2016
DOI: 10.1016/b978-0-444-63602-7.00004-7
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Comparative Studies in Relation to the Structure and Biochemical Properties of the Active Compounds in the Volatile and Nonvolatile Fractions of Turmeric (C. longa) and Ginger (Z. officinale)

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Cited by 20 publications
(14 citation statements)
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“…It was active against human mouth epidermal carcinoma (KB) cells and mouse leukemia (P388) cells, with respective IC 50 values of 1.088 and 0.084 mg/mL [ 177 ]. It was also cytotoxic to the pancreatic cancer (PANC-1), melanoma (B16), prostate cancer (LNCaP), and human cervical adenocarcinoma (HeLa) cell lines due to the presence of ar -turmerone, α-turmerone, β-turmerone, curlone, ar -curcumene, zingiberene, and β-sesquiphellandrene [ 23 , 74 , 175 , 176 ]. Crude organic extracts of turmeric-inhibited lipopolysaccharide (LPS)-induced production of tumor necrosis factor (TNF)-α (IC 50 = 15.2 μg/mL) and prostaglandin E2 (PGE2; IC 50 = 0.92μg/mL) in human leukemia (HL-60) cells [ 181 ].…”
Section: Biological Activities Of Curcuma Oilsmentioning
confidence: 99%
“…It was active against human mouth epidermal carcinoma (KB) cells and mouse leukemia (P388) cells, with respective IC 50 values of 1.088 and 0.084 mg/mL [ 177 ]. It was also cytotoxic to the pancreatic cancer (PANC-1), melanoma (B16), prostate cancer (LNCaP), and human cervical adenocarcinoma (HeLa) cell lines due to the presence of ar -turmerone, α-turmerone, β-turmerone, curlone, ar -curcumene, zingiberene, and β-sesquiphellandrene [ 23 , 74 , 175 , 176 ]. Crude organic extracts of turmeric-inhibited lipopolysaccharide (LPS)-induced production of tumor necrosis factor (TNF)-α (IC 50 = 15.2 μg/mL) and prostaglandin E2 (PGE2; IC 50 = 0.92μg/mL) in human leukemia (HL-60) cells [ 181 ].…”
Section: Biological Activities Of Curcuma Oilsmentioning
confidence: 99%
“…Cyclocurcumin,(E)-2-4-hydroxy-3-methoxyphenyl-6-(4-hydrox-3-methoxystyryl)2H-pyra-4(3H)-one, isolated and identified from turmeric have some structural similarities to curcumin. They are formed by the addition of enol oxygen group through intramolecular Michael addition to enone group [9]. They have shown inhibitory action on breast cancer (MCF-7) cells [12].…”
Section: Non-curcuminoids As Anticancer Agentsmentioning
confidence: 99%
“…This rhizomatous herbaceous perennial plant found abundantly in Asia is renowned for its cosmetic, culinary, color, and medicinal applications for centuries [7,8]. Basically, its volatile oil and nonvolatile oleoresin constitutes of bioactive components, which are classified as diphenylheptanoids (nonvolatile) diphenylpentanoids (nonvolatile), phenyl propene (cinnamic acid type) derivatives (nonvolatile), turmeric oil containing terpenoids (volatile) [9]. Major diphenylheptanoids are curcumin, demethoxycurcumin, and bisdemethoxycurcumin, which are collectively called curcuminoids [10,11].…”
Section: Introductionmentioning
confidence: 99%
“…Several studies indicated that the bioactive ingredients of Curcuma rhizome are the non-volatile curcuminoids (curcumin, demethoxycurcumin, and bisdemethoxycurcumin) and the volatile oil (sesquiterpenoids and monoterpenoids) [14,18]. Curcumin, the most active curcuminoid in turmeric rhizome, has anticancer [19], anti-inflammatory [20], antioxidant [21], antibacterial, anti-fungal [22], analgesic, digestive, antidepressant [23], and hypoglycemic [23] properties and has shown potential against cardiovascular diseases [24] and Alzheimer’s disease [25]. Curcuma essential oil (EO) is often extracted by distillation of the fresh or dry rhizome [26], or by supercritical fluid extraction [27].…”
Section: Introductionmentioning
confidence: 99%