1.Study on Medication Rules of TCM Treatment for Primary Hepatic Carcinoma in Recent ;Ten Years
Minghao LIU ; Keke LI ; Lihui ZHANG ; Hanting JIA ; Wenxia ZHAO
Chinese Journal of Information on Traditional Chinese Medicine 2016;23(9):45-47
Objective To analyze medication rules of TCM treatment for primary hepatic carcinoma in recent ten years;To provide references for clinical medication. Methods Literature about primary hepatic carcinoma in CNKI, VIP and Wanfang database from January 2005 to September 2015 was searched by computers to carry out statistical analysis of medicine classification and frequency of usage. Results Through screening, 131 articles were included, covering 131 compound TCM prescriptions, 228 kinds of medicine, and 1416 times of frequency of usage. Medicines with relatively high frequency were tonifying deficiency medicine 430 times (30.37%), damp-clearing medicine 233 times (16.45%), medicine for invigorating blood circulation and eliminating stasis (12.99%). Medicines with relatively high frequency were Atractylodis Macrocephalae Rhizoma 64 times (4.52%), Poria 62 times (4.38%), Glycyrrhizae Radix et Rhizoma 52 times (3.67%), Bupleuri Radix 49 times (3.46%), Paeoniae Radix Alba 45 times (3.18%), Astragali Radix 44 times (3.22%), Curcumae Rhizoma 43 times (3.04%), and Artemisiae Scopariae Herba 41 times (2.90%). Conclusion This study summarizes the medicine classification and frequency of usage of TCM treatment for primary hepatic carcinoma in recent ten years, which can provide data support for clinical treatment.
2.A new diphenyl ether from the endophytic fungus Verticillium sp. isolated from Rehmannia glutinosa.
Wei PENG ; Fei YOU ; Xiao-Li LI ; Min JIA ; Cheng-Jian ZHENG ; Ting HAN ; Lu-Ping QIN
Chinese Journal of Natural Medicines (English Ed.) 2013;11(6):673-675
AIM:
To investigate the chemical constituents of the endophytic fungus Verticillium sp. isolated from Rehmannia glutinosa.
METHODS:
The compounds were isolated and purified by repeated column chromatography, and their structures were determined on the basis of physicochemical properties and spectral analysis. Their cytotoxic and antifungal activities were evaluated.
RESULTS:
Ten compounds were obtained and their structures were identified as 2, 4-dihydroxy-2', 6-diacetoxy-3'-methoxy-5'-methyl-diphenyl ether (1), paecilospirone (2), α-acetylorcinol (3), 2-methoxy-1,8-dimethyl-xanthen-9-one (4), 4-hydroxy-α-lapachone (5), enalin A (6), 2,3,4-trimethyl-5,7-dihydroxy-2,3-dihydrobenzofuran (7), 4-hydroxyethyl-phenol (8), 2,4-dihydroxy-3,5,6-trimethyl- methylbenzoate (9), and 3-isopropenyl-(Z)-monomethyl maleate (10).
CONCLUSIONS
Compound 1 is a new diphenyl ether, and showed cytotoxic activity against HL-60 cells (IC50 2.24 μg · mL(-1)), and antifungal activities against Candida albicans (MIC 8 μg · mL(-1)) and Aspergillus fumigatus (MIC 16 μg · mL(-1)).
Antifungal Agents
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chemistry
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isolation & purification
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metabolism
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pharmacokinetics
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Antineoplastic Agents
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chemistry
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isolation & purification
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metabolism
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pharmacokinetics
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Aspergillus fumigatus
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drug effects
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Candida albicans
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drug effects
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Cell Line, Tumor
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Endophytes
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chemistry
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metabolism
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Humans
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Phenyl Ethers
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chemistry
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isolation & purification
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metabolism
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pharmacokinetics
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Rehmannia
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microbiology
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Verticillium
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chemistry
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metabolism