Wednesday, July 11, 2018
Withania somnifera Published articles अश्वगंधा அமுக்கிரா అశ్వగంధ ಅಶ್ವಗಂಧಾ അമുക്കുരം અશ્વગંધા ਅਸ਼ਵਗੰਧਾ
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http://medplants.blogspot.com/2018/07/withania-somnifera.html
1. Vinay, K., N.A. Gajbhiye, and P. Manivel, Assessment of the genetic diversity of Ashwagandha (Withania somnifera L. Dunal) using agro-morphological, phytochemical and molecular markers. Research Journal of Biotechnology, 2018. 13(7): p. 59-68.
2. Sudeep, H.V., et al., Viwithan, a Standardized Withania somnifera Root Extract Induces Apoptosis in Murine Melanoma Cells. Pharmacognosy magazine, 2018. 13(Suppl 4): p. S801-S806.
3. Srivastava, S., et al., Comparative Study of Withanolide Biosynthesis-Related miRNAs in Root and Leaf Tissues of Withania somnifera. Applied biochemistry and biotechnology, 2018.
4. Srivastava, A., et al., Genetic variability, associations, and path analysis of chemical and morphological traits in Indian ginseng Withania somnifera (L.) Dunal for selection of higher yielding genotypes. Journal of Ginseng Research, 2018. 42(2): p. 158-164.
5. Sood, A., et al., Indian Ginseng (Withania somnifera) supplementation ameliorates oxidative stress and mitochondrial dysfunctions in experimental model of stroke. Metabolic brain disease, 2018.
6. Singh, R., et al., Modulations in primary and secondary metabolic pathways and adjustment in physiological behaviour of Withania somnifera under drought stress. Plant science : an international journal of experimental plant biology, 2018. 272: p. 42-54.
7. Shasmita, M.K. Rai, and S.K. Naik, Exploring plant tissue culture in Withania somnifera (L.) Dunal: in vitro propagation and secondary metabolite production. Critical Reviews in Biotechnology, 2018. 38(6): p. 836-850.
8. Sharma, R., et al., Adaptive physiological response, carbon partitioning, and biomass production of Withania somnifera (L.) Dunal grown under elevated CO2 regimes. 3 Biotech, 2018. 8(6).
9. Sengupta, P., et al., Role of Withania somnifera (Ashwagandha) in the management of male infertility. Reproductive Biomedicine Online, 2018. 36(3): p. 311-326.
10. Sathiyabama, M. and R. Parthasarathy, Withanolide production by fungal endophyte isolated from Withania somnifera. Natural Product Research, 2018. 32(13): p. 1573-1577.
11. Pandey, S.S., et al., Endophytes of Withania somnifera modulate in planta content and the site of withanolide biosynthesis. Scientific Reports, 2018. 8.
12. Pandey, A., et al., Multifunctional neuroprotective effect of Withanone, a compound from Withania somnifera roots in alleviating cognitive dysfunction. Cytokine, 2018. 102: p. 211-221.
13. Nasimi Doost Azgomi, R., et al., Comparative evaluation of the effects of Withania somnifera with pentoxifylline on the sperm parameters in idiopathic male infertility: A triple-blind randomised clinical trial. Andrologia, 2018: p. e13041-e13041.
14. Naidoo, D.B., et al., Withania somnifera modulates cancer cachexia associated inflammatory cytokines and cell death in leukaemic THP-1 cells and peripheral blood mononuclear cells (PBMC's). Bmc Complementary and Alternative Medicine, 2018. 18.
15. Mishra, A., et al., Endophyte-Mediated Modulation of Defense-Related Genes and Systemic Resistance in Withania somnifera (L.) Dunal under Alternaria alternata Stress. Applied and Environmental Microbiology, 2018. 84(8).
16. Mishra, A., et al., Bacterial endophytes modulates the withanolide biosynthetic pathway and physiological performance in Withania somnifera under biotic stress. Microbiological research, 2018. 212-213: p. 17-28.
17. Mahrous, R.S.R., et al., Validated thin-layer chromatographic method for the identification and monitoring of the effect of the extraction method on the yield and phytochemical constituents of Egyptian Withania somnifera leaves. Journal of Separation Science, 2018. 41(2): p. 518-524.
18. Lim, D.W., et al., Antihyperalgesic effects of ashwagandha (Withania somnifera root extract) in rat models of postoperative and neuropathic pain. Inflammopharmacology, 2018. 26(1): p. 207-215.
19. Kumar, S., et al., Extraction Optimization for Phenolic- and Withanolide-Rich Fractions from Withania somnifera Roots: Identification and Quantification of Withaferin A, 12-Deoxywithastromonolide, and Withanolide A in Plant Materials and Marketed Formulations Using a Reversed-Phase HPLC-Photodiode Array Detection Method. Journal of AOAC International, 2018.
20. Kumar, R., et al., Comparative study of effect of Withania somnifera as an adjuvant to DOTS in patients of newly diagnosed sputum smear positive pulmonary tuberculosis. The Indian journal of tuberculosis, 2018. 65(3): p. 246-251.
21. Johny, L., et al., Growth kinetics and withanolide production in novel transformed roots of Withania somnifera and measurement of their antioxidant potential using chemiluminescence. Plant Cell Tissue and Organ Culture, 2018. 132(3): p. 479-495.
22. Jain, J., et al., In Vivo Evaluation of Withania somnifera-Based Indian Traditional Formulation ( Amukkara Choornam), Against Chikungunya Virus-Induced Morbidity and Arthralgia. Journal of evidence-based integrative medicine, 2018. 23: p. 2156587218757661-2156587218757661.
23. Hameed, A. and N. Akhtar, Comparative chemical investigation and evaluation of antioxidant and tyrosinase inhibitory effects of Withania somnifera (L.) Dunal and Solanum nigrum (L.) berries. Acta Pharmaceutica, 2018. 68(1): p. 47-60.
24. Gupta, M. and G. Kaur, Withania somnifera as a Potential Anxiolytic and Anti-inflammatory Candidate Against Systemic Lipopolysaccharide-Induced Neuroinflammation. Neuromolecular medicine, 2018.
25. George, B.S., et al., Characterization of an Insecticidal Protein from Withania somnifera Against Lepidopteran and Hemipteran Pest. Molecular Biotechnology, 2018. 60(4): p. 290-301.
26. Elhadidy, M.E., et al., Protective effect of ashwagandha (Withania somnifera) against neurotoxicity induced by aluminum chloride in rats. Asian Pacific Journal of Tropical Biomedicine, 2018. 8(1): p. 59-66.
27. Deshpande, A., N. Irani, and R. Balakrishnan, Study protocol and rationale for a prospective, randomized, double-blind, placebo-controlled study to evaluate the effects of Ashwagandha (Withania somnifera) extract on nonrestorative sleep. Medicine, 2018. 97(26): p. e11299-e11299.
28. Caputi, F.F., et al., The standardized Withania somnifera Dunal root extract alters basal and morphine-induced opioid receptor gene expression changes in neuroblastoma cells. Bmc Complementary and Alternative Medicine, 2018. 18.
29. Azgomi, R.N.D., et al., Effects of Withania somnifera on Reproductive System: A Systematic Review of the Available Evidence. Biomed Research International, 2018.
30. Alrashidi, A.A., E.A. Kalashnikova, and R.N. Kirakosyan, THE PREPARATION AND CHARACTERIZATION OF SUSPENSION CELL CULTURES OF WITHANIA SOMNIFERA L. Voprosy biologicheskoi, meditsinskoi i farmatsevticheskoi khimii, 2018. 21(3): p. 32-36.
31. Akhtar, R. and A. Javaid, BIOLOGICAL MANAGEMENT OF BASAL ROT OF ONION BY Trichoderma harzianum AND Withania somnifera. Planta Daninha, 2018. 36.
32. Ahmed, W., et al., Antioxidant activity and apoptotic induction as mechanisms of action of Withania somnifera (Ashwagandha) against a hepatocellular carcinoma cell line. Journal of International Medical Research, 2018. 46(4): p. 1358-1369.
33. Agarwal, A.V., et al., Virus-Induced Silencing of Key Genes Leads to Differential Impact on Withanolide Biosynthesis in the Medicinal Plant, Withania somnifera. Plant and Cell Physiology, 2018. 59(2): p. 262-274.
34. Abul Qais, F., Samreen, and I. Ahmad, Broad-spectrum inhibitory effect of green synthesised silver nanoparticles from Withania somnifera (L.) on microbial growth, biofilm and respiration: a putative mechanistic approach. Iet Nanobiotechnology, 2018. 12(3): p. 325-335.
35. Zaka, M., et al., Comparative in silico analyses of Cannabis sativa, Prunella vulgaris and Withania somnifera compounds elucidating the medicinal properties against rheumatoid arthritis. Journal of Molecular Graphics & Modelling, 2017. 74: p. 296-304.
36. Trivedi, M.K., et al., Metabolite Profiling in Withania somnifera Roots Hydroalcoholic Extract Using LC/MS, GC/MS and NMR Spectroscopy. Chemistry & Biodiversity, 2017. 14(3).
37. Trivedi, M.K., et al., Immunomodulatory properties and biomarkers characterization of novel Withania somnifera based formulation supplemented with minerals in Sprague Dawley rats. Oriental Pharmacy and Experimental Medicine, 2017. 17(1): p. 59-69.
38. Tripathi, S., et al., Transcription factor repertoire in Ashwagandha (Withania somnifera) through analytics of transcriptomic resources: Insights into regulation of development and withanolide metabolism. Scientific Reports, 2017. 7.
39. Tripathi, C.D.P., et al., Withania somnifera chemotype NMITLI 101R significantly increases the efficacy of antileishmanial drugs by generating strong IFN-gamma and IL-12 mediated immune responses in Leishmania donovani infected hamsters. Phytomedicine, 2017. 24: p. 87-95.
40. Thakur, S., et al., Nutritional enrichment of broiler breast meat through dietary supplementation of Indian ginseng Withania somnifera and synbiotic substances under semi-arid climatic conditions. Veterinary World, 2017. 10(11): p. 1301-1306.
41. Tarique, A., et al., Preventive role of Withania somnifera on hyperlipidemia and cardiac oxidative stress in streptozotocin induced type 2 diabetic rats. Tropical Journal of Pharmaceutical Research, 2017. 16(1): p. 119-125.
42. Takshak, S. and S.B. Agrawal, Exogenous application of IAA alleviates effects of supplemental ultraviolet-B radiation in the medicinal plant Withania somnifera Dunal. Plant Biology, 2017. 19(6): p. 904-916.
43. Takshak, S. and S.B. Agrawal, Effect of supplemental ultraviolet-B radiation on Withania somnifera L. (Dunal): An appraisal of morphological, physiological and biochemical characteristics. Indian Journal of Experimental Biology, 2017. 55(12): p. 845-852.
44. Sumaira, A., et al., Current status of Withania somnifera (L.) dunal: an endangered medicinal plant from Himalaya. American Journal of Plant Sciences, 2017. 8(5): p. 1159-1169.
45. Sood, A. and R. Sandhir, Neuroprotective potential of Withania somnifera prophylaxis in experimental stroke reasearch. Cerebrovascular Diseases, 2017. 43.
46. Solanki, S. and D. Basudeb, First report of leaf spot of Aswagandha (Withania somnifera Dunal) caused by Colletotrichum gloeosporioides from West Bengal, India. Journal of Mycopathological Research, 2017. 55(3): p. 257-259.
47. Singla, M., et al., Impact of Ashwagandha (Withania somnifera) supplementation on the performance of Beetal kids under stall-fed conditions. Indian Journal of Animal Research, 2017. 51(6): p. 1086-1090.
48. Singh, V., et al., Leaf spot disease adversely affects human health-promoting constituents and withanolide biosynthesis in Withania somnifera (L.) Dunal. Journal of Applied Microbiology, 2017. 122(1): p. 153-165.
49. Singh, V., et al., Changes in the leaf proteome profile of Withania somnifera (L.) Dunal in response to Alternaria alternata infection. Plos One, 2017. 12(6).
50. Singh, P., et al., Addressing Challenges to Enhance the Bioactives of Withania somnifera through Organ, Tissue, and Cell Culture Based Approaches. Biomed Research International, 2017.
51. Singh, M.K., et al., Effect of dietary supplementation of Ashwagandha (Withania somnifera) and Selenium on growth performance and carcass quality of broilers. Asian Journal of Animal Science, 2017. 12(2): p. 129-133.
52. Singh, M. and C. Ramassamy, In vitro screening of neuroprotective activity of Indian medicinal plant Withania somnifera. Journal of Nutritional Science, 2017. 6.
53. Singh, G., et al., Sterol glycosyltransferases required for adaptation of Withania somnifera at high temperature. Physiologia Plantarum, 2017. 160(3): p. 297-311.
54. Singh, G., et al., Effect of antioxidant protection system on regeneration potential of different chemotypes of Withania somnifera (L.) Dunal-A comparative analysis. Indian Journal of Experimental Biology, 2017. 55(4): p. 242-250.
55. Singh, A.K., et al., A WRKY transcription factor from Withania somnifera regulates triterpenoid withanolide accumulation and biotic stress tolerance through modulation of phytosterol and defense pathways. New Phytologist, 2017. 215(3): p. 1115-1131.
56. Sharma, D., V. Roy, and A. Saraf, An Update on Phytochemicals Analysis and Medicinal Prospects of Indian Herb Withania somnifera. Ambient Science, 2017. 4(2).
57. Shah, R.A., et al., EVALUATION OF ANTIDIABETIC POTENTIAL OF WITHANIA SOMNIFERA BY GLUCOSE UPTAKE ASSAY ON 3T3 F442A FIBROBLAST (ADIPOCYTE) CELLS. International Journal of Pharmaceutical Sciences and Research, 2017. 8(1): p. 120-125.
58. Shaffi, M. and K. Gurcharan, Withania somnifera leaf alleviates cognitive dysfunction by enhancing hippocampal plasticity in high fat diet induced obesity model. BMC Complementary and Alternative Medicine, 2017. 17(136): p. (3 March 2017)-(3 March 2017).
59. Saykally, J.N., et al., Withania somnifera Extract Protects Model Neurons from In Vitro Traumatic Injury. Cell Transplantation, 2017. 26(7): p. 1193-1201.
60. Saxena, P., et al., Gene expression analysis of the withanolide biosynthetic pathway in hairy root cultures of Withania somnifera elicited with methyl jasmonate and the fungus Piriformospora indica. Symbiosis, 2017. 71(2): p. 143-154.
61. Reddy, K.B. and R.K. Jat, Isolation and characterization of Withaferin-A from the Withania somnifera (Ashwagandha). Journal of Drug Delivery and Therapeutics, 2017. 7(1): p. 65-69.
62. Razdan, S., et al., Molecular characterization of DWF1 from Withania somnifera (L.) Dunal: its implications in withanolide biosynthesis. Journal of Plant Biochemistry and Biotechnology, 2017. 26(1): p. 52-63.
63. Raju, S.K., et al., A study on the anticonvulsant activity of Withania somnifera (Dunal) in albino rats. National Journal of Physiology, Pharmacy and Pharmacology, 2017. 7(1): p. 17-21.
64. Pradhan, R., et al., Longevity and healthy ageing genes FOXO3A and SIRT3: Serum protein marker and new road map to burst oxidative stress by Withania somnifera. Experimental Gerontology, 2017. 95: p. 9-15.
65. Pandey, V., et al., Withania somnifera : Advances and Implementation of Molecular and Tissue Culture Techniques to Enhance Its Application. Frontiers in Plant Science, 2017. 8.
66. Pal, S., et al., Nitrogen treatment enhances sterols and withaferin A through transcriptional activation of jasmonate pathway, WRKY transcription factors, and biosynthesis genes in Withania somnifera (L.) Dunal. Protoplasma, 2017. 254(1): p. 389-399.
67. Nikhil, M., et al., Effect of integrated nutrient management on growth, yield and quality of Ashwagandha (Withania somnifera (L.) Dunal.). Environment and Ecology, 2017. 35(4B): p. 3206-3210.
68. Mukherjee, S., G. Kumar, and R. Patnaik, Identification of potential inhibitors of PARP-1, a regulator of caspase-independent cell death pathway, from Withania somnifera phytochemicals for combating neurotoxicity: A structure-based in-silico study. Journal of Theoretical & Computational Chemistry, 2017. 16(7).
69. Mishra, S.K., B.A. Venkatachalapathy, and H.M. Khanli, Safety and efficacy of Ashwagandha (Withania somnifera). Neuroprotective natural products: clinical aspects and mode of action, ed. G. Brahmachari. 2017. 313-319.
70. Mishra, M.K., et al., Overexpression of Withania somnifera SGTL1 gene resists the interaction of fungus Alternaria brassicicola in Arabidopsis thaliana. Physiological and Molecular Plant Pathology, 2017. 97: p. 11-19.
71. Mirakzehi, M.T., S.J. Hosseini, and H. Saleh, The effects of hydroalcoholic extracts of Withania somnifera root, Withania coagulans fruit and 1,25-dihydroxycholecalciferol on immune response and small intestinal morphology of broiler chickens. Journal of Applied Animal Research, 2017. 45(1): p. 591-597.
72. Marell, P., et al., PILOT STUDY ON THE EFFECTS OF WITHANIA SOMNIFERA ON ELECTROPHYSIOLOGICAL MEASURES OF SENSORY AND COGNITIVE PROCESSING IN SCHIZOPHRENIA. Schizophrenia Bulletin, 2017. 43: p. S185-S185.
73. Manchanda, S., et al., Aqueous Leaf Extract of Withania somnifera as a Potential Neuroprotective Agent in Sleep-deprived Rats: a Mechanistic Study. Molecular Neurobiology, 2017. 54(4): p. 3050-3061.
74. Manchanda, S. and G. Kaur, Withania somnifera leaf alleviates cognitive dysfunction by enhancing hippocampal plasticity in high fat diet induced obesity model. Bmc Complementary and Alternative Medicine, 2017. 17.
75. Kumar, G. and R. Patnaik, Inhibition of Gelatinases (MMP-2 and MMP-9) by Withania somnifera Phytochemicals Confers Neuroprotection in Stroke: An In Silico Analysis. Interdisciplinary sciences, computational life sciences, 2017.
76. Kumar, G., P. Paliwal, and R. Patnaik, Withania somnifera Phytochemicals Confer Neuroprotection by Inhibition of the Catalytic Domain of Human Matrix Metalloproteinase-9. Letters in Drug Design & Discovery, 2017. 14(6): p. 718-726.
77. Kumar, G., et al., Withania somnifera phytochemicals confer neuroprotection by selective inhibition of nNos: An in silico study to search potent and selective inhibitors for human nNOS. Journal of Theoretical & Computational Chemistry, 2017. 16(5).
78. Koshy, R., et al., Determination of Withanolides in Withania somnifera by Liquid Chromatography: Single-Laboratory Validation, First Action 2015.17. Journal of AOAC International, 2017. 100(1): p. 277-279.
79. Khan, B.M., et al., Process for transformation in withania somnifera plants to increase secondary metabolite content. 2017, Council of Scientific and Industrial Research.
80. Kaushik, M.K., et al., Triethylene glycol, an active component of Ashwagandha (Withania somnifera) leaves, is responsible for sleep induction. Plos One, 2017. 12(2).
81. Kaur, T., et al., Withania somnifera as a potential anxiolytic and immunomodulatory agent in acute sleep deprived female Wistar rats. Molecular and Cellular Biochemistry, 2017. 427(1-2): p. 91-101.
82. Kaur, T. and G. Kaur, Withania somnifera ameliorates neuroinflammation caused by high fat diet consumption in rat model of obesity. Journal of Neurochemistry, 2017. 142: p. 99-99.
83. Kaur, T. and G. Kaur, Withania somnifera as a potential candidate to ameliorate high fat diet-induced anxiety and neuroinflammation. Journal of Neuroinflammation, 2017. 14.
84. Kasar, S.S., et al., A glycoprotein alpha-amylase inhibitor from Withania somnifera differentially inhibits various alpha-amylases and affects the growth and development of Tribolium castaneum. Pest Management Science, 2017. 73(7): p. 1382-1390.
85. Kamaljit, K., K. Gurpreet, and K. Ritesh, Withania somnifera: an important herb in ayurveda and indigenous medicinal system. Journal of Plant Science Research, 2017. 33(2): p. 209-222.
86. Kalra, R. and N. Kaushik, Withania somnifera (Linn.) Dunal: a review of chemical and pharmacological diversity. Phytochemistry Reviews, 2017. 16(5): p. 953-987.
87. Jeannin, J.-M., Withania somnifera. Schweizerische Zeitschrift Fuer Ganzheitsmedizin, 2017. 29(1): p. 1-1.
88. Jadaun, J.S., et al., Over-expression of DXS gene enhances terpenoidal secondary metabolite accumulation in rose-scented geranium and Withania somnifera: active involvement of plastid isoprenogenic pathway in their biosynthesis. Physiologia Plantarum, 2017. 159(4): p. 381-400.
89. Hussein, Y.A., S.S. Al-Shokair, and K.M. Ashry, Acute and sub-chronic toxicological potential of Withania somnifera extract on rats. Alexandria Journal of Veterinary Sciences, 2017. 55(2): p. 10-18.
90. Henley, A.B., et al., Withania somnifera Root Extract Enhances Chemotherapy through 'Priming'. Plos One, 2017. 12(1).
91. Hamood, A.K. and B.H. Majeed, EFFECT OF SOME PlANT GROWTH REGULATORS ON TOTAL ALKALOIDS PRODUCTION OF ASHWAGANDHA (Withania somnifera L.) In Vitro. Iraqi Journal of Agricultural Sciences, 2017. 48(3): p. 690-700.
92. Hamood, A.K. and B.H. Majeed, EFFECT OF BENZYL ADENINE AND SALICYLIC ACID ON GROWTH AND TOTAL ALKALOIDS PRODUCTION OF WETHINIA (Withania somnifera L.) In Vitro. Iraqi Journal of Agricultural Sciences, 2017. 48(1): p. 256-265.
93. Girish, C. and Y.N. Reddy, EVALUATION OF ANTIANAPHYLACTIC ACTIVITY OF VARIOUS EXTRACTS OF WITHANIA SOMNIFERA IN RATS. International Journal of Pharmaceutical Sciences and Research, 2017. 8(4): p. 1717-1722.
94. Gaur, S.K. and K. Kumar, Withania somnifera acts as a potential insect growth regulator in the polyphagous pest, Pericallia ricini. Journal of Plant Protection Research, 2017. 57(4): p. 379-388.
95. Gaur, S.K. and K. Krishna, Bioefficacy of root extracts of a medicinal plant, Withania somnifera (Dunal) against a polyphagous pest, Spodoptera litura (Fabricius) (Lepidoptera: Noctuidae). Archives of Phytopathology and Plant Protection, 2017. 50(15/16): p. 802-814.
96. Dwivedi, D., B. Yadav, and N. Sengar, Extraction and Isolation of Withaferin A (Steroidal Lactone) from Withania somnifera Leafs and It's TLC and HPLC Analysis. Oriental Journal of Chemistry, 2017. 33(3): p. 1550-1554.
97. Dutta, K., et al., Withania somnifera Reverses Transactive Response DNA Binding Protein 43 Proteinopathy in a Mouse Model of Amyotrophic Lateral Sclerosis/Frontotemporal Lobar Degeneration. Neurotherapeutics, 2017. 14(2): p. 447-462.
98. Dhanani, T., et al., Effect of extraction methods on yield, phytochemical constituents and antioxidant activity of Withania somnifera. Arabian Journal of Chemistry, 2017. 10: p. S1193-S1199.
99. Desai, C.D., et al., Effect of spacing and fertilizer levels on growth, yield and quality of Ashwagandha (Withania somnifera Dunal) cv. JA-20. International Journal of Minor Fruits, Medicinal and Aromatic Plants, 2017. 3(2): p. 8-10.
100. Dehdashti, S.M., et al., An efficient Agrobacterium rhizogenes-mediated transformation protocol of Withania somnifera. Plant Cell Tissue and Organ Culture, 2017. 128(1): p. 55-65.
101. Dar, N.J., et al., Withanone, an Active Constituent from Withania somnifera, Affords Protection Against NMDA-Induced Excitotoxicity in Neuron-Like Cells. Molecular Neurobiology, 2017. 54(7): p. 5061-5073.
102. Choudhary, D., S. Bhattacharyya, and S. Bose, Efficacy and Safety of Ashwagandha (Withania somnifera (L.) Dunal) Root Extract in ImprovingMemory and Cognitive Functions. Journal of Dietary Supplements, 2017. 14(6): p. 599-612.
103. Chinembiri, T.N., et al., Topical Delivery of Withania somnifera Crude Extracts in Niosomes and Solid Lipid Nanoparticles. Pharmacognosy Magazine, 2017. 13(51): p. S663-S671.
104. Chaudhary, S.R., et al., Organic nutrient sources influence yield and quality of ashwagandha (Withania somnifera), and soil biochemical properties. Agrochimica, 2017. 61(3): p. 221-236.
105. Chandrasekaran, S., et al., Alcoholic Fractions F5 and F6 from Withania somnifera Leaves Show a Potent Antileishmanial and Immunomodulatory Activities to Control Experimental Visceral Leishmaniasis. Frontiers in Medicine, 2017. 4.
106. Chandran, U. and B. Patwardhan, Network ethnopharmacological evaluation of the immunomodulatory activity of Withania somnifera. Journal of Ethnopharmacology, 2017. 197: p. 250-256.
107. Bhatnagar, M., et al., Complete Comparison Display (CCD) evaluation of ethanol extracts of Centella asiatica and Withania somnifera shows that they can non-synergistically ameliorate biochemical and behavioural damages in MPTP induced Parkinson's model of mice. Plos One, 2017. 12(5).
108. Balakrishnan, A.S., et al., Withania somnifera targets interleukin-8 and cyclooxygenase-2 in human prostate cancer progression. Prostate International, 2017. 5(2): p. 75-83.
109. Balakrishnan, A.S., R. Kalyanasundaram, and A.A. Nathan, THERAPEUTIC POTENTIAL OF WITHANIA SOMNIFERA IN FILARIAL INDUCED SECONDARY LYMPHEDEMA. American Journal of Tropical Medicine and Hygiene, 2017. 97(5): p. 563-563.
110. Aswani, P., et al., Characterization of bioactive metabolites of endophytic Fusarium solani isolated from Withania somnifera. Journal of Biologically Active Products from Nature, 2017. 7(6): p. 411-426.
111. Archana, K., P.M. Gangadharappa, and J.S. Hiremath, Effect of organic and inorganic sources of nutrients on root and seed yield of Ashwagandha (Withania somnifera Dunal). Environment and Ecology, 2017. 35(4D): p. 3601-3604.
112. Anwer, T., et al., Preventive role of Withania somnifera on hyperlipidemia and cardiac oxidative stress in streptozotocin induced type 2 diabetic rats. Tropical Journal of Pharmaceutical Research, 2017. 16(1): p. 119-125.
113. Anuroopa, N., et al., Inoculation with Selected Microbial Consortia Not Only Enhances Growth and Yield of Withania somnifera but also Reduces Fertilizer Application by 25% Under Field Conditions. Proceedings of the Indian National Science Academy, 2017. 83(4): p. 957-971.
114. Anuroopa, N. and D.J. Bagyaraj, Selection of an Efficient Plant Growth Promoting Rhizobacteria for Inoculating Withania Somnifera. Journal of Scientific & Industrial Research, 2017. 76(4): p. 244-248.
115. Ankad, G.M., et al., Evaluation of Kunapa jala and Pancha gavya on plant quality, physiology, biochemistry, yield and growth attributes - A case study of Withania somnifera Dun. Journal of Ayurveda and Integrative Medicine, 2017. 8(4): p. 247-251.
116. Alrashedi, A.A., A.S. Mohamed, and R.Y. Pavlikov, INFLUENCE OF CULTIVATION CONDITIONS ON CLONAL MICRO PROPAGATION OF ASHWAGANDHA (WITANIA SOMNIFERA L.). Izvestiya Timiryazevskoi Sel'skokhozyaistvennoi Akademii, 2017(3): p. 30-38.
117. Aljubory, I.S., et al., Pharmacognostical with preliminary phytochemical studies of Iraqi Aswagandha (withania somnifera L.) plant. Research Journal of Pharmaceutical Biological and Chemical Sciences, 2017. 8(2): p. 1934-1939.
118. Ahmad, M. and N.J. Dar, Withania somnifera: Ethnobotany, Pharmacology, and Therapeutic Functions. Sustained Energy for Enhanced Human Functions and Activity, ed. D. Bagchi. 2017. 137-154.
119. Ahlawat, S., et al., Comparative study of withanolide production and the related transcriptional responses of biosynthetic genes in fungi elicited cell suspension culture of Withania somnifera in shake flask and bioreactor. Plant Physiology and Biochemistry, 2017. 114: p. 19-28.
120. Agarwal, A.V., et al., Comprehensive assessment of the genes involved in withanolide biosynthesis from Withania somnifera: chemotype-specific and elicitor-responsive expression. Functional & Integrative Genomics, 2017. 17(4): p. 477-490.
121. Yenisetti, S.C., M.J. Manjunath, and C. Muralidhara, Neuropharmacological Properties of Withania somnifera - Indian Ginseng: An Overview on Experimental Evidence with Emphasis on Clinical Trials and Patents. Recent patents on CNS drug discovery, 2016. 10(2): p. 204-215.
122. Vibha and U. Anubha, Effect of bioagents on Alternaria leaf spot and withaferin content of Withania somnifera (L.) Dunal. Indian Phytopathology, 2016. 69(4s): p. 333-337.
123. Vasantharaja, R. and J.R. Subramaniam, Withania somnifera root extract enhances telomerase activity in the human HeLa cell line. Advances in Bioscience and Biotechnology, 2016. 7(4): p. 199-204.
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500. Sivanandhan, G., et al., Increased production of withanolide A, withanone, and withaferin A in hairy root cultures of Withania somnifera (L.) Dunal elicited with methyl jasmonate and salicylic acid. Plant Cell Tissue and Organ Culture, 2013. 114(1): p. 121-129.
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505. Singh, S., et al., Withania somnifera Root Extract Inhibits Mammary Cancer Metastasis and Epithelial to Mesenchymal Transition. Figshare, 2013.
506. Singh, R.B., Determination of polyalcohols by Smith degradation technique from Withania somnifera Dunal seeds oxo-polysaccharide. Advances in Applied Science Research, 2013. 4(1): p. 71-73.
507. Singh, R.B., Periodate oxidation method used for the confirmation of seeds polysaccharide structure of Withania somnifera Dunal plant. Archives of Applied Science Research, 2013. 5(5): p. 8-10.
508. Singh, R., et al., Overexpression of WsSGTL1 Gene of Withania somnifera Enhances Salt Tolerance, Heat Tolerance and Cold Acclimation Ability in Transgenic Arabidopsis Plants. Figshare, 2013.
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534. Prakash, J., et al., Neuroprotective Role of Withania somnifera Root Extract in Maneb-Paraquat Induced Mouse Model of Parkinsonism. Neurochemical Research, 2013. 38(5): p. 972-980.
535. Prabu, P.C., S. Panchapakesan, and C.D. Raj, Acute and Sub-Acute Oral Toxicity Assessment of the Hydroalcoholic Extract of Withania somnifera Roots in Wistar Rats. Phytotherapy Research, 2013. 27(8): p. 1169-1178.
536. Pottabathini, R., S. Meena, and A. Kumar, Protectiveeffect of Ashwagandha (Withania Somnifera) Against Chronic Constriction Induced Behavioral and Biochemical Alterations: Possible Involvement of Nitric Oxide Mechanism. Indian Journal of Pharmacology, 2013. 45: p. S235-S236.
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550. Monika, J. and G. Munish, Formulation and evaluation of standardised Withania somnifera leaf extract loaded transdermal gel. Journal of Medical Sciences (Pakistan), 2013. 13(8): p. 814-818.
551. Mishra, S.K., N.S. Sangwan, and R.S. Sangwan, Comparative physico-kinetic properties of a homogenous purified beta-glucosidase from Withania somnifera leaf. Acta Physiologiae Plantarum, 2013. 35(5): p. 1439-1451.
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553. Mirakzehi, M.T., et al., The effects of dietary 1,25-dihydroxycholecalciferol and hydroalcoholic extract of Withania somnifera root on bone mineralisation, strength and histological characteristics in broiler chickens. British Poultry Science, 2013. 54(6): p. 789-800.
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555. Manwar, J., et al., Comparative antioxidant potential of Withania somnifera based herbal formulation prepared by traditional and non-traditional fermentation processes. Integrative medicine research, 2013. 2(2): p. 56-61.
556. Manjunath, M.J. and Muralidhara, Effect of Withania somnifera Supplementation on Rotenone-Induced Oxidative Damage in Cerebellum and Striatum of the Male Mice Brain. Central Nervous System Agents in Medicinal Chemistry, 2013. 13(1): p. 43-56.
557. Manisha, S., S. Ashok, and R. Nema, Bio-efficacy of non-conventional pesticides against Tetranychus urticae Koch infesting ashwagandha (Withania somnifera Dunal). Pest Management in Horticultural Ecosystems, 2013. 19(2): p. 254-255.
558. Maliyakkal, N., et al., Cytotoxic and apoptotic activities of extracts of Withania somnifera and Tinospora cordifolia in human breast cancer cells. International Journal of Applied Research in Natural Products, 2013. 6(4): p. 1-10.
559. Maheep, B., et al., Neuroprotective response of the hippocampus region of the brain to Withania somnifera and Asparagus racemosus root extract: an in vitro study. Journal of Medicinal Plants Research, 2013. 7(30): p. 2259-2264.
560. Latheef, S.K., et al., Ameliorative effects of Withania somnifera, Azadirachta indica, Tinospora cordifolia and E care Se herbal preparations on chicken infectious anaemia virus induced haematological changes in chicks and their live body weights. South Asian Journal of Experimental Biology, 2013. 3(4): p. 172-182.
561. Kushwaha, A.K., et al., Tropine Forming Tropinone Reductase Gene from Withania somnifera (Ashwagandha): Biochemical Characteristics of the Recombinant Enzyme and Novel Physiological Overtones of Tissue-Wide Gene Expression Patterns. Plos One, 2013. 8(9).
562. Kushwaha, A.K., et al., Kinetic parameters of Withania somnifera tropine forming tropinone reductase (WsTR-I) catalyzed reaction. Figshare, 2013. 1.
563. Kushwaha, A.K., et al., Gas chromatography-based quantification of tropinone and tropine in different tissues of Withania somnifera. Figshare, 2013. 1.
564. Kushwaha, A.K., et al., Tropine Forming Tropinone Reductase Gene from Withania somnifera (Ashwagandha): Biochemical Characteristics of the Recombinant Enzyme and Novel Physiological Overtones of Tissue-Wide Gene Expression Patterns. Figshare, 2013.
565. Kurapati, V.K.R., et al., ASHWAGANDHA (WITHANIA SOMNIFERA) REVERSES B-AMYLOID INDUCED NEURONAL TOXICITY: IMPLICATIONS IN HAND. Journal of Neuroimmune Pharmacology, 2013. 8(2): p. 422-422.
566. Kurapati, K.R.V., et al., Ashwagandha (Withania somnifera) Reverses beta-Amyloid(1-42) Induced Toxicity in Human Neuronal Cells: Implications in HIV-Associated Neurocognitive Disorders (HAND). Plos One, 2013. 8(10).
567. Kumar, S.S. and S. Edla, Isolation and incidence of thermophilic fungi from various thermogenic habitats in Andhra Pradesh. International Journal of Pharma and Bio Sciences, 2013. 4(4): p. B-1312-B-1318.
568. Kumar, S., N. Kaushik, and P. Proksch, Identification of antifungal principle in the solvent extract of an endophytic fungus Chaetomium globosum from Withania somnifera. Springerplus, 2013. 2.
569. Kumar, R.J.S., et al., Functional Characterization of a Glucosyltransferase Specific to Flavonoid 7-O-Glucosides from Withania somnifera. Plant Molecular Biology Reporter, 2013. 31(5): p. 1100-1108.
570. Kumar, R., et al., Withania somnifera root extract extends lifespan of Caenorhabditis elegans. Annals of neurosciences, 2013. 20(1): p. 13-6.
571. Kumar, O.A., G. Jyothirmayee, and S.S. Tata, In vitro conservation of Withania somnifera (L) Dunal (Ashwagandha) - a multipurpose medicinal plant. Journal of Asian Scientific Research, 2013. 3(8): p. 852-861.
572. Koppalkar, B.G., B.T. Pujari, and B.K. Desai, Influence of row proportions on yield and yield components of pigeonpea in intercropping system of pigeonpea Cajanus cajan (L.) Millsp. and ashwagandha (Withania somnifera Dunal). International Journal of Agricultural Sciences, 2013. 9(1): p. 100-103.
573. Khazal, K.F., et al., Withania somnifera extract inhibits invasion and metastasis of MDA-MB-231 cells by inhibiting CCL2 and CD44 high/CD24Iow stem cells. Cancer Research, 2013. 73.
574. Khazal, K.F., et al., Effect of an Extract of Withania somnifera Root on Estrogen Receptor-positive Mammary Carcinomas. Anticancer Research, 2013. 33(4): p. 1519-1523.
575. Khanna, P.K., et al., Germination behaviour of seeds of Withania somnifera (L.) Dunal: a high value medicinal plant. Physiology and Molecular Biology of Plants, 2013. 19(3): p. 449-454.
576. Kaushal, K., et al., Effect of integrated nutrient management on growth and yield of ashwagandha (Withania somnifera Dunal) under water stress condition. Progressive Research, 2013. 8(Special issue): p. 516-520.
577. Kataria, H., et al., Withania somnifera Water Extract as a Potential Candidate for Differentiation Based Therapy of Human Neuroblastomas. Plos One, 2013. 8(1).
578. Kanungo, S., J.R. Rout, and S.L. Sahoo, Evaluation of Antioxidant Enzyme Activities in Withania somnifera L. in vitro and in vivo Grown Explants. Iranian Journal of Biotechnology, 2013. 11(4): p. 260-264.
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585. Jasuja, N.D., S. Preeti, and S.C. Joshi, Ameliorating effect of Withania somnifera on acephate administered male albino rats. African Journal of Pharmacy and Pharmacology, 2013. 7(23): p. 1554-1559.
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Cissus quadrangularis
Citrullus lanatus
Cleistanthus patulus
Clematis gouriana
Clematis montana
Cleome gynandra
Clerodendrum chinense
Clerodendrum indicum
Clerodendrum infortunatum
Clerodendrum laevifolium
Clerodendrum philippinum
Clerodendrum phlomidis
Clerodendrum serratum
Clerodendrum splendens
Clerodendrum wallichii
Coccinia grandis
Cocculus hirsutus
Cocculus laurifolius
Cochlospermum religiosum
Coix lacryma-jobi
Colebrookea oppositifolia
Coleus aromaticus
Colocasia esculenta
Combretum indicum
Commelina benghalensis
Commelina maculata
Commelina paludosa
Commiphora caudata
Commiphora mukul
Commiphora wightii
Conocarpus lancifolius
Consolida ajacis
Convolvulus pluricaulis
Cordyline fruticosa
Corydalis cornuta
Cosmos sulphureus
Costus speciosus
Cotinus coggygria
Couroupita guianensis
Crinum asiaticum
Crocus sativus
Crossandra infundibuliformis
Crotalaria alata
Crotalaria pallida
Crotalaria prostrata
Croton klotzschianus
Croton scabiosus
Croton tiglium
Cryptolepis buchananii
Cryptolepis dubia
Cryptostegia grandiflora
Cucumis sativus
Cuminum cyminum
Cupressus torulosa
Curculigo orchioides
Curcuma amada
Curcuma longa
Cuscuta reflexa
Cyananthus lobatus
Cyanthillium cinereum
Cycas revoluta
Cyclanthera pedata
Cymbopogon nardus
Cynodon dactylon
Cyperus laevigatus
Cyperus malaccensis
Cyperus rotundus
Dactyloctenium aegyptium
Dactylorhiza hatagirea
Dalbergia latifolia
Datisca cannabina
Datura metel
Datura stramonium
Daucus carota
Delphinium ajacis
Delphinium denudatum
Delphinium elatum
Dendrobium densiflorum
Dendrobium ovatum
Derris scandens
Derris trifoliata
Desmodium concinnum
Desmodium gangeticum
Desmodium heterocarpon
Desmodium multiflorum
Desmodium triflorum
Dichrocephala integrifolia
Dicliptera paniculata
Didymocarpus pedicellatus
Dillenia indica
Dimorphocalyx glabellus
Dimorphoteca ecklonis
Dioscorea alata
Dioscorea pentaphylla
Dioscorea polygonoides
Diospyros kaki
Diospyros malabarica
Dipteracanthus patulus
Dipteracanthus prostratus
Dolichandrone spathacea
Dolichos biflorus
Dregea volubilis
Drimia indica
Drosera peltata
Duranta erecta
Dysoxylum binectariferum
Dysoxylum gotadhora
Dysphania ambrosioides
Echinocereus pentalophus
Echinops niveus
Echium plantagineum
Edgeworthia gardneri
Eichhornia crassipes
Elaeagnus umbellata
Elaeocarpus ganitrus
Elephantopus scaber
Eleutheranthera ruderalis
Elsholtzia fruticosa
Elytraria acaulis
Embelia ribes
Emblica officinalis
Enterolobium cyclocarpum
Ephedra foliata
Ephedra gerardiana
Epipactis helleborine
Eranthemum pulchellum
Eryngium foetidum
Erysimum hieraciifolium
Erythrina suberosa
Erythrina variegata
Euonymus echinatus
Euonymus japonicus
Eupatorium capillifolium
Eupatorium perfoliatum
Euphorbia antiquorum
Euphorbia cornigera
Euphorbia cotinifolia
Euphorbia granulata
Euphorbia heterophylla
Euphorbia hirta
Euphorbia hypericifolia
Euphorbia milii
Euphorbia nivulia
Euphorbia peplus
Euphorbia tirucalli
Fagonia cretica
Fagopyrum acutatum
Ferula foetida
Ficus elastica
Ficus religiosa
Filicium decipiens
Filipendula vestita
Flacourtia indica
Flemingia procumbens
Flemingia semialata
Foeniculum vulgare
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Fumaria indica
Fumaria parviflora
Furcraea foetida
Galega officinalis
General
Gentiana kurroo
Geranium lucidum
Geranium nepalense
Geranium pratense
Geranium wallichianum
Ghee
Globba schomburgkii
Glochidion hohenackeri
Gloriosa superba
Glycyrrhiza glabra
Gmelina arborea
Gomphrena globosa
Gomphrena serrata
Goodyera repens
Grewia asiatica
Grewia optiva
Grewia serrulata
Grewia tenax
Gymnema sylvestre
Habenaria edgeworthii
Habenaria plantaginea
Handroanthus impetiginosus
Hedychium spicatum
Helianthus annuus
Helicteres isora
Helinus lanceolatus
Heliotropium indicum
Hemidesmus indicus
Hemigraphis alternata
Hemigraphis colorata
Hemigraphis hirta
Heracleum sphondylium
Herpetospermum pedunculosum
Hibiscus cannabinus
Hibiscus esculentus
Hibiscus hirtus
Hibiscus lobatus
Hibiscus radiatus
Hibiscus vitifolius
Hippophae rhamnoides
Holarrhena antidysenterica
Holarrhena pubescens
Holoptelea integrifolia
Hosta plantaginea
Hoya carnosa
Hydrocotyle sibthorpioides
Hydrolea zeylanica
Hygrophila auriculata
Hygrophila polysperma
Hygrophila schulli
Hylocereus undatus
Hymenocallis speciosa
Hymenodictyon orixense
Hyoscyamus niger
Hypericum dyeri
Hypericum elodeoides
Hypericum oblongifolium
Hyptis suaveolens
Ilex dipyrena
Impatiens balsamina
Impatiens bracteata
Impatiens racemosa
Indigofera aspalathoides
Indigofera astragalina
Indigofera glabra
Ipomoea alba
Ipomoea aquatica
Ipomoea marginata
Isodon rugosus
Ixeris polycephala
Jacaranda mimosifolia
Jacquemontia pentantha
Jasminum auriculatum
Jasminum multiflorum
Jatropha curcas
Jatropha gossypifolia
Juncus thomsonii
Justicia adhatoda
Justicia brandegeeana
Justicia carnea
Justicia gendarussa
Justicia pubigera
Kalanchoe blossfeldiana
Kallstroemia pubescens
Koelreuteria elegans
Koelreuteria paniculata
Koenigia delicatula
Kopsia fruticosa
Kydia calycina
Kyllinga brevifolia
Lablab purpureus
Lactuca dissecta
Lantana camara
Lathyrus sativus
Leea aequata
Lens culinaris
Leonotis nepetifolia
Leonurus cardiaca
Lepidium sativum
Lepisanthes rubiginosa
Leucas aspera
Leucas nutans
Leucostemma latifolium
Leycesteria formosa
Ligularia amplexicaulis
Ligularia fischeri
Lilium polyphyllum
Linum usitatissimum
Liparis nervosa
Liquidambar formosana
Litsea monopetala
Lupinus angustifolius
Lycium ferocissimum
Macaranga peltata
Maesa argentea
Magnolia champaca
Mahonia napaulensis
Malachra Capitata
Mallotus nudiflorus
Mallotus philippinensis
Malva sylvestris
Malvastrum coromandelianum
Marchantia polymorpha
Martynia annua
Medicago lupulina
Medicinal Plants of India
Melilotus indicus
Melochia corchorifolia
Memecylon edule
Memecylon umbellatum
Mercurialis annua
Meriandra strobilifera
Merremia cissoides
Mesua ferrea
Micrococca mercuriali
Micromeria biflora
Mikania micrantha
Millettia pinnata
Mimosa polyancistra
Mimosa pudica
Mitragyna parvifolia
Modiola caroliniana
Momordica charantia
Momordica cochinchinensis
Morinda citrifolia
Morinda pubescens
Moringa oleifera
Mucuna pruriens
Muehlenbeckia platyclada
Muehlenbeckia platyclados
Muntingia calabura
Murdannia nudiflora
Murraya koenigii
Muscari neglectum
Myriactis nepalensis
Myristica fragrans
Myrtus communis
Naravelia zeylanica
Nardostachys grandiflora
Nardostachys jatamansi
Naringi crenulata
Nasturtium officinale
Nelumbo nucifera
Neolamarckia cadamba
Nepeta laevigata
Nerium indicum
Nerium oleander
Nicotiana plumbaginifolia
Nicotiana rustica
Nicotiana tabacum
Nigella sativa
Nyctanthes arbor-tristis
Nymphaea nouchali
Nymphaea pubescens
Nymphoides indica
Ocimum basilicum
Ocimum gratissimum
Ocimum kilimandscharicum
Ocimum sanctum
Oldenlandia umbellata
Ononis natrix
Ononis repens
Ononis spinosa
Operculina turpethum
Origanum majorana
Oroxylum indicum
Osteospermum ecklonis
Others
Oxyria digyna
Pachygone ovata
Pachyrhizus erosus
Paederia foetida
Pandanus tectorius
Papaver somniferum
Passiflora caerulea
Passiflora vitifolia
Pavetta indica
Pentapetes phoenicea
Pentas lanceolata
Peperomia argyreia
Peperomia heyneana
Peperomia pellucida
Peperomia sandersii
Peperomia tetraphylla
Perilla frutescens
Persicaria amplexicaulis
Persicaria barbata
Persicaria capitata
Persicaria glabra
Persicaria nepalensis
Phalaenopsis taenialis
Phaulopsis dorsiflora
Philodendron bipinnatifidum
Phlomis bracteosa
Phlomoides bracteosa
Phyllanthus acidus
Phyllanthus amarus
Phyllanthus fraternus
Phyllanthus lawii
Phyllanthus rotundifolius
Physalis grisea
Physalis peruviana
Picrorhiza kurroa
Pilea microphylla
Pimpinella anisum
Piper betle
Piper longum
Piper nigrum
Pisonia aculeata
Pistia stratiotes
Pisum sativum
Plantago orbignyana
Plantago ovata
Platanthera edgeworthii
Platostoma elongatum
Plectranthus barbatus
Plectranthus scutellarioides
Plumbago auriculata
Plumbago capensis
Plumbago zeylanica
Plumeria rubra
Podranea ricasoliana
Polemonium caeruleum
Polygala crotalarioides
Polygala persicariifolia
Polygonatum cirrhifolium
Polygonatum verticillatum
Polygonum amplexicaule
Polygonum barbatum
Polygonum recumbens
Pongamia pinnata
Portulaca oleracea
Portulaca umbraticola
Portulacaria afra
Potentilla fruticosa
Potentilla supina
Premna corymbosa
Premna tomentosa
Primula denticulata
Primula floribunda
Primula vulgaris
Prunus Amygdalus
Prunus dulcis
Pseuderanthemum carruthersii
Pseudobombax ellipticum
Pseudocaryopteris foetida
Psidium guajava
Psidium guineense
Pterocarpus santalinus
Pterospermum acerifolium
Pterospermum lanceifolium
Pterygota alata
Pulicaria dysenterica
Punica granatum
Putranjiva roxburghii
Pyrostegia venusta
Quisqualis indica
Ranunculus arvensis
Ranunculus laetus
Ranunculus sceleratus
Raphanus sativus
Rauvolfia serpentina
Rauvolfia tetraphylla
Reinwardtia indica
Rhamphicarpa fistulosa
Rhodiola trifida
Rhodiola wallichiana
Rhododendron arboreum
Rhynchosia heynei
Rhynchosia himalensis
Rhynchosia viscosa
Ricinus communis
Rorippa indica
Roscoea purpurea
Rosmarinus officinalis
Ruellia patula
Ruellia prostrata
Ruellia tuberosa
Rumex dentatus
Rumex hastatus
Rungia pectinata
Saccharum officinarum
Saccharum spontaneum
Salix denticulata
Salix tetrasperma
Salvadora persica
Salvia involucrata
Salvia miltiorrhiza
Salvia nubicola
Salvia splendens
Sambucus canadensis
Sambucus mexicana
Sambucus nigra
Santalum album
Sapindus saponaria
Saussurea auriculata
Saussurea candicans
Saussurea obvallata
Scadoxus multiflorus
Scutellaria baicalensis
Scutellaria grossa
Scutellaria repens
Sedum oreades
Semecarpus anacardium
Senna auriculata
Senna occidentalis
Senna siamea
Senna sophera
Sesbania bispinosa
Sesbania grandiflora
Seseli diffusum
Sesuvium portulacastrum
Setaria verticillata
Shorea robusta
Sida cordata
Sida cordifolia
Sida retusa
Sida spinosa
Sideritis hirsuta
Silybum marianum
Smithia ciliata
Solanum chrysotrichum
Solanum erianthum
Solanum jasminoides
Solanum melongena
Solanum nigrum
Solanum sisymbriifolium
Solanum surattense
Solanum torvum
Solanum tuberosum
Solanum villosum
Sonchus oleraceus
Soymida febrifuga
Sphaeranthus amaranthoides
Sphenoclea zeylanica
Spiranthes australis
Spiranthes sinensis
Spondias pinnata
Stellaria media
Stellera chamaejasme
Stephania japonica
Sterculia alata
Sterculia foetida
Sterculia villosa
Stereospermum tetragonum
Stevia rebaudiana
Striga asiatica
Strophanthus boivinii
Strychnos minor
Strychnos nux-vomica
Strychnos potatorum
Suaeda maritima
Suregada multiflora
Swertia angustifolia
Swertia bimaculata
Swertia cordata
Swertia paniculata
Swietenia macrophylla
Swietenia mahagoni
Syzygium alternifolium
Syzygium aromaticum
Syzygium cumini
Syzygium jambos
Syzygium samarangense
Tabebuia aurea
Tabebuia avellanedae
Talinum portulacifolium
Tamarindus indica
Taxus baccata
Tecoma castanifolia
Tephrosia calophylla
Tephrosia purpurea
Teramnus labialis
Terminalia alata
Terminalia catappa
Terminalia chebula
Terminalia elliptica
Terminalia pallida
Teucrium botrys
Teucrium royleanum
Thalictrum foliolosum
Thespesia populnea
Thunbergia erecta
Thunbergia fragrans
Thunbergia grandiflora
Thymus linearis
Tiliacora acuminata
Tiliacora racemosa
Tinospora cordifolia
Tinospora crispa
Tinospora sinensis
Toona ciliata
Trewia nudiflora
Tribulus terrestris
Trichodesma indicum
Trichosanthes cucumerina
Trichosanthes palmata
Trichosanthes tricuspidata
Trifolium repens
Trigonella foenum-graecum
Triumfetta rhomboidea
Tylophora indica
Uraria picta
Urena lobata
Urena sinuata
Urginea coromandeliana
Vachellia horrida
Valeriana jatamansi
Vanda tessellata
Veronica serpyllifolia
Viburnum coriaceum
Vicia bakeri
Vicia faba
Vicia sativa
Vigna radiata
Vigna unguiculata
Vinca rosea
Viola rupestris
Viscum album
Vitex negundo
Vitis vinifera
Withania somnifera
Wrightia tinctoria
Wulfeniosis amherstiana
Zamia furfuracea
Ziziphus jujuba
Ziziphus mauritiana
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