Cytotoxicity; Prunella vulgaris var. lilacina; Triterpenoic acid
Indexed keywords
2 HYDROXY 3 (3',4' DIHYDROXYPHENYL)PROPANOIC ACID;
2ALPHA, 3ALPHA,24 TRIHYDROXYURS 12,20(30) DIEN 28 OIC ACID;
2ALPHA,3ALPHA DIHYDROXYURS 12 EN 28 OIC ACID;
2ALPHA,3ALPHA,19ALPHA TRIHYDROXYURS 12 EN 28 OIC ACID;
2ALPHA,3ALPHA,19ALPHA,23 TETRAHYDROXYURS 12 EN 28 OIC ACID;
2ALPHA,3ALPHA,19ALPHA,24 TETRAHYDROXYURS 12 EN 28 OIC AICD 28 O GLUCOPYRANOSIDE;
2ALPHA,3ALPHA,23 TRIHYDROXYURS 12 EN 28 OIC ACID;
2ALPHA,3ALPHA,24 TRIHYDROXY 12,13 CYCLOTARAXER 14 EN 28 OIC ACID;
2ALPHA,3ALPHA,24 TRIHYDROXYOLEA 12 EN 28 OIC ACID;
2ALPHA,3BETA DIHYDROXYURS 12 EN 28 OIC ACID;
2ALPHA,3BETA,19ALPHA,24 TETRAHYDROXYURS 12 EN 28 OIC ACID 28 O GLUCOPYRANOSIDE;
2ALPHA,3BETA,24 TRIHYDROXYOLEA 12 EN 28 OIC ACID;
ASTRAGALIN;
CAFFEIC ACID;
CYTOTOXIC AGENT;
HA GO CHO;
KAEMPFEROL 3 O ALPHA RHAMNOPYRANOSYL(1,6) BETA DEXTRO GLUCOPRANOSIDE;
MASLINIC ACID;
OLEANIC ACID;
PARA COUMARIC ACID;
PHYTOL;
PRUNELLA VULGARIS EXTRACT;
PRUNVULOSIDE A;
QUERCETIN 3 O ALPHA RHAMNOPYRANOSYL(1,6) BETA GLUCOPYRANOSIDE;
QUERCETIN 3 O BETA GLUCOPYRANOSIDE;
ROSMARINIC ACID;
SULFORHODAMINE B;
TRITERPENE DERIVATIVE;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
URSOLIC ACID;
ARTICLE;
BIOASSAY;
CELL STRAIN;
COLON CANCER;
COLUMN CHROMATOGRAPHY;
DRUG ANALYSIS;
DRUG CYTOTOXICITY;
HUMAN;
HUMAN CELL;
IN VITRO STUDY;
LUNG NON SMALL CELL CANCER;
MELANOMA;
OVARY CANCER;
PRUNELLA;
PRUNELLA VULGARIS VAR LILACINA;
STRUCTURE ANALYSIS;
ANTINEOPLASTIC AGENTS, PHYTOGENIC;
CELL LINE, TUMOR;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
COLORING AGENTS;
DRUG SCREENING ASSAYS, ANTITUMOR;
HUMANS;
INDICATORS AND REAGENTS;
MAGNETIC RESONANCE SPECTROSCOPY;
PRUNELLA;
RHODAMINES;
SPECTROPHOTOMETRY, ULTRAVIOLET;
TRITERPENES;
Antinociceptive and antiinflammatory effects of Niga-ichigoside F1 and 23-hydroxytormentic acid obtained from Rubus coreanus
J. W. Choi K. T. Lee J. H. Ha S. Y. Yun C. D. Ko H. J. Jung H. J. Park 2003 Antinociceptive and antiinflammatory effects of Niga-ichigoside F1 and 23-hydroxytormentic acid obtained from Rubus coreanus Biol. Pharm. Bull. 26 1436 1441
Configurational studies on hydroxy groups at C-2, 3 and 23 or 24 of oleanene and ursene-type triterpeneds by NMR spectroscopy
K. Hisashi O. Haruo 1989 Configurational studies on hydroxy groups at C-2, 3 and 23 or 24 of oleanene and ursene-type triterpeneds by NMR spectroscopy Phytochemistry 28 1703 1710
Identification and quantification of anthocyanins and flavonoids in Mulberry (Morus sp.) cultivars
J. Y. Lee S. O. Moon S. J. Rhee H. R. Park 2004 Identification and quantification of anthocyanins and flavonoids in Mulberry (Morus sp.) cultivars Food Sci. Biotechnol. 13 176 184
Phytochemicals of black bean seed coats: Isolation, structure elucidation, and their antiproliferative and antioxidative activities
D. Mei D. Xiangjiu 2007 Phytochemicals of black bean seed coats: isolation, structure elucidation, and their antiproliferative and antioxidative activities J. Agric. Food Chem. 55 6044 6051
Multi-component HPLC fingerprinting of radix salviae miltiorrhizae and its LC-MS-MS identification
H. Ping Q. L. Ling G. A. Luo Z. Z. Zhao Z. H. Jiang 2005 Multi-component HPLC fingerprinting of radix salviae miltiorrhizae and its LC-MS-MS identification Chem. Pharm. Bull. 53 677 683
Anti-allergic and anti-inflammatory triterpenes from the herb of Prunella vulgaris
S. Y. Ryu M. H. Oak S. K. Yoon D. I. Cho G. S. Yoo T. S. Kim K. M. Kim 2000 Anti-allergic and anti-inflammatory triterpenes from the herb of Prunella vulgaris Planta Med. 66 358 360
New colorimetric cytotoxicity assay for anticancer-drug screening
P. Skehan R. Storeng D. Scudiero A. Monks J. Mcmahon D. Vistica J. T. Warren H. Bokesch S. Kenney M. R. Boyd 1990 New colorimetric cytotoxicity assay for anticancer-drug screening J. Natl. Cancer Inst. 82 1107 1112
The cytotoxic principles of Hyptis capitata and the structures of the new triterpenes hyptatic acid-A and -B
Y. Takashi Z. De-Cheng C. Jer-Jang R. Donald Mcphail T. Andrew Mcphail K. H. Lee 1988 The cytotoxic principles of Hyptis capitata and the structures of the new triterpenes hyptatic acid-A and -B Phytochemistry 27 3213 3216
Cytotoxic activity of Perilla frutescens var. japonica leaf extract is due to high concentrations of oleanolic and ursolic acid
A. Toshihiro K. Satoshi U. Taketo A. Hiroyuki B. Norihiro 2006 Cytotoxic activity of Perilla frutescens var. japonica leaf extract is due to high concentrations of oleanolic and ursolic acid J. Nat. Med. 60 331 333
