<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>102(24)</volume><submitter>Boettcher C</submitter><pubmed_abstract>Recently, our laboratory demonstrated that human neuroblastoma cells (SH-SY5Y) are capable of synthesizing morphine, the major active metabolite of opium poppy. Now our experiments are further substantiated by extending the biochemical studies to the entire morphine pathway in this human cell line. L-[1,2,3-13C3]- and [ring-2',5',6'-2H3]dopa showed high isotopic enrichment and incorporation in both the isoquinoline and the benzyl moiety of the endogenous morphine. [2,2-2H2]Dopamine, however, was exclusively incorporated only into the isoquinoline moiety. Neither the trioxygenated (R,S)-[1,3-13C2]norcoclaurine, the precursor of morphine in the poppy plant, nor (R)-[1,3,4-2H3]norlaudanosoline showed incorporation into endogenous morphine. However, (S)-[1,3,4-2H3]norlaudanosoline furnished a </pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pagination>8495-500</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC1150847</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>How human neuroblastoma cells make morphine.</pubmed_title><pmcid>PMC1150847</pmcid><pubmed_authors>Fellermeier M</pubmed_authors><pubmed_authors>Drager B</pubmed_authors><pubmed_authors>Zenk MH</pubmed_authors><pubmed_authors>Boettcher C</pubmed_authors></additional><is_claimable>false</is_claimable><name>How human neuroblastoma cells make morphine.</name><description>Recently, our laboratory demonstrated that human neuroblastoma cells (SH-SY5Y) are capable of synthesizing morphine, the major active metabolite of opium poppy. Now our experiments are further substantiated by extending the biochemical studies to the entire morphine pathway in this human cell line. L-[1,2,3-13C3]- and [ring-2',5',6'-2H3]dopa showed high isotopic enrichment and incorporation in both the isoquinoline and the benzyl moiety of the endogenous morphine. [2,2-2H2]Dopamine, however, was exclusively incorporated only into the isoquinoline moiety. Neither the trioxygenated (R,S)-[1,3-13C2]norcoclaurine, the precursor of morphine in the poppy plant, nor (R)-[1,3,4-2H3]norlaudanosoline showed incorporation into endogenous morphine. However, (S)-[1,3,4-2H3]norlaudanosoline furnished a </description><dates><release>2005-01-01T00:00:00Z</release><publication>2005 Jun</publication><modification>2025-04-21T21:22:14.133Z</modification><creation>2019-03-27T01:09:00Z</creation></dates><accession>S-EPMC1150847</accession><cross_references><pubmed>15937106</pubmed><doi>10.1073/pnas.0503244102</doi></cross_references></HashMap>