substitution in Sulfur and Carbocyclic Analogs

Drugs Derived from Cannabinoids. Effect of Alkyl Substitution in Sulfur and Carbocyclic Analogs.pdf (99.0 KB)

(-)-3-Isothujone, a Small Nonnitrogenous Molecule with Antinociceptive Activity in Mice

“Cannabinoid Reference” The results are compared with those of several cannabinoids
we have tested previously5 and morphine and codeine.
"

(-)-3-Isothujone, a Small Nonnitrogenous Molecule with Antinociceptive Activity in Mice.pdf (131.4 KB)

9-Nor-9-hydroxyhexahydrocannabinols. Synthesis, Some Behavioral and Analgesic Properties, and Comparison with the Tetrahydrocannabinols

9-Nor-9-hydroxyhexahydrocannabinols. Synthesis, Some Behavioral and Analgesic Properties, and Comparison with the Tetrahydrocannabinols.pdf (95.9 KB)

Cannabinoids. 1. 1-Amino- and l-Mercapto-7,8,9,10-tetrahydro-6H-dibenzo[6,d]pyrans

Cannabinoids. 1. 1-Amino- and l-Mercapto-7,8,9,10-tetrahydro-6H-dibenzo[6,d]pyrans.pdf (180.0 KB)

Cannabinoids. 2. Synthesis and Central Nervous System Activities of Some B-Ring Homocannabinoid Derivatives and Related Lactones

Cannabinoids. 2. Synthesis and Central Nervous System Activities of Some B-Ring Homocannabinoid Derivatives and Related Lactones.pdf (172.1 KB)

Cannabinoids. Synthesis and Central Nervous System Activity of 8-Substituted 10-Hydroxy-5,5-dimethyl-5ff-[ 1 ]benzopyrano[4,3-c]pyridine and Derivatives

Cannabinoids. Synthesis and Central Nervous System Activity of 8-Substituted 10-Hydroxy-5,5-dimethyl-5ff-[ 1 ]benzopyrano[4,3-c]pyridine and Derivatives.pdf (147.2 KB)

Drugs Derived from Cannabinoids. 7.1 Tachycardia and Analgesia Structure-Activity Relationships in delta 9 Tetrahydrocannabinol and Some Synthetic Analogues

Drugs Derived from Cannabinoids. 7.1 Tachycardia and Analgesia Structure-Activity Relationships in delta 9 Tetrahydrocannabinol and Some Synthetic Analogues.pdf (91.6 KB)

Some 11-Substituted Tetrahydrocannabinols. Synthesis and Comparison with the Potent Cannabinoid Metabolites 11-Hydroxytetrahydrocannabinols

Some 11-Substituted Tetrahydrocannabinols. Synthesis and Comparison with the Potent Cannabinoid Metabolites 11-Hydroxytetrahydrocannabinols.pdf (128.8 KB)

3’Hydroxy- and (±)-3’,ll-Dihydroxy-A9-tetrahydrocannabinol: Biologically Active Metabolites of A^Tetrahydrocannabinol1

3’Hydroxy- and (±)-3’,ll-Dihydroxy-A9-tetrahydrocannabinol Biologically Active Metabolites of A^Tetrahydrocannabinol1.pdf (165.5 KB)

New Antihypertensive Cannabinoids

New Antihypertensive Cannabinoids.pdf (133.1 KB)

New Azacannabinoids Highly Active in the Central Nervous System

New Azacannabinoids Highly Active in the Central Nervous System.pdf (104.2 KB)

A Cannabinoid Derived Prototypical Analgesic

A Cannabinoid Derived Prototypical Analgesic.pdf (183.5 KB)

Synthesis and Pharmacological Activity of Some 9-Substituted A8-Tetrahydrocannabinol Analogues

Synthesis and Pharmacological Activity of Some 9-Substituted A8-Tetrahydrocannabinol Analogues.pdf (101.7 KB)

Hashish: Synthesis and Central Nervous System Activity of Some Novel Analogues of Cannabidiol and Oxepin Derivatives of A9-Tetrahydrocannabinol

Hashish 1 Synthesis and Central Nervous System Activity of Some Novel Analogues of Cannabidiol and Oxepin Derivatives of A9-Tetrahydrocannabinol.pdf (152.0 KB)

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Damn :joy:

Apparently we’ve just scratched the surface of all this

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yep like I said ill boost research a little enjoy my friend ill be here for some time and its going to take
a long time to get through what I have then ill get more.

I am interested in dumping the pharma journals and some more psych journals and then running
the search over them.

today I found that if you methylate the phenol like morphine it becomes inactive.

if you acetylate it increase activty due to change in its ability to attach to fats.

also I found that cutting the phenolic oxygen off the molecule increases its binding affinity
to the CB2 receptor.

at a guess I would say that the propionyl ester of THC delta 9 would be strong long and
real trippy :slight_smile:

still much to find.

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I’ll need to get a couple cabins built and fly you out and have a science weekend :relaxed: I’m trying to make a space for people to just mess around with stuff and see what comes up

5 Likes

Journal of Medicinal Chemistry

1951 - 2011

Synthesis and Analgesic Evaluation of 4-(2-Heptyloxy)-7-[(Z)-(3-hydroxycyclohexyl)]indole: A Caveat on Indole-Phenol Bioisosterism

“Cannabinoid Reference: Compound 8, an analgesic, is a member of a series of
simplified cannabinoids lacking the dihydropyran ring,
among which 9 (CP-47497) has been extensively studied

Synthesis and Analgesic Evaluation of 4-(2-Heptyloxy)-7-[(Z)-(3-hydroxycyclohexyl)]indole A Caveat on Indole-Phenol Bioisosterism.pdf (201.8 KB)

Synthesis and Anticonvulsant and Sedative-Hypnotic Activity of 4-(Alkylimino)-2,3-dihydro-4/f-l-benzopyrans and -benzothiopyrans

“Cannabinoid Reference: The wide range of activity of cannabinoids on the central
nervous system has stimulated the search for modified
analogues with selective action and increased potency but
devoid of hallucinogenic properties.1 Some considerable
success, leading to compounds with antinausea and analgesic
activity, has been obtained in recent years.

Synthesis and Anticonvulsant and Sedative-Hypnotic Activity of 4-(Alkylimino)-2,3-dihydro-4 f-l-benzopyrans and -benzothiopyrans.pdf (164.1 KB)

Antinociceptive (Aminoalkyl)indoles

“Cannabinoid Reference: The evidence is summarized which suggests that this second antinociceptive mechanism is associated with binding to the recently characterized cannabinoid
receptor.

Antinociceptive (Aminoalkyl)indoles.pdf (326.5 KB)

Synthesis and Structure-Activity Relationships of a Series of Novel Benzopyran-Containing Platelet Activating Factor Antagonists

“Cannabinoid Reference: These cannabinoid analogues were originally
prepared at Abbott as analgesic, antihypertensive,
and sedative hypnotic agents

Synthesis and Structure-Activity Relationships of a Series of Novel Benzopyran-Containing Platelet Activating Factor Antagonists.pdf (246.1 KB)

Journal of Organic Chemistry

1936 - 2010

The Synthesis of ( — )-A9(11)-trans-Tetrahydrocannabinol ( — )-A9(11)-trans-Tetrahydrocannabinol

The Synthesis of ( — )-A9(11)-trans-Tetrahydrocannabinol ( — )-A9(11)-trans-Tetrahydrocannabinol.pdf (116.5 KB)

Synthesis of Covalent Probes for the Radiolabeling of the Cannabinoid Receptor

Synthesis of Covalent Probes for the Radiolabeling of the Cannabinoid Receptor.pdf (122.1 KB)

Cannabinoids. 3.’ Synthetic Approaches to 9-Ketocannabinoids. Total Synthesis of Nabilone

Cannabinoids. 3.’ Synthetic Approaches to 9-Ketocannabinoids. Total Synthesis of Nabilone.pdf (1.1 MB)

Synthesis of ll-Nor-A8-tetrahydrocannabinol-9-carboxylic Acid Methyl Ester

Synthesis of ll-Nor-A8-tetrahydrocannabinol-9-carboxylic Acid Methyl Ester.pdf (134.1 KB)

Synthesis of Functionalized Cannabinoids

Synthesis of Functionalized Cannabinoids.pdf (96.8 KB)

General Synthesis of Side Chain Derivatives of Cannabinoids

General Synthesis of Side Chain Derivatives of Cannabinoids.pdf (1012.8 KB)

Regioselective Synthesis of (±)-ll-Nor-9-carboxy-A9-THC

Regioselective Synthesis of (±)-ll-Nor-9-carboxy-A9-THC.pdf (101.9 KB)

High Pressure Diels-Alder Approach to Hydroxy-Substituted 6a-Cyano-tetrahydro-6H-benzo[c]chromen-6-ones: A Route to Δ6-Cis-Cannabidiol

High Pressure Diels-Alder Approach to Hydroxy-Substituted 6a-Cyano-tetrahydro-6H-benzo[c]chromen-6-ones A Route to Δ6-Cis-Cannabidiol.pdf (157.4 KB)

Carbon-13 Nuclear Magnetic Resonance Spectroscopy of Naturally Occurring Substances. 47. Cannabinoid Compounds

Carbon-13 Nuclear Magnetic Resonance Spectroscopy of Naturally Occurring Substances. 47. Cannabinoid Compounds.pdf (243.0 KB)

Hashish:’ Factors Influencing Double-Bond Stability in Cannabinoids

Hashish Factors Influencing Double-Bond Stability in Cannabinoids.pdf (586.4 KB)

Hashish.’ Synthesis of ( &)-A1- and A6-3,4-cis-Cannabidiols and Their Isomerization by Acid Catalysis

please remember that it is the trans isomer that is in nature not the cis. 
this paper is on synthetic CBD not natural.

Hashish.’ Synthesis of ( &)-A1- and A6-3,4-cis-Cannabidiols and Their Isomerization by Acid Catalysis.pdf (695.0 KB)

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1 Like

Mechoulam, R. (1982). Chemistry of Cannabis. Handbook of Experimental Pharmacology, 119–134.

Mechoulam, R. (1982). Chemistry of Cannabis. Handbook of Experimental Pharmacology, 119–134…pdf (2.1 MB)

Cannabinoid chemistry: an overview

Cannabinoid chemistry an overview.pdf (326.5 KB)

Synthetic Route Sourcing of Illicit at Home Cannabidiol (CBD)Isomerization to Psychoactive Cannabinoids Using Ionmobility-coupled-LC-MS/MS

Synthetic Route Sourcing of Illicit at Home Cannabidiol (CBD)Isomerization to Psychoactive Cannabinoids Using Ionmobility-coupled-LC-MS MS.pdf (1.2 MB)

Journal of American Chemical Society

Total synthesis of .DELTA.8-(.DELTA.1(6)-tetrahydrocannabinol, a biologically active constituent of hashish (marijuana)

Total synthesis of .DELTA.8-(.DELTA.1(6)-tetrahydrocannabinol, a biologically active constituent of hashish (marijuana).pdf (259.9 KB)

Total synthesis of (.±.)-.DELTA.9-tetrahydrocannabinol and four of its isomers

This latter compound was then dehydrated
with p-toluenesulfonic acid to give a single
product, clearly an endocyclic olefin with an nmr spectrum
identical with that reportedI (3) the reference they talk of is the total synth of delta 8
*in joc above *
Hashish.’ Synthesis of ( &)-A1- and A6-3,4-cis-Cannabidiols and Their Isomerization by Acid Catalysis

procedure is:

A solution of 828 mg (2.5 mmoles)
of XXII and 50 mg of p-toluenesulfonic acid in 50 ml of benzene
was heated for 30 min under reflux. The cooled solution was
washed with dilute sodium bicarbonate, dried (Na2S04)a, nd evaporated
to give 770 mg (98%) of XXIII as a colorless oil.

Total synthesis of (.±.)-.DELTA.9-tetrahydrocannabinol and four of its isomers.pdf (1.1 MB)

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