The University of Massachusetts Amherst

The Plant Cell Culture Library

Vigna unguiculata Subsp. sesquipedalis
Cell Line ID VS-14400-C1
Media Type M128
Lowest Tolerable USDA Zone 9a
Drought Tolerance Average
Availability Low
Order Fabales
Family Leguminosae
Genus Vigna
Antiviral Genus Level ➡ 23 citations
Insecticidal Genus Level ➡ 5 citations
Anticancer Genus Level ➡ 203 citations
Antiviral Citations
  1. Ishimasa, S. et al., Yakugaku Zasshi, 1956, 76, 1210- 1211 (Sophoradiol)
  2. Ishimasa, S. et al., Yakugaku Zasshi, 1960, 80, 304- 310 (Sophoradiol) [https://doi.org/10.1248/yakushi1947.80.3_304]
  3. Mak, T.C.W. et al., Chem. Comm., 1982, 785- 786 (Sophoradiol, cryst struct) [https://doi.org/10.1039/c39820000785]
  4. Kitagawa, I. et al., Chem. Pharm. Bull., 1983, 31, 674- 682 (Azukisaponin I) [https://doi.org/10.1248/cpb.31.674]
  5. Kitagawa, I. et al., Yakugaku Zasshi, 1988, 108, 538- 546 (Kaikasaponins) [https://doi.org/10.1248/yakushi1947.108.6_538]
  6. Takeshita, T. et al., Chem. Pharm. Bull., 1989, 37, 846- 848 (Abrisapogenol F) [https://doi.org/10.1248/cpb.37.846]
  7. Ding, Y. et al., Chem. Pharm. Bull., 1991, 39, 496- 498 (Crotalaria albida constits) [https://doi.org/10.1248/cpb.39.496]
  8. Fish, P.V. et al., JOC, 1994, 59, 2324- 2335 (Sophoradiol, synth) [https://doi.org/10.1021/jo00088a011]
  9. Miyano, H. et al., Chem. Pharm. Bull., 1996, 44, 1222- 1227 (Kaikasaponin III, Phaseoside IV) [https://doi.org/10.1248/cpb.44.1228]
  10. Miyao, H. et al., Chem. Pharm. Bull., 1996, 44, 1228- 1231 (Abrisaponins F,So1,So2) [https://doi.org/10.1248/cpb.44.1228]
  11. Arao, T. et al., Chem. Pharm. Bull., 1996, 44, 1970- 1972 (Acetylkaikasaponin III) [https://doi.org/10.1248/cpb.44.1970]
  12. Udayama, M. et al., Phytochemistry, 1998, 48, 1233- 1235 (Baptisiasaponin I) [https://doi.org/10.1016/S0031-9422(98)00162-9]
  13. Kinjo, J. et al., Biol. Pharm. Bull., 2000, 73, 887- 889 (activity)
  14. Oh, S.-R. et al., Planta Med., 2000, 66, 506- 510 (activity)
  15. Ndom, J.C. et al., Bull. Chem. Soc. Ethiop., 2001, 15, 151- 156 (α-Sophoradiol)
  16. Kim, N.-C. et al., Nat. Prod. Lett., 2002, 16, 261- 266 (6-methylglucuronoside) [https://doi.org/10.1080/10575630290020596]
  17. Riaz, N. et al., Nat. Prod. Lett., 2002, 16, 415- 418 (Alysinol) [https://doi.org/10.1080/10575630290034258]
  18. Li, R. et al., Zhongguo Zhongyao Zazhi, 2005, 30, 1255- 1257 (Sophorea carbonisatus constit)
  19. Chiu, H.-L. et al., J. Nat. Prod., 2008, 71, 1829- 1832 (3-ketone) [https://doi.org/10.1021/np800253s]
  20. Mkounga, P. et al., Chem. Pharm. Bull., 2010, 58, 1100- 1102 (Cylicodiscus gabunensis constit) [https://doi.org/10.1248/cpb.58.1100]
  21. Abdou, A.M. et al., Arch. Pharmacal Res., 2013, 36, 715- 722 (Anabasis setifera saponin)
  22. Lu, J. et al., J. Asian Nat. Prod. Res., 2013, 15, 1065- 1072 (Kakkasaponins II,III)
  23. Ye, X.Y. et al., J. Protein Chem., 2001, 20, 353- 359 (Unguilin) [https://doi.org/10.1023/A:1012272518778]
[top⬆]
Insecticidal Citations
  1. Chen, K.C. et al., J. Agric. Food Chem., 2002, 50, 7258- 7263 (Vr-D1) [https://doi.org/10.1021/jf020527q]
  2. Chen, K.C. et al., J. Agric. Food Chem., 2004, 52, 2256- 2261 (Vr-D1) [https://doi.org/10.1021/jf030662i]
  3. Shiau, Y.S. et al., J. Mol. Recognit., 2006, 19, 441- 450 (struct)
  4. Liu, Y.J. et al., Proteins, 2006, 63, 777- 786 (soln struct)
  5. Sugawara, F. et al., J. Agric. Food Chem., 1996, 44, 3360- 3364 (isol, pmr, cmr, hplc) [https://doi.org/10.1021/jf960166c]
[top⬆]
Anticancer Citations
  1. Aljančić, I.S. et al., Phytochemistry, 2014, 98, 190- 196 (Tomoroside A)
  2. Linstedt, G. et al., Acta Chem. Scand., 1950, 4, 1042- 1046 (Pinostrobin, Pinocembrin,struct, S-form) [https://doi.org/10.3891/acta.chem.scand.04-1042]
  3. Linstedt, G. et al., Acta Chem. Scand., 1951, 5, 1- 12 (Pinus constits) [https://doi.org/10.3891/acta.chem.scand.05-0001]
  4. Linstedt, G. et al., Acta Chem. Scand., 1951, 5, 121- 128 (Pinus constits, chromatogr) [https://doi.org/10.3891/acta.chem.scand.05-0121]
  5. Hasegawa, M. et al., JACS, 1957, 79, 450- 452 (Verecundin) [https://doi.org/10.1021/ja01559a059]
  6. Hasegawa, M. et al., JACS, 1957, 79, 1738- 1740 (Verecundin) [https://doi.org/10.1021/ja01564a056]
  7. Arakawa, H. et al., Annalen, 1960, 636, 111- 117 (Pinocembrin, abs config)
  8. Batterham, T.J. et al., Aust. J. Chem., 1964, 17, 428- 439 (Alpinetin, pmr) [https://doi.org/10.1071/CH9640428]
  9. Mongkolsuk, S. et al., JCS, 1964, 4654- 4655 ((±)-Pinostrobin, (±)-Alpinetin)
  10. Audier, H., Bull. Soc. Chim. Fr., 1966, 2892- 2899 (ms)
  11. Aurnhammer, G. et al., Chem. Ber., 1970, 103, 3667- 3673 (Isosarotanoside, Sarotanoside)
  12. Asakawa, Y. et al., Bull. Chem. Soc. Jpn., 1971, 44, 2761- 2766 (Pinocembrin, Alpinetin,Alnus sieboldiana constit) [https://doi.org/10.1246/bcsj.44.2761]
  13. Bick, I.R.C. et al., Aust. J. Chem., 1972, 25, 449- 451 (Eucalyptus sieberi constits) [https://doi.org/10.1071/CH9720449]
  14. The Flavonoids, (eds. Harborne, J.B. et al), Chapman and Hall, 1975, 563 (occur)
  15. Miyakado, M. et al., Phytochemistry, 1976, 15, 846- 847 (Pinocembrin, activity) [https://doi.org/10.1016/S0031-9422(00)94481-9]
  16. Wagner, H. et al., Tet. Lett., 1976, 17, 1799- 1802 (cmr) [https://doi.org/10.1016/S0040-4039(00)93787-0]
  17. Pomilio, A.B. et al., Phytochemistry, 1979, 18, 1410- 1411 (Sarotanoside) [https://doi.org/10.1016/0031-9422(79)83040-X]
  18. Tanaka, N. et al., Chem. Pharm. Bull., 1980, 28, 2843- 2845 (Pinocembroside) [https://doi.org/10.1248/cpb.28.2843]
  19. González, M.D. et al., Phytochemistry, 1981, 20, 1174- 1175 (7-(2'''-acetylneohesperidoside)) [https://doi.org/10.1016/0031-9422(81)83063-4]
  20. Ripperberger, H., Phytochemistry, 1981, 20, 1757- 1758 (4'''-Acetylsarotanoside) [https://doi.org/10.1016/S0031-9422(00)98578-9]
  21. Jaipetch, T. et al., Aust. J. Chem., 1982, 35, 351- 361 ((±)-Pinocembrin, (±)-Pinostrobin,Boesenbergia pandurata constit) [https://doi.org/10.1071/CH9820351]
  22. González, M.D. et al., Phytochemistry, 1982, 21, 757- 759 (7-(6''-acetylneohesperidoside),7-(3'''-acetylneohesperidoside)) [https://doi.org/10.1016/0031-9422(82)83182-8]
  23. The Flavonoids: Advances in Research, (eds. Harborne, J.B. et al), Chapman and Hall, 1982, 360 (occur)
  24. Bohlmann, F. et al., Phytochemistry, 1984, 23, 1338- 1339 (7-O-Prenylpinocembrin) [https://doi.org/10.1016/S0031-9422(00)80458-6]
  25. Norbedo, C. et al., Phytochemistry, 1984, 23, 2698- 2700 (7-O-2,3-epoxy-3-methylbutyl) [https://doi.org/10.1016/S0031-9422(00)84139-4]
  26. Bohlmann, F. et al., Planta Med., 1984, 50, 271- 272 (5-Methoxy-7-prenyloxyflavanone) [https://doi.org/10.1055/s-2007-969699]
  27. Talapatra, B. et al., Indian J. Chem., Sect. B, 1985, 24, 561 (Pinocembrin, synth)
  28. Kaouadji, M. et al., J. Nat. Prod., 1986, 49, 153- 155 (7-O-Prenylpinocembrin) [https://doi.org/10.1021/np50043a023]
  29. Jakupovic, J. et al., Phytochemistry, 1987, 26, 803- 807 (hydroxyethylphenyl ether) [https://doi.org/10.1016/S0031-9422(00)84791-3]
  30. Fukui, H. et al., Chem. Pharm. Bull., 1988, 36, 4174- 4176 (Pinocembrin, activity) [https://doi.org/10.1248/cpb.36.4174]
  31. Kapetanidis, J. et al., Pharm. Acta Helv., 1988, 63, 206- 208 (7-rutinoside)
  32. Tomimori, T. et al., Shoyakugaku Zasshi, 1988, 42, 98- 101 (7-glucuronide)
  33. The Flavonoids: Advances in Research Since 1980, (ed. Harborne, J.B.), Chapman and Hall, 1988, 358 (occur)
  34. González, A.G. et al., Phytochemistry, 1989, 28, 2871- 2872 (Salvia texana constit) [https://doi.org/10.1016/S0031-9422(00)98114-7]
  35. Shoja, M., Z. Kristallogr., Kristallgeom., Kristallphys., Kristallchem., 1989, 189, 89- 93 (cryst struct, Pinostrobin)
  36. Krause, M. et al., J. Chromatogr., A, 1990, 502, 287- 296 (chiral hplc, Pinocembrin) [https://doi.org/10.1016/S0021-9673(01)89593-5]
  37. Jung, J.H. et al., Phytochemistry, 1990, 29, 1271- 1275 (cmr) [https://doi.org/10.1016/0031-9422(90)85441-H]
  38. Geibel, M. et al., Phytochemistry, 1991, 30, 1519- 1521 (Prunus cerasus constit) [https://doi.org/10.1016/0031-9422(91)84200-C]
  39. Randriaminahy, M. et al., Z. Naturforsch., C, 1992, 47, 10- 16 (neryl ether)
  40. Yuniong, X. et al., Phytochemistry, 1993, 33, 510- 511 (Onychin) [https://doi.org/10.1016/0031-9422(93)85552-3]
  41. Bilia, A.R. et al., Phytochemistry, 1993, 33, 1449- 1452 (7-Me ether 5-glucoside) [https://doi.org/10.1016/0031-9422(93)85108-4]
  42. Hoeneison, M. et al., Phytochemistry, 1993, 34, 1653 (7-benzoyl) [https://doi.org/10.1016/S0031-9422(00)90867-7]
  43. Fukui, H. et al., Phytochemistry, 1993, 34, 1653 (Pinocembrin, activity)
  44. Houghton, P.J. et al., Pharm. Pharmacol. Lett., 1997, 7, 96- 98 (Pinocembrin, activity)
  45. Huang, Y.-L. et al., J. Nat. Prod., 1998, 61, 523- 524 (HHDP derivs) [https://doi.org/10.1021/np970428k]
  46. Meekes, M. et al., Phytomedicine, 1998, 5, 459- 463 (Pinostrobin, activity) [https://doi.org/10.1016/S0944-7113(98)80042-1]
  47. Tip-Pyang, S. et al., ACGC Chem. Res. Commun., 2000, 10, 21- 26 (Pinocembrin,Pinostrobin, Alpinetin, activity)
  48. Le Bail, J.-C. et al., Cancer Lett., 2000, 156, 37- 44 (Pinostrobin, activity) [https://doi.org/10.1016/S0304-3835(00)00435-3]
  49. Yuldashev, M.P., Chem. Nat. Compd. (Engl. Transl.), 2001, 37, 224- 225 (Pinocembroside) [https://doi.org/10.1023/A:1012505721054]
  50. Hodgetts, K.J. et al., Tet. Lett., 2001, 42, 3763- 3766 (Pinostrobin, synth) [https://doi.org/10.1016/S0040-4039(01)00567-6]
  51. Lin, J.-H. et al., J. Nat. Prod., 2002, 65, 638- 640 (7-apiosylapiosylglucoside) [https://doi.org/10.1021/np010548z]
  52. Gu, J.-Q. et al., J. Nat. Prod., 2002, 65, 1616- 1620 (±-7-Me ether)
  53. Hegde, V.R. et al., Bioorg. Med. Chem. Lett., 2003, 13, 2925- 2928 (Sch 644343) [https://doi.org/10.1016/S0960-894X(03)00584-5]
  54. Leu, Y.-L. et al., Chem. Pharm. Bull., 2004, 52, 858- 860 (Viscum articulatum glycosides) [https://doi.org/10.1248/cpb.52.858]
  55. He, W. et al., Bioorg. Med. Chem., 2005, 13, 1837- 1845 (Alpinetin, activity) [https://doi.org/10.1016/j.bmc.2004.11.038]
  56. Caccamese, S. et al., J. Chromatogr., A, 2005, 1076, 155- 162 (chiral hplc-cd, Pinocembrin) [https://doi.org/10.1016/j.chroma.2005.04.024]
  57. Urgaonkar, S. et al., Org. Lett., 2005, 7, 5609- 5612 ((±)-Pinocembrin, synth) [https://doi.org/10.1021/ol052269z]
  58. Ma, X.-M. et al., Chem. Biodiversity, 2007, 4, 2172- 2181 (isol, pmr, cmr)
  59. Matus-Cádiz, M.A. et al., J. Agric. Food Chem., 2008, 56, 1644- 1653 (7-rhamnoside, occur) [https://doi.org/10.1021/jf072970c]
  60. Yuan, Y. et al., J. Asian Nat. Prod. Res., 2008, 10, 999- 1002 (Pinocembrin, resoln)
  61. Drewes, S.E. et al., Phytochemistry, 2008, 69, 1745- 1749 (Dibenzylpinocembrin, activity) [https://doi.org/10.1016/j.phytochem.2008.02.022]
  62. Jeong, K.-W. et al., J. Nat. Prod., 2009, 72, 719- 724 (Pinocembrin, activity) [https://doi.org/10.1021/np800698d]
  63. Lotti, C. et al., J. Agric. Food Chem., 2010, 58, 2209- 2213 (Mexican propolis constit) [https://doi.org/10.1021/jf100070w]
  64. Chou, T.-S. et al., J. Nat. Prod., 2010, 73, 1470- 1475 (S-form, Pinostrobin, activity) [https://doi.org/10.1021/np100014j]
  65. Pick, A. et al., Bioorg. Med. Chem., 2011, 19, 2090- 2102 (Leptospermum scoparium constit,activity) [https://doi.org/10.1016/j.bmc.2010.12.043]
  66. Xu, X. et al., J. Agric. Food Chem., 2011, 59, 1205- 1209 (7-neohesperidoside, 7-rutinoside,Litchioside D) [https://doi.org/10.1021/jf104387y]
  67. Allard, P.-M. et al., J. Nat. Prod., 2011, 74, 2446- 2453 (Cryptocarya chartacea constits) [https://doi.org/10.1021/np200715v]
  68. Korenaga, T. et al., Org. Lett., 2011, 13, 2022- 2025 ((-)-Pinostrobin, synth, bibl) [https://doi.org/10.1021/ol2004148]
  69. Katerere, D.R. et al., Fitoterapia, 2012, 83, 932- 940 (Alpinetin, Pinocembrin) [https://doi.org/10.1016/j.fitote.2012.04.011]
  70. Ullah, Z. et al., Nat. Prod. Commun., 2012, 7, 1011- 1014 (Pistacide A)
  71. Ukida, K. et al., Chem. Pharm. Bull., 2013, 61, 1136- 1142 (Schoepfiajasmin G) [https://doi.org/10.1248/cpb.c13-00466]
  72. Wang, M. et al., Nat. Prod. Res., 2014, 28, 70- 73 (S-form, 5-Me ether 7-glucoside)
  73. Vuppalapati, S.V.N. et al., Synthesis, 2014, 46, 465- 474 ((±)-di-Me ether)
  74. Briggs, L.H. et al., JCS, 1949, 2162- 2164 (Isokanugin)
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  76. Popa, G. et al., Fresenius' Z. Anal. Chem., 1959, 165, 16- 19 (use, detn, Ta) [https://doi.org/10.1007/BF00465908]
  77. Jurd, L., JOC, 1962, 27, 1294- 1297 (Retusin, synth) [https://doi.org/10.1021/jo01051a041]
  78. Hamaguchi, H. et al., Anal. Chim. Acta, 1963, 28, 61- 67 (detn, Sc) [https://doi.org/10.1016/S0003-2670(00)87196-2]
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  92. Nogradi, M. et al., Chem. Ber., 1970, 103, 3414- 3418 (synth)
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  98. Okonenko, V.U. et al., Rastit. Resur., 1973, 9, 250- 260 (Neorutin)
  99. Farkas, L. et al., Chem. Ber., 1974, 107, 1518- 1527 (4',7-diglucoside)
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  105. Rizk, A.M. et al., Pharmazie, 1976, 31, 405 (3'-xyloside)
  106. Urbatsch, L.E. et al., Phytochemistry, 1976, 15, 440- 441 (3,3',4'-tri-Me ether) [https://doi.org/10.1016/S0031-9422(00)86853-3]
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  109. Ghosal, S. et al., Phytochemistry, 1980, 19, 123- 126 (Tetramethylstearoylquercetin) [https://doi.org/10.1016/0031-9422(80)85027-8]
  110. Henning, W. et al., Phytochemistry, 1980, 19, 2727- 2729 (3-rutinoside 3',7-diglucoside) [https://doi.org/10.1016/S0031-9422(00)83951-5]
  111. Gehring, E. et al., Z. Naturforsch., C, 1980, 35, 380- 383 (3',5-di-Me 3-glucoside)
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  113. Aguinagalde, I. et al., Phytochemistry, 1982, 21, 2875- 2878 (Crambe cordifolia constit) [https://doi.org/10.1016/0031-9422(80)85059-X]
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  116. Nishino, H. et al., Experientia, 1984, 40, 184- 185 (Quercetin, tox)
  117. Wollenweber, E. et al., Z. Naturforsch., C, 1984, 39, 303- 306 (Pachypodol, isol)
  118. Clark, W.D. et al., Phytochemistry, 1985, 24, 1122- 1123 (5,7-Dihydroxy-3,3',4'-trimethoxyflavone, Pachypodol) [https://doi.org/10.1016/S0031-9422(00)83207-0]
  119. Cabrera, J.L. et al., Phytochemistry, 1985, 24, 1394- 1395 (3,3',7-trisulfate) [https://doi.org/10.1016/S0031-9422(00)81147-4]
  120. Rossi, M. et al., Bioorg. Chem., 1986, 14, 55- 69 (cryst struct) [https://doi.org/10.1016/0045-2068(86)90018-0]
  121. Kulanthaivel, P. et al., Can. J. Chem., 1986, 64, 514- 519 (Traversia baccharoides constits) [https://doi.org/10.1139/v86-081]
  122. Barron, D. et al., Phytochemistry, 1986, 25, 1719- 1721 (3-sulfate, struct, cmr) [https://doi.org/10.1016/S0031-9422(00)81243-1]
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  124. Wollenweber, E. et al., Z. Naturforsch., C, 1986, 41, 87- 93 (5,7-dihydroxy-3,3',4'-trimethoxyflavone, isol)
  125. Saxena, V.K. et al., Fitoterapia, 1987, 53, 571- 572 (3',4',5,7-tetra-Me ether 3-rhamnosylglucoside)
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