File:Fig5 Cicaloni Separ22 9-4.png

Fig. 5 Analysis of the top 25 correlated compounds based on Pearson correlation coefficient for δ-9-cis-tetrahydrocannabinol, α-pinene, β-caryophyllene, and β-myrcene. The numbers in the figure represent: 1: (1S,2S,4R)-1,3,3-trimethylbicyclo[2.2.1]hept-2-yl (6ar,10ar)-1-hydroxy-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromene-2-carboxylate; 2: 4-(6-hydroxy-1,2,3,9a-tetrahydro-3ah-spiro[cyclopenta[b]chromene-9,1′-cyclopentan]-3a-yl)-1,3-benzenediol; 3:(2R,3R,4R,5R)-2-{(1R)-5-[(5R,7R)-1,6-dioxaspiro[4.5]dec-7-yl]-1-hydroxypentyl}-5-(hydroxymethyl)-3,4-pyrrolidinediol; 4: (5Z,8Z,11Z,14Z)-N-(2-furylmethyl)-5,8,11,14-icosatetraenamide; 5: 3,19-diacetoxy-5,14-dihydroxycard-20(22)-enolide; 6: 5,7,4′-trihydroxy-3,6-dimethoxy-3′,5′-diprenylflavone; 7: 1,5-anhydro-2,4,6-tris-O-(3,4,5-trihydroxybenzoyl)-D-glucitol; 8: methyl (1R,2R,3S,3ar,8bs)-2,3,3a,8b-tetrahydro-1,6,8b-trihydroxy-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-1H-cyclopenta[b]benzofuran-2-carboxylate.

Cicaloni, V.; Salvini, L.; Vitalini, S.; Garzoli, S. (2022). "Chemical profiling and characterization of different cultivars of Cannabis sativa L. inflorescences by SPME-GC-MS and UPLC-MS". Separations 9 (4): 90. doi:10.3390/separations9040090. 

2022

Cicaloni, V.; Salvini, L.; Vitalini, S.; Garzoli, S.

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