[{"data":1,"prerenderedAt":20},["ShallowReactive",2],{"notifications-general-fr":3,"compound-S-HHCP-fr":4},"En raison des vacances d'été, le laboratoire fonctionnera selon un horaire modifié du 22 juillet au 9 août 2026. Les résultats d’analyse seront disponibles 7 à 10 jours après la réception de l’échantillon. Merci de votre compréhension.",{"name":5,"shortname":6,"synonyms":7,"cas":7,"molMass":8,"pubchemLink":7,"structure":9,"important":10,"synthetic":11,"compoundClass":12,"asociationImage":15,"summarySet":16,"compoundEffectSet":19},"9S-Hexahydrocannabiphorol","S-HHCP",null,344.5,"science\u002Fstructures\u002F9S-hhcp_AiVVfXY.png",true,false,{"id":13,"description":14},"2","Cannabinoids","",[17],{"summaryText":18,"language":7},"\u003Cp>\u003Cspan style=\"font-family: "Times New Roman";\">\u003C\u002Fspan>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">HHCP is a heptyl homolog of HHC. To be more specific, HHCP is made by adding two more carbons to its alkyl chain at the tail of the chemical structure. \u003C\u002Fspan>\u003Cspan style=\"font-family: "Times New Roman";\">It is believed that the increased length of the alkyl chain\u003C\u002Fspan>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">, similar to that of THCP, allows HHCP to have increased bonding to cannabinoid receptors such as CB1 in the brain.\u003C\u002Fspan>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px; color: rgb(51, 51, 51);\"> THCP has the impressive ability to bind to CB1 receptors in the brain\u003C\u002Fspan>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\"> \u003C\u002Fspan>\u003Ca href=\"https:\u002F\u002Fwww.ncbi.nlm.nih.gov\u002Fpmc\u002Farticles\u002FPMC6937300\u002F\" target=\"_blank\" rel=\"noopener\" style=\"font-family: Helvetica, sans-serif; font-size: 18px; background-color: rgb(255, 255, 255); color: rgb(0, 123, 255); transition: all 0.2s ease-in-out 0s;\">\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">33 times more than Delta-9 THC\u003C\u002Fspan>\u003C\u002Fa>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">.\u003C\u002Fspan>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\"> \u003C\u002Fspan>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px; color: rgb(51, 51, 51);\">According to users of THCP, the high is 10 times more potent than your average THC.\u003C\u002Fspan>\u003Cbr>\u003C\u002Fp>\u003Cp style=\"margin-bottom: 20px; font-size: 18px; font-family: Helvetica, sans-serif;\">\u003Cspan style=\"color: rgb(51, 51, 51); font-family: "Times New Roman"; font-size: 14px;\">Now the comparison of HHCP is more of an analogous situation with THCP. Both are hydrogenated versions of a THC derivative and, because of it, are believed to be better at binding creating a more potent effect. Anecdotally, it is believed that HHCP may even be more potent than THCP. There isn't a lot of information on the difference between R and S stereoisomer, but S is energetically less favored. However, if we apply what we know from stereoisomerism of HHC, R isomer might be psychoactive, while S isomer is not.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp style=\"margin-bottom: 20px; font-size: 18px; font-family: Helvetica, sans-serif;\">\u003Cspan style=\"color: rgb(51, 51, 51);\">\u003Cbr>\u003C\u002Fspan>\u003C\u002Fp>",[],1785925844961]