<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>68(Pt 4)</volume><submitter>Xie L</submitter><pubmed_abstract>The title compound, C(51)H(78)N(4)O(12), is a derivative of rapamycin, a triene macrolide anti-biotic mol-ecule isolated from Streptomyces hygroscopicus. The macrocyclic ring structure has 15 chiral centres, with one of the substituent hy-droxy groups giving an intra-molecular hydrogen bond to a ketone O-atom acceptor. The mol-ecules also form inter-molecular hy-droxy-ketone O-H⋯O hydrogen-bonding associations, giving one-dimensional chains extending along (010). The crystal has 108 Å(3) solvent-accessible voids.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>o1206-7</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3344143</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>41-Azido-41-de-oxy-rapamycin.</pubmed_title><pmcid>PMC3344143</pmcid><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Zuo J</pubmed_authors><pubmed_authors>Xie L</pubmed_authors><pubmed_authors>Yu H</pubmed_authors><pubmed_authors>Cheng Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>41-Azido-41-de-oxy-rapamycin.</name><description>The title compound, C(51)H(78)N(4)O(12), is a derivative of rapamycin, a triene macrolide anti-biotic mol-ecule isolated from Streptomyces hygroscopicus. The macrocyclic ring structure has 15 chiral centres, with one of the substituent hy-droxy groups giving an intra-molecular hydrogen bond to a ketone O-atom acceptor. The mol-ecules also form inter-molecular hy-droxy-ketone O-H⋯O hydrogen-bonding associations, giving one-dimensional chains extending along (010). The crystal has 108 Å(3) solvent-accessible voids.</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Apr</publication><modification>2025-04-04T09:12:34.617Z</modification><creation>2019-03-27T00:53:04Z</creation></dates><accession>S-EPMC3344143</accession><cross_references><pubmed>22606146</pubmed><doi>10.1107/S1600536812012548</doi></cross_references></HashMap>