The Plant Cell Culture Library

Bauhinia yunnanensis
Cell Line ID BY-14409 C1
Media Type B50
Availability Medium
Order Fabales
Family Fabaceae
Genus Bauhinia
Antibacterial Genus Level ➡ 14 citations
Antifungal Genus Level ➡ 105 citations
Trypanocidal Genus Level
Anthelmintic Genus Level ➡ 3 citations
Anticancer Genus Level ➡ 70 citations
Culture Start Material Seed
Plant Supplier Comm/Chiltern Seeds
Antibacterial Citations
  1. Cooke, R.G. et al., Aust. J. Chem., 1971, 24, 1257- 1265 (4'-Hydroxy-7-methoxyflavan) [https://doi.org/10.1071/CH9711257]
  2. Takasugi, M. et al., Chem. Lett., 1980, 9, 1459- 1460 (Broussin) [https://doi.org/10.1246/cl.1980.1459]
  3. Coxon, D.T. et al., Phytochemistry, 1980, 19, 889- 891 (isol, synth) [https://doi.org/10.1016/0031-9422(80)85132-6]
  4. Takasugi, M. et al., Chem. Lett., 1984, 13, 689- 692 (De-O-methylbroussin) [https://doi.org/10.1246/cl.1984.689]
  5. Ghosal, S. et al., Phytochemistry, 1986, 25, 1097- 1102 (Broussin, activity) [https://doi.org/10.1016/S0031-9422(00)81561-7]
  6. Achenbach, H. et al., Phytochemistry, 1988, 27, 1835- 1841 (Bauhinia manca constits,activity) [https://doi.org/10.1016/0031-9422(88)80455-2]
  7. Min, B.S. et al., Chem. Pharm. Bull., 2001, 49, 1217- 1219 (4-Hydroxy-7-methoxyflavan,activity) [https://doi.org/10.1248/cpb.49.1217]
  8. Li, Y. et al., J. Nat. Prod., 2001, 64, 214- 216 (7-Me ether, synth) [https://doi.org/10.1021/np0001171]
  9. Pan, W.-B. et al., J. Nat. Prod., 2003, 66, 161- 168 (Tupistra chinensis constit) [https://doi.org/10.1021/np0203382]
  10. Xue, J. et al., Synth. Commun., 2003, 33, 3527- 3536 (synth, ir, pmr, ms)
  11. Liu, J. et al., Z. Naturforsch., B, 2008, 63, 1407- 1410 (Dracaena cambodiana constit,activity)
  12. Awale, S. et al., J. Nat. Prod., 2009, 72, 1631- 1636 (Soymida febrifuga constits, activity) [https://doi.org/10.1021/np9003323]
  13. Lee, D.Y. et al., Bioorg. Med. Chem. Lett., 2010, 20, 3764- 3767 (Broussonetia kazinoki constit) [https://doi.org/10.1016/j.bmcl.2010.04.064]
  14. Fu, K.-L. et al., Helv. Chim. Acta, 2013, 96, 338- 344 (Narcissus tazetta constits, activity)
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Antifungal Citations
  1. Cooke, R.G. et al., Aust. J. Chem., 1971, 24, 1257- 1265 (4'-Hydroxy-7-methoxyflavan) [https://doi.org/10.1071/CH9711257]
  2. Takasugi, M. et al., Chem. Lett., 1980, 9, 1459- 1460 (Broussin) [https://doi.org/10.1246/cl.1980.1459]
  3. Coxon, D.T. et al., Phytochemistry, 1980, 19, 889- 891 (isol, synth) [https://doi.org/10.1016/0031-9422(80)85132-6]
  4. Takasugi, M. et al., Chem. Lett., 1984, 13, 689- 692 (De-O-methylbroussin) [https://doi.org/10.1246/cl.1984.689]
  5. Ghosal, S. et al., Phytochemistry, 1986, 25, 1097- 1102 (Broussin, activity) [https://doi.org/10.1016/S0031-9422(00)81561-7]
  6. Achenbach, H. et al., Phytochemistry, 1988, 27, 1835- 1841 (Bauhinia manca constits,activity) [https://doi.org/10.1016/0031-9422(88)80455-2]
  7. Min, B.S. et al., Chem. Pharm. Bull., 2001, 49, 1217- 1219 (4-Hydroxy-7-methoxyflavan,activity) [https://doi.org/10.1248/cpb.49.1217]
  8. Li, Y. et al., J. Nat. Prod., 2001, 64, 214- 216 (7-Me ether, synth) [https://doi.org/10.1021/np0001171]
  9. Pan, W.-B. et al., J. Nat. Prod., 2003, 66, 161- 168 (Tupistra chinensis constit) [https://doi.org/10.1021/np0203382]
  10. Xue, J. et al., Synth. Commun., 2003, 33, 3527- 3536 (synth, ir, pmr, ms)
  11. Liu, J. et al., Z. Naturforsch., B, 2008, 63, 1407- 1410 (Dracaena cambodiana constit,activity)
  12. Awale, S. et al., J. Nat. Prod., 2009, 72, 1631- 1636 (Soymida febrifuga constits, activity) [https://doi.org/10.1021/np9003323]
  13. Lee, D.Y. et al., Bioorg. Med. Chem. Lett., 2010, 20, 3764- 3767 (Broussonetia kazinoki constit) [https://doi.org/10.1016/j.bmcl.2010.04.064]
  14. Fu, K.-L. et al., Helv. Chim. Acta, 2013, 96, 338- 344 (Narcissus tazetta constits, activity)
  15. Reidel, V.L. et al., Annalen, 1942, 550, 146- 151 (2',3,4,4'-tetra-Me ether, synth)
  16. Rimpler, H. et al., Arch. Pharm. (Weinheim, Ger.), 1965, 298, 838- 847 (2'-glucoside, struct,synth)
  17. Wiermann, R., Planta, 1970, 95, 133- 145 (2,3,4,4',6'-Pentahydroxychalcone,flavonol/anthocyanin biosynth precursor)
  18. Fa-Ch'ing Ch'en, et al.T'ai-wan K'o Hsueh, 1972, 26, 46 (synth)
  19. US Pat., 1972, 3 686 319 (2',3,4,4',6'-Pentahydroxychalcone, synth)
  20. Fraser, A.W. et al., Phytochemistry, 1974, 13, 1561- 1564 (Merrillia caloxylon constits, struct) [https://doi.org/10.1016/0031-9422(74)80328-6]
  21. Chibber, S.S. et al., Curr. Sci., 1982, 51, 933- 934 (Tephrone, struct, synth)
  22. Imperato, F., Experientia, 1982, 38, 67- 68 (3-Me ether 2'-glucoside, struct)
  23. US Pat., 1986, 4 605 674, ( Hoffmann-La Roche) (2',4,4'-tri-Me ether, synth, viral replication inhibitor)
  24. Fukunaga, T. et al., Chem. Pharm. Bull., 1987, 35, 3292- 3297 (2',3,4'-tri-Me ether 4-glucoside, struct) [https://doi.org/10.1248/cpb.35.3292]
  25. Greenaway, W. et al., Phytochemistry, 1991, 30, 3005- 3009 (Populus sieboldii constits, gc-ms) [https://doi.org/10.1016/S0031-9422(00)98240-2]
  26. Tanaka, T. et al., Phytochemistry, 1992, 31, 993- 998 (2',3,4,4'-tetra-Me ether, struct, synth) [https://doi.org/10.1016/0031-9422(92)80055-J]
  27. Sogawa, S. et al., J. Med. Chem., 1993, 36, 3904- 3909 (2',3,4,4',6'-Pentahydroxychalcone,synth, 5-lipoxygenase inhibitor) [https://doi.org/10.1021/jm00076a019]
  28. Cechinel-Filho, V. et al., Eur. J. Med. Chem., 1996, 31, 833- 840 (3,4-methylene 2',4'-di-Me ether, synth, antiinflammatory activity) [https://doi.org/10.1016/0223-5234(96)83978-X]
  29. Martin, T. et al., Pharm. Biol., 1999, 37, 28- 31 (Hesperidin methylchalcone, struct)
  30. Phrutivorapongkul, A. et al., Chem. Pharm. Bull., 2003, 51, 187- 190 (Millettia leucantha constits, struct, cytotoxicity) [https://doi.org/10.1248/cpb.51.187]
  31. Chu, H.-W. et al., Tetrahedron, 2004, 60, 2647- 2655 (2',3,4,4'-tetra-Me ether, synth) [https://doi.org/10.1016/j.tet.2004.01.023]
  32. Maheswara, M. et al., Asian J. Chem., 2005, 18, 419- 422 (Tephrone, struct, antifungal activity)
  33. Zhao, L.-M. et al., Bioorg. Med. Chem. Lett., 2005, 15, 5027- 5029 (2',3,4,4',6'-Pentahydroxychalcone, 3-Me ether, 3,4-di-Me ether, synth, platelet aggregation inhibitor) [https://doi.org/10.1016/j.bmcl.2005.08.039]
  34. Boeck, P. et al., Bioorg. Med. Chem., 2006, 14, 1538- 1545 (3,4-methylene 2',4'-di-Me ether,synth, antileishmanial activity) [https://doi.org/10.1016/j.bmc.2005.10.005]
  35. Jun, N. et al., Biosci., Biotechnol., Biochem., 2006, 70, 193- 202 (2',3,4,4',6'-Pentahydroxychalcone, 2',4'-di-Me ether, synth, free-radical scavenging activity)
  36. Chiaradia, L.D. et al., Bioorg. Med. Chem., 2008, 16, 658- 667 (3,4-methylene 2',4',6'-tri-Me ether, synth) [https://doi.org/10.1016/j.bmc.2007.10.039]
  37. Boumendjel, A. et al., J. Med. Chem., 2008, 51, 2307- 2310 (3,4-methylene 2',4'-di-Me ether, synth) [https://doi.org/10.1021/jm0708331]
  38. Aponte, J.C. et al., J. Med. Chem., 2008, 51, 6230- 6234 (3,4-methylene 2'-Me ether, 3,4-methylene 2',4'-di-Me ether, synth, antitrypanosomal activity) [https://doi.org/10.1021/jm800812k]
  39. US Pat., 2008, 2008 260 869, ( Mary Kay Inc) (Hesperidin methylchalcone, treatment of skin conditions)
  40. Detsi, A. et al., Bioorg. Med. Chem., 2009, 17, 8073- 8085 (2',3,4,4',6'-Pentahydroxychalcone, 2',3,4,4'-tetra-Me ether, synth, antioxidative activity) [https://doi.org/10.1016/j.bmc.2009.10.002]
  41. Semwal, D.K. et al., J. Asian Nat. Prod. Res., 2009, 11, 1045- 1055 (2',3,4-tri-Me ether 4'-glucoside, struct, antimicrobial activity)
  42. Srinivasan, B. et al., J. Med. Chem., 2009, 52, 7228- 7235 (2',4,4'-tri-Me ether, synth) [https://doi.org/10.1021/jm901278z]
  43. Alqasoumi, S.I. et al., Alexandria J. Pharm. Sci., 2010, 24, 48- 50 (3-Methoxyneosakuranin,struct)
  44. US Pat., 2010, 2010 019 861 (3,4-methylene 2',4'-di-Me ether, synth)
  45. Shafaghat, A. et al., World Appl. Sci. J., 2010, 11, 473- 477 (Galium verum constit, struct)
  46. Juvale, K. et al., Bioorg. Med. Chem., 2012, 20, 346- 355 (2',3,4,4'-tetra-Me ether, BCRP inhibitor, potentiation of cytotoxicity) [https://doi.org/10.1016/j.bmc.2011.10.074]
  47. Sun, L.-P. et al., Chem. Biol. Drug Des., 2012, 80, 584- 590 (2',3,4,4',6'-Pentahydroxychalcone, 3-Me ether, PTP 1B inhibitor)
  48. Sui, X. et al., Med. Chem. Res., 2012, 21, 1290- 1296 (2',3,4,4',6'-Pentahydroxychalcone, 3-Me ether, 3,4-di-Me ether, synth, antidepressant activity)
  49. Geissman, T.A. et al., JACS, 1946, 68, 697- 700 (bibl) [https://doi.org/10.1021/ja01208a051]
  50. Bate-Smith, E.C. et al., JCS, 1953, 2185- 2187 (Dahlia variabilis constit)
  51. Duewell, H., JCS, 1954, 2562- 2564 (2',4-Dihydroxy-4'-methoxychalcone)
  52. Guilleman, P. et al., Gaz. Hop. Civ. Mil., 1958, 130, 215- 216 (Metochalcone)
  53. Harborne, J., Phytochemistry, 1962, 1, 203- 207 (Ulex europaeus constits) [https://doi.org/10.1016/S0031-9422(00)82823-X]
  54. Litvinenko, V.I., Dokl. Akad. Nauk SSSR, Ser. Khim., 1964, 155, 600- 602 (Neoisoliquiritin)
  55. Litvinenko, V.I. et al., Dokl. Chem. (Engl. Transl.), 1966, 169, 691- 694 (Licuroside)
  56. Kubota, T. et al., Nippon Kagaku Zasshi, 1966, 87, 1201- 1205 (synth) [https://doi.org/10.1246/nikkashi1948.87.11_1201]
  57. Wong, E., Phytochemistry, 1966, 5, 463- 467 (Isoliquiritigenin) [https://doi.org/10.1016/S0031-9422(00)82160-3]
  58. Wong, E. et al., Phytochemistry, 1968, 7, 2123- 2129 (Isoliquiritigenin) [https://doi.org/10.1016/S0031-9422(00)85667-8]
  59. Wong, E. et al., Phytochemistry, 1968, 7, 2139- 2142 (Isoliquiritigenin) [https://doi.org/10.1016/S0031-9422(00)85669-1]
  60. Winger, G. et al., Biochemistry, 1969, 8, 2067- 2074 (Neoisoliquiritin, synth)
  61. Tindale, M.D. et al., Phytochemistry, 1969, 8, 1713- 1727 (Acacia constit, occur, struct) [https://doi.org/10.1016/S0031-9422(00)85959-2]
  62. Van Hulle, C. et al., Planta Med., 1971, 20, 278- 282 (Rhamnoisoliquiritin) [https://doi.org/10.1055/s-0028-1099705]
  63. Manners, G.D. et al., Phytochemistry, 1974, 13, 292- 293 (Isoliquiritigenin) [https://doi.org/10.1016/S0031-9422(00)91322-0]
  64. Markham, K.R. et al., Tetrahedron, 1976, 32, 2607- 2612 (cmr) [https://doi.org/10.1016/0040-4020(76)88036-2]
  65. Srivastava, S.K. et al., Indian J. Chem., Sect. B, 1981, 20, 347- 348 (2'-O-rhamnosylglucoside)
  66. Carlson, R.E. et al., Phytochemistry, 1982, 21, 1733- 1736 (2'-Me ether) [https://doi.org/10.1016/S0031-9422(82)85049-8]
  67. Menichini, F. et al., Planta Med., 1982, 45, 243- 244 (4-Hydroxycordoin) [https://doi.org/10.1055/s-2007-971382]
  68. Ferrari, F. et al., Phytochemistry, 1983, 22, 1663- 1664 (Isoliquiritigenin) [https://doi.org/10.1016/0031-9422(83)80106-X]
  69. Maurya, R. et al., J. Nat. Prod., 1984, 47, 179- 181 (Isoliquiritigenin) [https://doi.org/10.1021/np50031a029]
  70. Namikoshi, M. et al., Chem. Pharm. Bull., 1987, 35, 3568- 3575 (4,4'-Dihydroxy-2'-methoxychalcone) [https://doi.org/10.1248/cpb.35.3568]
  71. Achenbach, H. et al., Phytochemistry, 1988, 27, 1835- 1841 (2',4'-Dihydroxy-4-methoxychalcone, Acrobil) [https://doi.org/10.1016/0031-9422(88)80455-2]
  72. Miething, H. et al., Arch. Pharm. (Weinheim, Ger.), 1989, 322, 141- 143 (Neolicuroside)
  73. Dagne, E. et al., Phytochemistry, 1990, 29, 2671- 2673 (4'-O-Geranylisoliquiritigenin) [https://doi.org/10.1016/0031-9422(90)85210-7]
  74. Tawata, M. et al., Eur. J. Pharmacol., 1992, 212, 87- 92 (props) [https://doi.org/10.1016/0014-2999(92)90076-G]
  75. Kitagawa, I. et al., Chem. Pharm. Bull., 1993, 41, 1567- 1572 (Licuroside) [https://doi.org/10.1248/cpb.41.1567]
  76. Sogawa, S. et al., J. Med. Chem., 1993, 36, 3904- 3909 (Isoliquiritigenin) [https://doi.org/10.1021/jm00076a019]
  77. Majumder, P.L. et al., Phytochemistry, 1995, 40, 271- 274 (Luisia volucris constit) [https://doi.org/10.1016/0031-9422(95)00060-K]
  78. Kitagawa, I. et al., Chem. Pharm. Bull., 1998, 46, 1511- 1517 (Glucoisoliquiritin apioside) [https://doi.org/10.1248/cpb.46.1511]
  79. Reyes-Chilpa, R. et al., Holzforschung, 1998, 52, 459- 462 (Isoliquiritigenin, activity)
  80. Hatano, T. et al., Phytochemistry, 1998, 47, 287- 293 (liquorice glycosides) [https://doi.org/10.1016/S0031-9422(97)00560-8]
  81. Huang, C. et al., Synth. Commun., 1999, 29, 1383- 1392 (4'-O-Geranylisoliquiritigenin)
  82. Wang, Y.P. et al., Chin. Chem. Lett., 2002, 13, 929- 930 (Isoliquiritin, synth)
  83. Liu, M. et al., Bioorg. Med. Chem., 2003, 11, 2729- 2738 (Acrobil, activity) [https://doi.org/10.1016/S0968-0896(03)00233-5]
  84. Veitch, N.C. et al., J. Nat. Prod., 2003, 66, 210- 216 (4'-Me ether) [https://doi.org/10.1021/np020425u]
  85. Shi, Y. et al., Zhongcaoyao, 2003, 34, 676- 678 (2'-apiosylglucoside)
  86. Fu, W. et al., J. Agric. Food Chem., 2005, 53, 7408- 7414 (Licuroside, activity) [https://doi.org/10.1021/jf051258h]
  87. Lee, M.-H. et al., Phytochemistry, 2006, 67, 1262- 1270 (Neoisoliquiritin, activity) [https://doi.org/10.1016/j.phytochem.2006.05.008]
  88. Avila, H.P. et al., Bioorg. Med. Chem., 2008, 16, 9790- 9794 (4-Hydroxycordoin, activity) [https://doi.org/10.1016/j.bmc.2008.09.064]
  89. Ducki, S. et al., Bioorg. Med. Chem., 2009, 17, 7698- 7710 (Acrobil, activity) [https://doi.org/10.1016/j.bmc.2009.09.039]
  90. Krohn, K. et al., Synthesis, 2009, 779- 786 (2'-Hydroxy-4,4'-dimethoxychalcone) [https://doi.org/10.1055/s-0028-1083361]
  91. Evidente, A. et al., J. Agric. Food Chem., 2010, 58, 2902- 2907 (4-Me ether, pea constit) [https://doi.org/10.1021/jf904247k]
  92. Wang, J.-G. et al., Acta Cryst. E, 2011, 67, o732 (synth, cryst struct)
  93. Thippeswamy, G.B. et al., Acta Cryst. E, 2011, 67, o829 (4'-Me ether, cryst struct)
  94. Rayanil, K.-O. et al., Arch. Pharmacal Res., 2011, 34, 881- 886 (Millettia leucantha constit,uv)
  95. Sano, S. et al., Chem. Pharm. Bull., 2011, 59, 885- 888 (synth) [https://doi.org/10.1248/cpb.59.885]
  96. Zhao, Z.-X. et al., Fitoterapia, 2011, 82, 1102- 1105 (Entada phaseoloides constits) [https://doi.org/10.1016/j.fitote.2011.07.005]
  97. Musa, A.M. et al., J. Med. Plants Res., 2011, 5, 5444- 5449 (Indigofera prenyl ether)
  98. Feldman, M. et al., J. Nat. Prod., 2011, 74, 26- 31 (4-Hydroxycordoin, activity) [https://doi.org/10.1021/np100547b]
  99. Hermange, P. et al., Org. Lett., 2011, 13, 2444- 2447 (Metochalcone) [https://doi.org/10.1021/ol200686h]
  100. Birari, R.B. et al., Phytomedicine, 2011, 18, 795- 801 (Isoliquiritin, Licuroside, activity) [https://doi.org/10.1016/j.phymed.2011.01.002]
  101. Moreira, O. et al., Bioorg. Med. Chem. Lett., 2012, 22, 225- 230 (activity) [https://doi.org/10.1016/j.bmcl.2011.11.059]
  102. Min, B.S. et al., Bioorg. Med. Chem. Lett., 2012, 22, 7436- 7439 (3-Deoxysappanchalcone,activity) [https://doi.org/10.1016/j.bmcl.2012.10.055]
  103. Li, X. et al., Nat. Prod. Res., 2013, 27, 554- 557 (Oxytropis ochrocephala constit)
  104. Ezhilarasi, K.S. et al., Acta Cryst. E, 2014, 70, o608- o609 (4-Me ether, synth, cryst struct)
  105. Maillard, M.P. et al., Helv. Chim. Acta, 1991, 74, 791- 799 (Bauhinia rufescens constits, cryst struct, activity)
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Anthelmintic Citations
  1. Panda SK, Padhi L, Leyssen P, Liu M, Neyts J, Luyten W. Antimicrobial, Anthelmintic, and Antiviral Activity of Plants Traditionally Used for Treating Infectious Disease in the Similipal Biosphere Reserve, Odisha, India. Front Pharmacol. 2017 Oct 23;8:658. [https://doi.org/10.3389/fphar.2017.00658.] eCollection 2017. PubMed PMID: 29109684; PubMed Central PMCID: PMC5660100.
  2. Lopes SG, Barros LB, Louvandini H, Abdalla AL, Costa Junior LM. Effect of tanniniferous food from Bauhinia pulchella on pasture contamination with gastrointestinal nematodes from goats. Parasit Vectors. 2016 Feb 24;9:102. [https://doi.org/10.1186/s13071-016-1370-3.] PubMed PMID: 26911140; PubMed Central PMCID: PMC4765232.
  3. Sashidhara KV, Singh SP, Misra S, Gupta J, Misra-Bhattacharya S. Galactolipids from Bauhinia racemosa as a new class of antifilarial agents against human lymphatic filarial parasite, Brugia malayi. Eur J Med Chem. 2012 Apr;50:230-5. [https://doi.org/10.1016/j.ejmech.2012.01.057.] Epub 2012 Feb 3. PubMed PMID: 22348826.
[top⬆]
Anticancer Citations
  1. Fujise, S. et al., Ber., 1933, 66, 929- 930 (synth)
  2. Fujise, S. et al., Ber., 1936, 69, 1893- 1896 (R-form, synth, struct, resoln)
  3. Arakawa, H. et al., Annalen, 1960, 636, 111- 117 (abs config)
  4. Mitscher, L.A. et al., J. Nat. Prod., 1973, 36, 422- 425 (Eugenia javanica constits)
  5. Joshi, B.S. et al., Indian J. Chem., Sect. B, 1974, 12, 1033- 1037 (7-Me ether)
  6. Cannon, J.R. et al., Aust. J. Chem., 1977, 30, 2099- 2101 (Agonis spathulata constit, bibl) [https://doi.org/10.1071/CH9772099]
  7. Hiraoka, A., Biochem. Syst. Ecol., 1978, 6, 171- 175 (glucoside) [https://doi.org/10.1016/0305-1978(78)90003-0]
  8. Wollenweber, E. et al., Z. Pflanzenphysiol., 1979, 94, 241- 246 (Pityrogramma pallida constit) [https://doi.org/10.1016/S0044-328X(79)80163-4]
  9. Hufford, C.D. et al., JOC, 1981, 46, 3073- 3078 (Uvaria afzelii constit) [https://doi.org/10.1021/jo00328a017]
  10. Tanrisever, N. et al., Phytochemistry, 1987, 26, 175- 179 (Ceratiola ericoides constit, cryst struct) [https://doi.org/10.1016/S0031-9422(00)81505-8]
  11. Kadota, S. et al., Chem. Pharm. Bull., 1994, 42, 1712- 1714 (Matteuorienate B) [https://doi.org/10.1248/cpb.42.1712]
  12. Basnet, P. et al., Chem. Pharm. Bull., 1995, 43, 1558- 1564 (Matteuccia orientalis constit) [https://doi.org/10.1248/cpb.43.1558]
  13. Wu, J.-H. et al., Bioorg. Med. Chem. Lett., 2003, 13, 1813- 1816 (S-form, activity) [https://doi.org/10.1016/S0960-894X(03)00197-5]
  14. Kuo, Y.-C. et al., Planta Med., 2004, 70, 1237- 1239 (5-Me ether) [https://doi.org/10.1055/s-2004-835859]
  15. Mustafa, K.A. et al., Biochem. Syst. Ecol., 2005, 33, 1049- 1059 (Metrosideros excelsa constit, cd, struct) [https://doi.org/10.1016/j.bse.2005.02.003]
  16. Salem, M.M. et al., J. Nat. Prod., 2005, 68, 108- 111 (S-form, activity) [https://doi.org/10.1021/np049682k]
  17. Boonphong, S. et al., J. Nat. Prod., 2007, 70, 795- 801 (Bauhinia purpurea constit, activity) [https://doi.org/10.1021/np070010e]
  18. Dacunha-Marinho, B. et al., Acta Cryst. C, 2008, 64, o353- o356 (5-Me ether, cryst struct)
  19. Lee, J.S. et al., Chem. Pharm. Bull., 2008, 56, 711- 714 (R-form, activity) [https://doi.org/10.1248/cpb.56.711]
  20. Zhang, D. et al., J. Asian Nat. Prod. Res., 2013, 15, 1163- 1167 (7-6-acetylglucoside, cd)
  21. Memon, A.H. et al., Molecules, 2015, 20, 14212- 14233 (cryst struct)
  22. Cooke, R.G. et al., Aust. J. Chem., 1971, 24, 1257- 1265 (4'-Hydroxy-7-methoxyflavan) [https://doi.org/10.1071/CH9711257]
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Inquiries regarding the purchase of Plant cell lines or other PCCL services can be directed to Michael Daley mpdaley@umass.edu

Acknowledgements

The establishment of the PCCL has been sponsored by National Science Foundation (NSF/DBI-156 1572), United States Department of Agriculture Massachusetts Experiment Station Award (MAS00496), the Science and Technology fund from the President's office of the University of Massachusetts, and the 2016 UMass Amherst Armstrong Fund for Science.

National Science FoundationCenter for Agriculture, Food and the Environment

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