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    <responseDate>2026-10-13T23:35:28Z</responseDate>
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    <identifier>10.57760/sciencedb.nprd.00329</identifier>
    <datestamp>2026-07-23T13:23:49Z</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>2026-07-23</dc:date>
  <dc:title>Alkaloids and phenolic constituents from Buteae Monospermae semen-raw data</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.nprd.00329</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>In order to study the chemical composition of purple rivet, the ethyl acetate part of purple rivet was separated and purified by silica gel, ODS, MC Ⅰ, Sephadex LH_20 gel and semi preparative HPLC, and its structure was identified by modern spectral techniques such as 1 H NMR, 13 NMR and MS. Finally, 20 compounds were obtained, including 3R_ [(3, s_format_ &amp;beta; _ lactam), ethyl acetate] _ hydroxyindole (1), oleurol (2), 2 (3,4,5-dihydroxyphenyl) _1,3-dioxaldehyde-5-aldehyde (3), lanceolatin B (4), dihydroquercetin (5), and o Ⅴ alifolin(6) 、2_(2_methoxyphenyl)furo[2 ,3_h]chromen_ 4_one(7) 、pongapin(8) 、desmethoxy kanugin (9) 、2_(1 ,3_benzodioxol_5_yl)_3 ,6_dimethoxy_4H_1_benzopyran_4_one (10) 、 (2s)_3 ,4 , _methylenedioxy_6 Nie, 6 Nie, dimethylchromeno_ [2 Nie, 3 Nie: 7,8] _fla V anone (11), 6, 6, d_dimethylpyrano [2, 3,: 7,8] fla_ V one(12) 、3_hydroxyisolanchoearpin(13) 、_(4_hydroxyphenyl)_3_methoxy_4H_chromen_4_one (14) 、 Dye lignin (15), dye lignin 7_0_ &amp;beta; - d_furanosyl_ (1 &amp;rarr; 6) _0_ &amp;beta; - d_glucopyranoside (16), _ (4_ hydroxy_3 methoxyphenyl) _ 5_ ethoxydecan_3 _one (17), anti hydroxycinnamic acid (18), ethyl paraben (19), uridine (20). Among them, compounds 1 and 20 are alkaloids, compounds 2-15, 17-19 are phenolic acids, and compound 16 is a phenolic glycoside. Compounds 1~3 and 13~20 were isolated from purple rivet for the first time. The MTS method was used to evaluate the cell proliferation activity of compound 1 at concentrations greater than 25 0 &amp;mu; mol/L can promote the proliferation of RAW 264.7 macrophages.&amp;nbsp;</dc:description>
  <dc:subject>alkaloids; phenolic constituents; Butea monospermae</dc:subject>
  <dc:creator>Hongfang Li</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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