The Plant Cell Culture Library
Gossypium darwinii
Cell Line ID GD-13212 C1
Media Type B50
Availability Medium
Order Malvales
Family Malvaceae
Genus Gossypium
Antibacterial Genus Level ➡ 1 citations
Insecticidal Genus Level ➡ 1 citations
Anticancer Genus Level ➡ 118 citations
Common Names Cotton
Culture Initiation Site Dusseldorf
Plant Habitat Warm Temp/Tropical
Culture Start Material Seed
Native Range Genus : Warm Temperate and Tropical Region
Plant Supplier Inst/Nat. Plant Germplasm System USDA
Antibacterial Citations
- 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.
Insecticidal Citations
- 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.
Anticancer Citations
- Aldrich Library of FT-IR Spectra, 1st edn., 1985, 1, 1120D (ir)
- Aldrich Library of 13C and 1H FT-NMR Spectra, 1992, 2, 326A (nmr)
- Bokada, M.M. et al., Proc. Chem. Soc., London, 1960, 280 (stereochem)
- Batterham, T.J. et al., Aust. J. Chem., 1964, 17, 428- 439 (pmr) [https://doi.org/10.1071/CH9640428]
- Dority, G.H., Diss. Abstr., 1965, 26, 3036 (Mailein)
- Clark-Lewis, J.W., Aust. J. Chem., 1968, 21, 3025- 3054 (ms) [https://doi.org/10.1071/CH9683025]
- Haslam, E., JCS(C), 1969, 1824- 1828 (3-Galloylcatechin)
- Weinges, K. et al., Annalen, 1970, 734, 46- 55 (Polydine)
- Karrer, W. et al., Konstitution und Vorkommen der Organischen Pflanzenstoffe, 2nd edn., Birkhäuser Verlag, 1972, nos. 1762-1764 (occur)
- Coxon, D.T. et al., Tetrahedron, 1972, 28, 2819- 2826 (3,5-Digalloylepicatechin) [https://doi.org/10.1016/0040-4020(72)80118-2]
- Doskotch, R.W. et al., Phytochemistry, 1973, 12, 1153- 1155 (7-xyloside) [https://doi.org/10.1016/0031-9422(73)85032-0]
- Chumbalov, T.K. et al., Chem. Nat. Compd. (Engl. Transl.), 1976, 12, 94- 95 (Catechin 7-xyloside)
- Chumbalov, T.K. et al., Chem. Nat. Compd. (Engl. Transl.), 1976, 12, 232- 233 (Catechin 7-rhamnoside) [https://doi.org/10.1007/BF00566356]
- Markham, K.R. et al., Tetrahedron, 1976, 32, 2607- 2612 (cmr) [https://doi.org/10.1016/0040-4020(76)88036-2]
- Takani, M. et al., Chem. Pharm. Bull., 1977, 25, 3388- 3390 (7-glucoside) [https://doi.org/10.1248/cpb.25.3388]
- Alhadeff, M., Drugs of Today (Barcelona), 1977, 13, 60- 69 (Catechin, rev)
- Jacques, D. et al., JCS Perkin 1, 1977, 1637- 1643 (biosynth) [https://doi.org/10.1039/p19770001637]
- Barrett, M.W. et al., JCS Perkin 1, 1979, 2375- 2377 (cd) [https://doi.org/10.1039/p19790002375]
- Tschesche, R. et al., Phytochemistry, 1980, 19, 1825- 1829 (Symplocoside) [https://doi.org/10.1016/S0031-9422(00)83821-2]
- Eur. Pat., 1981, 37 800 (synth, pharmacol, Meciadanol, Cinnamomum Me ethers, Lindera umbellata Me ethers)
- Nonaka, G.-I. et al., Phytochemistry, 1982, 21, 429- 432 (Polygonum multiflorum constit) [https://doi.org/10.1016/S0031-9422(00)95282-8]
- Karl, C. et al., Z. Naturforsch., C, 1982, 37, 148- 151 (7-apioside, 7-arabinofuranoside)
- Nonaka, G. et al., Chem. Pharm. Bull., 1983, 31, 3906- 3914 (hydroxybenzoyl derivs, oolong tea) [https://doi.org/10.1248/cpb.31.3906]
- Foo, L.Y. et al., JCS Perkin 1, 1983, 1535- 1543 (ent-Catechin, synth, cmr) [https://doi.org/10.1039/p19830001535]
- 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]
- 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]
- Tanaka, T. et al., Phytochemistry, 1983, 22, 2575- 2578 (7-Galloylcatechin) [https://doi.org/10.1016/0031-9422(83)80168-X]
- Spek, A.L. et al., Acta Cryst. C, 1984, 40, 2068- 2071 (cryst struct, Epicatechin) [https://doi.org/10.1107/S0108270184010659]
- 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]
- Morimoto, S. et al., Chem. Pharm. Bull., 1985, 33, 2281- 2286 (Cinnamomum constits,Lindera constits) [https://doi.org/10.1248/cpb.33.2281]
- Malterud, K.E. et al., J. Nat. Prod., 1985, 48, 559- 563 ((+)-Catechin, isol, activity) [https://doi.org/10.1021/np50040a007]
- Foo, L.Y. et al., Phytochemistry, 1985, 24, 1495- 1498 (Phylloflavan) [https://doi.org/10.1016/S0031-9422(00)81052-3]
- Hsu, F.L. et al., Phytochemistry, 1985, 24, 2089- 2092 (cyclohexenecarboxylates) [https://doi.org/10.1016/S0031-9422(00)83128-3]
- Miyata, T. et al., Yakugaku Zasshi, 1985, 105, 59- 64 (Catechin, cryst struct) [https://doi.org/10.1248/yakushi1947.105.1_59]
- Murakami, T. et al., Yakugaku Zasshi, 1985, 105, 649- 654 (Epicatechin allosides) [https://doi.org/10.1248/yakushi1947.105.7_649]
- Morimoto, S. et al., Chem. Pharm. Bull., 1986, 34, 633- 642 (Cinnamomum cassia constits) [https://doi.org/10.1248/cpb.34.633]
- 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]
- Kashiwada, Y. et al., Chem. Pharm. Bull., 1986, 34, 3208- 3222 (rhubarb glucosides) [https://doi.org/10.1248/cpb.34.3208]
- Porter, L.J. et al., J. Chem. Res., Synop., 1986, 86- 87 (pmr, conformn)
- Bonefeld, M. et al., Phytochemistry, 1986, 25, 1205- 1207 (3-rhamnoside) [https://doi.org/10.1016/S0031-9422(00)81581-2]
- Perrissoud, D., Prog. Clin. Biol. Res., 1986, 213, 559- 569 (rev, pharmacol)
- Hashimoto, F. et al., Chem. Pharm. Bull., 1987, 35, 611- 616 (oolong tea epicatechin derivs) [https://doi.org/10.1248/cpb.35.611]
- Ishimaru, K. et al., Phytochemistry, 1987, 26, 1167- 1170 (3-glucoside, 3-rhamnoside) [https://doi.org/10.1016/S0031-9422(00)82371-7]
- Malan, E. et al., Phytochemistry, 1987, 26, 2049- 2051 (Acacia gerrardii constits) [https://doi.org/10.1016/S0031-9422(00)81756-2]
- Foo, L.Y. et al., Phytochemistry, 1987, 26, 2825- 2830 (Phylloflavan, (-)-Epicatechin) [https://doi.org/10.1016/S0031-9422(00)83598-0]
- Yamazaki, M. et al., Yakugaku Zasshi, 1987, 107, 914- 916 (Artocarpus integra constit) [https://doi.org/10.1248/yakushi1947.107.11_914]
- Kiehlmann, E. et al., Magn. Reson. Chem., 1988, 26, 204- 210 (cmr)
- Son, B.W. et al., Arch. Pharmacal Res., 1989, 12, 219- 222 (Uldavioside)
- Morisaka, N. et al., J. Nat. Prod., 1989, 52, 1221- 1226 (3-Galloylcatechin, isol)
- Law, K.-H. et al., Phytochemistry, 1989, 28, 1099- 1100 (Uncaria elliptica constit) [https://doi.org/10.1016/0031-9422(89)80191-8]
- Foo, L.Y. et al., Phytochemistry, 1989, 28, 1237- 1240 (Pseudotsuga menziesii constit,Epicatechin 7-glucoside)
- Nakane, H., Biochemistry, 1990, 29, 2841- 2845 (Epicatechin gallate, anti-HIV activity) [https://doi.org/10.1021/bi00463a029]
- Malan, E., Phytochemistry, 1990, 29, 1334- 1335 (Acacia gerrardii constit) [https://doi.org/10.1016/0031-9422(90)85459-S]
- Rossouw, W. et al., Tetrahedron, 1990, 50, 12477- 12488 (pmr, abs config) [https://doi.org/10.1016/S0040-4020(01)89554-5]
- Urano, M. et al., J. Het. Chem., 1991, 28, 1845- 1847 (synth)
- Malan, E., Phytochemistry, 1991, 30, 2737- 2739 (Acacia nilotica constits) [https://doi.org/10.1016/0031-9422(91)85134-L]
- Jin, Q.D. et al., Yaoxue Xuebao, 1991, 26, 841- 845 (Epigeoside)
- Cui, C.B. et al., Chem. Pharm. Bull., 1992, 40, 2035- 2040 (Epicatechin 5-glucoside) [https://doi.org/10.1248/cpb.40.2035]
- Lee, M.W. et al., Phytochemistry, 1992, 31, 2117- 2120 (Pithecellobium lobatum constits)
- Martindale, The Extra Pharmacopoeia, 30th edn., Pharmaceutical Press, 1993, 1353
- Shen, C.-C. et al., Phytochemistry, 1993, 34, 843- 845 (pmr, cmr) [https://doi.org/10.1016/0031-9422(93)85370-7]
- Bae, Y.S. et al., Phytochemistry, 1994, 35, 473- 478 (Catechin 3-rutinoside) [https://doi.org/10.1016/S0031-9422(00)94785-X]
- 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]
- Pan, H. et al., Phytochemistry, 1995, 39, 1423- 1428 (3'-O-Methylcatechin 7-glucoside) [https://doi.org/10.1016/0031-9422(95)00144-V]
- Davis, A.L. et al., Magn. Reson. Chem., 1996, 34, 887- 890 (pmr, cmr, gallates)
- Pan, H. et al., Phytochemistry, 1996, 42, 1185- 1189 (3'-O-Methylcatechin) [https://doi.org/10.1016/0031-9422(96)00122-7]
- Bilia, A.R. et al., Phytochemistry, 1996, 43, 887- 892 (7-O-Methylcatechin) [https://doi.org/10.1016/0031-9422(96)00291-9]
- Seto, R. et al., Biosci., Biotechnol., Biochem., 1997, 61, 1434- 1439 (tea catechins)
- Van Rensberg, H. et al., Tet. Lett., 1997, 38, 3089- 3092 (synth, Catechin isomers) [https://doi.org/10.1016/S0040-4039(97)00552-2]
- 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]
- Miketova, P. et al., J. Nat. Prod., 1998, 61, 461- 467 (Catechins, ms) [https://doi.org/10.1021/np9703959]
- Ferrari, F. et al., Phytochemistry, 1998, 47, 1165- 1166 (Epicatechin 5-xyloside) [https://doi.org/10.1016/S0031-9422(98)80094-0]
- Zhang, H.L. et al., Phytochemistry, 1998, 48, 665- 668 (Gossypium hirsutum constit) [https://doi.org/10.1016/S0031-9422(98)00075-2]
- Nakao, M. et al., Phytochemistry, 1998, 49, 2379- 2382 (Catechins, Epicatechin gallate,activity) [https://doi.org/10.1016/S0031-9422(98)00333-1]
- Xiong, Q. et al., Planta Med., 2000, 66, 127- 133 (2R,3S-form) [https://doi.org/10.1055/s-2000-11135]
- Nay, B. et al., Tet. Lett., 2000, 41, 9049- 9051 (synth) [https://doi.org/10.1016/S0040-4039(00)01649-X]
- Kinjo, J. et al., Biol. Pharm. Bull., 2001, 24, 1443- 1445 (7-Galloylcatechin, activity) [https://doi.org/10.1248/bpb.24.1443]
- Otsuka, H. et al., Chem. Pharm. Bull., 2001, 49, 921- 923 (Glochiflavanosides) [https://doi.org/10.1248/cpb.49.921]
- Hwang, B.Y. et al., J. Nat. Prod., 2001, 64, 82- 84 ((-)-Epicatechin, 3-Benzoylepicatechin 5-glucoside, activity) [https://doi.org/10.1021/np000251l]
- Akdemir, Z.S. et al., Phytochemistry, 2001, 56, 189- 193 (6-Chloroepicatechin) [https://doi.org/10.1016/S0031-9422(00)00367-8]
- Demirezer, L.O. et al., Phytochemistry, 2001, 58, 1213- 1217 (6-chloro) [https://doi.org/10.1016/S0031-9422(01)00337-5]
- Su, B.-N. et al., J. Nat. Prod., 2002, 65, 163- 169 (2R,3S-form)
- Qi, S.-H. et al., Acta Bot. Sin., 2003, 45, 1129- 1133 (3-3,5-Dimethylgalloylepicatechin)
- Lokvam, J. et al., Phytochemistry, 2004, 65, 351- 358 (3-cinnamoylglycosides) [https://doi.org/10.1016/j.phytochem.2003.11.012]
- Gao, S. et al., Planta Med., 2004, 70, 1128- 1134 (Lysidicichin, activity) [https://doi.org/10.1055/s-2004-835839]
- Flavonoids: Chemistry and Biochemistry, (ed. Andersen, O.M. et al), CRC Press, 2005
- 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]
- Bekker, M. et al., Phytochemistry, 2006, 67, 818- 823 (Epicatechin 7-xyloside) [https://doi.org/10.1016/j.phytochem.2006.01.015]
- Iida, N. et al., Chem. Biodiversity, 2007, 4, 32- 42 (3'-Me 5-glucoside, 4'-Me 5-glucoside)
- Li, D.-L. et al., Molecules, 2007, 12, 1163- 1169 (3-Acetylepicatechin, 3,7-Diacetylepicatechin, Pentaacetylepicatechin)
- Kofink, M. et al., Molecules, 2007, 12, 1274- 1288 (cocoa, occur)
- Dib, M.A. et al., Asian J. Chem., 2008, 20, 3926- 3934 (Arbutus 3-4-hydroxybenzoate)
- Ölschläger, C. et al., Phytochemistry, 2008, 69, 1389- 1397 (3-(3,4-Dimethylgalloyl)epicatechin) [https://doi.org/10.1016/j.phytochem.2008.01.001]
- Ramanandraibe, V. et al., Planta Med., 2008, 74, 417- 421 (5-Galloylcatechin, 7-Galloylcatechin, activity) [https://doi.org/10.1055/s-2008-1034328]
- Kim, H.J. et al., Fitoterapia, 2009, 80, 73- 76 (Epicatechin gallates, activity) [https://doi.org/10.1016/j.fitote.2008.10.003]
- Nishanbaev, S.Z. et al., Chem. Nat. Compd. (Engl. Transl.), 2010, 46, 357- 362 (Epicatechin)
- Rinaldo, D. et al., Chirality, 2010, 22, 726- 733 (Catechin, ent-Catechin, Epicatechin, ent-Epicatechin, cd, sepn)
- Tian, L.-W. et al., Helv. Chim. Acta, 2010, 93, 2194- 2202 (7-O-Methylcatechin 5-glucoside)
- Schmidt, C.A. et al., J. Nat. Prod., 2010, 73, 2035- 2041 (Symplocosidin, activity) [https://doi.org/10.1021/np100523s]
- Meng, D. et al., Phytochemistry, 2010, 71, 325- 331 (Breynia fruticosa 3-acetylepicatechins) [https://doi.org/10.1016/j.phytochem.2009.10.002]
- 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]
- Zhang, D. et al., Eur. J. Med. Chem., 2011, 46, 4548- 4558 (Epicatechin, activity) [https://doi.org/10.1016/j.ejmech.2011.07.031]
- Ivanov, S.A. et al., Fitoterapia, 2011, 82, 212- 218 (3,5-Digalloylcatechin) [https://doi.org/10.1016/j.fitote.2010.09.013]
- Chira, K. et al., Molecules, 2011, 16, 1519- 1532 (grape constits) [https://doi.org/10.3390/molecules16021519]
- Wungsintaweekul, B. et al., Phytochemistry, 2011, 72, 495- 502 (ent-Catechin, activity) [https://doi.org/10.1016/j.phytochem.2010.12.018]
- 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]
- Dong, Y. et al., Chem. Biodiversity, 2012, 9, 68- 79 (Epicatechin, activity)
- Stadlbauer, S. et al., Chem. Comm., 2012, 48, 8425- 8427 (synth)
- Wu, X.-D. et al., Fitoterapia, 2012, 83, 1068- 1071 (Malaferins B,C)
- Al-Taweel, A.M. et al., Fitoterapia, 2012, 83, 1610- 1615 (5-gallate) [https://doi.org/10.1016/j.fitote.2012.09.010]
- Agbo, M.O. et al., Fitoterapia, 2013, 86, 78- 83 (Tri-O-methylgalloylepicatechin) [https://doi.org/10.1016/j.fitote.2013.02.006]
- Qiu, L. et al., Phytochem. Lett., 2013, 6, 368- 371 (3-Nitropropanoylepicatechin) [https://doi.org/10.1016/j.phytol.2013.04.010]
- Hosny, M. et al., Arch. Pharmacal Res., 2014, 37, 698- 705 (Ulmus davidiana constits)
- Wang, N. et al., Molecules, 2014, 19, 6623- 6634 (3',7-di-Me ether 5-glucoside, activity, rel config)
- Şöhretoğlu, D. et al., Rec. Nat. Prod., 2014, 8, 323- 329 (8-Chlorocatechin)
- Liu, F. et al., Phytochemistry, 2015, 110, 150- 159 (3-Curvulinoylepicatechin, 3-Caffeoylepicatechin) [https://doi.org/10.1016/j.phytochem.2014.12.007]
- Jin, H.-G. et al., Arch. Pharmacal Res., 2016, 39, 755- 761 (Symplocoside)
- Sax's Dangerous Properties of Industrial Materials, 11th edn., J. Wiley, 2004, CCP875 (Catechin)