Manetto et al., 2024 - Google Patents

Cannabichromene (CBC) Shows Matrix-Dependent Thermal Configurational Stability

Manetto et al., 2024

Document ID
3338897875626888594
Author
Manetto S
Caprioglio D
Grassi G
Botta B
Gasparrini F
Mazzoccanti G
Appendino G
Publication year
Publication venue
Journal of Natural Products

External Links

Snippet

The optical purity of cannabichromene (CBC, 1a) is affected by the matrix in which it is generated by thermolysis from its native carboxylated form (cannabichromenic acid, CBCA, 1b). Thus, thermolysis at 130° C in planta caused a marked decrease of the enantiomeric …
Continue reading at pubs.acs.org (other versions)

Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02—Column chromatography
    • G01N30/62—Detectors specially adapted therefor
    • G01N30/72—Mass spectrometers
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/90—Plate chromatography, e.g. thin layer or paper chromatography
    • G01N30/94—Development
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02—Column chromatography
    • G01N30/88—Integrated analysis systems specially adapted therefor, not covered by a single one of the groups G01N30/04 - G01N30/86
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02—Column chromatography
    • G01N30/26—Conditioning of the fluid carrier; Flow patterns
    • G01N30/38—Flow patterns

Similar Documents

Publication Publication Date Title
Schafroth et al. Δ9-cis-Tetrahydrocannabinol: natural occurrence, chirality, and pharmacology
Linciano et al. Isolation of a high-affinity cannabinoid for the human CB1 receptor from a medicinal Cannabis sativa variety: Δ9-tetrahydrocannabutol, the butyl homologue of Δ9-tetrahydrocannabinol
Sarker et al. Natural product isolation: an overview
Sarker et al. An introduction to natural products isolation
Tu et al. Automated high-throughput system to fractionate plant natural products for drug discovery
Jiang et al. Eco-friendly deep eutectic solvents contribute to improving the separation of isoquinoline alkaloids in supercritical fluid chromatography
Guoruoluo et al. Isolation and characterization of sesquiterpenoids from Cassia buds and their antimicrobial activities
Wan et al. Isolation, structure elucidation, semi-synthesis, and structural modification of C19-diterpenoid alkaloids from Aconitum apetalum and their neuroprotective activities
Hu et al. (±)-Japonones A and B, two pairs of new enantiomers with anti-KSHV activities from Hypericum japonicum
Covington et al. Atropoisomerism in biflavones: the absolute configuration of (−)-agathisflavone via chiroptical spectroscopy
Du et al. Discovery of new muscarinic acetylcholine receptor antagonists from Scopolia tangutica
Fukuda et al. (±)-Tylopilusins, diphenolic metabolites from the fruiting bodies of Tylopilus eximius
Jiao et al. Three pairs of enantiomeric sesquiterpenoids from Syringa pinnatifolia
Huang et al. Fast analysis of alkaloids from different parts of Mahonia bealei (Fort.) Carr. studied for their anti‐Alzheimer's activity using supercritical fluid chromatography
Reinhardt et al. Compounds from Toddalia asiatica: immunosuppressant activity and absolute configurations
Li et al. Purification of spinosin from Ziziphi Spinosae Semen using macroporous resins followed by preparative high‐performance liquid chromatography
Xia et al. Simultaneous determination of brazilin and protosappanin B in Caesalpinia sappan by ionic-liquid dispersive liquid-phase microextraction method combined with HPLC
Williams et al. Antibiotic indole sesquiterpene alkaloid from Greenwayodendron suaveolens with a new natural product framework
Liu et al. Extraction and preparation of 5‐lipoxygenase and acetylcholinesterase inhibitors from Astragalus membranaceus stems and leaves
Du et al. Efficient determination of the enantiomeric purity and absolute configuration of flavanones by using (S)-3, 3′-dibromo-1, 1′-bi-2-naphthol as a chiral solvating agent
Manetto et al. Cannabichromene (CBC) Shows Matrix-Dependent Thermal Configurational Stability
Wang et al. Attenuated structural transformation of aconitine during sand frying process and antiarrhythmic effect of its converted products
Coelho et al. Milligram scale enantioresolution of promethazine and its main metabolites, determination of their absolute configuration and assessment of enantioselective effects on human SY-SY5Y cells
Xia et al. (+)/(−)-Phaeocaulin AD, four pairs of new enantiomeric germacrane-type sesquiterpenes from Curcuma phaeocaulis as natural nitric oxide inhibitors
Xiao et al. Six unusual meroterpenoids from the leaves of Psidium guajava L. and their PTP1B inhibitory activities