1. Academic Validation
  2. Biological activities of pyrrolidinoindoline alkaloids from Calycodendron milnei

Biological activities of pyrrolidinoindoline alkaloids from Calycodendron milnei

  • Planta Med. 1995 Aug;61(4):313-6. doi: 10.1055/s-2006-958090.
H E Saad 1 S H el-Sharkawy W T Shier
Affiliations

Affiliation

  • 1 Department of Pharmacognosy, Faculty of Pharmacy, University of Mansoura, Egypt.
Abstract

Certain genera of the tribe Psychotrieae, specifically Calycodendron and Psychotria, found on Pacific Islands, synthesize a series of Nb-methyltryptamine-derived Alkaloids made by linking together 2 to 8 pyrrolidinoindoline units. Nine Alkaloids of this class have been isolated from the aerial parts and stem bark of Calycodendron milnei, a species endemic to the Vaté Islands (New Hebrides), and examined for potential application as anti-cancer and anti-infective agents. All members of the series exhibited readily detected cytotoxic activity against proliferating and non-proliferating Vero African green monkey kidney cells in culture, with the most potent activity being exhibited by vatamine and quadrigemine C. Only hodgkinsine A exhibited substantial Antiviral activity against a DNA virus, herpes simplex type 1, and an RNA virus, vesicular stomatitis virus. All members of the series showed readily detected anti-bacterial, anti-fungal, and anti-candidal activities using both tube dilution and disc diffusion assay methods. The most potent anti-microbial Alkaloids were hodgkinsine A and quadrigemine C, which exhibited minimum inhibitory concentration (MIC) values as low as 5 micrograms/ml.

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