New prenylated benzoic acid derivatives of Piper hispidum.Pharmazie. 2005 Jun; 60(6):455-7.P
Abstract
Three new 4-hydroxy-benzoic acid derivatives, 4-methoxy-3,5-bis-(3-hydroxy-3-methyl-1-butenyl)benzoate, 3-hydroxy-2-(1-hydroxy-1-methylethyl)-2,3-dihydrobenzofuran-5-carboxylic acid, and 3-hydroxy-2-(1-hydroxy-1-methylethyl)-2,3-dihydrobenzofuran-5-carboxylic acid methyl ester together with eight known compounds, have been isolated from the stems of Piper hispidum. Their structures were elucidated by a detailed spectroscopic analysis. In addition, the cytotoxicity of seven isolated compounds has been evaluated, revealing a moderate activity for three derivatives of dillapiole.
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
15997836
Citation
Friedrich, U, et al. "New Prenylated Benzoic Acid Derivatives of Piper Hispidum." Die Pharmazie, vol. 60, no. 6, 2005, pp. 455-7.
Friedrich U, Siems K, Solis PN, et al. New prenylated benzoic acid derivatives of Piper hispidum. Pharmazie. 2005;60(6):455-7.
Friedrich, U., Siems, K., Solis, P. N., Gupta, M. P., & Jenett-Siems, K. (2005). New prenylated benzoic acid derivatives of Piper hispidum. Die Pharmazie, 60(6), 455-7.
Friedrich U, et al. New Prenylated Benzoic Acid Derivatives of Piper Hispidum. Pharmazie. 2005;60(6):455-7. PubMed PMID: 15997836.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - New prenylated benzoic acid derivatives of Piper hispidum.
AU - Friedrich,U,
AU - Siems,K,
AU - Solis,P N,
AU - Gupta,M P,
AU - Jenett-Siems,K,
PY - 2005/7/7/pubmed
PY - 2005/8/24/medline
PY - 2005/7/7/entrez
SP - 455
EP - 7
JF - Die Pharmazie
JO - Pharmazie
VL - 60
IS - 6
N2 - Three new 4-hydroxy-benzoic acid derivatives, 4-methoxy-3,5-bis-(3-hydroxy-3-methyl-1-butenyl)benzoate, 3-hydroxy-2-(1-hydroxy-1-methylethyl)-2,3-dihydrobenzofuran-5-carboxylic acid, and 3-hydroxy-2-(1-hydroxy-1-methylethyl)-2,3-dihydrobenzofuran-5-carboxylic acid methyl ester together with eight known compounds, have been isolated from the stems of Piper hispidum. Their structures were elucidated by a detailed spectroscopic analysis. In addition, the cytotoxicity of seven isolated compounds has been evaluated, revealing a moderate activity for three derivatives of dillapiole.
SN - 0031-7144
UR - https://www.unboundmedicine.com/medline/citation/15997836/New_prenylated_benzoic_acid_derivatives_of_Piper_hispidum_
DB - PRIME
DP - Unbound Medicine
ER -