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    <identifier>10.57760/sciencedb.nprd.000e8</identifier>
    <datestamp>2026-09-29T09:49:12Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2026-09-29</dc:date>
  <dc:title>Chemical constituents from the roots of Urtica fissa and their 5&amp;alpha;-reductase inhibitory activities-raw data</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.nprd.000e8</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>To investigate the 5&amp;alpha;-reductase inhibitory constituents from the roots of Urtica fissa E. Pritz, the chemical constituents in the ethanol extract from the roots of U. fissa were systematically separated and identified in this study by using silica gel column chromatography, preparative HPLC, NMR and other modern chromatographic and spectral techniques. Subsequently, the obtained compounds were subjected to molecular docking and further 5&amp;alpha;‑reductase inhibitory assays. 42 compounds were obtained, which were identified as 2-(5-(hydroxymethyl)furan-2-yl)-5-(2,3,4-trihydroxybutyl)-oxazole (1), cycloolivil (2), olivil-4,4&amp;prime;-di-O-&amp;beta;-D-glucopyranoside (3), (7R,7'R,8S,8'S)-neoolivil-4-O-&amp;beta;-D-glucopyranoside (4), pinoresinol-4-O-&amp;beta;-D-glucopyranoside (5), tangutorid E (6), tangutorid F (7), 2-(furan-2-yl)-5-(2,3,4-trihydroxybutyl)-1,4-diazine (8), perlolyrine (9), erythro-glehlinoside C (10), threo-glehlinoside C (11), 3,5-dihydroxyphenethyl alcohol-3-O-&amp;beta;-D-glucopyranoside (12), p-hydroxyphenethyl alcohol-8-O-&amp;beta;-D-glucopyranoside (13), 4-hydroxy-3-methoxyphenthyl alcohol-8-O-&amp;beta;-D-glucopyranoside (14), 3,4'-dihydroxy-3'-methoxypropiophenone-3-O-&amp;beta;-D-glucopyranoside (15), 3,4&amp;prime;-dihydroxypropiophenone-3-O-&amp;beta;-D-glucopyranoside (16), 3-(4-hydroxyphenyl)-1,2-propandiol (17), ficuscarpanoside A (18), chavicol-4-O-&amp;beta;-D-glucopyranoside (19), citrusin C (20), fraxin-7-O-&amp;beta;-D-glucopyranoside (21), dihydrophaseic acid-3&amp;prime;-O-&amp;beta;-D-glucopyranoside (22), isomaltol-3-O-&amp;alpha;-D-mannopyranoside (23), hypofuran B (24), aneglycoside D (25), (2E,4E)-8-hydroxy-2,7-dimethyl-2,4-decadiene-1,10-dioic acid-8-O-&amp;beta;-D-glucopyranoside (26), 2&amp;prime;-O-methyladenosine (27), N6-threonylcarbamoyladenosine (28), urticene (29), urticol (30), cycloolivil-6-O-&amp;beta;-D-glucopyranoside (31), olivil-4&amp;prime;-O-&amp;beta;-D-glucopyranoside (32), isolariciresinol (33), isolariciresinol-4'-O-&amp;beta;-D-glucopyranoside (34), 2,3,4,9-tetrahydro-1H-pyrido-[3,4-b]indole-3-carboxylic acid (35), vanillic acid (36), ferulic acid (37), p-hydroxybenzaldehyde (38), scopolin (39), (9R,7E)-9-hydroxy-5,7-mengatigmadien-4-one-9-O-&amp;beta;-D-glucopyranoside (40), 5-hydroxymethyl-2-furfural (41), adenosine (42). Compounds 1 was a new compound. Compounds 2-28 were isolated from genus Urtica for the first time. Compounds 29 and 33 exhibited good inhibitory activity against 5&amp;alpha;-reductase.</dc:description>
  <dc:subject>roots of Urtica fissa; chemical constituents; structure identification; molecular docking; 5α-reductase</dc:subject>
  <dc:creator>Zhou Chenglin</dc:creator>
  <dc:creator>Shen Xia</dc:creator>
  <dc:creator>Dong Yichen</dc:creator>
  <dc:creator>Li Xiaobo</dc:creator>
  <dc:creator>Wang Mengyue</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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