National Center for Natural Products Research
The University of Mississippi

Below is a list of publications produced within the National Center for Natural Products Research, organized by year (click on each year to expand the relevant list). If you have any questions or concerns, feel free to contact us!

2017 Publications
  1. Ali A, Cantrell CL, Khan IA. A New In Vitro Bioassay System for the Discovery and Quantitative Evaluation of Mosquito Repellents. J Med Entomol. 2017;54(5):1328-36. doi: 10.1093/jme/tjx100.
  2. Andrioli WJ, Lopes AA, Cavalcanti BC, Pessoa C, Nanayakkara NPD, Bastos JK. Isolation and characterization of 2-pyridone alkaloids and alloxazines from Beauveria bassiana. Nat Prod Res. 2017;31(16):1920-9. doi: 10.1080/14786419.2016.1269091.
  3. Avonto C, Rua D, Lasonkar PB, Chittiboyina AG, Khan IA. Identification of a compound isolated from German chamomile (Matricaria chamomilla) with dermal sensitization potential. Toxicol Appl Pharmacol. 2017;318:16-22. doi: 10.1016/j.taap.2017.01.009.
  4. Avula B, Wang Y-H, Isaac G, Yuk J, Wrona M, Yu K, Khan IA. Metabolic Profiling of Hoodia, Chamomile, Terminalia Species and Evaluation of Commercial Preparations Using Ultrahigh-Performance Liquid Chromatography Quadrupole-Time-of-Flight Mass Spectrometry. Planta Med. 2017;83(16):1297-308. doi: 10.1055/s-0043-109239.
  5. Bacherikov VA, Chittiboyina AG, Avery MA. Design, Synthesis, and Biological Evaluation of Peptidomimetic N-Substituted Cbz-4-Hyp-Hpa-Amides as Novel Inhibitors of Plasmodium falciparum. Chem Biodivers. 2017;14(8). doi: 10.1002/cbdv.201700037. 
  6. Chandra S, Lata H, ElSohly MA, Walker LA, Potter D. Cannabis cultivation: Methodological issues for obtaining medical-grade product. Epilepsy Behav. 2017;70(Pt B):302-12. doi: 10.1016/j.yebeh.2016.11.029.
  7. Chaurasiya ND, Leon F, Ding Y, Gomez-Betancur I, Benjumea D, Walker LA, Cutler SJ, Tekwani BL. Interactions of Desmethoxyyangonin, a Secondary Metabolite from Renealmia alpinia, with Human Monoamine Oxidase-A and Oxidase-B. Evid Based Complement Alternat Med. 2017;2017:4018724. doi: 10.1155/2017/4018724.
  8. Chaurasiya ND, Shukla S, Tekwani BL. A Combined In Vitro Assay for Evaluation of Neurotrophic Activity and Cytotoxicity. SLAS Discovery. 2017;22(6):667-75. doi: 10.1177/2472555217698677.
  9. Chen Y, Zhao J, Qiu Y, Yuan H, Khan SI, Hussain N, Iqbal CM, Zeng F, Guo D-A, Khan IA, Wang W. Prenylated flavonoids from the stems and roots of Tripterygium wilfordii. Fitoterapia. 2017;119:64-8. doi: 10.1016/j.fitote.2017.04.003.
  10. Cohen PA, Avula B, Khan IA. Variability in strength of red yeast rice supplements purchased from mainstream retailers. Eur J Prev Cardiol. 2017;24(13):1431-4. doi: 10.1177/2047487317715714.
  11. Cohen PA, Avula B, Venhuis B, Travis JC, Wang Y-H, Khan IA. Pharmaceutical doses of the banned stimulant oxilofrine found in dietary supplements sold in the USA. Drug Test Anal. 2017;9(1):135-42. doi: 10.1002/dta.1976.
  12. Cortese A, Pantaleo G, Borri A, Amato M, Claudio PP. Necrotizing odontogenic fasciitis of head and neck extending to anterior mediastinum in elderly patients: innovative treatment with a review of the literature. Aging Clin Exp Res. 2017;29(Suppl 1):159-65. doi: 10.1007/s40520-016-0650-2.
  13. Dasmahapatra AK, Carty DR, Khan IA. Developmental ethanol exposure impairs locomotor movement in Japanese medaka (Oryzias latipes) larvae targeting epigenome. Chemosphere. 2017;186:901-10. doi: 10.1016/j.chemosphere.2017.08.048.
  14. El-Hawary SS, Sayed AM, Rateb ME, Bakeer W, AbouZid SF, Mohammed R. Secondary metabolites from fungal endophytes of Solanum nigrum. Nat Prod Res. 2017;31(21):2568-71. doi: 10.1080/14786419.2017.1327859.
  15. Elshemy HAH, Zaki MA. Design and synthesis of new coumarin hybrids and insight into their mode of antiproliferative action. Bioorg Med Chem. 2017;25(3):1066-75. doi: 10.1016/j.bmc.2016.12.019.
  16. ElSohly MA, Radwan MM, Gul W, Chandra S, Galal A. Phytochemistry of Cannabis sativa L. Prog Chem Org Nat Prod. 2017;103(Phytocannabinoids):1-36. doi: 10.1007/978-3-319-45541-9_1.
  17. Fasinu PS, Manda VK, Dale OR, Egiebor NO, Walker LA, Khan SI. Modulation of Cytochrome P450, P-glycoprotein and Pregnane X Receptor by Selected Antimalarial Herbs-Implication for Herb-Drug Interaction. Molecules. 2017;22(12). doi: 10.3390/molecules22122049.
  18. Fawzy GA, Al-Taweel AM, Perveen S, Khan SI, Al-Omary FA. Bioactivity and chemical characterization of Acalypha fruticosa Forssk. growing in Saudi Arabia. Saudi Pharm J. 2017;25(1):104-9. doi: 10.1016/j.jsps.2016.05.004.
  19. Ferreira MC, Cantrell CL, Wedge DE, Goncalves VN, Jacob MR, Khan S, Rosa CA, Rosa LH,. Antimycobacterial and antimalarial activities of endophytic fungi associated with the ancient and narrowly endemic neotropical plant Vellozia gigantea from Brazil. Mem Inst Oswaldo Cruz. 2017;112(10):692-7. doi: 10.1590/0074-02760170144.
  20. Ferreira MC, Cantrell CL, Duke SO, Ali A, Rosa LH. New Pesticidal Diterpenoids from Vellozia gigantea (Velloziaceae), an Endemic Neotropical Plant Living in the Endangered Brazilian Biome Rupestrian Grasslands. Molecules. 2017;22(1). doi: 10.3390/molecules22010175.
  21. Gadetskaya AV, Mohamed SM, Tarawneh AH, Mohamed NM, Ma G, Ponomarev BN, Zhusupova GE, Cantrell CL, Cutler SJ, Ross SA. Phytochemical characterization and biological activity of secondary metabolites from three Limonium species. Med Chem Res. 2017;26(11):2743-50. doi: 10.1007/s00044-017-1973-z.
  22. Greco A, Albanese S, Auletta L, De CF, Salvatore M, Howard CM, Claudio PP. Advances in molecular preclinical therapy mediated by imaging. Q J Nucl Med Mol Imaging. 2017;61(1):76-94. doi: 10.23736/S1824-4785.16.02944-7.
  23. Gross AD, Tabanca N, Islam R, Ali A, Khan IA, Kaplancikli ZA, Altintop MD, Ozdemir A, Bloomquist JR. Toxicity and Synergistic Activities of Chalcones Against Aedes aegypti (Diptera: Culicidae) and Drosophila melanogaster (Diptera: Drosophilidae). J Med Entomol. 2017;54(2):382-6. doi: 10.1093/jme/tjw183.
  24. Helal MA, Habib ES, Chittiboyina AG. Selective kappa opioid antagonists for treatment of addiction, are we there yet? Eur J Med Chem. 2017;141:632-47. doi: 10.1016/j.ejmech.2017.10.012.
  25. Howard CM, Valluri J, Alberico A, Julien T, Mazagri R, Marsh R, Alastair H, Cortese A, Griswold M, Wang W, Denning K, Brown L, Claudio PP. Analysis of Chemopredictive Assay for Targeting Cancer Stem Cells in Glioblastoma Patients. Transl Oncol. 2017;10(2):241-54. doi: 10.1016/j.tranon.2017.01.008.
  26. Hu S, Wang Y-H, Avula B, Wang M, Khan IA. Separation of cucurbitane triterpenoids from bitter melon drinks and determination of partition coefficients using vortex-assisted dispersive liquid-phase microextraction followed by UHPLC analysis. J Sep Sci. 2017;40(10):2238-45. doi: 10.1002/jssc.201700023.
  27. Hussain H, Al-Harrasi A, Csuk R, Shamraiz U, Green IR, Ahmed I, Khan IA, Ali Z. Therapeutic potential of boswellic acids: a patent review (1990-2015). Expert Opin Ther Pat. 2017;27(1):81-90.
  28. Hussain H, Green IR, Ali I, Khan IA, Ali Z, Al-Sadi AM, Ahmed I. Ursolic acid derivatives for pharmaceutical use: a patent review (2012-2016). Expert Opin Ther Pat. 2017;27(9):1061-72. doi: 10.1080/13543776.2017.1344219.
  29. Ibrahim MA, El-Alfy AT, Ezel K, Radwan MO, Shilabin AG, Kochanowska-Karamyan AJ, Abd-Alla HI, Otsuka M, Hamann MT. Marine Inspired 2-(5-Halo-1H-indol-3-yl)-N,N-dimethylethanamines as Modulators of Serotonin Receptors: An Example Illustrating the Power of Bromine as Part of the Uniquely Marine Chemical Space. Mar Drugs. 2017;15(8). doi: 10.3390/md15080248.
  30. Ibrahim MK, Eissa IH, Abdallah AE, Metwaly AM, Radwan MM, ElSohly MA. Design, synthesis, molecular modeling and anti-hyperglycemic evaluation of novel quinoxaline derivatives as potential PPARγ and SUR agonists. Bioorg Med Chem. 2017;25(4):1496-513. doi: 10.1016/j.bmc.2017.01.015.
  31. Ibrahim MK, Eissa IH, Alesawy MS, Metwaly AM, Radwan MM, ElSohly MA. Design, synthesis, molecular modeling and anti-hyperglycemic evaluation of quinazolin-4(3H)-one derivatives as potential PPARγ and SUR agonists. Bioorg Med Chem. 2017;25(17):4723-44. doi: 10.1016/j.bmc.2017.07.015.
  32. Ibrahim SRM, Mohamed GA, Ross SA. Aspernolides L and M, new butyrolactones from the endophytic fungus Aspergillus versicolor. Z Naturforsch C. 2017;72(5-6):155-60. doi: 10.1515/znc-2016-0138.
  33. Ibrahim SRM, Mohamed GA, Zayed MF, Ross SA. 8-Hydroxyirilone 5-methyl ether and 8-hydroxyirilone, new antioxidant and α-amylase inhibitors isoflavonoids from Iris germanica rhizomes. Bioorg Chem. 2017;70:192-8. doi: 10.1016/j.bioorg.2016.12.010.
  34. Jain J, Jain SK, Walker LA, Tekwani BL. Inhibitors of ubiquitin E3 ligase as potential new antimalarial drug leads. BMC Pharmacol Toxicol. 2017;18:40/1-/10. doi: 10.1186/s40360-017-0147-4.
  35. Kama-Kama F, Omosa LK, Nganga J, Maina N, Osanjo G, Yaouba S, Ilias M, Midiwo J, Naessens J. Antimycoplasmal Activities of Compounds from Solanum aculeastrum and Piliostigma thonningii against Strains from the Mycoplasma mycoides Cluster. Front Pharmacol. 2017;8:920. doi: 10.3389/fphar.2017.00920.
  36. Kang N-X, Zhu Y-J, Zhao J-P, Zhu W-F, Liu Y-L, Xu Q-M, Zhuge H-X, Khan IA, Yang S-L. Antischistosomal activity of hederacochiside C against Schistosoma japonicum harbored in experimentally infected animals. J Asian Nat Prod Res. 2017;19(4):402-15. doi: 10.1080/10286020.2016.1208181.
  37. Kholiya R, Khan SI, Bahuguna A, Tripathi M, Rawat DS. N-Piperonyl substitution on aminoquinoline-pyrimidine hybrids: Effect on the antiplasmodial potency. Eur J Med Chem. 2017;131:126-40. doi: 10.1016/j.ejmech.2017.03.007.
  38. Labib RM, Youssef FS, Ashour ML, Abdel-Daim MM, Ross SA. Chemical Composition of Pinus roxburghii Bark Volatile Oil and Validation of Its Anti-Inflammatory Activity Using Molecular Modelling and Bleomycin-Induced Inflammation in Albino Mice. Molecules. 2017;22(9). doi: 10.3390/molecules22091384.
  39. Lan X, Deng K, Zhao J, Chen Y, Xin X, Liu Y, Khan IA, Yang S, Wang T, Xu Q. New Triterpenoid Saponins from Green Vegetable Soya Beans and Their Anti-Inflammatory Activities. J Agric Food Chem. 2017;65(50):11065-72. doi: 10.1021/acs.jafc.7b04134.
  40. Li B, Ali Z, Chan M, Li J, Wang M, Abe N, Wu C-R, Khan IA, Wang W, Li S-X. Chemical constituents of Pholidota cantonensis. Phytochemistry. 2017;137:132-8. doi: 10.1016/j.phytochem.2017.02.005.
  41. Li J, Zhao J, Wang W, Li L, Zhang L, Zhao X-F, Liu Q-R, Liu F, Yang M, Khan IA, Li S-X. New Acorane-Type Sesquiterpene from Acorus calamus L. Molecules. 2017;22(4). doi: 10.3390/molecules22040529.
  42. Li J, Li Z-X, Zhao J-P, Wang W, Zhao X-F, Xu B, Li L, Zhang L, Ren J, Khan IA, Li S-X. A Novel Tropoloisoquinoline Alkaloid, Neotatarine, from Acorus calamus L. Chem Biodivers. 2017;14(10). doi: 10.1002/cbdv.201700201.
  43. Liu Q, Li B, Zhao J, Khan SI, Liu W-B, Zeng T, Peng C-Y, Cai X, Peng Q, Huang H, Khan IA, Wang W. A new sucrosephenylpropanoid ester from Polygonum pubescens Blume. Nat Prod Res. 2017;31(15):1725-32. doi: 10.1080/14786419.2017.1289208.
  44. Manda VK, Avula B, Dale OR, Ali Z, Khan IA, Walker LA, Khan SI. PXR mediated induction of CYP3A4, CYP1A2, and P-gp by Mitragyna speciosa and its alkaloids. Phytother Res. 2017;31(12):1935-45. doi: 10.1002/ptr.5942.
  45. Manda VK, Avula B, Mohammad K A, Abe N, Khan IA, Khan SI. Quantification of mesembrine and mesembrenone in mouse plasma using UHPLC-QToF-MS: Application to a pharmacokinetic study. Biomed Chromatogr. 2017;31(3):n/a. doi: 10.1002/bmc.3815.
  46. Maurya SS, Khan SI, Bahuguna A, Kumar D, Rawat DS. Synthesis, antimalarial activity, heme binding and docking studies of N-substituted 4-aminoquinoline-pyrimidine molecular hybrids. Eur J Med Chem. 2017;129:175-85. doi: 10.1016/j.ejmech.2017.02.024.
  47. Miousse IR, Skinner CM, Lin H, Ewing LE, Kosanke SD, Williams DK, Avula B, Khan IA, ElSohly MA, Gurley BJ, Koturbash I. Safety assessment of the dietary supplement OxyELITE® Pro (New Formula) in inbred and outbred mouse strains. Food Chem Toxicol. 2017;109(Pt 1):194-209. doi: 10.1016/j.fct.2017.08.025.
  48. Mohamed NM, Makboul MA, Farag SF, Tarawneh AH, Khan SI, Brooks TA, Wang Y-H, Ross SA. Iridoid and phenylpropanoid glycosides from the roots of Lantana montevidensis. Med Chem Res. 2017;26(6):1117-26. doi: 10.1007/s00044-017-1817-x.
  49. Morimoto M, Cantrell CL, Khan S, Tekwani BL, Duke SO. Antimalarial and Antileishmanial Activities of Phytophenolics and Their Synthetic Analogues. Chem Biodivers. 2017;14(12).  doi: 10.1002/cbdv.201700324.
  50. Park Y-N, Srikantha T, Daniels KJ, Jacob MR, Agarwal AK, Li X-C, Soll DR. Protocol for Identifying Natural Agents That Selectively Affect Adhesion, Thickness, Architecture, Cellular Phenotypes, Extracellular Matrix, and Human White Blood Cell Impenetrability of Candida albicans Biofilms. Antimicrob Agents Chemother. 2017;61(11). doi: 10.1128/AAC.01319-17.
  51. Parveen I, Singh HK, Malik S, Raghuvanshi S, Babbar SB. Evaluating five different loci (rbcL, rpoB, rpoC1, matK, and ITS) for DNA barcoding of Indian orchids. Genome. 2017;60(8):665-71. doi: 10.1139/gen-2016-0215.
  52. Peng Y, Jian Y, Zulfiqar A, Li B, Zhang K, Long F, Peng C, Cai X, Khan IA, Wang W. Two new sesquiterpene lactone glycosides from Cnicus benedictus. Nat Prod Res. 2017;31(19):2211-7. doi: 10.1080/14786419.2017.1295239.
  53. Perera WH, Avula B, Khan IA, McChesney JD. Assignment of sugar arrangement in branched steviol glycosides using electrospray ionization quadrupole time-of-flight tandem mass spectrometry. Rapid Commun Mass Spectrom. 2017;31(3):315-24. doi: 10.1002/rcm.7784.
  54. Perera WH, Ghiviriga I, Rodenburg DL, Alves K, Bowling JJ, Avula B, Khan IA, McChesney JD. Rebaudiosides T and U, minor C-19 xylopyranosyl and arabinopyranosyl steviol glycoside derivatives from Stevia rebaudiana (Bertoni) Bertoni. Phytochemistry. 2017;135:106-14. doi: 10.1016/j.phytochem.2016.12.001.
  55. Porta EOJ, Jager SN, Nocito I, Lepesheva GI, Serra EC, Tekwani BL, Labadie GR. Antitrypanosomal and antileishmanial activity of prenyl-1,2,3-triazoles. Medchemcomm. 2017;8(5):1015-21.  doi: 10.1039/C7MD00008A.
  56. Ragab FAF, Abou-Seri SM, Abdel-Aziz SA, Alfayomy AM, Aboelmagd M. Design, synthesis and anticancer activity of new monastrol analogues bearing 1,3,4-oxadiazole moiety. Eur J Med Chem. 2017;138:140-51. doi: 10.1016/j.ejmech.2017.06.026.
  57. Raman V, Bussmann RW, Khan IA. Which Bay Leaf is in Your Spice Rack? – A Quality Control Study. Planta Med. 2017;83(12/13):1058-67. doi: 10.1055/s-0043-103963.
  58. Raman V, Tabanca N, Demirci B, Khan IA. Studies on the floral anatomy and scent chemistry of titan arum (Amorphophallus titanum, Araceae). Turk J Bot. 2017;41(1):63-74. doi: 10.3906/bot-1604-34.
  59. Reddy PL, Khan SI, Ponnan P, Tripathi M, Rawat DS. Design, synthesis and evaluation of 4-aminoquinoline-purine hybrids as potential antiplasmodial agents. Eur J Med Chem. 2017;126:675-86. doi: 10.1016/j.ejmech.2016.11.057.
  60. Selim KA, Abdelrasoul H, Aboelmagd M, Tawila AM. The Role of the MAPK Signaling, Topoisomerase and Dietary Bioactives in Controlling Cancer Incidence. Diseases. 2017;5(2). doi: 10.3390/diseases5020013.
  61. Sharma KK, Maurya IK, Khan SI, Jacob MR, Kumar V, Tikoo K, Jain R. Discovery of a Membrane-Active, Ring-Modified Histidine Containing Ultrashort Amphiphilic Peptide That Exhibits Potent Inhibition of Cryptococcus neoformans. J Med Chem. 2017;60(15):6607-21. doi: 10.1021/acs.jmedchem.7b00481.
  62. Shenmar K, Sharma KK, Wangoo N, Maurya IK, Kumar V, Khan SI, Jacob MR, Tikoo K, Jain R. Synthesis, stability and mechanistic studies of potent anticryptococcal hexapeptides. Eur J Med Chem. 2017;132:192-203. doi: 10.1016/j.ejmech.2017.03.046.
  63. Shi Y-N, Liu F-F, Jacob MR, Li X-C, Zhu H-T, Wang D, Cheng R-R, Yang C-R, Xu M, Zhang Y-J. Antifungal Amide Alkaloids from the Aerial Parts of Piper flaviflorum and Piper sarmentosum. Planta Med. 2017;83(1-02):143-50. doi: 10.1055/s-0042-109778.
  64. Singh A, Agarwal A, Xu Y-J. Novel Cell-Killing Mechanisms of Hydroxyurea and the Implication toward Combination Therapy for the Treatment of Fungal Infections. Antimicrob Agents Chemother. 2017;61(11). doi: 10.1128/AAC.00734-17.
  65. Srivedavyasasri R, Hayes T, Ross SA. Phytochemical and biological evaluation of Salvia apiana. Nat Prod Res. 2017;31(17):2058-61. doi: 10.1080/14786419.2016.1269096.
  66. Stamper B, Gul W, Godfrey M, Gul SW, ElSohly MA,. LC-MS-MS Method for Analysis of Benzodiazepines in Wastewater During Football Games IV. J Anal Toxicol. 2017;41(3):205-13.
  67. Techen N, Parveen I, Khan IA. A single molecular marker to distinguish between species of Dioscorea. Genome. 2017;60(3):201-7. doi: 10.1139/gen-2015-0105.
  68. Tekwani BL. Meet Our Editorial Board Member. Infect Disord: Drug Targets. 2017;17(1):1. doi: 10.2174/187152651701170320182626.
  69. Tripathi SK, Xu T, Feng Q, Avula B, Shi X, Pan X, Mask MM, Baerson SR, Jacob MR, Ravu RR, Khan SI, Li X-C, Khan IA, Clark AM, Agarwal AK. Two plant-derived aporphinoid alkaloids exert their antifungal activity by disrupting mitochondrial iron-sulfur cluster biosynthesis. J Biol Chem. 2017;292(40):16578-93. doi: 10.1074/jbc.M117.781773.
  70. Wang J, Jia Z, Zhang Z, Wang Y, Liu X, Wang L, Lin R. Analysis of Chemical Constituents of Melastoma dodecandrum Lour. by UPLC-ESI-Q-Exactive Focus-MS/MS. Molecules. 2017;22(3). doi: 10.3390/molecules22030476.
  71. Wang M, Wang Y-H, Avula B, Radwan MM, Wanas AS, Mehmedic Z, van Antwerp J, El Sohly MA, Khan IA. Quantitative Determination of Cannabinoids in Cannabis and Cannabis Products Using Ultra-High-Performance Supercritical Fluid Chromatography and Diode Array/Mass Spectrometric Detection. J Forensic Sci. 2017;62(3):602-11. doi: 10.1111/1556-4029.13341.
  72. Xiang C-P, Han J-X, Li X-C, Li H-Z, Zhang Y, Chen L, Qu Y, Hao C-Y, Li Y-H, Yang C-R, Zhao S-J, Xu M. Chemical Composition and Acetylcholinesterase Inhibitory Activity of Essential Oils from Piper Species. J Agric Food Chem. 2017;65(18):3702-10. doi: 10.1021/acs.jafc.7b01350.
  73. Xiao H, Rao RR, Tekwani BL, Li W, Liu W-B, Jacob MR, Khan SI, Cai X, Peng C-Y, Khan IA, Li X-C, Wang W. Biological evaluation of phytoconstituents from Polygonum hydropiper. Nat Prod Res. 2017;31(17):2053-7.  doi: 10.1080/14786419.2016.1269094.
  74. Yalamanchili C, Manda VK, Chittiboyina AG, Guernieri RL, Harrell WA, Jr., Webb RP, Smith LA, Khan IA. Utilizing Ayurvedic literature for the identification of novel phytochemical inhibitors of botulinum neurotoxin A. J Ethnopharmacol. 2017;197:211-7. doi: 10.1016/j.jep.2016.07.069.
  75. Yan Y, An Y, Wang X, Chen Y, Jacob MR, Tekwani BL, Dai L, Li X-C. Synthesis and Antimicrobial Evaluation of Fire Ant Venom Alkaloid Based 2-Methyl-6-alkyl-Δ(1,6)-piperideines. J Nat Prod. 2017;80(10):2795-8. doi: 10.1021/acs.jnatprod.7b00625.
  76. Yassin AM, El-Deeb NM, Metwaly AM, El FGF, Radwan MM, Hafez EE. Induction of Apoptosis in Human Cancer Cells Through Extrinsic and Intrinsic Pathways by Balanites aegyptiaca Furostanol Saponins and Saponin-Coated SilverNanoparticles. Appl Biochem Biotechnol. 2017;182(4):1675-93. doi: 10.1007/s12010-017-2426-3.
  77. Yuan H, Zhao J, Wang M, Khan SI, Zhai C, Xu Q, Huang J, Peng C, Xiong G, Wang W, Khan IA. Benzophenone glycosides from the flower buds of Aquilaria sinensis. Fitoterapia. 2017;121:170-4. doi: 10.1016/j.fitote.2017.07.013.
  78. Yuan W-J, Yuan J-B, Peng J-B, Ding Y-Q, Zhu J-X, Ren G. Flavonoids from the roots of Artocarpus heterophyllus. Fitoterapia. 2017;117:133-7.  doi: 10.1016/j.fitote.2017.01.016
  79. Zaki AA, Ali Z, Wang Y-H, El-Amier YA, Khan SI, Khan IA. Cytotoxic steroidal saponins from Panicum turgidum Forssk. Steroids. 2017;125:14-9. doi: 10.1016/j.steroids.2017.06.003.
  80. Zhai C, Wang M, Raman V, Rehman JU, Meng Y, Zhao J, Avula B, Wang Y-H, Khan Z, Khan IA. Eleutherococcus senticosus (Araliaceae) Leaf Morpho-Anatomy, Essential Oil Composition, and Its Biological Activity Against Aedes aegypti (Diptera: Culicidae). J Med Entomol. 2017;54(3):658-69. doi: 10.1093/jme/tjw221.
  81. Zulfiqar F, Khan SI, Ross SA, Ali Z, Khan IA. Prenylated flavonol glycosides from Epimedium grandiflorum: Cytotoxicity and evaluation against inflammation and metabolic disorder. Phytochem Lett. 2017;20:160-7. doi: 10.1016/j.phytol.2017.04.027.