4.3 Article

Isolation of Acridone Alkaloids and N-[(4-Monoterpenyloxy)phenylethyl]-Substituted Sulfur-Containing Propanamide Derivatives from Glycosmis parva and Their Anti-herpes Simplex Virus Activity

Journal

CHEMICAL & PHARMACEUTICAL BULLETIN
Volume 57, Issue 11, Pages 1246-1250

Publisher

PHARMACEUTICAL SOC JAPAN
DOI: 10.1248/cpb.57.1246

Keywords

Glycosmis parva; glycosparvarine; S-deoxydihydroglyparvin, S-deoxytetrahydroglyparvin; anti-herpes simplex virus activity

Funding

  1. Royal Golden Jubilee (RGJ) [PHD/0212/2547]
  2. Thailand Research Fund

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Six acridone alkaloids including a new glycosparvarine (1), three limonoids, and four N-[4-monoterpenyloxy)phenylethyl]-substituted sulfur-containing propanamide derivatives including two new species, (+)-S-deoxydihydroglyparvin (10) and (+)-S-deoxytetrahydroglyparvin (11), were isolated from the branches and the leaves of Glycosmis parva CRAM collected in the east of Thailand. Antiviral activity evaluation of isolates against herpes simplex virus (HSV) type 1 and 2 disclosed that two acridone alkaloids, glycosparvarine (1) and glycofolinine (4), showed moderate inhibitory activities with 50% effective concentration (EC50) of 348 mu M and 151 mu M respectively; as well, (+)-S-deoxydihydroglyparvin (10) exhibited anti-HSV activity at the lower concentration.

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