HPLC isolation of the anti-plasmodially active bisbenzylisoquinone alkaloids present in roots of Cissampelos mucronata

The methanolic extract of dried, powdered Cissampelos mucronata roots possesses significant in vitro activity against Plasmodium falciparum. In order to enable further pharmacological testing, the substances responsible for the observed activity were purified, mainly by HPLC, using various stationar...

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Published inPhytochemical analysis Vol. 14; no. 1; pp. 13 - 22
Main Authors Tshibangu, J.N, Wright, A.D, Konig, G.M
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 2003
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Abstract The methanolic extract of dried, powdered Cissampelos mucronata roots possesses significant in vitro activity against Plasmodium falciparum. In order to enable further pharmacological testing, the substances responsible for the observed activity were purified, mainly by HPLC, using various stationary and mobile phases. The active principles were determined to be a series of bisbenzylisoquinoline alkaloids, a group of natural products for which one of the first routine preparative HPLC separation methods is described. Copyright © 2003 John Wiley & Sons, Ltd.
AbstractList The methanolic extract of dried, powdered Cissampelos mucronata roots possesses significant in vitro activity against Plasmodium falciparum. In order to enable further pharmacological testing, the substances responsible for the observed activity were purified, mainly by HPLC, using various stationary and mobile phases. The active principles were determined to be a series of bisbenzylisoquinoline alkaloids, a group of natural products for which one of the first routine preparative HPLC separation methods is described.
Abstract The methanolic extract of dried, powdered Cissampelos mucronata roots possesses significant in vitro activity against Plasmodium falciparum . In order to enable further pharmacological testing, the substances responsible for the observed activity were purified, mainly by HPLC, using various stationary and mobile phases. The active principles were determined to be a series of bisbenzylisoquinoline alkaloids, a group of natural products for which one of the first routine preparative HPLC separation methods is described. Copyright © 2003 John Wiley & Sons, Ltd.
The methanolic extract of dried, powdered Cissampelos mucronata roots possesses significant in vitro activity against Plasmodium falciparum. In order to enable further pharmacological testing, the substances responsible for the observed activity were purified, mainly by HPLC, using various stationary and mobile phases. The active principles were determined to be a series of bisbenzylisoquinoline alkaloids, a group of natural products for which one of the first routine preparative HPLC separation methods is described. Copyright © 2003 John Wiley & Sons, Ltd.
Author König, Gabriele M.
Wright, Anthony D.
Tshibangu, Jeannette Ndaya
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Cites_doi 10.1039/jr9610001896
10.1016/S0031-9422(00)88152-2
10.1139/v89-045
10.1039/jr9530003893
10.1039/JR9400000737
10.1248/yakushi1947.72.10_1219
10.1021/jo00324a036
10.1002/jccs.197000030
10.1007/978-3-642-68773-0
10.1016/S0040-4039(01)95519-4
10.1021/jo950767n
10.1021/np50052a001
10.1021/np50001a001
10.1016/S0040-4020(01)90186-3
10.1016/S0040-4039(00)77898-1
10.1016/S0021-9673(97)01065-0
10.1039/c29700001020
10.1016/0040-4020(72)80168-6
10.1016/S0040-4039(00)70400-X
10.1016/S0040-4020(01)81727-0
10.1021/np970257j
10.1007/978-3-662-09141-8
10.1016/S0021-9673(98)00416-6
10.1021/np9702042
10.1055/s-2000-8610
10.1128/AAC.16.6.710
10.1021/np50025a001
10.1016/S0021-9673(00)00629-4
10.1128/AAC.40.8.1846
10.1021/np50075a001
10.1055/s-2007-969398
10.1021/np9700174
10.3891/acta.chem.scand.15-1130
10.1039/p29730000716
10.1016/S0378-8741(01)00409-3
10.1021/np9602527
10.1016/S0040-4039(00)00299-9
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References Egan RS, Stanaszek RS and Williamson DE. 1973. Solution conformation of (+)-tubocurarine chloride. J Chem Soc Perkin Trans II 716-717.
Guha KP, Mukherjee B and Mukherjee R. 1979. Bisbenzylisoquinoline alkaloids. Reviews. J Nat Prod 42: 1-85 [and references therein].
Koike L, Marsaioli AJ and Reis F de AM. 1981. Proton and carbon-13 nuclear magnetic resonance spectroscopy and conformational aspects of the curine class of bisbenzylisoquinoline alkaloids. J Org Chem 46: 2385-2389.
Berthou S, Jossang A, Guinaudeau H, Leboeuf M and Cavé A. 1988. Alcaloïdes bisbenzylisoquinoleiques biphenyliques de Guatteria guainensis. Tetrahedron 44: 1293-2201.
Kanyinda B, Vanhaelen-Fastré R and Vanhaelen M. 1996. Two new seco-bisbenzylisoquinoline alkaloids from the leaves of Anisocycla jollyana. J Nat Prod 59: 498-500.
Saa JM, Lakshimikantham MV, Mitchell MJ and Cava MP. 1976. Thalibrunimine, a new iminobisbenzylisoquinoline alkaloid; conformers of thalsimine. Tetrahedron Lett 7: 513-516.
Koike L, Marsaioli AJ, Rúveda EA and Reis F de AM. 1979. Stereochemical aspects and 13C-NMR spectroscopy of the berbamine class of bisbenzylisoquinoline alkaloids. Tetrahedron Lett 39: 3765-3768.
Wang XK, Zhao TF, Lai S, Shizuri Y and Yamamura S. 1993. Three cissampareine-type bisbenzylisoquinoline alkaloids from Cyclea species. Phytochemistry 33: 5, 1249-1252.
Kanyinda B, Vanhaelen-Fastré R and Vanhaelen M. 1997. Two new isochondodendrine-type alkaloids from the root of Anisocycla jollyana. J Nat Prod 60: 1121-1124.
Sun SW and Wu AC. 1998. Optimisation of the capillary electrophoretic separation of bisbenzylisoquinoline alkaloids by an overlapping resolution mapping scheme. J Chromatogr A 814: 223-231.
Schiff PL. 1997. Bisbenzylisoquinoline alkaloids. Reviews. J Nat Prod 60: 934-953 [and references therein].
Bhakuni SD, Satish S and Dhar MM. 1972. Absolute configuration of isococlaurine. Tetrahedron 28: 1093-1095.
Hall AM and Chang CJ. 1997. Multi-drug-resistance modulators from Stephania japonica. J Nat Prod 60: 1193-1195.
Bick IRC and Clezy PS. 1953. The cleavage of biscoclaurine alkaloids with sodium in liquid ammonia. Part I. Curine and chondrocurine. J Chem Soc 3893-3896.
Galinis DL, Wiemer DF and Cazin J. 1993. Cissampentin: a new bisbenzylisoquinoline alkaloid from Cissampelos fasciculata. Tetrahedron 49: 7, 1337-1342.
King H. 1940. Curare alkaloids. Part V. Alkaloids from Chondrodendron species and the origin of radix pareirae bravae. J Chem Soc 737-746.
Yang TH and Chen CM. 1970. Alkaloids of Nelumbo nucifera. J Chin Chem Soc 17: 4, 235-242 [Chem Abs 1971, 74: 100254g].
Cava MP, Kunitomo J and DaRocha AI. 1969. The alkaloids of Chondrodendron toxicoferum. Phytochemistry 8: 2341-2343.
Schiff PL. 1991. Bisbenzylisoquinoline alkaloids. J Nat Prod 54: 645-749 [and references therein].
Sun SW, Kuo CH, Lee SS and Chen CK. 2000. Determination of bisbenzylisoquinoline alkaloids by high-performance liquid chromatography (II). J Chromatogr A 891: 189-194.
Bhatnagar AK and Polpi SP. 1966. Chemical examination of the roots of Cissampelos pareira Linn. Part V. Structure and stereochemistry of Hayatidin. Experientia 23: 4, 242-243.
Tomita M and Yamaguchi H. 1952. Alkaloids of menispermaceous plants. XCVI. Syntheses of coclaurine and analogous compounds. 4. Synthesis of dl-isococlaurine. J Pharm Soc Japan 72: 1219-1222.
Ndaya Tshibangu JN, Chifundera K, Kaminsky R, Wright AD and König GM. 2002. Screening of African medicinal plants for anti-microbial and enzyme inhibitory activity. J Ethnopharmac 80: 25-35.
Tomita M, Furukawa H, Yang TH and Lin TJ. 1964. Studies on the alkaloids of loti embryo (1). Structure of isoliensinine. Tetrahedron Lett 37: 2637-2642.
Desjardins RE, Canfield CJ, Haynes DM and Chulay JD. 1979. Quantitative assessment of anti-malarial activity in vitro by a semi-automated microdilution technique. Antimicrob Agents Chemother 16: 710-718.
Mambu L, Martin MT, Razafimahefa D, Ramanitrahasimbola D, Rasoanaivo P and Frappier F. 2000. Spectral characterisation and anti-plasmodial activity of bisbenzylisoquinolines from Isolona ghesquiereina. Planta Med 66: 537-540.
Schiff PL. 1987. Bisbenzylisoquinoline alkaloids. J Nat Prod 50: 529-599 [and references therein].
Sun SW, Lee SS, Wu AC and Chen CK. 1998. Determination of bisbenzylisoquinoline alkaloids by high-performance liquid chromatography. J Chromatogr A 799: 337-342.
Chowdhury AP and Roy R. 1972. Chemical investigations on Cissampelos pareira Linn. Sci Cult 38: 358-359.
Jossang A, Cavé A, Saez J, Bartoli MH, Cavé A and Jossang P. 1996. Two highly populated conformations at room temperature of monterine and granjine, anti-tumour bisbenzylisoquinoline alkaloids: origin and three dimensional structures. J Org Chem 61: 3023-3030.
Bhattacharji S, Roy AC and Dhar ML. 1962. Isolation and structure of hayatidin. J Sci Ind Res 21 B: 428-433.
Haynes LJ, Herbert EJ and Plimmer JR. 1966. (++)-4″-O-methylcurine from Cissampelos pareira L. J Chem Soc 615-617.
Ridley GR, Hofheinz W, Matile H, Jaquet C, Dorn A, Masciadri R, Jolidon S, Richter WF, Guenzi A, Girometta MA, Urwyler H, Huber W, Thaithong S and Peters W. 1996. 4-Aminoquinoline analogues of chloroquine with shortened side chains retain activity against chloroquine-resistant Plasmodium falciparum. Antimicrob Agents Chemother 40: 1846-1854.
Schiff PL. 1983. Bisbenzylisoquinoline alkaloids. J Nat Prod 46: 1-43 [and references therein].
Wagner H, Bladt S and Zgainski EM. 1983. Drogenanalyse. Springer: Berlin.
Telezhenetskaya MV and Yunusov SY. 1965. Structure of thalmine and thalmidine. Dokl Akad Nauk SSSR 162: 254 [Chem Abs 63: 5689].
Hultin E. 1961. Bisbenzylisoquinoline alkaloids. II. Methods for preparing the two monomethyl ethers of d-chondrocurine. Acta Chem Scand 15: 5, 1130-1140.
Saez J, Fernandez E, Jossang A, Cavé A and Cavé A. 1988. Nouveaux alcaloïdes bisbenzylisoquinoléiques biphényliques de Crematosperma sp. Can J Chem 67: 275-278.
Lemli J, Galeffi C, Messana I, Nicoletti M and Marini-Bettolo GB. 1985. A new bisbenzylisoquinoline alkaloid from a Peruvian curare. Planta Med 51: 68-69.
Menachery MD, Stern EW, Steinbeiser RJ, Freyer AJ and Killmer LB. 2000. Cavanine, a novel α-hydroxybisbenzylisoquinoline alkaloid from Sciadotenia toxifera (Krukoff and A.C. Smith). Tetrahedron Lett 41: 2843-2846.
Bick IRC, Harley-Mason J, Sheppard N and Vernengo MJ. 1961. Structural correlations in the nuclear magnetic resonance spectra of bisbenzylisoquinoline and aporphine alkaloids. J Chem Soc 1896-1903.
Latscha HP and Klein HA. 1993. Organische Chemie- Basiswissen II, 3rd ed. Springer: Berlin; 52.
Everett AJ, Lowe LA and Wilkinson S. 1970. Revision of the structures of (+)-tubocurine chloride and (+)-chondrocurine. Chem Commun 1020-1021.
1979; 39
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Chowdhury AP (e_1_2_1_9_1) 1972; 38
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Wang XK (e_1_2_1_44_1) 1993; 33
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Telezhenetskaya MV (e_1_2_1_40_1) 1965; 162
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References_xml – volume: 59
  start-page: 498
  year: 1996
  end-page: 500
  article-title: Two new seco‐bisbenzylisoquinoline alkaloids from the leaves of
  publication-title: J Nat Prod
– volume: 41
  start-page: 2843
  year: 2000
  end-page: 2846
  article-title: Cavanine, a novel α‐hydroxybisbenzylisoquinoline alkaloid from (Krukoff and A.C. Smith)
  publication-title: Tetrahedron Lett
– year: 1983
– volume: 49
  start-page: 7
  year: 1993
  end-page: 1342
  article-title: Cissampentin: a new bisbenzylisoquinoline alkaloid from
  publication-title: Tetrahedron
– volume: 40
  start-page: 1846
  year: 1996
  end-page: 1854
  article-title: 4‐Aminoquinoline analogues of chloroquine with shortened side chains retain activity against chloroquine‐resistant
  publication-title: Antimicrob Agents Chemother
– volume: 23
  start-page: 4
  year: 1966
  end-page: 243
  article-title: Chemical examination of the roots of Linn. Part V. Structure and stereochemistry of Hayatidin
  publication-title: Experientia
– start-page: 737
  year: 1940
  end-page: 746
  article-title: Curare alkaloids. Part V. Alkaloids from species and the origin of radix pareirae bravae
  publication-title: J Chem Soc
– start-page: 1896
  year: 1961
  end-page: 1903
  article-title: Structural correlations in the nuclear magnetic resonance spectra of bisbenzylisoquinoline and aporphine alkaloids
  publication-title: J Chem Soc
– volume: 17
  start-page: 4
  year: 1970
  end-page: 242
  article-title: Alkaloids of
  publication-title: J Chin Chem Soc
– start-page: 1020
  year: 1970
  end-page: 1021
  article-title: Revision of the structures of (+)‐tubocurine chloride and (+)‐chondrocurine
  publication-title: Chem Commun
– volume: 28
  start-page: 1093
  year: 1972
  end-page: 1095
  article-title: Absolute configuration of isococlaurine
  publication-title: Tetrahedron
– volume: 33
  start-page: 5
  year: 1993
  end-page: 1252
  article-title: Three cissampareine‐type bisbenzylisoquinoline alkaloids from species
  publication-title: Phytochemistry
– volume: 38
  start-page: 358
  year: 1972
  end-page: 359
  article-title: Chemical investigations on Linn
  publication-title: Sci Cult
– volume: 54
  start-page: 645
  year: 1991
  end-page: 749
  article-title: Bisbenzylisoquinoline alkaloids
  publication-title: J Nat Prod
– volume: 72
  start-page: 1219
  year: 1952
  end-page: 1222
  article-title: Alkaloids of menispermaceous plants. XCVI. Syntheses of coclaurine and analogous compounds. 4. Synthesis of dl‐isococlaurine
  publication-title: J Pharm Soc Japan
– start-page: 52
  year: 1993
– volume: 891
  start-page: 189
  year: 2000
  end-page: 194
  article-title: Determination of bisbenzylisoquinoline alkaloids by high‐performance liquid chromatography (II)
  publication-title: J Chromatogr A
– volume: 51
  start-page: 68
  year: 1985
  end-page: 69
  article-title: A new bisbenzylisoquinoline alkaloid from a Peruvian curare
  publication-title: Planta Med
– volume: 162
  start-page: 254
  year: 1965
  article-title: Structure of thalmine and thalmidine
  publication-title: Dokl Akad Nauk SSSR
– volume: 44
  start-page: 1293
  year: 1988
  end-page: 2201
  article-title: Alcaloïdes bisbenzylisoquinoleiques biphenyliques de
  publication-title: Tetrahedron
– volume: 42
  start-page: 1
  year: 1979
  end-page: 85
  article-title: Bisbenzylisoquinoline alkaloids. Reviews
  publication-title: J Nat Prod
– start-page: 615
  year: 1966
  end-page: 617
  article-title: (++)‐4″‐O‐methylcurine from L
  publication-title: J Chem Soc
– volume: 61
  start-page: 3023
  year: 1996
  end-page: 3030
  article-title: Two highly populated conformations at room temperature of monterine and granjine, anti‐tumour bisbenzylisoquinoline alkaloids: origin and three dimensional structures
  publication-title: J Org Chem
– volume: 39
  start-page: 3765
  year: 1979
  end-page: 3768
  article-title: Stereochemical aspects and C‐NMR spectroscopy of the berbamine class of bisbenzylisoquinoline alkaloids
  publication-title: Tetrahedron Lett
– volume: 80
  start-page: 25
  year: 2002
  end-page: 35
  article-title: Screening of African medicinal plants for anti‐microbial and enzyme inhibitory activity
  publication-title: J Ethnopharmac
– volume: 7
  start-page: 513
  year: 1976
  end-page: 516
  article-title: Thalibrunimine, a new iminobisbenzylisoquinoline alkaloid; conformers of thalsimine
  publication-title: Tetrahedron Lett
– start-page: 428
  year: 1962
  end-page: 433
  article-title: Isolation and structure of hayatidin
  publication-title: J Sci Ind Res
– volume: 60
  start-page: 934
  year: 1997
  end-page: 953
  article-title: Bisbenzylisoquinoline alkaloids. Reviews
  publication-title: J Nat Prod
– volume: 46
  start-page: 2385
  year: 1981
  end-page: 2389
  article-title: Proton and carbon‐13 nuclear magnetic resonance spectroscopy and conformational aspects of the curine class of bisbenzylisoquinoline alkaloids
  publication-title: J Org Chem
– volume: 50
  start-page: 529
  year: 1987
  end-page: 599
  article-title: Bisbenzylisoquinoline alkaloids
  publication-title: J Nat Prod
– volume: 66
  start-page: 537
  year: 2000
  end-page: 540
  article-title: Spectral characterisation and anti‐plasmodial activity of bisbenzylisoquinolines from
  publication-title: Planta Med
– volume: 8
  start-page: 2341
  year: 1969
  end-page: 2343
  article-title: The alkaloids of
  publication-title: Phytochemistry
– volume: 60
  start-page: 1121
  year: 1997
  end-page: 1124
  article-title: Two new isochondodendrine‐type alkaloids from the root of
  publication-title: J Nat Prod
– year: 2002
– volume: 67
  start-page: 275
  year: 1988
  end-page: 278
  article-title: Nouveaux alcaloïdes bisbenzylisoquinoléiques biphényliques de sp
  publication-title: Can J Chem
– volume: 814
  start-page: 223
  year: 1998
  end-page: 231
  article-title: Optimisation of the capillary electrophoretic separation of bisbenzylisoquinoline alkaloids by an overlapping resolution mapping scheme
  publication-title: J Chromatogr A
– volume: 16
  start-page: 710
  year: 1979
  end-page: 718
  article-title: Quantitative assessment of anti‐malarial activity by a semi‐automated microdilution technique
  publication-title: Antimicrob Agents Chemother
– volume: 46
  start-page: 1
  year: 1983
  end-page: 43
  article-title: Bisbenzylisoquinoline alkaloids
  publication-title: J Nat Prod
– volume: 37
  start-page: 2637
  year: 1964
  end-page: 2642
  article-title: Studies on the alkaloids of loti embryo (1). Structure of isoliensinine
  publication-title: Tetrahedron Lett
– start-page: 716
  year: 1973
  end-page: 717
  article-title: Solution conformation of (+)‐tubocurarine chloride
  publication-title: J Chem Soc Perkin Trans II
– volume: 15
  start-page: 5
  year: 1961
  end-page: 1140
  article-title: Bisbenzylisoquinoline alkaloids. II. Methods for preparing the two monomethyl ethers of ‐chondrocurine
  publication-title: Acta Chem Scand
– start-page: 3893
  year: 1953
  end-page: 3896
  article-title: The cleavage of biscoclaurine alkaloids with sodium in liquid ammonia. Part I. Curine and chondrocurine
  publication-title: J Chem Soc
– volume: 799
  start-page: 337
  year: 1998
  end-page: 342
  article-title: Determination of bisbenzylisoquinoline alkaloids by high‐performance liquid chromatography
  publication-title: J Chromatogr A
– volume: 60
  start-page: 1193
  year: 1997
  end-page: 1195
  article-title: Multi‐drug‐resistance modulators from
  publication-title: J Nat Prod
– ident: e_1_2_1_7_1
  doi: 10.1039/jr9610001896
– ident: e_1_2_1_8_1
  doi: 10.1016/S0031-9422(00)88152-2
– ident: e_1_2_1_32_1
  doi: 10.1139/v89-045
– ident: e_1_2_1_6_1
  doi: 10.1039/jr9530003893
– ident: e_1_2_1_21_1
  doi: 10.1039/JR9400000737
– ident: e_1_2_1_41_1
  doi: 10.1248/yakushi1947.72.10_1219
– ident: e_1_2_1_23_1
  doi: 10.1021/jo00324a036
– ident: e_1_2_1_45_1
  doi: 10.1002/jccs.197000030
– ident: e_1_2_1_43_1
  doi: 10.1007/978-3-642-68773-0
– ident: e_1_2_1_22_1
  doi: 10.1016/S0040-4039(01)95519-4
– ident: e_1_2_1_18_1
  doi: 10.1021/jo950767n
– ident: e_1_2_1_34_1
  doi: 10.1021/np50052a001
– ident: e_1_2_1_14_1
  doi: 10.1021/np50001a001
– start-page: 615
  year: 1966
  ident: e_1_2_1_16_1
  article-title: (++)‐4″‐O‐methylcurine from Cissampelos pareira L
  publication-title: J Chem Soc
  contributor:
    fullname: Haynes LJ
– volume: 162
  start-page: 254
  year: 1965
  ident: e_1_2_1_40_1
  article-title: Structure of thalmine and thalmidine
  publication-title: Dokl Akad Nauk SSSR
  contributor:
    fullname: Telezhenetskaya MV
– ident: e_1_2_1_13_1
  doi: 10.1016/S0040-4020(01)90186-3
– volume: 23
  start-page: 4
  year: 1966
  ident: e_1_2_1_4_1
  article-title: Chemical examination of the roots of Cissampelos pareira Linn. Part V. Structure and stereochemistry of Hayatidin
  publication-title: Experientia
  contributor:
    fullname: Bhatnagar AK
– ident: e_1_2_1_31_1
  doi: 10.1016/S0040-4039(00)77898-1
– ident: e_1_2_1_38_1
  doi: 10.1016/S0021-9673(97)01065-0
– ident: e_1_2_1_12_1
  doi: 10.1039/c29700001020
– ident: e_1_2_1_3_1
  doi: 10.1016/0040-4020(72)80168-6
– ident: e_1_2_1_42_1
  doi: 10.1016/S0040-4039(00)70400-X
– ident: e_1_2_1_2_1
  doi: 10.1016/S0040-4020(01)81727-0
– ident: e_1_2_1_20_1
  doi: 10.1021/np970257j
– ident: e_1_2_1_24_1
  doi: 10.1007/978-3-662-09141-8
– ident: e_1_2_1_37_1
  doi: 10.1016/S0021-9673(98)00416-6
– ident: e_1_2_1_15_1
  doi: 10.1021/np9702042
– ident: e_1_2_1_26_1
  doi: 10.1055/s-2000-8610
– ident: e_1_2_1_10_1
  doi: 10.1128/AAC.16.6.710
– volume: 38
  start-page: 358
  year: 1972
  ident: e_1_2_1_9_1
  article-title: Chemical investigations on Cissampelos pareira Linn
  publication-title: Sci Cult
  contributor:
    fullname: Chowdhury AP
– ident: e_1_2_1_33_1
  doi: 10.1021/np50025a001
– ident: e_1_2_1_39_1
  doi: 10.1016/S0021-9673(00)00629-4
– volume: 40
  start-page: 1846
  year: 1996
  ident: e_1_2_1_30_1
  article-title: 4‐Aminoquinoline analogues of chloroquine with shortened side chains retain activity against chloroquine‐resistant Plasmodium falciparum
  publication-title: Antimicrob Agents Chemother
  doi: 10.1128/AAC.40.8.1846
  contributor:
    fullname: Ridley GR
– ident: e_1_2_1_35_1
  doi: 10.1021/np50075a001
– ident: e_1_2_1_25_1
  doi: 10.1055/s-2007-969398
– ident: e_1_2_1_36_1
  doi: 10.1021/np9700174
– ident: e_1_2_1_17_1
  doi: 10.3891/acta.chem.scand.15-1130
– start-page: 428
  year: 1962
  ident: e_1_2_1_5_1
  article-title: Isolation and structure of hayatidin
  publication-title: J Sci Ind Res
  contributor:
    fullname: Bhattacharji S
– ident: e_1_2_1_11_1
  doi: 10.1039/p29730000716
– ident: e_1_2_1_29_1
  doi: 10.1016/S0378-8741(01)00409-3
– volume: 33
  start-page: 5
  year: 1993
  ident: e_1_2_1_44_1
  article-title: Three cissampareine‐type bisbenzylisoquinoline alkaloids from Cyclea species
  publication-title: Phytochemistry
  contributor:
    fullname: Wang XK
– ident: e_1_2_1_19_1
  doi: 10.1021/np9602527
– ident: e_1_2_1_27_1
  doi: 10.1016/S0040-4039(00)00299-9
– ident: e_1_2_1_28_1
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Snippet The methanolic extract of dried, powdered Cissampelos mucronata roots possesses significant in vitro activity against Plasmodium falciparum. In order to enable...
Abstract The methanolic extract of dried, powdered Cissampelos mucronata roots possesses significant in vitro activity against Plasmodium falciparum . In order...
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SubjectTerms alkaloids
Alkaloids - isolation & purification
Alkaloids - pharmacology
Animals
anti-malarial
anti-plasmodial
antimalarials
Antimalarials - isolation & purification
Antimalarials - pharmacology
Benzylisoquinolines
bisbenzylisoquinoline alkaloids
bisbenzylisoquinone alkaloids
cell lines
Cells, Cultured
chemical analysis
chemical structure
Chromatography, High Pressure Liquid
Cissampelos
Cissampelos - chemistry
Cissampelos mucronata
cytotoxicity
gas chromatography
high performance liquid chromatography
HPLC
humans
isolation
Isoquinolines - isolation & purification
Isoquinolines - pharmacology
Magnoliaceae
mass spectrometry
medicinal plants
Molecular Structure
natural product isolation
phytochemicals
plant extracts
Plant Roots - chemistry
Plasmodium falciparum
Plasmodium falciparum - drug effects
qualitative analysis
quantitative analysis
roots
Schisandra chinensis
spectral analysis
volatile compounds
Title HPLC isolation of the anti-plasmodially active bisbenzylisoquinone alkaloids present in roots of Cissampelos mucronata
URI https://api.istex.fr/ark:/67375/WNG-MQHBXR6Z-D/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fpca.673
https://www.ncbi.nlm.nih.gov/pubmed/12597251
https://search.proquest.com/docview/73046642
Volume 14
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