Alkaloids of the leaves of Voacanga grandifolia

Besides vobtusine and vobtusine-lactone, deoxyvobtusine was isolated from the leaves of Voacanga grandifolia (Miq. Rolfe. Spectral and chemical evi     

Chemical constituents of Melodinus hemsleyanus diels

Phytochemical investigation on the aerial parts of Melodinus hemsleyanus diels (Jahrb, Syst, 1995) led to the isolation and identification of 27 compounds, including fifteen aspidosperma-type alkaloids (1–15), four quinoline-type alkaloids (16–19), three quebrachamine-type alkaloids (20–22), and five eburna-type alkaloids (23–27). The structure of compound 1 was elucidated by means of spectroscopic analysis, including HRESIMS, and 1D and 2D NMR experiments. Compounds 1–2, 6, 10, 12, 13, 15, 16 and 20–27 are herein reported for the first time from the studied plant, while the compounds 1–2 and 21 have not previously been recorded in the genus Melodinus. The aspidosperma-type monoterpenoid indole alkaloids in M. hemsleyanus could serve as chemotaxonomic markers.     

Alkaloids of Dyera costulata

Six bisindole alkaloids have been isolated from the leaves of Dyera costulata (Apocynaceae). One is the known ochrolifuanine A and the others are the novel ochrolifuanines E and F, and the 18-dehydroochrolifuanines A, E and F.     

Alkaloids of melodinus guillauminii

Fourteen alkaloids were isolated from the stem bark and aerial parts of Melodinus guillauminii. They were 11-hydroxytabersonine, venalstonine, venalstonidine, 14,15-seco-3-oxokopsinal, 3-oxovenalstonine, 11-methoxy-Δ¹⁴– vincamenine, 3-oxo-hydroxykopsinine, 11-methoxy-Δ¹⁴-vincanol, kopsinine, 15-α-hydroxykopsinine, 11-methoxy- tabersonine, pleiocarpamine, 19-β-hydroxyvenalstonine and guillauminiine.     

Majvinine: A new indole alkaloid of Vinca major

A new alkaloid, majvinine, was isolated from aerial parts of Vinca major. Its structure was determined by chemical and spectroscopic investigations     

Corolla tube formation in six species of apocynaceae

Corolla tube formation inTrachelospermum asiaticum, Nerium indicum var.leucanthum, Anodendrom affine, Vinca major, Catharanthus roseus andAmsonia elliptica was investigated anatomically. The corolla tube formation among these species is basically similar. The bases of petal primordia extend laterally to the interprimordial regions, the upward growth occurrig at those regions just beside the petal bases. The extending petal bases connect with each other at the bases of the abaxial side of stamen primordia in the early stage of the corolla development. The upward growth at the coonnected regions results in the formation of a short corolla tube but is weakened rapidly. At the stage of the mutual connection of petal bases, a common base of petal and stamen primordia is initiated. This common base develops into the lower portion of the corolla tube, i.e. the portion below the stamen insertion. In a relatively late stage, adjacent margins, of the corolla lobes fuse postgenitally at their lower portions, resulting in the formation of almost all of the upper portion of the corolla tube. The corona inNerium andVinca is initiated by the active adaxial growth of the upper portion of the corolla tube.     

Formation of catharanthine,akuammicine and vindoline in Catharanthus roseus suspension cells

Catharanthine and akuammicine, together with ajmalicine and strictosidine, were isolated from a culture strain of Catharanthus roseus suspension cells. The biosynthetic capability of the cultured cells to produce akuammicine, catharanthine and vindoline was confirmed by feeding experiments with dl-tryptophan-[3-¹⁴C] to yield the radioactive alkaloids.     

19-hydroxycoronaridin und 19-hydroxyibogamin,zwei antibiotisch wirksame alkaloide vom ibogamin-typ

During the separation of an extract from Tabernaemontana glandulosa, small amounts of a new alkaloid were obtained for which the structure 19-hydroxycoronaridine was deduced. This new alkaloid and 19-hydroxyibogamine, which can be obtained from it, show marked antibiotic activity in the agar plate diffusion test.