261 results on '"Citti, Cinzia"'
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2. A three-years survey of microbial contaminants in industrial hemp inflorescences from two Italian cultivation sites
3. An emerging trend in Novel Psychoactive Substances (NPSs): designer THC
4. Δ9-Tetrahydrocannabiphorol: Identification and quantification in recreational products
5. Analysis of phytocannabinoids in hemp seeds, sprouts and microgreens
6. One-phase extraction coupled with photochemical reaction allows the in-depth lipid characterization of hempseeds by untargeted lipidomics
7. Bidimensional heart-cut achiral-chiral liquid chromatography coupled to high-resolution mass spectrometry for the separation of the main chiral phytocannabinoids and enantiomerization studies of cannabichromene and cannabichromenic acid
8. Untargeted cannabinomics reveals the chemical differentiation of industrial hemp based on the cultivar and the geographical field location
9. Phytocannabinoids biosynthesis during early stages of development of young Cannabis sativa L. seedlings: Integrating biochemical and transcription data
10. Kratom: The analytical challenge of an emerging herbal drug
11. Enantioseparation of chiral phytocannabinoids in medicinal cannabis
12. Evaluation of the carotenoid and fat-soluble vitamin profile of industrial hemp inflorescence by liquid chromatography coupled to mass spectrometry and photodiode-array detection
13. Cis-Δ9-tetrahydrocannabinolic acid occurrence in Cannabis sativa L.
14. Kynurenine and kynurenic acid: Two human neuromodulators found in Cannabis sativa L.
15. HPLC-MS/MS method applied to an untargeted metabolomics approach for the diagnosis of “olive quick decline syndrome”
16. Targeted and untargeted characterization of underivatized policosanols in hemp inflorescence by liquid chromatography-high resolution mass spectrometry
17. The novel heptyl phorolic acid cannabinoids content in different Cannabis sativa L. accessions
18. nalysis of phytocannabinoids in hemp seeds, sprouts and microgreens
19. Recent applications of mass spectrometry for the characterization of cannabis and hemp phytocannabinoids: From targeted to untargeted analysis
20. HPLC-UV-HRMS analysis of cannabigerovarin and cannabigerobutol, the two impurities of cannabigerol extracted from hemp
21. Phytocannabinomics: Untargeted metabolomics as a tool for cannabis chemovar differentiation
22. Techno-economic study of a small scale gasifier applied to an indoor hemp farm: From energy savings to biochar effects on productivity
23. Improved identification of phytocannabinoids using a dedicated structure-based workflow
24. Is cannabidiol a scheduled controlled substance? Origin makes the difference
25. A new software-assisted analytical workflow based on high-resolution mass spectrometry for the systematic study of phenolic compounds in complex matrices
26. Pitfalls in the analysis of phytocannabinoids in cannabis inflorescence
27. New insights in hemp chemical composition: a comprehensive polar lipidome characterization by combining solid phase enrichment, high-resolution mass spectrometry, and cheminformatics
28. Analysis of impurities of cannabidiol from hemp. Isolation, characterization and synthesis of cannabidibutol, the novel cannabidiol butyl analog
29. Analytical Methodologies for Lipidomics in Hemp Plant
30. Untargeted rat brain metabolomics after oral administration of a single high dose of cannabidiol
31. Development of a simple and sensitive liquid chromatography triple quadrupole mass spectrometry (LC–MS/MS) method for the determination of cannabidiol (CBD), Δ9-tetrahydrocannabinol (THC) and its metabolites in rat whole blood after oral administration of a single high dose of CBD
32. Analysis of cannabinoids in commercial hemp seed oil and decarboxylation kinetics studies of cannabidiolic acid (CBDA)
33. Pharmaceutical and biomedical analysis of cannabinoids: A critical review
34. Identification of a new cannabidiol n-hexyl homolog in a medicinal cannabis variety with an antinociceptive activity in mice: cannabidihexol
35. Synthesis and pharmacological activity of the epimers of hexahydrocannabinol (HHC)
36. A novel phytocannabinoid isolated from Cannabis sativa L. with an in vivo cannabimimetic activity higher than Δ9-tetrahydrocannabinol: Δ9-Tetrahydrocannabiphorol
37. Analytical and preparative enantioseparation and main chiroptical properties of Iridium(III) bis(4,6-difluorophenylpyridinato)picolinato
38. Medicinal cannabis: Principal cannabinoids concentration and their stability evaluated by a high performance liquid chromatography coupled to diode array and quadrupole time of flight mass spectrometry method
39. “Heart-cut” bidimensional achiral-chiral liquid chromatography applied to the evaluation of stereoselective metabolism, in vivo biological activity and brain response to chiral drug candidates targeting the central nervous system
40. Impact of Chitosan-Based Foliar Application on the Phytochemical Content and the Antioxidant Activity in Hemp (Cannabis sativa L.) Inflorescences.
41. Enantioseparation of Chiral Phytocannabinoids in Medicinal Cannabis
42. Analysis of Phytocannabinoids in Hemp Seeds, Sprouts and Microgreens
43. Synthesis and pharmacological activity of the epimers of hexahydrocannabinol (HHC)
44. Design, stereoselective synthesis, configurational stability and biological activity of 7-chloro-9-(furan-3-yl)-2,3,3a,4-tetrahydro-1H-benzo[e]pyrrolo[2,1-c][1,2,4]thiadiazine 5,5-dioxide
45. Evaluation of the Carotenoid and Fat-Soluble Vitamin Profile of Industrial Hemp Inflorescence by Liquid Chromatography Coupled to Mass Spectrometry and Photodiode-Array Detection
46. Cis-Δ9-Tetrahydrocannabinolic Acid Occurrence in Cannabis Sativa L
47. Oxidative Stress and Multi-Organel Damage Induced by Two Novel Phytocannabinoids, CBDB and CBDP, in Breast Cancer Cells
48. Analysis of Sequence Variability and Transcriptional Profile of Cannabinoid synthase Genes in Cannabis sativa L. Chemotypes with a Focus on Cannabichromenic acid synthase
49. HPLC-MS/MS method applied to an untargeted metabolomics approach for the diagnosis of “olive quick decline syndrome”
50. Origin of Δ9-Tetrahydrocannabinol Impurity in Synthetic Cannabidiol
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