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Volumn , Issue , 2012, Pages 53-66

Novel Biomedical Agents from Plants

Author keywords

glucosidase; Acetylcholinesterase; Bioactivity; Biosynthesis; Enzyme inhibition; Glutathione s transferase; Isolation; Natural products; Pharmacophore; Phytochemistry

Indexed keywords


EID: 84882754203     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.2174/978160805114411201010053     Document Type: Chapter
Times cited : (1)

References (56)
  • 1
    • 34447096207 scopus 로고    scopus 로고
    • Plant natural products: Back to the future or into extinction
    • McChesney JD, Venkataraman SK, Henri JT. Plant natural products: Back to the future or into extinction? Phytochemistry 2007; 68: 2015-22.
    • (2007) Phytochemistry , vol.68 , pp. 2015-2022
    • McChesney, J.D.1    Venkataraman, S.K.2    Henri, J.T.3
  • 2
    • 34247109045 scopus 로고    scopus 로고
    • Natural products as source of new drugs over the last 25 years
    • Newman DJ, Cragg GM. Natural products as source of new drugs over the last 25 years. J Nat Prod 2007; 70: 461-77.
    • (2007) J Nat Prod , vol.70 , pp. 461-477
    • Newman, D.J.1    Cragg, G.M.2
  • 3
    • 0034082239 scopus 로고    scopus 로고
    • The influence of natural products upon drug discovery
    • Newman DJ, Craig GM, Sanderb KM. The influence of natural products upon drug discovery. Nat Prod Rep 2000; 17: 215-34.
    • (2000) Nat Prod Rep , vol.17 , pp. 215-234
    • Newman, D.J.1    Craig, G.M.2    Sanderb, K.M.3
  • 4
    • 77956342834 scopus 로고    scopus 로고
    • Innovations in Chemical Biology
    • In: Sener B, Ed, New York, Springer
    • Ata A. In: Sener B, Ed. Innovations in Chemical Biology. New York, Springer 2009; pp. 51-60.
    • (2009) , pp. 51-60
    • Ata, A.1
  • 5
    • 37149045604 scopus 로고    scopus 로고
    • Gluthathione S-transferase and acetylcholinesterase inhibiting natural products from medicinally important plants
    • Ata A, Van Den Bosch SA, Harwanik DJ, Pidsinski GE. Gluthathione S-transferase and acetylcholinesterase inhibiting natural products from medicinally important plants. Pure Appl Chem 2007; 70: 2269-76.
    • (2007) Pure Appl Chem , vol.70 , pp. 2269-2276
    • Ata, A.1    Van Den Bosch, S.A.2    Harwanik, D.J.3    Pidsinski, G.E.4
  • 6
    • 54749133402 scopus 로고    scopus 로고
    • The discovery and application of inhibitors of glutathione S-transferase as therapeutic agents -a review
    • Ata A, Udenigwe CC. The discovery and application of inhibitors of glutathione S-transferase as therapeutic agents -a review. Curr Bioactive Compds 2008; 4: 41-50.
    • (2008) Curr Bioactive Compds , vol.4 , pp. 41-50
    • Ata, A.1    Udenigwe, C.C.2
  • 7
    • 34447509879 scopus 로고    scopus 로고
    • New chemical constituents of Ambrosia psilostachya
    • ARKIVOC
    • Ata A, Diduck C, Udenigwe CC, Zahid S, Decken A. New chemical constituents of Ambrosia psilostachya. ARKIVOC 2007; 13: 195-203.
    • (2007) , vol.13 , pp. 195-203
    • Ata, A.1    Diduck, C.2    Udenigwe, C.C.3    Zahid, S.4    Decken, A.5
  • 8
    • 0023173876 scopus 로고
    • Mechanism of action of glutathione-dependent enzymes
    • Douglas KT. Mechanism of action of glutathione-dependent enzymes. Adv Enzymol Relat Areas Mol Biol 1987; 59: 103-67.
    • (1987) Adv Enzymol Relat Areas Mol Biol , vol.59 , pp. 103-167
    • Douglas, K.T.1
  • 9
    • 0025340142 scopus 로고
    • The glutathione binding site in glutathione S-transferases. Investigation of the cysteinyl, glycyl and gamma-glutamyl domains
    • Adang AE, Brussee J, Gen A van der, Mulder GJ. The glutathione binding site in glutathione S-transferases. Investigation of the cysteinyl, glycyl and gamma-glutamyl domains. Biochem J 1990; 269: 47-54.
    • (1990) Biochem J , vol.269 , pp. 47-54
    • Adang, A.E.1    Brussee, J.2    Der, G.A.V.3    Mulder, G.J.4
  • 10
    • 0023845218 scopus 로고
    • Characterization and localization of glutathione- S-transferases in rat brain and binding of hormones, neurotransmitters, and drugs
    • Abramovitz M, Homma H, Ishigaki S, Tansey F, Cammer W, Listowsky I. Characterization and localization of glutathione- S-transferases in rat brain and binding of hormones, neurotransmitters, and drugs. J Neurochem 1988; 50: 50-57.
    • (1988) J Neurochem , vol.50 , pp. 50-57
    • Abramovitz, M.1    Homma, H.2    Ishigaki, S.3    Tansey, F.4    Cammer, W.5    Listowsky, I.6
  • 11
    • 0025303623 scopus 로고
    • Characterization of glutathione Stransferase expression in lymphocytes from chronic lymphocytic leukemia patients
    • Schisselbauer JC, Silber R, Papadopoulos E, Abrams K, LaCreta FP, Tew KD. Characterization of glutathione Stransferase expression in lymphocytes from chronic lymphocytic leukemia patients. Cancer Res 1990; 50: 3562-68.
    • (1990) Cancer Res , vol.50 , pp. 3562-3568
    • Schisselbauer, J.C.1    Silber, R.2    Papadopoulos, E.3    Abrams, K.4    LaCreta, F.P.5    Tew, K.D.6
  • 12
    • 67650872625 scopus 로고    scopus 로고
    • Bioactive chemical constituents of Caesalpinia bonduc (Fabaceae)
    • Ata A, Gale EM, Samarasekera R. Bioactive chemical constituents of Caesalpinia bonduc (Fabaceae). Phytochem Lett 2009; 2: 106-9.
    • (2009) Phytochem Lett , vol.2 , pp. 106-109
    • Ata, A.1    Gale, E.M.2    Samarasekera, R.3
  • 14
    • 34047153270 scopus 로고    scopus 로고
    • Glutathione S-transferase inhibiting chemical constituents of Caesalpinia bonduc
    • Udenigwe CC, Ata A, Samarasekera R. Glutathione S-transferase inhibiting chemical constituents of Caesalpinia bonduc. Chem Pharm Bull 2007; 55: 442-45.
    • (2007) Chem Pharm Bull , vol.55 , pp. 442-445
    • Udenigwe, C.C.1    Ata, A.2    Samarasekera, R.3
  • 15
    • 78649526216 scopus 로고    scopus 로고
    • Glutathione S-transferase inhibitory, free radical scavenging, and anti-leishmanial activities of chemical constituents of Artocarpus nobilis and Matricaria chamomilla
    • Iverson CD, Zahid S, Li Y, Shoqafi AH, Ata A, Samarasekera R. Glutathione S-transferase inhibitory, free radical scavenging, and anti-leishmanial activities of chemical constituents of Artocarpus nobilis and Matricaria chamomilla. Phytochem Lett 2010; 3: 207-11.
    • (2010) Phytochem Lett , vol.3 , pp. 207-211
    • Iverson, C.D.1    Zahid, S.2    Li, Y.3    Shoqafi, A.H.4    Ata, A.5    Samarasekera, R.6
  • 16
    • 73349136790 scopus 로고    scopus 로고
    • Chemical constituents of Nauclea latifolia and their anti-GST and anti-fungal activities
    • Ata A, Udenigwe CC, Matochko W, Holloway P, Eze MO, Uzoegwu, PN. Chemical constituents of Nauclea latifolia and their anti-GST and anti-fungal activities. Nat Prod Comm 2009; 4: 1185-88.
    • (2009) Nat Prod Comm , vol.4 , pp. 1185-1188
    • Ata, A.1    Udenigwe, C.C.2    Matochko, W.3    Holloway, P.4    Eze, M.O.5    Uzoegwu, P.N.6
  • 17
    • 60649094943 scopus 로고    scopus 로고
    • Chemical constituents of Barleria prionitis and their enzyme inhibitory and free radical scavenging activities
    • Ata A, Kalhari KS, Samarasekera R. Chemical constituents of Barleria prionitis and their enzyme inhibitory and free radical scavenging activities. Phytochem Lett 2009; 2: 37-40.
    • (2009) Phytochem Lett , vol.2 , pp. 37-40
    • Ata, A.1    Kalhari, K.S.2    Samarasekera, R.3
  • 18
    • 33846622079 scopus 로고    scopus 로고
    • Mucoralactone A: an unusual steroid from the liquid culture of Mucor plumbeus
    • Ata A, Conci LJ, Orhan I. Mucoralactone A: an unusual steroid from the liquid culture of Mucor plumbeus. Heterocycles 2006; 68: 2097-2106.
    • (2006) Heterocycles , vol.68 , pp. 2097-2106
    • Ata, A.1    Conci, L.J.2    Orhan, I.3
  • 20
    • 0027429837 scopus 로고
    • Brain selective inhibition of acetylcholinesterase: a novel approach to therapy for Alzheimer's disease
    • Enz A, Amstutz R, Boddeke H, Gmelin G, Malonowski J. Brain selective inhibition of acetylcholinesterase: a novel approach to therapy for Alzheimer's disease. Prog Brain Res 1993; 98: 431-45.
    • (1993) Prog Brain Res , vol.98 , pp. 431-445
    • Enz, A.1    Amstutz, R.2    Boddeke, H.3    Gmelin, G.4    Malonowski, J.5
  • 21
    • 78650197817 scopus 로고    scopus 로고
    • Advances in the researches on cholinesterase inhibitors for the treatment of Alzheimer's disease
    • Fang L, Chen Y, Zhang Y. Advances in the researches on cholinesterase inhibitors for the treatment of Alzheimer's disease. Yaoxue Jinzhan 2009; 33: 289-96.
    • (2009) Yaoxue Jinzhan , vol.33 , pp. 289-296
    • Fang, L.1    Chen, Y.2    Zhang, Y.3
  • 23
    • 77949771090 scopus 로고    scopus 로고
    • Cholinesterase inhibitors as adjunctive therapy in patients with schizophrenia and schizoaffective disorder: a review and meta-analysis of the literature
    • Ribeiz SRI, Bassitt DP, Arrais JA, Avila R, Steffens DC, Bottino CMC. Cholinesterase inhibitors as adjunctive therapy in patients with schizophrenia and schizoaffective disorder: a review and meta-analysis of the literature. CNS Drugs 2010; 24: 303-17.
    • (2010) CNS Drugs , vol.24 , pp. 303-317
    • Ribeiz, S.R.I.1    Bassitt, D.P.2    Arrais, J.A.3    Avila, R.4    Steffens, D.C.5    Bottino, C.M.C.6
  • 24
    • 77952312984 scopus 로고    scopus 로고
    • Alkaloids
    • In Cordell GA, Ed, San Diego, CA, Elsevier
    • Heinrich M. In Cordell GA, Ed. Alkaloids. San Diego, CA, Elsevier. 2010; pp. 157-65.
    • (2010) , pp. 157-165
    • Heinrich, M.1
  • 25
    • 73249133781 scopus 로고    scopus 로고
    • Rivastigmine for the treatment of dementia in patients with progressive supranuclear palsy: Clinical observations as a basis for power calculations and safety analysis
    • Liepelt I, Gaenslen A, Godau J, et al. Rivastigmine for the treatment of dementia in patients with progressive supranuclear palsy: Clinical observations as a basis for power calculations and safety analysis. Alzheimers Demen 2010; 6: 70-74.
    • (2010) Alzheimers Demen , vol.6 , pp. 70-74
    • Liepelt, I.1    Gaenslen, A.2    Godau, J.3
  • 26
    • 0033917296 scopus 로고    scopus 로고
    • Hepatotoxicity of tacrine: occurrence of membrane fluidity alterations without involvement of lipid peroxidation
    • Galisteo M, Rissel M, Sergent O, et al. Hepatotoxicity of tacrine: occurrence of membrane fluidity alterations without involvement of lipid peroxidation. J Pharmacol Exp Ther 2000; 294: 160-67.
    • (2000) J Pharmacol Exp Ther , vol.294 , pp. 160-167
    • Galisteo, M.1    Rissel, M.2    Sergent, O.3
  • 27
    • 0034113018 scopus 로고    scopus 로고
    • Lack of adverse pharmacodynamic drug interactions with rivastigmine and twenty-two classes of medications
    • Grossberg GT, Stahelin HB, Messina JC, Anand R. Lack of adverse pharmacodynamic drug interactions with rivastigmine and twenty-two classes of medications. Int J Geriatr Psychiatry 2000; 15: 242-47.
    • (2000) Int J Geriatr Psychiatry , vol.15 , pp. 242-247
    • Grossberg, G.T.1    Stahelin, H.B.2    Messina, J.C.3    Anand, R.4
  • 28
    • 0034098363 scopus 로고    scopus 로고
    • Molecular modelling and QSAR of reversible acetylcholinesterase inhibitors
    • Kaur J, Zhang M-Q. Molecular modelling and QSAR of reversible acetylcholinesterase inhibitors. Curr Med Chem 2000; 7: 273-94.
    • (2000) Curr Med Chem , vol.7 , pp. 273-294
    • Kaur, J.1    Zhang, M.-Q.2
  • 29
    • 38549085277 scopus 로고    scopus 로고
    • In-vitro screening assays to identify natural or synthetic acetylcholinesterase inhibitors: Thin layer chromatography versus microplate methods
    • Di Giovanni S, Borloz A, Urbain A et al. In-vitro screening assays to identify natural or synthetic acetylcholinesterase inhibitors: Thin layer chromatography versus microplate methods. Eur J Pharm Sci 2008; 33: 109-19.
    • (2008) Eur J Pharm Sci , vol.33 , pp. 109-119
    • Di Giovanni, S.1    Borloz, A.2    Urbain, A.3
  • 30
    • 38049168553 scopus 로고    scopus 로고
    • Hopeahainol A: An acetylcholinesterase inhibitor from Hopea hainanensis
    • Ge HM, Zhu CH, Shi DH, et al. Hopeahainol A: An acetylcholinesterase inhibitor from Hopea hainanensis. Chem Eur J 2008; 14: 376-81.
    • (2008) Chem Eur J , vol.14 , pp. 376-381
    • Ge, H.M.1    Zhu, C.H.2    Shi, D.H.3
  • 31
    • 41249090622 scopus 로고    scopus 로고
    • N - Alkylated galanthamine derivatives: Potent acetylcholinesterase inhibitors from Leucojum aestivum
    • Berkov S, Codina C, Viladomat F, Bastida J. N - Alkylated galanthamine derivatives: Potent acetylcholinesterase inhibitors from Leucojum aestivum. Bioorg Med Chem Lett 2008; 18: 2263-66.
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 2263-2266
    • Berkov, S.1    Codina, C.2    Viladomat, F.3    Bastida, J.4
  • 32
    • 38149105897 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of helicid analogues as novel acetylcholinesterase inhibitors
    • Wen H, Lin C, Ling Q, et al. Synthesis and biological evaluation of helicid analogues as novel acetylcholinesterase inhibitors. Eur J Med Chem 2008: 43:166-73.
    • (2008) Eur J Med Chem , vol.43 , pp. 166-173
    • Wen, H.1    Lin, C.2    Ling, Q.3
  • 33
    • 73649106915 scopus 로고    scopus 로고
    • Acetylcholinesterase inhibitory activity of lycopodane-type alkaloids from the Icelandic Lycopodium annotinum ssp
    • Halldorsdottir ES, Jaroszewski JW, Olafsdottir ES. Acetylcholinesterase inhibitory activity of lycopodane-type alkaloids from the Icelandic Lycopodium annotinum ssp. alpestre. Phytochemistry 2010; 71: 149-57.
    • (2010) alpestre. Phytochemistry , vol.71 , pp. 149-157
    • Halldorsdottir, E.S.1    Jaroszewski, J.W.2    Olafsdottir, E.S.3
  • 34
    • 77953138321 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of a new series of berberine derivatives as dual inhibitors of acetylcholinesterase and butyrylcholinesterase
    • Huang L, Luo Z, He F, Lu J, Li X. Synthesis and biological evaluation of a new series of berberine derivatives as dual inhibitors of acetylcholinesterase and butyrylcholinesterase. Bioorg Med Chem 2010; 18: 4475-84.
    • (2010) Bioorg Med Chem , vol.18 , pp. 4475-4484
    • Huang, L.1    Luo, Z.2    He, F.3    Lu, J.4    Li, X.5
  • 35
    • 33751258231 scopus 로고    scopus 로고
    • New bioactive steroidal alkaloids from Buxus hyrcana
    • Babar ZU, Ata A, Meshkatalsadat MH. New bioactive steroidal alkaloids from Buxus hyrcana. Steroids 2006; 71: 1045-51.
    • (2006) Steroids , vol.71 , pp. 1045-1051
    • Babar, Z.U.1    Ata, A.2    Meshkatalsadat, M.H.3
  • 36
    • 0038204368 scopus 로고    scopus 로고
    • New triterpenoid alkaloid cholinesterase inhibitors from Buxus hyrcana
    • Choudhary MI, Shahnaz S, Parveen S, et al. New triterpenoid alkaloid cholinesterase inhibitors from Buxus hyrcana. J Nat Prod 2003; 66: 739-42.
    • (2003) J Nat Prod , vol.66 , pp. 739-742
    • Choudhary, M.I.1    Shahnaz, S.2    Parveen, S.3
  • 37
    • 15044358936 scopus 로고    scopus 로고
    • Recent studies on bioactive natural products
    • Atta-ur-Rahman, Choudhary MI. Recent studies on bioactive natural products. Pure Appl Chem 1999; 71: 1079-1081.
    • (1999) Pure Appl Chem , vol.71 , pp. 1079-1081
    • Atta-ur-rahman1    Choudhary, M.I.2
  • 39
    • 35848934607 scopus 로고    scopus 로고
    • New potent acetylcholinesterase inhibitors in the tetracyclic triterpene series
    • Sauvaitre T, Barlier M., Herlem D, et al. New potent acetylcholinesterase inhibitors in the tetracyclic triterpene series. J Med Chem 2007; 50: 5311-23.
    • (2007) J Med Chem , vol.50 , pp. 5311-5323
    • Sauvaitre, T.1    Barlier, M.2    Herlem, D.3
  • 40
    • 0034170289 scopus 로고    scopus 로고
    • Protection from vascular risk in diabetic hypertension
    • Corry DB, Tuck ML. Protection from vascular risk in diabetic hypertension. Curr Hypertens Resp 2000; 2: 154-59.
    • (2000) Curr Hypertens Resp , vol.2 , pp. 154-159
    • Corry, D.B.1    Tuck, M.L.2
  • 41
    • 79952039167 scopus 로고    scopus 로고
    • Chemical constituents of Drypetes gossweileri and their enzyme inhibitory and anti-fungal activities
    • Ata A, Tan DS, Matochko WL, Adesanwo JK. Chemical constituents of Drypetes gossweileri and their enzyme inhibitory and anti-fungal activities. Phytochem Lett 2011; 4: 34-37.
    • (2011) Phytochem Lett , vol.4 , pp. 34-37
    • Ata, A.1    Tan, D.S.2    Matochko, W.L.3    Adesanwo, J.K.4
  • 42
    • 37149008949 scopus 로고    scopus 로고
    • Sciences at the interface of chemistry and biology: Discoveries of α-glucosidase inhibitors and antiglycation agents
    • Atta-ur-Rahman, Choudhary MI, Basha FZ, Abbad G, Khan SN, Shah SAA. Sciences at the interface of chemistry and biology: Discoveries of α-glucosidase inhibitors and antiglycation agents. Pure Appl Chem 2007; 70; 2263-68.
    • (2007) Pure Appl Chem , vol.70 , pp. 2263-2268
    • Atta-ur-rahman1    Choudhary, M.I.2    Basha, F.Z.3    Abbad, G.4    Khan, S.N.5    Shah, S.A.A.6
  • 43
    • 51549116862 scopus 로고    scopus 로고
    • Phenylethyl cinnamides: A new series of α-glucosidase inhibitors from the leaves of Aegle marmelos
    • Phuwapraisirisan P, Puksasook T, Jong-aramruang J, Kokpol U. Phenylethyl cinnamides: A new series of α-glucosidase inhibitors from the leaves of Aegle marmelos. Bioorg Med Chem Lett 2008; 18: 4956-58.
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 4956-4958
    • Phuwapraisirisan, P.1    Puksasook, T.2    Jong-aramruang, J.3    Kokpol, U.4
  • 44
    • 45749132973 scopus 로고    scopus 로고
    • α-Glucosidase inhibitors ellagic acid derivatives with immunoinhibitory properties from Terminalia superba
    • Tabopda TK, Ngoupayo J, Liu J, et al. α-Glucosidase inhibitors ellagic acid derivatives with immunoinhibitory properties from Terminalia superba. Chem Pharm Bull 2008; 56: 847-50.
    • (2008) Chem Pharm Bull , vol.56 , pp. 847-850
    • Tabopda, T.K.1    Ngoupayo, J.2    Liu, J.3
  • 46
    • 84865069950 scopus 로고    scopus 로고
    • Research on method for synthesis of salacinol, a natural antidiabetic drug
    • Zhang L, Wang Y, Wang Z. Research on method for synthesis of salacinol, a natural antidiabetic drug. Huagong Shikan 2008; 22: 42-44.
    • (2008) Huagong Shikan , vol.22 , pp. 42-44
    • Zhang, L.1    Wang, Y.2    Wang, Z.3
  • 47
    • 46549085471 scopus 로고    scopus 로고
    • Synthesis of 2-amido, 2-amino, and 2-azido derivatives of the nitrogen analog of the naturally occurring glycosidase inhibitor salacinol and their inhibitory activities against OGlcNAcase and NagZ enzymes
    • Choubdar N, Bhat, RG, Stubbs KA, Yuzwa S, Pinto BM. Synthesis of 2-amido, 2-amino, and 2-azido derivatives of the nitrogen analog of the naturally occurring glycosidase inhibitor salacinol and their inhibitory activities against OGlcNAcase and NagZ enzymes. Carbohydrate Res 2008; 343:1766-77.
    • (2008) Carbohydrate Res , vol.343 , pp. 1766-1777
    • Choubdar, N.1    Bhat, R.G.2    Stubbs, K.A.3    Yuzwa, S.4    Pinto, B.M.5
  • 48
    • 74949102237 scopus 로고    scopus 로고
    • New glucosidase inhibitors from an ayurvedic herbal treatment for type 2 diabetes: Structures and inhibition of human intestinal maltase-glucoamylase with compounds from Salacia reticulata
    • Sim L, Jayakanthan K, Mohan S, et al. New glucosidase inhibitors from an ayurvedic herbal treatment for type 2 diabetes: Structures and inhibition of human intestinal maltase-glucoamylase with compounds from Salacia reticulata. Biochemistry 2010; 49: 443-51.
    • (2010) Biochemistry , vol.49 , pp. 443-451
    • Sim, L.1    Jayakanthan, K.2    Mohan, S.3
  • 49
    • 47549112929 scopus 로고    scopus 로고
    • α -Glucosidase inhibitor from kothala-himbutu (Salacia reticulata WIGHT)
    • Ozaki S, Oe H, Kitamura S. α -Glucosidase inhibitor from kothala-himbutu (Salacia reticulata WIGHT). J Nat. Prod 2008; 71: 981-84.
    • (2008) J Nat. Prod , vol.71 , pp. 981-984
    • Ozaki, S.1    Oe, H.2    Kitamura, S.3
  • 50
    • 65649134270 scopus 로고    scopus 로고
    • Triterpene acids isolated from Lagerstroemia speciosa leaves as α-glucosidase inhibitors
    • Hou W, Li Y, Zhang Q, et al. Triterpene acids isolated from Lagerstroemia speciosa leaves as α-glucosidase inhibitors. Phytother Res 2009; 23: 614-18.
    • (2009) Phytother Res , vol.23 , pp. 614-618
    • Hou, W.1    Li, Y.2    Zhang, Q.3
  • 51
    • 54349083268 scopus 로고    scopus 로고
    • α -Glucosidase inhibitors from Garcinia brevipedicellata (Clusiaceae)
    • Ngoupayo J, Tabopda, Turibio K, Ali MS,Tsamo E. α -Glucosidase inhibitors from Garcinia brevipedicellata (Clusiaceae). Chem Pharm Bull 2008; 56: 1466-69.
    • (2008) Chem Pharm Bull , vol.56 , pp. 1466-1469
    • Ngoupayo, J.1    Tabopda, T.K.2    Ali, M.S.3    Tsamo, E.4
  • 52
    • 64249171799 scopus 로고    scopus 로고
    • New Labdane diterpenes as intestinal α - glucosidase inhibitor from antihyperglycemic extract of Hedychium spicatum (Ham. Ex Smith) rhizomes
    • Reddy PP, Tiwari, AK, Rao RR, et al. New Labdane diterpenes as intestinal α - glucosidase inhibitor from antihyperglycemic extract of Hedychium spicatum (Ham. Ex Smith) rhizomes. Bioorg Med Chem Lett 2009; 19: 2562-65.
    • (2009) Bioorg Med Chem Lett , vol.19 , pp. 2562-2565
    • Reddy, P.P.1    Tiwari, K.A.2    Rao, R.R.3
  • 53
    • 64549084589 scopus 로고    scopus 로고
    • Dolichandroside A, A new α -glucosidase inhibitor and DPPH free-radical scavenger from Dolichandrone falcata Seem
    • Aparna P, Tiwari AK, Srinivas PV, Ali AZ, Anuradha V, Rao JM. Dolichandroside A, A new α -glucosidase inhibitor and DPPH free-radical scavenger from Dolichandrone falcata Seem. Phytother Res 2009; 23: 591-96.
    • (2009) Phytother Res , vol.23 , pp. 591-596
    • Aparna, P.1    Tiwari, A.K.2    Srinivas, P.V.3    Ali, A.Z.4    Anuradha, V.5    Rao, J.M.6
  • 54
    • 0001187230 scopus 로고
    • Biosynthesis of the 3-benzylchroman-4-one eucomin in Euconis bicolor
    • Dewick PM. Biosynthesis of the 3-benzylchroman-4-one eucomin in Euconis bicolor. Phytochemistry 1975; 14: 983-88.
    • (1975) Phytochemistry , vol.14 , pp. 983-988
    • Dewick, P.M.1
  • 55
    • 0343798333 scopus 로고
    • Biosynthesis of coumestrol in Phaseolus aureous Phytochemistry
    • Dewick PM, Baz W, Grisebach H. Biosynthesis of coumestrol in Phaseolus aureous Phytochemistry 1970; 9: 775-83.
    • (1970) , vol.9 , pp. 775-783
    • Dewick, P.M.1    Baz, W.2    Grisebach, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.