ABFC Cape St. George, named after Cape St. George in the Jervis Bay Territory, is a Cape-class patrol boat of the marine unit of the Australian Border Force.
"}{"type":"standard","title":"The Bodysnatchers (novel)","displaytitle":"The Bodysnatchers (novel)","namespace":{"id":0,"text":""},"wikibase_item":"Q7719013","titles":{"canonical":"The_Bodysnatchers_(novel)","normalized":"The Bodysnatchers (novel)","display":"The Bodysnatchers (novel)"},"pageid":5413317,"thumbnail":{"source":"https://upload.wikimedia.org/wikipedia/en/2/2b/Bodysnatchers.jpg","width":251,"height":399},"originalimage":{"source":"https://upload.wikimedia.org/wikipedia/en/2/2b/Bodysnatchers.jpg","width":251,"height":399},"lang":"en","dir":"ltr","revision":"1290229504","tid":"5657114c-3005-11f0-a6f7-23c2e8602021","timestamp":"2025-05-13T14:19:53Z","description":"1997 novel by Mark Morris","description_source":"local","content_urls":{"desktop":{"page":"https://en.wikipedia.org/wiki/The_Bodysnatchers_(novel)","revisions":"https://en.wikipedia.org/wiki/The_Bodysnatchers_(novel)?action=history","edit":"https://en.wikipedia.org/wiki/The_Bodysnatchers_(novel)?action=edit","talk":"https://en.wikipedia.org/wiki/Talk:The_Bodysnatchers_(novel)"},"mobile":{"page":"https://en.m.wikipedia.org/wiki/The_Bodysnatchers_(novel)","revisions":"https://en.m.wikipedia.org/wiki/Special:History/The_Bodysnatchers_(novel)","edit":"https://en.m.wikipedia.org/wiki/The_Bodysnatchers_(novel)?action=edit","talk":"https://en.m.wikipedia.org/wiki/Talk:The_Bodysnatchers_(novel)"}},"extract":"The Bodysnatchers is an original novel written by Mark Morris and based on the long-running British science fiction television series Doctor Who.","extract_html":"
The Bodysnatchers is an original novel written by Mark Morris and based on the long-running British science fiction television series Doctor Who.
"}{"type":"standard","title":"CBD-DMH","displaytitle":"CBD-DMH","namespace":{"id":0,"text":""},"wikibase_item":"Q28654981","titles":{"canonical":"CBD-DMH","normalized":"CBD-DMH","display":"CBD-DMH"},"pageid":53052196,"thumbnail":{"source":"https://upload.wikimedia.org/wikipedia/commons/thumb/0/00/CBD-DMH_structure.png/330px-CBD-DMH_structure.png","width":320,"height":166},"originalimage":{"source":"https://upload.wikimedia.org/wikipedia/commons/0/00/CBD-DMH_structure.png","width":652,"height":338},"lang":"en","dir":"ltr","revision":"1264606535","tid":"a007a39f-c07f-11ef-acd6-8249b9f7d8b9","timestamp":"2024-12-22T16:13:05Z","description":"Chemical compound with cannabinoid effects","description_source":"local","content_urls":{"desktop":{"page":"https://en.wikipedia.org/wiki/CBD-DMH","revisions":"https://en.wikipedia.org/wiki/CBD-DMH?action=history","edit":"https://en.wikipedia.org/wiki/CBD-DMH?action=edit","talk":"https://en.wikipedia.org/wiki/Talk:CBD-DMH"},"mobile":{"page":"https://en.m.wikipedia.org/wiki/CBD-DMH","revisions":"https://en.m.wikipedia.org/wiki/Special:History/CBD-DMH","edit":"https://en.m.wikipedia.org/wiki/CBD-DMH?action=edit","talk":"https://en.m.wikipedia.org/wiki/Talk:CBD-DMH"}},"extract":"Cannabidiol-dimethylheptyl (CBD-DMH or DMH-CBD) is a synthetic homologue of cannabidiol where the pentyl chain has been replaced by a dimethylheptyl chain. Several isomers of this compound are known. The most commonly used isomer in research is (−)-CBD-DMH, which has the same stereochemistry as natural cannabidiol, and a 1,1-dimethylheptyl side chain. This compound is not psychoactive and acts primarily as an anandamide reuptake inhibitor, but is more potent than cannabidiol as an anticonvulsant and has around the same potency as an antiinflammatory. Unexpectedly the “unnatural” enantiomer (+)-CBD-DMH, which has reversed stereochemistry from cannabidiol, was found to be a directly acting cannabinoid receptor agonist with a Ki of 17.4nM at CB1 and 211nM at CB2, and produces typical cannabinoid effects in animal studies, as does its 7-OH derivative.","extract_html":"
Cannabidiol-dimethylheptyl (CBD-DMH or DMH-CBD) is a synthetic homologue of cannabidiol where the pentyl chain has been replaced by a dimethylheptyl chain. Several isomers of this compound are known. The most commonly used isomer in research is (−)-CBD-DMH, which has the same stereochemistry as natural cannabidiol, and a 1,1-dimethylheptyl side chain. This compound is not psychoactive and acts primarily as an anandamide reuptake inhibitor, but is more potent than cannabidiol as an anticonvulsant and has around the same potency as an antiinflammatory. Unexpectedly the “unnatural” enantiomer (+)-CBD-DMH, which has reversed stereochemistry from cannabidiol, was found to be a directly acting cannabinoid receptor agonist with a Ki of 17.4nM at CB1 and 211nM at CB2, and produces typical cannabinoid effects in animal studies, as does its 7-OH derivative.
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