[{"data":1,"prerenderedAt":44},["ShallowReactive",2],{"notifications-general-hr":3,"compound-CBC-hr":4},"Zbog ljetnih praznika laboratorij će raditi prema izmijenjenom rasporedu od 22. srpnja do 9. kolovoza 2026. Rezultati analiza bit će dostupni 7 do 10 dana nakon primitka uzorka. Hvala na razumijevanju.",{"name":5,"shortname":6,"synonyms":7,"cas":8,"molMass":9,"pubchemLink":10,"structure":11,"important":12,"synthetic":13,"compoundClass":14,"asociationImage":17,"summarySet":18,"compoundEffectSet":22},"Cannabichromene","CBC","cannabichrome, pentylcannabichromene or cannabinochromene","20675-51-8",314.469,"https:\u002F\u002Fpubchem.ncbi.nlm.nih.gov\u002Fcompound\u002Fcannabichromene","science\u002Fstructures\u002FRS-Cannabichromene.png",true,false,{"id":15,"description":16},"2","Cannabinoids","science\u002Fimages\u002FCBC.png",[19],{"summaryText":20,"language":21},"\u003Cp class=\"MsoNoSpacing\">\u003Cspan style=\"background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;\">CBC is considered one of\r\nthe “big six” cannabinoids prominent in medical research. \u003C\u002Fspan>\u003Cspan style=\"text-align: justify;\">For CBC,\r\nit converts from CBGA into cannabichrome carboxylic acid (CBCA), and then\r\nfinally to CBC after exposure to heat or ultraviolet light. \u003C\u002Fspan>\u003Cspan style=\"text-align: justify;\">CBC is non-intoxicating, so it\r\ndoesn’t produce a euphoric high like THC. The reason it is non-intoxicating is\r\nbecause it binds poorly to CB1 cannabinoid receptors in the brain. But CBC does\r\nbind with other receptors in the body, such as the vanilloid receptor 1 (TRPV1)\r\nand transient receptor potential ankyrin 1 (TRPA1), both of which are linked to\r\npain perception. When CBC activates these receptors, increased levels of the\r\nbody’s natural endocannabinoids like anandamide are released.\u003C\u002Fspan>\u003C\u002Fp>",null,[23,28,32,36,40],{"effectName":24,"LiteratureReferences":27},{"effectName":25,"effectType":26},"Anti-inflamation - Colitis","A_0","\u003Cp>\u003Ca href=\"http:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fbph.12120\u002Ffull\">The cannabinoid TRPA1 agonist cannabichromene inhibits nitric oxide production in macrophages and ameliorates murine colitis\u003C\u002Fa>\u003Cbr>\u003C\u002Fp>",{"effectName":29,"LiteratureReferences":31},{"effectName":30,"effectType":26},"Antidepresant","\u003Cp>\u003Ca href=\"https:\u002F\u002Fwww.ncbi.nlm.nih.gov\u002Fpubmed\u002F20332000\">Antidepressant-like effect of delta9-tetrahydrocannabinol and other cannabinoids isolated from Cannabis sativa L\u003C\u002Fa>\u003Cbr>\u003C\u002Fp>",{"effectName":33,"LiteratureReferences":35},{"effectName":34,"effectType":26},"Anti inflamation - Edema","\u003Cp>\u003Ca href=\"http:\u002F\u002Fdruglibrary.org\u002Fcrl\u002Fpain\u002FTurner%20&%20Elsohly%2081Cannabichromene_%20JClinPharmacol.pdf\">Biological Activity of Cannabichromene, its Homologs and Isomers\u003C\u002Fa>\u003C\u002Fp>\u003Cp>\u003Ca href=\"http:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002F0024320580906311\">Anti-inflammatory properties of cannabichromene\u003C\u002Fa>\u003C\u002Fp>\u003Cp>\u003Ca href=\"http:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002F0024320580906311\">Anti-inflammatory properties of cannabichromene\u003C\u002Fa>\u003Cbr>\u003Cbr>\u003Cbr>\u003C\u002Fp>",{"effectName":37,"LiteratureReferences":39},{"effectName":38,"effectType":26},"Anti inflamation - Inflammation-induced hypermotility","\u003Cp>\u003Ca href=\"http:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002F0024320580906311\">Inhibitory effect of cannabichromene, a non-psychotropic cannabinoid extracted from Cannabis sativa, on inflammation-induced hypermotility in mice\u003C\u002Fa>\u003Cbr>\u003C\u002Fp>",{"effectName":41,"LiteratureReferences":43},{"effectName":42,"effectType":26},"Antimicrobial","\u003Cp>\u003Ca href=\"http:\u002F\u002Fdruglibrary.org\u002Fcrl\u002Fpain\u002FTurner%20&%20Elsohly%2081Cannabichromene_%20JClinPharmacol.pdf\">Biological Activity of Cannabichromene, its Homologs and Isomers\u003C\u002Fa>\u003C\u002Fp>\u003Cp>\u003Ca href=\"http:\u002F\u002Fdruglibrary.org\u002Fcrl\u002Fpain\u002FTurner%20&%20Elsohly%2081Cannabichromene_%20JClinPharmacol.pdf\">Biological Activity of Cannabichromene, its Homologs and Isomers\u003C\u002Fa>\u003C\u002Fp>\u003Cp>\u003Ca href=\"http:\u002F\u002Fpubs.acs.org\u002Fdoi\u002Fpdf\u002F10.1021\u002Fnp8002673\">Antibacterial Cannabinoids from Cannabis satiWa: A Structure-Activity Study\u003C\u002Fa>\u003Cbr>\u003Cbr>\u003Cbr>\u003C\u002Fp>",1785925837251]