The Plant Cell Culture Library

Acacia aneura

Cell Line ID: AA-08778 C2
Media Type: M42
Availability: Medium
Order: Fabales
Family: Fabaceae
Genus: Acacia
Antiviral:
Genus Level ➡ 4 citations
Antibacterial:
Genus Level ➡ 73 citations
Antifungal:
Genus Level ➡ 105 citations
Anthelmintic:
Genus Level ➡ 26 citations
Insecticidal:
Genus Level ➡ 7 citations
Anticancer:
Genus Level ➡ 166 citations
Common Names: Mulga
Culture Initiation Site: Taastrup
Plant Habit: Shrub/Tree
Plant Habitat: Warm Temp/SubTrop
Culture Start Material: Seed
Native Range: Australia
Plant Supplier: Comm/J.L. Hudson
Antiviral Citations:
  1. Ghoke, S. S., Sood, R., Kumar, N., Pateriya, A. K., Bhatia, S., Mishra, A., Dixit, R., Singh, V. K., Desai, D. N., Kulkarni, D. D., Dimri, U., … Singh, V. P. (2018). Evaluation of antiviral activity of Ocimum sanctum and Acacia arabica leaves extracts against H9N2 virus using embryonated chicken egg model. BMC complementary and alternative medicine, 18(1), 174. [https://doi.org/10.1186/s12906-018-2238-1]
  2. Nutan, Modi, M., Dezzutti, C. S., Kulshreshtha, S., Rawat, A. K., Srivastava, S. K., Malhotra, S., Verma, A., Ranga, U., … Gupta, S. K. (2013). Extracts from Acacia catechu suppress HIV-1 replication by inhibiting the activities of the viral protease and Tat. Virology journal, 10, 309. [https://doi.org/10.1186/1743-422X-10-309]
  3. Arbab, A. H., Parvez, M. K., Al-Dosari, M. S., Al-Rehaily, A. J., Al-Sohaibani, M., Zaroug, E. E., AlSaid, M. S., … Rafatullah, S. (2015). Hepatoprotective and antiviral efficacy of Acacia mellifera leaves fractions against hepatitis B virus. BioMed research international, 2015, 929131.
  4. Rehman, S., Ashfaq, U. A., Riaz, S., Javed, T., & Riazuddin, S. (2011). Antiviral activity of Acacia nilotica against Hepatitis C Virus in liver infected cells. Virology journal, 8, 220. [https://doi.org/10.1186/1743-422X-8-220]
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Antibacterial Citations:
  1. 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]
  2. Linstedt, G. et al., Acta Chem. Scand., 1951, 5, 1- 12 (Pinus constits) [https://doi.org/10.3891/acta.chem.scand.05-0001]
  3. Linstedt, G. et al., Acta Chem. Scand., 1951, 5, 121- 128 (Pinus constits, chromatogr) [https://doi.org/10.3891/acta.chem.scand.05-0121]
  4. Hasegawa, M. et al., JACS, 1957, 79, 450- 452 (Verecundin) [https://doi.org/10.1021/ja01559a059]
  5. Hasegawa, M. et al., JACS, 1957, 79, 1738- 1740 (Verecundin) [https://doi.org/10.1021/ja01564a056]
  6. Arakawa, H. et al., Annalen, 1960, 636, 111- 117 (Pinocembrin, abs config)
  7. Batterham, T.J. et al., Aust. J. Chem., 1964, 17, 428- 439 (Alpinetin, pmr) [https://doi.org/10.1071/CH9640428]
  8. Mongkolsuk, S. et al., JCS, 1964, 4654- 4655 ((±)-Pinostrobin, (±)-Alpinetin)
  9. Audier, H., Bull. Soc. Chim. Fr., 1966, 2892- 2899 (ms)
  10. Aurnhammer, G. et al., Chem. Ber., 1970, 103, 3667- 3673 (Isosarotanoside, Sarotanoside)
  11. 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]
  12. Bick, I.R.C. et al., Aust. J. Chem., 1972, 25, 449- 451 (Eucalyptus sieberi constits) [https://doi.org/10.1071/CH9720449]
  13. The Flavonoids, (eds. Harborne, J.B. et al), Chapman and Hall, 1975, 563 (occur)
  14. Miyakado, M. et al., Phytochemistry, 1976, 15, 846- 847 (Pinocembrin, activity) [https://doi.org/10.1016/S0031-9422(00)94481-9]
  15. Wagner, H. et al., Tet. Lett., 1976, 17, 1799- 1802 (cmr) [https://doi.org/10.1016/S0040-4039(00)93787-0]
  16. Pomilio, A.B. et al., Phytochemistry, 1979, 18, 1410- 1411 (Sarotanoside) [https://doi.org/10.1016/0031-9422(79)83040-X]
  17. Tanaka, N. et al., Chem. Pharm. Bull., 1980, 28, 2843- 2845 (Pinocembroside) [https://doi.org/10.1248/cpb.28.2843]
  18. González, M.D. et al., Phytochemistry, 1981, 20, 1174- 1175 (7-(2'''-acetylneohesperidoside)) [https://doi.org/10.1016/0031-9422(81)83063-4]
  19. Ripperberger, H., Phytochemistry, 1981, 20, 1757- 1758 (4'''-Acetylsarotanoside) [https://doi.org/10.1016/S0031-9422(00)98578-9]
  20. Jaipetch, T. et al., Aust. J. Chem., 1982, 35, 351- 361 ((±)-Pinocembrin, (±)-Pinostrobin,Boesenbergia pandurata constit) [https://doi.org/10.1071/CH9820351]
  21. 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]
  22. The Flavonoids: Advances in Research, (eds. Harborne, J.B. et al), Chapman and Hall, 1982, 360 (occur)
  23. Bohlmann, F. et al., Phytochemistry, 1984, 23, 1338- 1339 (7-O-Prenylpinocembrin) [https://doi.org/10.1016/S0031-9422(00)80458-6]
  24. 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]
  25. Bohlmann, F. et al., Planta Med., 1984, 50, 271- 272 (5-Methoxy-7-prenyloxyflavanone) [https://doi.org/10.1055/s-2007-969699]
  26. Talapatra, B. et al., Indian J. Chem., Sect. B, 1985, 24, 561 (Pinocembrin, synth)
  27. Kaouadji, M. et al., J. Nat. Prod., 1986, 49, 153- 155 (7-O-Prenylpinocembrin) [https://doi.org/10.1021/np50043a023]
  28. Jakupovic, J. et al., Phytochemistry, 1987, 26, 803- 807 (hydroxyethylphenyl ether) [https://doi.org/10.1016/S0031-9422(00)84791-3]
  29. Fukui, H. et al., Chem. Pharm. Bull., 1988, 36, 4174- 4176 (Pinocembrin, activity) [https://doi.org/10.1248/cpb.36.4174]
  30. Kapetanidis, J. et al., Pharm. Acta Helv., 1988, 63, 206- 208 (7-rutinoside)
  31. Tomimori, T. et al., Shoyakugaku Zasshi, 1988, 42, 98- 101 (7-glucuronide)
  32. The Flavonoids: Advances in Research Since 1980, (ed. Harborne, J.B.), Chapman and Hall, 1988, 358 (occur)
  33. González, A.G. et al., Phytochemistry, 1989, 28, 2871- 2872 (Salvia texana constit) [https://doi.org/10.1016/S0031-9422(00)98114-7]
  34. Shoja, M., Z. Kristallogr., Kristallgeom., Kristallphys., Kristallchem., 1989, 189, 89- 93 (cryst struct, Pinostrobin)
  35. Krause, M. et al., J. Chromatogr., A, 1990, 502, 287- 296 (chiral hplc, Pinocembrin) [https://doi.org/10.1016/S0021-9673(01)89593-5]
  36. Jung, J.H. et al., Phytochemistry, 1990, 29, 1271- 1275 (cmr) [https://doi.org/10.1016/0031-9422(90)85441-H]
  37. Geibel, M. et al., Phytochemistry, 1991, 30, 1519- 1521 (Prunus cerasus constit) [https://doi.org/10.1016/0031-9422(91)84200-C]
  38. Randriaminahy, M. et al., Z. Naturforsch., C, 1992, 47, 10- 16 (neryl ether)
  39. Yuniong, X. et al., Phytochemistry, 1993, 33, 510- 511 (Onychin) [https://doi.org/10.1016/0031-9422(93)85552-3]
  40. 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]
  41. Hoeneison, M. et al., Phytochemistry, 1993, 34, 1653 (7-benzoyl) [https://doi.org/10.1016/S0031-9422(00)90867-7]
  42. Fukui, H. et al., Phytochemistry, 1993, 34, 1653 (Pinocembrin, activity)
  43. Houghton, P.J. et al., Pharm. Pharmacol. Lett., 1997, 7, 96- 98 (Pinocembrin, activity)
  44. Huang, Y.-L. et al., J. Nat. Prod., 1998, 61, 523- 524 (HHDP derivs) [https://doi.org/10.1021/np970428k]
  45. Meekes, M. et al., Phytomedicine, 1998, 5, 459- 463 (Pinostrobin, activity) [https://doi.org/10.1016/S0944-7113(98)80042-1]
  46. Tip-Pyang, S. et al., ACGC Chem. Res. Commun., 2000, 10, 21- 26 (Pinocembrin,Pinostrobin, Alpinetin, activity)
  47. Le Bail, J.-C. et al., Cancer Lett., 2000, 156, 37- 44 (Pinostrobin, activity) [https://doi.org/10.1016/S0304-3835(00)00435-3]
  48. Yuldashev, M.P., Chem. Nat. Compd. (Engl. Transl.), 2001, 37, 224- 225 (Pinocembroside) [https://doi.org/10.1023/A:1012505721054]
  49. Hodgetts, K.J. et al., Tet. Lett., 2001, 42, 3763- 3766 (Pinostrobin, synth) [https://doi.org/10.1016/S0040-4039(01)00567-6]
  50. Lin, J.-H. et al., J. Nat. Prod., 2002, 65, 638- 640 (7-apiosylapiosylglucoside) [https://doi.org/10.1021/np010548z]
  51. Gu, J.-Q. et al., J. Nat. Prod., 2002, 65, 1616- 1620 (±-7-Me ether)
  52. 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]
  53. Leu, Y.-L. et al., Chem. Pharm. Bull., 2004, 52, 858- 860 (Viscum articulatum glycosides) [https://doi.org/10.1248/cpb.52.858]
  54. He, W. et al., Bioorg. Med. Chem., 2005, 13, 1837- 1845 (Alpinetin, activity) [https://doi.org/10.1016/j.bmc.2004.11.038]
  55. 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]
  56. Urgaonkar, S. et al., Org. Lett., 2005, 7, 5609- 5612 ((±)-Pinocembrin, synth) [https://doi.org/10.1021/ol052269z]
  57. Ma, X.-M. et al., Chem. Biodiversity, 2007, 4, 2172- 2181 (isol, pmr, cmr)
  58. Matus-Cádiz, M.A. et al., J. Agric. Food Chem., 2008, 56, 1644- 1653 (7-rhamnoside, occur) [https://doi.org/10.1021/jf072970c]
  59. Yuan, Y. et al., J. Asian Nat. Prod. Res., 2008, 10, 999- 1002 (Pinocembrin, resoln)
  60. Drewes, S.E. et al., Phytochemistry, 2008, 69, 1745- 1749 (Dibenzylpinocembrin, activity) [https://doi.org/10.1016/j.phytochem.2008.02.022]
  61. Jeong, K.-W. et al., J. Nat. Prod., 2009, 72, 719- 724 (Pinocembrin, activity) [https://doi.org/10.1021/np800698d]
  62. Lotti, C. et al., J. Agric. Food Chem., 2010, 58, 2209- 2213 (Mexican propolis constit) [https://doi.org/10.1021/jf100070w]
  63. Chou, T.-S. et al., J. Nat. Prod., 2010, 73, 1470- 1475 (S-form, Pinostrobin, activity) [https://doi.org/10.1021/np100014j]
  64. 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]
  65. Xu, X. et al., J. Agric. Food Chem., 2011, 59, 1205- 1209 (7-neohesperidoside, 7-rutinoside,Litchioside D) [https://doi.org/10.1021/jf104387y]
  66. Allard, P.-M. et al., J. Nat. Prod., 2011, 74, 2446- 2453 (Cryptocarya chartacea constits) [https://doi.org/10.1021/np200715v]
  67. Korenaga, T. et al., Org. Lett., 2011, 13, 2022- 2025 ((-)-Pinostrobin, synth, bibl) [https://doi.org/10.1021/ol2004148]
  68. Katerere, D.R. et al., Fitoterapia, 2012, 83, 932- 940 (Alpinetin, Pinocembrin) [https://doi.org/10.1016/j.fitote.2012.04.011]
  69. Ullah, Z. et al., Nat. Prod. Commun., 2012, 7, 1011- 1014 (Pistacide A)
  70. Ukida, K. et al., Chem. Pharm. Bull., 2013, 61, 1136- 1142 (Schoepfiajasmin G) [https://doi.org/10.1248/cpb.c13-00466]
  71. Wang, M. et al., Nat. Prod. Res., 2014, 28, 70- 73 (S-form, 5-Me ether 7-glucoside)
  72. Vuppalapati, S.V.N. et al., Synthesis, 2014, 46, 465- 474 ((±)-di-Me ether)
  73. Badr, J.M. et al., Phytochem. Lett., 2013, 6, 113- 117 (Loranthin) [https://doi.org/10.1016/j.phytol.2012.11.008]
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Antifungal Citations:
  1. Nigam, S.K. et al., Indian J. Chem., 1967, 5, 395 (α-Spinasterol glucoside)
  2. Thompson, M.J. et al., Phytochemistry, 1972, 11, 1781- 1790 (pmr) [https://doi.org/10.1016/0031-9422(72)85036-2]
  3. Kircher, H.W. et al., JOC, 1973, 38, 2259- 2260 (α-Spinasterol, synth) [https://doi.org/10.1021/jo00952a041]
  4. Armarego, W.L.F. et al., Phytochemistry, 1973, 12, 2181- 2187 (biosynth) [https://doi.org/10.1016/0031-9422(73)85117-9]
  5. Sarin, J.P.S. et al., Indian J. Chem., 1975, 13, 199- 200 (Vittadinoside)
  6. Sucrow, W. et al., Phytochemistry, 1976, 15, 1533- 1535 (pmr, config) [https://doi.org/10.1016/S0031-9422(00)88932-3]
  7. Iyer, C.S. et al., Phytochemistry, 1978, 17, 2036- 2037 (Chondrillasterone) [https://doi.org/10.1016/S0031-9422(00)88763-4]
  8. Banerji, N., J. Indian Chem. Soc., 1980, 57, 417- 419 (Amaranthus spinosus saponins)
  9. Banerji, R. et al., J. Indian Chem. Soc., 1980, 57, 1043- 1044 (Acacia concinna constits,Acacia caesia constits)
  10. Smetanina, O.F. et al., Chem. Nat. Compd. (Engl. Transl.), 1981, 17, 422- 424 (Parathyona sulfate)
  11. Anastasia, M. et al., JCS Perkin 1, 1981, 2561- 2562 (α-Spinasterol, Chondrillasterol, synth) [https://doi.org/10.1039/P19810002561]
  12. Goodfellow, R.M. et al., Comp. Biochem. Physiol., B: Comp. Biochem., 1983, 76, 575- 578 (3β,5α,22E,24ξ-form, occur, sulfate) [https://doi.org/10.1016/0305-0491(83)90296-1]
  13. Itoh, T. et al., JCS Perkin 1, 1983, 147- 153 (Axinella cannabina constit) [https://doi.org/10.1039/p19830000147]
  14. Dini, A. et al., Comp. Biochem. Physiol., B: Comp. Biochem., 1984, 78, 741- 744 (Ircinia variabilis constit) [https://doi.org/10.1016/0305-0491(84)90128-7]
  15. Seldes, A.M. et al., Comp. Biochem. Physiol., B: Comp. Biochem., 1985, 80, 337- 339 (3β,5α,22E,24ξ-form, occur) [https://doi.org/10.1016/0305-0491(85)90215-9]
  16. Ikram, M. et al., Planta Med., 1987, 53, 389 (Artemisia absinthium constit) [https://doi.org/10.1055/s-2006-962748]
  17. Makarieva, T.N. et al., Steroids, 1993, 58, 508- 517 (Eupentacta fraudatrix constits) [https://doi.org/10.1016/0039-128X(93)90026-J 492034]
  18. Jahan, N. et al., J. Nat. Prod., 1995, 58, 1244- 1247 (Mimusops elengi glycosides) [https://doi.org/10.1021/np50122a014]
  19. Jahan, N. et al., Fitoterapia, 1996, 67, 91- 92 (3-Epichondrillasterol)
  20. Stonik, V.A., Comp. Biochem. Physiol., B: Biochem. Mol. Biol., 1998, 120, 337- 347 (sea cucumber constits) [https://doi.org/10.1016/S0305-0491(98)10023-8]
  21. Pearce, G.E.S. et al., Org. Geochem., 1998, 28, 3- 10 (sediment constit) [https://doi.org/10.1016/S0146-6380(97)00124-1]
  22. Gomes, D. de C.F. et al., Phytochemistry, 1998, 49, 1365- 1367 (Pithecellobium caulifolium constits) [https://doi.org/10.1016/S0031-9422(97)00925-4]
  23. Hearth, H.M.T.B. et al., ACGC Chem. Res. Commun., 1999, 9, 3- 8 (α-Spinasterol, activity)
  24. Wandji, J. et al., Planta Med., 2002, 68, 822- 826 (Chondrillasterol xyloside,Chondrillasterone) [https://doi.org/10.1055/s-2002-34416]
  25. Paulo, A. et al., Fitoterapia, 2005, 76, 765- 767 (Autonoe madeirensis constit) [https://doi.org/10.1016/j.fitote.2005.06.002]
  26. Zhang, L.-J. et al., J. Asian Nat. Prod. Res., 2005, 7, 649- 653 (Securisteroside)
  27. Badreddine, A. et al., Steroids, 2015, 99, 119- 124 (synth) [https://doi.org/10.1016/j.steroids.2015.01.005]
  28. Yang, X. et al., Fitoterapia, 2017, 119, 12- 19 (α-Spinasterol, synth) [https://doi.org/10.1016/j.fitote.2017.03.011]
  29. Breton, J.L. et al., JCS, 1963, 1401- 1406 (synth)
  30. Mahato, S.B. et al., Phytochemistry, 1972, 11, 2116- 2117 (Careya arborea constits) [https://doi.org/10.1016/S0031-9422(00)90189-4]
  31. Nakano, Y. et al., Mokuzai Gakkaishi, 1975, 21, 577- 580 (Albizzia julibrissin constits)
  32. Iyer, C. et al., Phytochemistry, 1978, 17, 2036- 2037 (Grangea maderaspatana constit) [https://doi.org/10.1016/S0031-9422(00)88763-4]
  33. Lee, I.-R. et al., Yakhak Hoechi, 1979, 23, 57- 61 (Codonopsis pilosula constit)
  34. Brooks, C.J.W. et al., Lipids, 1980, 15, 745- 755 (synth)
  35. Herath, H.M.T.B. et al., ACGC Chem. Res. Commun., 1999, 9, 3- 8 (α-Spinasterone,activity)
  36. Akihisa, T. et al., Chem. Pharm. Bull., 1999, 47, 1161- 1163 (pmr, cmr) [https://doi.org/10.1248/cpb.47.1161]
  37. Bargellini, G. et al., Gazz. Chim. Ital., 1914, 44, 25- 34 (3',4'-di-Me ether, synth)
  38. Marquardt, F.H., Helv. Chim. Acta, 1965, 48, 1476- 1485 (tri-Me ether, synth)
  39. Pederiva, R. et al., An. Asoc. Quim. Argent. (1921-2001), 1975, 63, 85- 90 (Larrea nitida constit)
  40. Starkov, S.P. et al., J. Gen. Chem. USSR (Engl. Transl.), 1982, 52, 1214- 1217 (3'-Me ether,synth)
  41. Wollenweber, E. et al., Phytochemistry, 1982, 21, 1063- 1066 (Acacia neovernicosa constit) [https://doi.org/10.1016/S0031-9422(00)82416-4]
  42. Anto, R.J. et al., Cancer Lett., 1995, 97, 33- 37 (3',4'-di-Me ether, activity) [https://doi.org/10.1016/0304-3835(95)03945-S]
  43. Liu, M. et al., J. Med. Chem., 2001, 44, 4443- 4452 (tri-Me ether, activity) [https://doi.org/10.1021/jm0101747]
  44. De La Rocha, N. et al., Pharmacol. Res., 2003, 48, 97- 99 (3'-Me ether, activity)
  45. Svetaz, L. et al., Planta Med., 2007, 73, 1074- 1080 (Larrein, activity) [https://doi.org/10.1055/s-2007-981561]
  46. Aguero, M.B. et al., J. Agric. Food Chem., 2010, 58, 194- 201 (3'-Me ether, activity) [https://doi.org/10.1021/jf902991t]
  47. Chou, T.H., J. Nat. Prod., 2010, 73, 1470- 1475 (Larrein, activity) [https://doi.org/10.1021/np100014j]
  48. Tran, V.H. et al., Phytochemistry, 2012, 81, 126- 132 (Acacia paradoxa constits, activity) [https://doi.org/10.1016/j.phytochem.2012.06.002]
  49. Ghani, N.A. et al., Res. J. Med. Plant, 2012, 6, 74- 82 (3'-Me ether, activity)
  50. Geissman, T.A. et al., JACS, 1946, 68, 697- 700 (bibl) [https://doi.org/10.1021/ja01208a051]
  51. Bate-Smith, E.C. et al., JCS, 1953, 2185- 2187 (Dahlia variabilis constit)
  52. Duewell, H., JCS, 1954, 2562- 2564 (2',4-Dihydroxy-4'-methoxychalcone)
  53. Guilleman, P. et al., Gaz. Hop. Civ. Mil., 1958, 130, 215- 216 (Metochalcone)
  54. Harborne, J., Phytochemistry, 1962, 1, 203- 207 (Ulex europaeus constits) [https://doi.org/10.1016/S0031-9422(00)82823-X]
  55. Litvinenko, V.I., Dokl. Akad. Nauk SSSR, Ser. Khim., 1964, 155, 600- 602 (Neoisoliquiritin)
  56. Litvinenko, V.I. et al., Dokl. Chem. (Engl. Transl.), 1966, 169, 691- 694 (Licuroside)
  57. Kubota, T. et al., Nippon Kagaku Zasshi, 1966, 87, 1201- 1205 (synth) [https://doi.org/10.1246/nikkashi1948.87.11_1201]
  58. Wong, E., Phytochemistry, 1966, 5, 463- 467 (Isoliquiritigenin) [https://doi.org/10.1016/S0031-9422(00)82160-3]
  59. Wong, E. et al., Phytochemistry, 1968, 7, 2123- 2129 (Isoliquiritigenin) [https://doi.org/10.1016/S0031-9422(00)85667-8]
  60. Wong, E. et al., Phytochemistry, 1968, 7, 2139- 2142 (Isoliquiritigenin) [https://doi.org/10.1016/S0031-9422(00)85669-1]
  61. Winger, G. et al., Biochemistry, 1969, 8, 2067- 2074 (Neoisoliquiritin, synth)
  62. Tindale, M.D. et al., Phytochemistry, 1969, 8, 1713- 1727 (Acacia constit, occur, struct) [https://doi.org/10.1016/S0031-9422(00)85959-2]
  63. Van Hulle, C. et al., Planta Med., 1971, 20, 278- 282 (Rhamnoisoliquiritin) [https://doi.org/10.1055/s-0028-1099705]
  64. Manners, G.D. et al., Phytochemistry, 1974, 13, 292- 293 (Isoliquiritigenin) [https://doi.org/10.1016/S0031-9422(00)91322-0]
  65. Markham, K.R. et al., Tetrahedron, 1976, 32, 2607- 2612 (cmr) [https://doi.org/10.1016/0040-4020(76)88036-2]
  66. Srivastava, S.K. et al., Indian J. Chem., Sect. B, 1981, 20, 347- 348 (2'-O-rhamnosylglucoside)
  67. Carlson, R.E. et al., Phytochemistry, 1982, 21, 1733- 1736 (2'-Me ether) [https://doi.org/10.1016/S0031-9422(82)85049-8]
  68. Menichini, F. et al., Planta Med., 1982, 45, 243- 244 (4-Hydroxycordoin) [https://doi.org/10.1055/s-2007-971382]
  69. Ferrari, F. et al., Phytochemistry, 1983, 22, 1663- 1664 (Isoliquiritigenin) [https://doi.org/10.1016/0031-9422(83)80106-X]
  70. Maurya, R. et al., J. Nat. Prod., 1984, 47, 179- 181 (Isoliquiritigenin) [https://doi.org/10.1021/np50031a029]
  71. Namikoshi, M. et al., Chem. Pharm. Bull., 1987, 35, 3568- 3575 (4,4'-Dihydroxy-2'-methoxychalcone) [https://doi.org/10.1248/cpb.35.3568]
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  73. Miething, H. et al., Arch. Pharm. (Weinheim, Ger.), 1989, 322, 141- 143 (Neolicuroside)
  74. Dagne, E. et al., Phytochemistry, 1990, 29, 2671- 2673 (4'-O-Geranylisoliquiritigenin) [https://doi.org/10.1016/0031-9422(90)85210-7]
  75. Tawata, M. et al., Eur. J. Pharmacol., 1992, 212, 87- 92 (props) [https://doi.org/10.1016/0014-2999(92)90076-G]
  76. Kitagawa, I. et al., Chem. Pharm. Bull., 1993, 41, 1567- 1572 (Licuroside) [https://doi.org/10.1248/cpb.41.1567]
  77. Sogawa, S. et al., J. Med. Chem., 1993, 36, 3904- 3909 (Isoliquiritigenin) [https://doi.org/10.1021/jm00076a019]
  78. Majumder, P.L. et al., Phytochemistry, 1995, 40, 271- 274 (Luisia volucris constit) [https://doi.org/10.1016/0031-9422(95)00060-K]
  79. Kitagawa, I. et al., Chem. Pharm. Bull., 1998, 46, 1511- 1517 (Glucoisoliquiritin apioside) [https://doi.org/10.1248/cpb.46.1511]
  80. Reyes-Chilpa, R. et al., Holzforschung, 1998, 52, 459- 462 (Isoliquiritigenin, activity)
  81. Hatano, T. et al., Phytochemistry, 1998, 47, 287- 293 (liquorice glycosides) [https://doi.org/10.1016/S0031-9422(97)00560-8]
  82. Huang, C. et al., Synth. Commun., 1999, 29, 1383- 1392 (4'-O-Geranylisoliquiritigenin)
  83. Wang, Y.P. et al., Chin. Chem. Lett., 2002, 13, 929- 930 (Isoliquiritin, synth)
  84. Liu, M. et al., Bioorg. Med. Chem., 2003, 11, 2729- 2738 (Acrobil, activity) [https://doi.org/10.1016/S0968-0896(03)00233-5]
  85. Veitch, N.C. et al., J. Nat. Prod., 2003, 66, 210- 216 (4'-Me ether) [https://doi.org/10.1021/np020425u]
  86. Shi, Y. et al., Zhongcaoyao, 2003, 34, 676- 678 (2'-apiosylglucoside)
  87. Fu, W. et al., J. Agric. Food Chem., 2005, 53, 7408- 7414 (Licuroside, activity) [https://doi.org/10.1021/jf051258h]
  88. Lee, M.-H. et al., Phytochemistry, 2006, 67, 1262- 1270 (Neoisoliquiritin, activity) [https://doi.org/10.1016/j.phytochem.2006.05.008]
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  91. Krohn, K. et al., Synthesis, 2009, 779- 786 (2'-Hydroxy-4,4'-dimethoxychalcone) [https://doi.org/10.1055/s-0028-1083361]
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  94. Thippeswamy, G.B. et al., Acta Cryst. E, 2011, 67, o829 (4'-Me ether, cryst struct)
  95. Rayanil, K.-O. et al., Arch. Pharmacal Res., 2011, 34, 881- 886 (Millettia leucantha constit,uv)
  96. Sano, S. et al., Chem. Pharm. Bull., 2011, 59, 885- 888 (synth) [https://doi.org/10.1248/cpb.59.885]
  97. Zhao, Z.-X. et al., Fitoterapia, 2011, 82, 1102- 1105 (Entada phaseoloides constits) [https://doi.org/10.1016/j.fitote.2011.07.005]
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  103. 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]
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[top⬆]
Anthelmintic Citations:
  1. Saiyad, I.Z. et al., JCS, 1937, 1737- 1739 (synth)
  2. Jurd, L. et al., JOC, 1961, 26, 2561- 2563 (uv) [https://doi.org/10.1021/jo01351a622]
  3. Audier, H., Bull. Soc. Chim. Fr., 1966, 2892- 2899 (ms)
  4. Obara, H. et al., Bull. Chem. Soc. Jpn., 1969, 42, 560- 561 (synth) [https://doi.org/10.1246/bcsj.42.560]
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  7. Khanna, R.N. et al., Indian J. Chem., 1973, 11, 1225- 1227 (synth)
  8. Lupi, A. et al., Farmaco, Ed. Sci., 1975, 30, 449- 455 (Cordoin)
  9. Braz Filho, R. et al., Phytochemistry, 1975, 14, 1454- 1456 (Derricidin) [https://doi.org/10.1016/S0031-9422(00)98664-3]
  10. Delle Monache, F. et al., Phytochemistry, 1978, 17, 1812- 1813 (Cordoin) [https://doi.org/10.1016/S0031-9422(00)88713-0]
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  12. Patra, A. et al., Org. Magn. Reson., 1982, 18, 241- 242 (cmr)
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  15. Bohlmann, F. et al., Planta Med., 1984, 50, 271- 272 (Helichrysum ruglosum constit) [https://doi.org/10.1055/s-2007-969699]
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  22. Mativandlela, S.P. et al., J. Nat. Prod., 2009, 72, 2169- 2171 (Galena africana constit) [https://doi.org/10.1021/np800778b]
  23. Lou, C. et al., Toxicol. in Vitro, 2009, 23, 906- 910 (2',4'-Dihydroxychalcone, activity) [https://doi.org/10.1016/j.tiv.2009.05.002]
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[top⬆]
Insecticidal Citations:
  1. Benelli G, Kadaikunnan S, Alharbi NS, Govindarajan M. Biophysical characterization of Acacia caesia-fabricated silver nanoparticles: effectiveness on mosquito vectors of public health relevance and impact on non-target aquatic biocontrol agents.Environ Sci Pollut Res Int. 2018 Apr;25(11):10228-10242. [https://doi.org/10.1007/s11356-017-8482-y.] Epub 2017 Feb 5. PubMed PMID: 28161865.
  2. Vivekanandhan P, Venkatesan R, Ramkumar G, Karthi S, Senthil-Nathan S, Shivakumar MS. Comparative Analysis of Major Mosquito Vectors Response to Seed-Derived Essential Oil and Seed Pod-Derived Extract from Acacia nilotica. Int J Environ Res Public Health. 2018 Feb 23;15(2). pii: E388. [https://doi.org/10.3390/ijerph15020388.] PubMed PMID: 29473901; PubMed Central PMCID: PMC5858457.
  3. Thongwat D, Ganranoo L, Chokchaisiri R. LARVICIDAL AND PUPICIDAL ACTIVITIES OF CRUDE AND FRACTIONATED EXTRACTS OF ACACIA PENNATA (L.) WILLD. SUBSP INSUAVIS SHOOT TIPS AGAINST AEDES AEGYPTI (L.) (DIPTERA: CULICIDAE). Southeast Asian J Trop Med Public Health. 2017 Jan;48(1):27-36. PubMed PMID: 29644817.
  4. Nazeefullah S, Dastagir G, Ahmad B. Effect of cold water extracts of Acacia modesta Wall. and Glycyrrhiza glabra Linn. on Tribolium castaneum and Lemna minor. Pak J Pharm Sci. 2014 Mar;27(2):217-22. PubMed PMID: 24577905.
  5. Machado SW, de Oliveira CF, Bezerra Cda S, Freire Md, Regina Kill M, Machado OL, Marangoni S, Macedo ML. Purification of a Kunitz-type inhibitor from Acacia polyphyllaDC seeds: characterization and insecticidal properties against Anagasta kuehniella Zeller (Lepidoptera: Pyralidae). J Agric Food Chem. 2013 Mar 13;61(10):2469-78. [https://doi.org/10.1021/jf3049565.] Epub 2013 Feb 27. PubMed PMID: 23418748.
  6. Chaubal R, Pawar PV, Hebbalkar GD, Tungikar VB, Puranik VG, Deshpande VH, Deshpande NR. Larvicidal activity of Acacia nilotica extracts and isolation of D-pinitol--a bioactive carbohydrate. Chem Biodivers. 2005 May;2(5):684-8. PubMed PMID: 17192011.
  7. Vahitha R, Venkatachalam MR, Murugan K, Jebanesan A. Larvicidal efficacy of Pavonia zeylanica L. and Acacia ferruginea D.C. against Culex quinquefasciatus Say. Bioresour Technol. 2002 Apr;82(2):203-4. PubMed PMID: 12003324.
[top⬆]
Anticancer Citations:
  1. De Oliveira, A.B. et al., Ann. Acad. Bras. Ciènc., (Suppl.), 1970, 42, 109- 110 (Platymiscium praecox constit)
  2. Cardillo, G. et al., JCS(C), 1971, 3967- 3970 (R-form)
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  4. Do Nascimento, M.C. et al., Phytochemistry, 1972, 11, 3023- 3028 (Isoderricidin) [https://doi.org/10.1016/0031-9422(72)80097-9]
  5. de Oliveira, A.B. et al., Phytochemistry, 1972, 11, 3515- 3519 (Platymiscium praecox constit) [https://doi.org/10.1016/S0031-9422(00)89849-0]
  6. Bohlmann, F. et al., Phytochemistry, 1979, 18, 1189- 1194 (Flourensia heterolepsis constit) [https://doi.org/10.1016/0031-9422(79)80132-6]
  7. Wollenweber, E. et al., Phytochemistry, 1982, 21, 1063- 1066 (Acacia neovernicosa constit) [https://doi.org/10.1016/S0031-9422(00)82416-4]
  8. Maurya, R. et al., J. Nat. Prod., 1984, 47, 179- 181 (Pterocarpus marsupium constit) [https://doi.org/10.1021/np50031a029]
  9. Furlong, J.J.P. et al., JCS Perkin 2, 1985, 633- 639 ((±)-form, synth) [https://doi.org/10.1039/P29850000633]
  10. Talapatra, B. et al., Indian J. Chem., Sect. B, 1986, 25, 1122- 1125 (synth)
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  12. Roy, R. et al., Phytochemistry, 1994, 37, 1775- 1776 (glucoside) [https://doi.org/10.1016/S0031-9422(00)89613-2]
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  21. Vuppalapati, S.V.N. et al., Synthesis, 2014, 46, 465- 474 ((±)-Me ether)
  22. Bedane, K.G. et al., Synth. Commun., 2016, 46, 1803- 1809 ((±)-form, synth, ir, pmr, cmr)
  23. Aldrich Library of FT-IR Spectra, 1st edn., 1985, 1, 1120D (ir)
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  26. Batterham, T.J. et al., Aust. J. Chem., 1964, 17, 428- 439 (pmr) [https://doi.org/10.1071/CH9640428]
  27. Dority, G.H., Diss. Abstr., 1965, 26, 3036 (Mailein)
  28. Clark-Lewis, J.W., Aust. J. Chem., 1968, 21, 3025- 3054 (ms) [https://doi.org/10.1071/CH9683025]
  29. Haslam, E., JCS(C), 1969, 1824- 1828 (3-Galloylcatechin)
  30. Weinges, K. et al., Annalen, 1970, 734, 46- 55 (Polydine)
  31. Karrer, W. et al., Konstitution und Vorkommen der Organischen Pflanzenstoffe, 2nd edn., Birkhäuser Verlag, 1972, nos. 1762-1764 (occur)
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  33. Doskotch, R.W. et al., Phytochemistry, 1973, 12, 1153- 1155 (7-xyloside) [https://doi.org/10.1016/0031-9422(73)85032-0]
  34. Chumbalov, T.K. et al., Chem. Nat. Compd. (Engl. Transl.), 1976, 12, 94- 95 (Catechin 7-xyloside)
  35. Chumbalov, T.K. et al., Chem. Nat. Compd. (Engl. Transl.), 1976, 12, 232- 233 (Catechin 7-rhamnoside) [https://doi.org/10.1007/BF00566356]
  36. Markham, K.R. et al., Tetrahedron, 1976, 32, 2607- 2612 (cmr) [https://doi.org/10.1016/0040-4020(76)88036-2]
  37. Takani, M. et al., Chem. Pharm. Bull., 1977, 25, 3388- 3390 (7-glucoside) [https://doi.org/10.1248/cpb.25.3388]
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  39. Jacques, D. et al., JCS Perkin 1, 1977, 1637- 1643 (biosynth) [https://doi.org/10.1039/p19770001637]
  40. Barrett, M.W. et al., JCS Perkin 1, 1979, 2375- 2377 (cd) [https://doi.org/10.1039/p19790002375]
  41. Tschesche, R. et al., Phytochemistry, 1980, 19, 1825- 1829 (Symplocoside) [https://doi.org/10.1016/S0031-9422(00)83821-2]
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  43. Nonaka, G.-I. et al., Phytochemistry, 1982, 21, 429- 432 (Polygonum multiflorum constit) [https://doi.org/10.1016/S0031-9422(00)95282-8]
  44. Karl, C. et al., Z. Naturforsch., C, 1982, 37, 148- 151 (7-apioside, 7-arabinofuranoside)
  45. Nonaka, G. et al., Chem. Pharm. Bull., 1983, 31, 3906- 3914 (hydroxybenzoyl derivs, oolong tea) [https://doi.org/10.1248/cpb.31.3906]
  46. Foo, L.Y. et al., JCS Perkin 1, 1983, 1535- 1543 (ent-Catechin, synth, cmr) [https://doi.org/10.1039/p19830001535]
  47. Miyamura, M. et al., Phytochemistry, 1983, 22, 215- 218 (3-Hydroxy-5,7-dimethoxy-3',4'-methylenedioxyflavan) [https://doi.org/10.1016/S0031-9422(00)80092-8]
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  49. Tanaka, T. et al., Phytochemistry, 1983, 22, 2575- 2578 (7-Galloylcatechin) [https://doi.org/10.1016/0031-9422(83)80168-X]
  50. Spek, A.L. et al., Acta Cryst. C, 1984, 40, 2068- 2071 (cryst struct, Epicatechin) [https://doi.org/10.1107/S0108270184010659]
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  52. Morimoto, S. et al., Chem. Pharm. Bull., 1985, 33, 2281- 2286 (Cinnamomum constits,Lindera constits) [https://doi.org/10.1248/cpb.33.2281]
  53. Malterud, K.E. et al., J. Nat. Prod., 1985, 48, 559- 563 ((+)-Catechin, isol, activity) [https://doi.org/10.1021/np50040a007]
  54. Foo, L.Y. et al., Phytochemistry, 1985, 24, 1495- 1498 (Phylloflavan) [https://doi.org/10.1016/S0031-9422(00)81052-3]
  55. Hsu, F.L. et al., Phytochemistry, 1985, 24, 2089- 2092 (cyclohexenecarboxylates) [https://doi.org/10.1016/S0031-9422(00)83128-3]
  56. Miyata, T. et al., Yakugaku Zasshi, 1985, 105, 59- 64 (Catechin, cryst struct) [https://doi.org/10.1248/yakushi1947.105.1_59]
  57. Murakami, T. et al., Yakugaku Zasshi, 1985, 105, 649- 654 (Epicatechin allosides) [https://doi.org/10.1248/yakushi1947.105.7_649]
  58. Morimoto, S. et al., Chem. Pharm. Bull., 1986, 34, 633- 642 (Cinnamomum cassia constits) [https://doi.org/10.1248/cpb.34.633]
  59. Morimoto, S. et al., Chem. Pharm. Bull., 1986, 34, 643- 649 (Cinnamomum cassia constits,Cinnamomum obtusifolium constits) [https://doi.org/10.1248/cpb.34.643]
  60. Kashiwada, Y. et al., Chem. Pharm. Bull., 1986, 34, 3208- 3222 (rhubarb glucosides) [https://doi.org/10.1248/cpb.34.3208]
  61. Porter, L.J. et al., J. Chem. Res., Synop., 1986, 86- 87 (pmr, conformn)
  62. Bonefeld, M. et al., Phytochemistry, 1986, 25, 1205- 1207 (3-rhamnoside) [https://doi.org/10.1016/S0031-9422(00)81581-2]
  63. Perrissoud, D., Prog. Clin. Biol. Res., 1986, 213, 559- 569 (rev, pharmacol)
  64. Hashimoto, F. et al., Chem. Pharm. Bull., 1987, 35, 611- 616 (oolong tea epicatechin derivs) [https://doi.org/10.1248/cpb.35.611]
  65. Ishimaru, K. et al., Phytochemistry, 1987, 26, 1167- 1170 (3-glucoside, 3-rhamnoside) [https://doi.org/10.1016/S0031-9422(00)82371-7]
  66. Malan, E. et al., Phytochemistry, 1987, 26, 2049- 2051 (Acacia gerrardii constits) [https://doi.org/10.1016/S0031-9422(00)81756-2]
  67. Foo, L.Y. et al., Phytochemistry, 1987, 26, 2825- 2830 (Phylloflavan, (-)-Epicatechin) [https://doi.org/10.1016/S0031-9422(00)83598-0]
  68. Yamazaki, M. et al., Yakugaku Zasshi, 1987, 107, 914- 916 (Artocarpus integra constit) [https://doi.org/10.1248/yakushi1947.107.11_914]
  69. Kiehlmann, E. et al., Magn. Reson. Chem., 1988, 26, 204- 210 (cmr)
  70. Son, B.W. et al., Arch. Pharmacal Res., 1989, 12, 219- 222 (Uldavioside)
  71. Morisaka, N. et al., J. Nat. Prod., 1989, 52, 1221- 1226 (3-Galloylcatechin, isol)
  72. Law, K.-H. et al., Phytochemistry, 1989, 28, 1099- 1100 (Uncaria elliptica constit) [https://doi.org/10.1016/0031-9422(89)80191-8]
  73. Foo, L.Y. et al., Phytochemistry, 1989, 28, 1237- 1240 (Pseudotsuga menziesii constit,Epicatechin 7-glucoside)
  74. Nakane, H., Biochemistry, 1990, 29, 2841- 2845 (Epicatechin gallate, anti-HIV activity) [https://doi.org/10.1021/bi00463a029]
  75. Malan, E., Phytochemistry, 1990, 29, 1334- 1335 (Acacia gerrardii constit) [https://doi.org/10.1016/0031-9422(90)85459-S]
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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 Foundation Center for Agriculture, Food and the Environment