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・ Dihydroisocodeine
・ Dihydroisocoumarin
・ Dihydroisoindole
・ Dihydrokaempferide
・ Dihydrokaempferol 4-reductase
・ Dihydrokanakugiol
・ Dihydrokavain
・ Dihydrolipoamide
・ Dihydrolipoamide dehydrogenase
・ Dihydrolipoic acid
・ Dihydrolipoyl transacetylase
・ Dihydrolipoyllysine-residue (2-methylpropanoyl)transferase
・ Dihydrolipoyllysine-residue succinyltransferase
・ Dihydromethysticin
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Dihydromorphine
・ Dihydroneopterin aldolase
・ Dihydronicotinamide adenine dinucleotide-coenzyme Q reductase
・ Dihydroorotase
・ Dihydroorotate dehydrogenase
・ Dihydroorotate dehydrogenase (fumarate)
・ Dihydroorotate dehydrogenase (quinone)
・ Dihydrophloroglucinol
・ Dihydroprogesterone
・ Dihydropteroate
・ Dihydropteroate synthase
・ Dihydropteroate synthase inhibitor
・ Dihydropyran
・ Dihydropyridine
・ Dihydropyrimidinase


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Dihydromorphine : ウィキペディア英語版
Dihydromorphine

Dihydromorphine (Paramorfan, Paramorphan) is a semi-synthetic opioid structurally related to and derived from morphine. The 7,8-double bond in morphine is reduced to a single bond to get dihydromorphine.〔Rama Rao Nadendla. Principles Of Organic Medicinal Chemistry pp. 215〕 Dihydromorphine is a moderately strong analgesic and is used clinically in the treatment of pain and also is an active metabolite of the analgesic opioid drug dihydrocodeine.〔(DrugBank: Dihydromorphine (DB01565) )〕〔(Dihydromorphine - PubChem )〕 Dihydromorphine occurs in trace quantities in assays of opium on occasion, as does dihydrocodeine, dihydrothebaine, tetrahydrothebaine, etc. The process for manufacturing dihydromorphine from morphine for pharmaceutical use was developed in Germany in the late 19th Century, with the synthesis being published in 1900 and the drug introduced clinically as Paramorfan shortly thereafter. A high-yield synthesis from tetrahydrothebaine was later developed〔http://www.scribd.com/doc/55812020/dihydromorphine〕
==Uses==


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