The University of Massachusetts Amherst

The Plant Cell Culture Library

Gossypium armourianum
Cell Line ID GA-13211 C1
Media Type B50
Availability medium
Order Malvales
Family Malvaceae
Genus Gossypium
Antiviral Genus Level ➡ 4 citations
Antibacterial Genus Level ➡ 1 citations
Insecticidal Genus Level ➡ 1 citations
Anticancer Genus Level ➡ 118 citations
Common Names Cotton
Culture Initiation Site Dusseldorf
Plant Habit Herb Annual/Perennial
Plant Habitat Temperate
Culture Start Material Seed
Native Range Genus : Asia to Australia
Plant Supplier Inst/Nat. Plant Germplasm System USDA
Antiviral Citations
  1. Nazeer W, Tipu AL, Ahmad S, Mahmood K, Mahmood A, Zhou B. Evaluation of cotton leaf curl virus resistance in BC1, BC2, and BC3 progenies from an interspecific cross between Gossypium arboreum and Gossypium hirsutum. PLoS One. 2014 Nov 5;9(11):e111861. [https://doi.org/10.1371/journal.pone.0111861.] eCollection 2014. PubMed PMID: 25372141; PubMed Central PMCID: PMC4221200.
  2. Nazeer W, Ahmad S, Mahmood K, Tipu AL, Mahmood A, Zhou B. Introgression of genes for cotton leaf curl virus resistance and increased fiber strength from Gossypium stocksii into upland cotton (G. hirsutum). Genet Mol Res. 2014 Feb 21;13(1):1133-43. [https://doi.org/10.4238/2014.February.21.2.] PubMed PMID: 24634169.
  3. Ahmad S, Mahmood K, Hanif M, Nazeer W, Malik W, Qayyum A, Hanif K, Mahmood A, Islam N. Introgression of cotton leaf curl virus-resistant genes from Asiatic cotton (Gossypium arboreum) into upland cotton (G. hirsutum). Genet Mol Res. 2011 Oct 7;10(4):2404-14. [https://doi.org/10.4238/2011.October.7.2.] PubMed PMID: 22002133.
  4. Hashmi JA, Zafar Y, Arshad M, Mansoor S, Asad S. Engineering cotton (Gossypium hirsutum L.) for resistance to cotton leaf curl disease using viral truncated AC1 DNA sequences. Virus Genes. 2011 Apr;42(2):286-96. [https://doi.org/10.1007/s11262-011-0569-9.] Epub 2011 Feb 15. Erratum in: Virus Genes. 2011 Dec;43(3):476. PubMed PMID: 21327530.
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Antibacterial Citations
  1. Annan K, Houghton PJ. Antibacterial, antioxidant and fibroblast growth stimulation of aqueous extracts of Ficus asperifolia Miq. and Gossypium arboreum L., wound-healing plants of Ghana. J Ethnopharmacol. 2008 Sep 2;119(1):141-4. [https://doi.org/10.1016/j.jep.2008.06.017.] Epub 2008 Jun 27. PubMed PMID: 18638536.
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Insecticidal Citations
  1. Patil CD, Borase HP, Salunkhe RB, Suryawanshi RK, Narkhade CP, Salunke BK, Patil SV. Mosquito Larvicidal Potential of Gossypium hirsutum (Bt cotton) Leaves Extracts against Aedes aegypti and Anopheles stephensi larvae. J Arthropod Borne Dis. 2013 Dec 18;8(1):91-101. eCollection 2014. PubMed PMID: 25629069; PubMed Central PMCID: PMC4289515.
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Anticancer Citations
  1. Aldrich Library of FT-IR Spectra, 1st edn., 1985, 1, 1120D (ir)
  2. Aldrich Library of 13C and 1H FT-NMR Spectra, 1992, 2, 326A (nmr)
  3. Bokada, M.M. et al., Proc. Chem. Soc., London, 1960, 280 (stereochem)
  4. Batterham, T.J. et al., Aust. J. Chem., 1964, 17, 428- 439 (pmr) [https://doi.org/10.1071/CH9640428]
  5. Dority, G.H., Diss. Abstr., 1965, 26, 3036 (Mailein)
  6. Clark-Lewis, J.W., Aust. J. Chem., 1968, 21, 3025- 3054 (ms) [https://doi.org/10.1071/CH9683025]
  7. Haslam, E., JCS(C), 1969, 1824- 1828 (3-Galloylcatechin)
  8. Weinges, K. et al., Annalen, 1970, 734, 46- 55 (Polydine)
  9. Karrer, W. et al., Konstitution und Vorkommen der Organischen Pflanzenstoffe, 2nd edn., Birkhäuser Verlag, 1972, nos. 1762-1764 (occur)
  10. Coxon, D.T. et al., Tetrahedron, 1972, 28, 2819- 2826 (3,5-Digalloylepicatechin) [https://doi.org/10.1016/0040-4020(72)80118-2]
  11. Doskotch, R.W. et al., Phytochemistry, 1973, 12, 1153- 1155 (7-xyloside) [https://doi.org/10.1016/0031-9422(73)85032-0]
  12. Chumbalov, T.K. et al., Chem. Nat. Compd. (Engl. Transl.), 1976, 12, 94- 95 (Catechin 7-xyloside)
  13. Chumbalov, T.K. et al., Chem. Nat. Compd. (Engl. Transl.), 1976, 12, 232- 233 (Catechin 7-rhamnoside) [https://doi.org/10.1007/BF00566356]
  14. Markham, K.R. et al., Tetrahedron, 1976, 32, 2607- 2612 (cmr) [https://doi.org/10.1016/0040-4020(76)88036-2]
  15. Takani, M. et al., Chem. Pharm. Bull., 1977, 25, 3388- 3390 (7-glucoside) [https://doi.org/10.1248/cpb.25.3388]
  16. Alhadeff, M., Drugs of Today (Barcelona), 1977, 13, 60- 69 (Catechin, rev)
  17. Jacques, D. et al., JCS Perkin 1, 1977, 1637- 1643 (biosynth) [https://doi.org/10.1039/p19770001637]
  18. Barrett, M.W. et al., JCS Perkin 1, 1979, 2375- 2377 (cd) [https://doi.org/10.1039/p19790002375]
  19. Tschesche, R. et al., Phytochemistry, 1980, 19, 1825- 1829 (Symplocoside) [https://doi.org/10.1016/S0031-9422(00)83821-2]
  20. Eur. Pat., 1981, 37 800 (synth, pharmacol, Meciadanol, Cinnamomum Me ethers, Lindera umbellata Me ethers)
  21. Nonaka, G.-I. et al., Phytochemistry, 1982, 21, 429- 432 (Polygonum multiflorum constit) [https://doi.org/10.1016/S0031-9422(00)95282-8]
  22. Karl, C. et al., Z. Naturforsch., C, 1982, 37, 148- 151 (7-apioside, 7-arabinofuranoside)
  23. Nonaka, G. et al., Chem. Pharm. Bull., 1983, 31, 3906- 3914 (hydroxybenzoyl derivs, oolong tea) [https://doi.org/10.1248/cpb.31.3906]
  24. Foo, L.Y. et al., JCS Perkin 1, 1983, 1535- 1543 (ent-Catechin, synth, cmr) [https://doi.org/10.1039/p19830001535]
  25. 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]
  26. Nonaka, G.-I. et al., Phytochemistry, 1983, 22, 1659- 1661 (Rheum constit, Rhaphiolepis umbellata constit) [https://doi.org/10.1016/0031-9422(83)80105-8]
  27. Tanaka, T. et al., Phytochemistry, 1983, 22, 2575- 2578 (7-Galloylcatechin) [https://doi.org/10.1016/0031-9422(83)80168-X]
  28. Spek, A.L. et al., Acta Cryst. C, 1984, 40, 2068- 2071 (cryst struct, Epicatechin) [https://doi.org/10.1107/S0108270184010659]
  29. Delgado, G. et al., Phytochemistry, 1984, 23, 675- 678 (Viguiera quinqueradiata constit,3',5,7-Trimethylcatechin) [https://doi.org/10.1016/S0031-9422(00)80405-7]
  30. Morimoto, S. et al., Chem. Pharm. Bull., 1985, 33, 2281- 2286 (Cinnamomum constits,Lindera constits) [https://doi.org/10.1248/cpb.33.2281]
  31. Malterud, K.E. et al., J. Nat. Prod., 1985, 48, 559- 563 ((+)-Catechin, isol, activity) [https://doi.org/10.1021/np50040a007]
  32. Foo, L.Y. et al., Phytochemistry, 1985, 24, 1495- 1498 (Phylloflavan) [https://doi.org/10.1016/S0031-9422(00)81052-3]
  33. Hsu, F.L. et al., Phytochemistry, 1985, 24, 2089- 2092 (cyclohexenecarboxylates) [https://doi.org/10.1016/S0031-9422(00)83128-3]
  34. Miyata, T. et al., Yakugaku Zasshi, 1985, 105, 59- 64 (Catechin, cryst struct) [https://doi.org/10.1248/yakushi1947.105.1_59]
  35. Murakami, T. et al., Yakugaku Zasshi, 1985, 105, 649- 654 (Epicatechin allosides) [https://doi.org/10.1248/yakushi1947.105.7_649]
  36. Morimoto, S. et al., Chem. Pharm. Bull., 1986, 34, 633- 642 (Cinnamomum cassia constits) [https://doi.org/10.1248/cpb.34.633]
  37. 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]
  38. Kashiwada, Y. et al., Chem. Pharm. Bull., 1986, 34, 3208- 3222 (rhubarb glucosides) [https://doi.org/10.1248/cpb.34.3208]
  39. Porter, L.J. et al., J. Chem. Res., Synop., 1986, 86- 87 (pmr, conformn)
  40. Bonefeld, M. et al., Phytochemistry, 1986, 25, 1205- 1207 (3-rhamnoside) [https://doi.org/10.1016/S0031-9422(00)81581-2]
  41. Perrissoud, D., Prog. Clin. Biol. Res., 1986, 213, 559- 569 (rev, pharmacol)
  42. Hashimoto, F. et al., Chem. Pharm. Bull., 1987, 35, 611- 616 (oolong tea epicatechin derivs) [https://doi.org/10.1248/cpb.35.611]
  43. Ishimaru, K. et al., Phytochemistry, 1987, 26, 1167- 1170 (3-glucoside, 3-rhamnoside) [https://doi.org/10.1016/S0031-9422(00)82371-7]
  44. Malan, E. et al., Phytochemistry, 1987, 26, 2049- 2051 (Acacia gerrardii constits) [https://doi.org/10.1016/S0031-9422(00)81756-2]
  45. Foo, L.Y. et al., Phytochemistry, 1987, 26, 2825- 2830 (Phylloflavan, (-)-Epicatechin) [https://doi.org/10.1016/S0031-9422(00)83598-0]
  46. Yamazaki, M. et al., Yakugaku Zasshi, 1987, 107, 914- 916 (Artocarpus integra constit) [https://doi.org/10.1248/yakushi1947.107.11_914]
  47. Kiehlmann, E. et al., Magn. Reson. Chem., 1988, 26, 204- 210 (cmr)
  48. Son, B.W. et al., Arch. Pharmacal Res., 1989, 12, 219- 222 (Uldavioside)
  49. Morisaka, N. et al., J. Nat. Prod., 1989, 52, 1221- 1226 (3-Galloylcatechin, isol)
  50. Law, K.-H. et al., Phytochemistry, 1989, 28, 1099- 1100 (Uncaria elliptica constit) [https://doi.org/10.1016/0031-9422(89)80191-8]
  51. Foo, L.Y. et al., Phytochemistry, 1989, 28, 1237- 1240 (Pseudotsuga menziesii constit,Epicatechin 7-glucoside)
  52. Nakane, H., Biochemistry, 1990, 29, 2841- 2845 (Epicatechin gallate, anti-HIV activity) [https://doi.org/10.1021/bi00463a029]
  53. Malan, E., Phytochemistry, 1990, 29, 1334- 1335 (Acacia gerrardii constit) [https://doi.org/10.1016/0031-9422(90)85459-S]
  54. Rossouw, W. et al., Tetrahedron, 1990, 50, 12477- 12488 (pmr, abs config) [https://doi.org/10.1016/S0040-4020(01)89554-5]
  55. Urano, M. et al., J. Het. Chem., 1991, 28, 1845- 1847 (synth)
  56. Malan, E., Phytochemistry, 1991, 30, 2737- 2739 (Acacia nilotica constits) [https://doi.org/10.1016/0031-9422(91)85134-L]
  57. Jin, Q.D. et al., Yaoxue Xuebao, 1991, 26, 841- 845 (Epigeoside)
  58. Cui, C.B. et al., Chem. Pharm. Bull., 1992, 40, 2035- 2040 (Epicatechin 5-glucoside) [https://doi.org/10.1248/cpb.40.2035]
  59. Lee, M.W. et al., Phytochemistry, 1992, 31, 2117- 2120 (Pithecellobium lobatum constits)
  60. Martindale, The Extra Pharmacopoeia, 30th edn., Pharmaceutical Press, 1993, 1353
  61. Shen, C.-C. et al., Phytochemistry, 1993, 34, 843- 845 (pmr, cmr) [https://doi.org/10.1016/0031-9422(93)85370-7]
  62. Bae, Y.S. et al., Phytochemistry, 1994, 35, 473- 478 (Catechin 3-rutinoside) [https://doi.org/10.1016/S0031-9422(00)94785-X]
  63. Mukherjee, R.K. et al., Phytochemistry, 1994, 37, 1641- 1643 (5,7-di-Me, 3',4'-methylene ether) [https://doi.org/10.1016/S0031-9422(00)89583-7]
  64. Pan, H. et al., Phytochemistry, 1995, 39, 1423- 1428 (3'-O-Methylcatechin 7-glucoside) [https://doi.org/10.1016/0031-9422(95)00144-V]
  65. Davis, A.L. et al., Magn. Reson. Chem., 1996, 34, 887- 890 (pmr, cmr, gallates)
  66. Pan, H. et al., Phytochemistry, 1996, 42, 1185- 1189 (3'-O-Methylcatechin) [https://doi.org/10.1016/0031-9422(96)00122-7]
  67. Bilia, A.R. et al., Phytochemistry, 1996, 43, 887- 892 (7-O-Methylcatechin) [https://doi.org/10.1016/0031-9422(96)00291-9]
  68. Seto, R. et al., Biosci., Biotechnol., Biochem., 1997, 61, 1434- 1439 (tea catechins)
  69. Van Rensberg, H. et al., Tet. Lett., 1997, 38, 3089- 3092 (synth, Catechin isomers) [https://doi.org/10.1016/S0040-4039(97)00552-2]
  70. Matsuda, H. et al., Bioorg. Med. Chem. Lett., 1998, 8, 2939- 2944 (Catechin 7-xyloside,activity) [https://doi.org/10.1016/S0960-894X(98)00528-9]
  71. Miketova, P. et al., J. Nat. Prod., 1998, 61, 461- 467 (Catechins, ms) [https://doi.org/10.1021/np9703959]
  72. Ferrari, F. et al., Phytochemistry, 1998, 47, 1165- 1166 (Epicatechin 5-xyloside) [https://doi.org/10.1016/S0031-9422(98)80094-0]
  73. Zhang, H.L. et al., Phytochemistry, 1998, 48, 665- 668 (Gossypium hirsutum constit) [https://doi.org/10.1016/S0031-9422(98)00075-2]
  74. Nakao, M. et al., Phytochemistry, 1998, 49, 2379- 2382 (Catechins, Epicatechin gallate,activity) [https://doi.org/10.1016/S0031-9422(98)00333-1]
  75. Xiong, Q. et al., Planta Med., 2000, 66, 127- 133 (2R,3S-form) [https://doi.org/10.1055/s-2000-11135]
  76. Nay, B. et al., Tet. Lett., 2000, 41, 9049- 9051 (synth) [https://doi.org/10.1016/S0040-4039(00)01649-X]
  77. Kinjo, J. et al., Biol. Pharm. Bull., 2001, 24, 1443- 1445 (7-Galloylcatechin, activity) [https://doi.org/10.1248/bpb.24.1443]
  78. Otsuka, H. et al., Chem. Pharm. Bull., 2001, 49, 921- 923 (Glochiflavanosides) [https://doi.org/10.1248/cpb.49.921]
  79. Hwang, B.Y. et al., J. Nat. Prod., 2001, 64, 82- 84 ((-)-Epicatechin, 3-Benzoylepicatechin 5-glucoside, activity) [https://doi.org/10.1021/np000251l]
  80. Akdemir, Z.S. et al., Phytochemistry, 2001, 56, 189- 193 (6-Chloroepicatechin) [https://doi.org/10.1016/S0031-9422(00)00367-8]
  81. Demirezer, L.O. et al., Phytochemistry, 2001, 58, 1213- 1217 (6-chloro) [https://doi.org/10.1016/S0031-9422(01)00337-5]
  82. Su, B.-N. et al., J. Nat. Prod., 2002, 65, 163- 169 (2R,3S-form)
  83. Qi, S.-H. et al., Acta Bot. Sin., 2003, 45, 1129- 1133 (3-3,5-Dimethylgalloylepicatechin)
  84. Lokvam, J. et al., Phytochemistry, 2004, 65, 351- 358 (3-cinnamoylglycosides) [https://doi.org/10.1016/j.phytochem.2003.11.012]
  85. Gao, S. et al., Planta Med., 2004, 70, 1128- 1134 (Lysidicichin, activity) [https://doi.org/10.1055/s-2004-835839]
  86. Flavonoids: Chemistry and Biochemistry, (ed. Andersen, O.M. et al), CRC Press, 2005
  87. Aguiar, R.M. et al., Phytochemistry, 2005, 66, 2388- 2392 (Byrsonima microphylla tri-Me ether) [https://doi.org/10.1016/j.phytochem.2005.07.011]
  88. Bekker, M. et al., Phytochemistry, 2006, 67, 818- 823 (Epicatechin 7-xyloside) [https://doi.org/10.1016/j.phytochem.2006.01.015]
  89. Iida, N. et al., Chem. Biodiversity, 2007, 4, 32- 42 (3'-Me 5-glucoside, 4'-Me 5-glucoside)
  90. Li, D.-L. et al., Molecules, 2007, 12, 1163- 1169 (3-Acetylepicatechin, 3,7-Diacetylepicatechin, Pentaacetylepicatechin)
  91. Kofink, M. et al., Molecules, 2007, 12, 1274- 1288 (cocoa, occur)
  92. Dib, M.A. et al., Asian J. Chem., 2008, 20, 3926- 3934 (Arbutus 3-4-hydroxybenzoate)
  93. Ölschläger, C. et al., Phytochemistry, 2008, 69, 1389- 1397 (3-(3,4-Dimethylgalloyl)epicatechin) [https://doi.org/10.1016/j.phytochem.2008.01.001]
  94. Ramanandraibe, V. et al., Planta Med., 2008, 74, 417- 421 (5-Galloylcatechin, 7-Galloylcatechin, activity) [https://doi.org/10.1055/s-2008-1034328]
  95. Kim, H.J. et al., Fitoterapia, 2009, 80, 73- 76 (Epicatechin gallates, activity) [https://doi.org/10.1016/j.fitote.2008.10.003]
  96. Nishanbaev, S.Z. et al., Chem. Nat. Compd. (Engl. Transl.), 2010, 46, 357- 362 (Epicatechin)
  97. Rinaldo, D. et al., Chirality, 2010, 22, 726- 733 (Catechin, ent-Catechin, Epicatechin, ent-Epicatechin, cd, sepn)
  98. Tian, L.-W. et al., Helv. Chim. Acta, 2010, 93, 2194- 2202 (7-O-Methylcatechin 5-glucoside)
  99. Schmidt, C.A. et al., J. Nat. Prod., 2010, 73, 2035- 2041 (Symplocosidin, activity) [https://doi.org/10.1021/np100523s]
  100. Meng, D. et al., Phytochemistry, 2010, 71, 325- 331 (Breynia fruticosa 3-acetylepicatechins) [https://doi.org/10.1016/j.phytochem.2009.10.002]
  101. Anderson, J.C. et al., Bioorg. Med. Chem. Lett., 2011, 21, 6996- 7000 (Epicatechin 3-gallate,activity) [https://doi.org/10.1016/j.bmcl.2011.09.116]
  102. Zhang, D. et al., Eur. J. Med. Chem., 2011, 46, 4548- 4558 (Epicatechin, activity) [https://doi.org/10.1016/j.ejmech.2011.07.031]
  103. Ivanov, S.A. et al., Fitoterapia, 2011, 82, 212- 218 (3,5-Digalloylcatechin) [https://doi.org/10.1016/j.fitote.2010.09.013]
  104. Chira, K. et al., Molecules, 2011, 16, 1519- 1532 (grape constits) [https://doi.org/10.3390/molecules16021519]
  105. Wungsintaweekul, B. et al., Phytochemistry, 2011, 72, 495- 502 (ent-Catechin, activity) [https://doi.org/10.1016/j.phytochem.2010.12.018]
  106. Manir, M.M. et al., Bioorg. Med. Chem., 2012, 20, 2376- 2381 (2R,3S-form, activity) [https://doi.org/10.1016/j.bmc.2012.02.002]
  107. Dong, Y. et al., Chem. Biodiversity, 2012, 9, 68- 79 (Epicatechin, activity)
  108. Stadlbauer, S. et al., Chem. Comm., 2012, 48, 8425- 8427 (synth)
  109. Wu, X.-D. et al., Fitoterapia, 2012, 83, 1068- 1071 (Malaferins B,C)
  110. Al-Taweel, A.M. et al., Fitoterapia, 2012, 83, 1610- 1615 (5-gallate) [https://doi.org/10.1016/j.fitote.2012.09.010]
  111. Agbo, M.O. et al., Fitoterapia, 2013, 86, 78- 83 (Tri-O-methylgalloylepicatechin) [https://doi.org/10.1016/j.fitote.2013.02.006]
  112. Qiu, L. et al., Phytochem. Lett., 2013, 6, 368- 371 (3-Nitropropanoylepicatechin) [https://doi.org/10.1016/j.phytol.2013.04.010]
  113. Hosny, M. et al., Arch. Pharmacal Res., 2014, 37, 698- 705 (Ulmus davidiana constits)
  114. Wang, N. et al., Molecules, 2014, 19, 6623- 6634 (3',7-di-Me ether 5-glucoside, activity, rel config)
  115. Şöhretoğlu, D. et al., Rec. Nat. Prod., 2014, 8, 323- 329 (8-Chlorocatechin)
  116. Liu, F. et al., Phytochemistry, 2015, 110, 150- 159 (3-Curvulinoylepicatechin, 3-Caffeoylepicatechin) [https://doi.org/10.1016/j.phytochem.2014.12.007]
  117. Jin, H.-G. et al., Arch. Pharmacal Res., 2016, 39, 755- 761 (Symplocoside)
  118. Sax's Dangerous Properties of Industrial Materials, 11th edn., J. Wiley, 2004, CCP875 (Catechin)
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