Secondary Metabolites of Medicinal Plants. Bharat SinghЧитать онлайн книгу.
of alphatocopherol and pigments in callus and cell suspension cultures of Carthamus tinctorius L. World J. Pharm. Res. 4: 1734–1742.
7 Fan, L., Zhao, H.Y., Xu, M. et al. (2009). Qualitative evaluation and quantitative determination of 10 major active components in Carthamus tinctorius L. by high-performance liquid chromatography coupled with diode array detector. J. Chromatogr. A 1216: 2063–2070.
8 Fan, L., Zhao, H.-Y., Pu, R. et al. (2011). Study on flavonoids in the flower of Carthamus tinctorius L. Chin. Pharm. J. 46: 333–337.
9 Farshadfar, E., Elyasi, P., and Aghaee, M. (2012). In vitro selection for drought tolerance in common wheat (Triticum aestivum L.) genotypes by mature embryo culture. Am. J. Sci. Res. 48: 102–115.
10 Gawande, N.D., Mahurkar, D.G., Rathod, T.H. et al. (2005). In vitro screening of wheat genotypes for drought tolerance. Ann. Plant Physiol. 19: 162–168.
11 Hassan, N.M., Serag, M.S., and El-Feky, F.M. (2004). Changes in nitrogen content and protein profiles following in vitro selection of NaCl resistant mung bean and tomato. Acta Physiol. Plant. 26: 165–175.
12 Kakaei, M., Mansouri, M., Abdollahi, M.R., and Moradi, F. (2013). Effect of NaCl and PEG induced osmotic stress on callus growth parameters of two safflower (Carthamus tinctorius L.) cultivars. Int. J. Agric. Crop Sci. 6: 127–132.
13 Karakaya, A., Başalma, D., and Uranbey, S. (2004). Response of safflower (Carthamus tinctorius L.) genotypes to rust disease. Tarim Bilim. Derg. 10: 93–95.
14 Knowles, P.F. (1989). Safflower. In: Oil Crops of the World (eds. R.K. Downey, G. Robellen and A. Ashri), 363–374. New York, NY: McGraw-Hill.
15 Kurkin, V.A. and Kharisova, A.V. (2014). Flavonoids of Carthamus tinctorius flowers. Chem. Nat. Compd. 50: 446–448.
16 Li, Y. and Che, Q. (1998). Studies on chemical components of Carthamus tinctorius petals. Yao Xue Xue Bao 33: 626–628.
17 Li, F., He, Z.-S., and Ye, Y. (2002). Flavonoids from Carthamus tinctorius. Chin. J. Chem. 20: 699–702.
18 Mahmood, I., Razzaq, A., Ashraf, M. et al. (2012). In vitro selection of tissue culture induced somaclonal variants of wheat for drought tolerance. J. Agric. Res. 50: 177–188.
19 Namjooyan, S., Khavari-Nejad, R., Bernard, F. et al. (2012). The effect of cadmium on growth and antioxidant responses in the safflower (Carthamus tinctorius L.) callus. Turk. J. Agric. For. 36: 145–152.
20 Nikam, T.D. and Shitole, M.G. (1998). In vitro culture of Safflower L. cv. Bhima: initiation, growth optimization and organogenesis. Plant Cell Tissue Organ Cult. 55: 15–22.
21 Saito, K., Daimon, E., Kusaka, K. et al. (1988). Accumulation of a novel red pigment in cell suspension cultures of floral meristem tissues from Carthamus tinctorius L. Z. Naturforsch. 43c: 862–870.
22 Saito, K., Kanehira, T., Horimoto, M. et al. (1993). Biosynthesis of carthamin in florets and cultured cells of Carthamus tinctorius. Biol. Planta 35: 537–546.
23 Shabani, A., Sepaskhah, A.R., and Kamgar-Haghighi, A.A. (2013). Growth and physiologic response of rapeseed (Brassica napus L.) to deficit irrigation, water salinity and planting method. Int. J. Plant Prod. 7: 569–596.
24 Shirwaikar, A., Khan, S., Kamariya, Y.H. et al. (2010). Medicinal plants for the management of postmenopausal osteoporosis: a review. Open Bone J. 2: 1–13.
25 Tayefi-Nasrabadi, H., Dehghan, G., Daeihassani, B. et al. (2011). Some biochemical properties of catalase from safflower (Carthamus tinctorius L. cv. M-CC-190). Afr. J. Agric. Res. 6: 5221–5226.
26 Wang, G. and Li, Y. (1985). Clinical application of safflower (Carthamus tinctorius). Zhejiang Tradit. Chin. Med. Sci. J. 1: 42–43.
27 Yamamoto, H. (1980). Effect of berberine on growth of the callus cultures of several species. Shokubutsu-Gaku-Zasshi 93: 307–315.
28 Yao, D., Wang, Z., Miao, L., and Wang, L. (2016). Effects of extracts and isolated compounds from safflower on some index of promoting blood circulation and regulating menstruation. J. Ethnopharmacol. 191: 264–272.
29 Yue, S., Tang, Y., Li, S., and Duan, J.-A. (2013). Chemical and biological properties of quinochalcone C-glycosides from the florets of Carthamus tinctorius. Molecules 18: 15220–15254.
30 Yue, S.J., Tang, Y.P., Wang, L.Y. et al. (2014). Separation and evaluation of antioxidant constituents from Carthamus tinctorius. Zhongguo Zhong Yao Za Zhi 39: 3295–3300.
31 Yue, S.J., Qu, C., Zhang, P.X. et al. (2016). Carthorquinosides A and B, quinochalcone C-glycosides with diverse dimeric skeletons from Carthamus tinctorius. J. Nat. Prod. 79: 2644–2651.
32 Zair, I., Chlyah, A., Sabounji, K. et al. (2003). Salt tolerance improvement in some wheat cultivars after application of in vitro selection pressure. Plant Cell Tissue Organ Cult. 73: 237–244.
33 Zhou, Y.Z., Ma, H.Y., Chen, H. et al. (2006). New acetylenic glucosides from Carthamus tinctorius. Chem. Pharm. Bull. 54: 1455–1456.
34 Zhou, Y.Z., Chen, H., Qiao, L. et al. (2008). Two new compounds from Carthamus tinctorius. J. Asian Nat. Prod. Res. 10: 429–433.
35 Zhou, F.R., Zhao, M.B., and Tu, P.F. (2009). Simultaneous determination of four nucleosides in Carthamus tinctorius L. and safflower injection using high-performance liquid chromatography. J. Chin. Pharm. Sci. 18: 326–330.
2.22 Cassia Species
2.22.1 Ethnopharmacological Properties and Phytochemistry
Cassia tora Linn. (Fam. – Caesalpiniaceae) is a well-known medicinal plant commonly found in India and other tropical countries (Nadkarni 1954). Various medicinal properties have been attributed to this plant in the traditional system of Indian medicine. Several anthraquinones have been isolated from the seeds of C. tora (Shibata et al. 1969; Raghunathan et al. 1974). Sennosides, which are well known for their medicinal importance, have been detected in the leaves of the plants (Lohar et al. 1975). The extracts of C. tora have been used as a remedy for various skin ailments and rheumatic disease and as laxatives (Kirtikar and Basu 1975a; Jain 1968). The extract of C. tora leaves has been found to possess significant hepatoprotective activity and anti-inflammatory activity (Maitya et al. 1997, 1998).
The chrysoeriol-7-O-(2″-O-β-D-mannopyranosyl)-β-D-allopyranoside and rhamnetin-3-O-(2″-O-β-D-mannopyranosyl)-β-D-allopyranoside were separated from the seeds of Cassia alata (Gupta and Singh 1991). Luteolin-7-O-β-glucopyranoside, quercetin-3-O-β-D-glucuronide, and formononetin-7-O-β-D-glucoside were isolated from the ethanol extract of C. tora leaves (Vijayalakshmi and Madhira 2014). The phenolic, proanthocyanidin, and flavonoid-rich extracts of Cassia fistula showed antioxidant activity (Luximon-Ramma et al. 2002). The Cassia species showed antioxidant activity against 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical scavenging, metal chelating activity, phosphomolybdenum-reducing power, hydrogen peroxide radical scavenging, hydroxyl radical scavenging, deoxyribose degradation, and β-carotene bleaching models (Kolar et al. 2018).
The seeds of Cassia absu showed the presence of linoleic acid, luteolin, palmitic acid, stearic acid, and arachidic acid, and their identities were confirmed by HPLC–DAD analysis (Zribi et al. 2017). The cassgranon D, rutin, afzelin, quercitrin, epicatechin, (−)-epiafzelechin, isoquercitrin, and aloe emodin were isolated from the ethyl acetate and methanol extracts of leaf of Cassia grandis. This plant species is also used for the treatment of skin disorders, back pain, and aches (Trinh et al. 2017). The fistula flavonoids B and C were isolated from the bark and stems of C. fistula (Zhao et al. 2013; Bahorun et al. 2005) and the ethyl acetate fraction of pods C. fistula showed anticonvulsant and anxiolytic activities (Kalaiyarasia et al. 2015).
The (−)-3-O-acetylspectaline, (−)-7-hydroxyspectaline, (−)-7-hydroxycassine, iso-6-spectaline, 3-O-acetylspectaline, (−)-cassine, (−)-spectaline, (−)-3-O-acetylspectaline, (−)-3-O-acetylspectaline, (−)-7-hydroxyspectaline,