Ibogan, tacaman, and cytotoxic bisindole alkaloids from tabernaemontana. Cononusine, an iboga alkaloid with unusual incorporation of a pyrrolidone moiety.

Six new indole alkaloids, viz., cononusine (1, a rare example of an iboga-pyrrolidone conjugate), ervaluteine (2), vincamajicine (3), tacamonidine (4), 6-oxoibogaine (5), and N(4)-chloromethylnorfluorocurarine chloride (6), and two new vobasinyl-iboga bisindole alkaloids, ervatensines A (7) and B (8), in addition to other known alkaloids, were isolated from the stem-bark extract of the Malayan Tabernaemontana corymbosa. The structures of these alkaloids were established on the basis of NMR and MS analyses and, in one instance (7), confirmed by X-ray diffraction analysis. Vincamajicine (3) showed appreciable activity in reversing multidrug resistance in vincristine-resistant KB cells (IC50 2.62 μM), while ervatensines A (7) and B (8) and two other known bisindoles displayed pronounced in vitro growth inhibitory activity against human KB cells (IC50 < 2 μM). Compounds 7 and 8 also showed good growth inhibitory activity against A549, MCF-7, MDA-468, HCT-116, and HT-29 cells (IC50 0.70-4.19 μM). Cell cycle and annexin V-FITC apoptosis assays indicated that compounds 7 and 8 inhibited proliferation of HCT-116 and MDA-468 cells, evoking apoptotic and necrotic cell death.

[1]  T. Kam,et al.  Five new iboga alkaloids from Tabernaemontana corymbosa. , 2002, Journal of natural products.

[2]  G. Tan,et al.  Four tetracyclic oxindole alkaloids and a taberpsychine derivative from a Malayan Tabernaemontana. , 2009, Phytochemistry.

[3]  Gérald Bernardinelli,et al.  Reporting and evaluating absolute-structure and absolute-configuration determinations , 2000 .

[4]  S. Pelletier Alkaloids: Chemical and Biological Perspectives , 1992, Alkaloids: Chemical and Biological Perspectives.

[5]  Jian-Ping Yu,et al.  Indole alkaloids from Ervatamia chinensis. , 2012, Phytochemistry.

[6]  J. Nuzillard,et al.  Alkaloids from stem bark and leaves of Peschiera buchtieni , 1995 .

[7]  T. Kam,et al.  Tronocarpine, a novel pentacyclic indole incorporating a seven-membered lactam moiety , 2000 .

[8]  T. Kam,et al.  Voastrictine, a novel pentacyclic quinolinic alkaloid from Tabernaemontana , 2001 .

[9]  C. Hootele,et al.  The alkaloids of voacanga thouarsii var. obtusa , 1970 .

[10]  D. J. Middleton Apocynaceae (subfamilies Rauvolfioideae and Apocynoideae) , 2007 .

[11]  T. Kam,et al.  Mersinines A and B and mersiloscine, novel quinolinic alkaloids from Kopsia , 2001 .

[12]  T. V. van Beek,et al.  Tabernaemontana L. (Apocynaceae): a review of its taxonomy, phytochemistry, ethnobotany and pharmacology. , 1984, Journal of ethnopharmacology.

[13]  T. Bradshaw,et al.  Novel antitumour indole alkaloid, Jerantinine A, evokes potent G2/M cell cycle arrest targeting microtubules , 2014, Investigational New Drugs.

[14]  T. A. Beek,et al.  Alkaloids of Tabernaemontana eglandulosa , 1984 .

[15]  M. Hayashi,et al.  Lundurines A-D, cytotoxic indole alkaloids incorporating a cyclopropyl moiety from Kopsia tenuis and revision of the structures of tenuisines A-C , 2004 .

[16]  M. Cava,et al.  Problems in chemotaxonomy. V. Alkaloids of Peschiera lundii. Isolation and structure elucidation of voacristine pseudoindoxyl and iboxygaine hydroxyindolenine , 1969 .

[17]  A. Leeuwenberg A revision of Tabernaemontana: the old world species. , 1991 .

[18]  K. Komiyama,et al.  Jerantinines A-G, cytotoxic Aspidosperma alkaloids from Tabernaemontana corymbosa. , 2008, Journal of natural products.

[19]  T. Kam,et al.  Cytotoxic vobasine, tacaman, and corynanthe-tryptamine bisindole alkaloids from Tabernaemontana and structure revision of tronoharine. , 2014, Journal of natural products.

[20]  T. Kam,et al.  Tronoharine, a novel hexacyclic indole alkaloid from a Malayan Tabernaemontana , 1999 .

[21]  K. Lim,et al.  Seco-tabersonine alkaloids from Tabernaemontana corymbosa. , 2009, Phytochemistry.

[22]  P. Clivio,et al.  Alkaloids from leaves and root bark ofErvatamia hirta , 1991 .

[23]  T. Kam,et al.  Conodirinines A and B, Novel Vobasine‐Iboga Bisindoles Incorporating an Additional Tetrahydro‐1,3‐oxazine Unit on the Vobasinyl Moiety , 2003 .

[24]  M. Hayashi,et al.  Structure, biological activity, and a biomimetic partial synthesis of the lirofolines, novel pentacylic indole alkaloids from Tabernaemontana , 2010 .

[25]  H. Flack,et al.  On enantiomorph‐polarity estimation , 1983 .

[26]  H. Gottlieb,et al.  The C(2) Stereochemistry of Iboluteine , 1977 .

[27]  H. L. Filho,et al.  13C NMR analysis of alkaloids from peschiera fuchsiaefolia , 1984 .

[28]  N. Bisset,et al.  Alkaloids from the leaves ofStrychnos icaja Baill. , 1973 .

[29]  T. Kam,et al.  New bisindole alkaloids from Tabernaemontana corymbosa. , 2003, Journal of natural products.

[30]  Juming Yan,et al.  Cytotoxic indole alkaloids from Tabernaemontana divaricata. , 2013, Journal of natural products.

[31]  K. Lim,et al.  Conoliferine and isoconoliferine, structurally novel alkaloid-lignan conjugates from Tabernaemontana corymbosa. , 2009 .

[32]  S. Pelletier Alkaloids: Chemical and Biological Perspectives , 1991, Alkaloids: Chemical and Biological Perspectives.

[33]  T. Kam,et al.  Conodurine, conoduramine, and ervahanine derivatives from Tabernaemontana corymbosa. , 2003, Phytochemistry.

[34]  M. Hayashi,et al.  Conolutinine, a hexacyclic indole alkaloid with a novel ring system incorporating a diazaspiro center and fused oxadiazepine–tetrahydrofuran rings , 2009 .

[35]  K. Lim,et al.  Conomicidines A and B, Unusual Alkaloid-Hydroxycinnamyl Alcohol Conjugates from Tabernaemontana corymbosa. , 2009 .