The University of Massachusetts Amherst

The Plant Cell Culture Library

Acacia aneura
Cell Line ID AA-08778 C2
Media Type M42
Availability medium
Order Fabales
Family Leguminosae
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]
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[top⬆]
Anthelmintic Citations
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[top⬆]
Insecticidal Citations
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  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.
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[top⬆]
Anticancer Citations
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  70. Son, B.W. et al., Arch. Pharmacal Res., 1989, 12, 219- 222 (Uldavioside)
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