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1.
Nat Prod Res ; 30(21): 2483-90, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27426217

ABSTRACT

Two new compounds, 19-hydroxy-melodinine K (1) and melodiside (2), and 25 known compounds were isolated from leaves and twigs of Melodinus suaveolens. Their structures were elucidated based on 1- and 2-D NMR, FTIR, UV and MS spectroscopic data. 19-hydroxy-melodinine K showed cytotoxic activity against MDA-MB-231 breast, BCG-823 gastric, SW480 colon and Hela cancer cells.


Subject(s)
Apocynaceae/chemistry , Antineoplastic Agents, Phytogenic/pharmacology , Cell Line, Tumor , Humans , Magnetic Resonance Spectroscopy , Plant Leaves/chemistry
2.
Phytochemistry ; 120: 46-52, 2015 Dec.
Article in English | MEDLINE | ID: mdl-25687604

ABSTRACT

Continued interest in cytotoxic alkaloids resulted in the isolation of 37 alkaloids including 29 known monoterpenoid indole alkaloids from the aerial parts of Tabernaemontana officinalis. Of the remaining 8 alkaloids, six were bisindole alkaloids named taberdivarines A-F (1-6) and the two were monomers named taberdivarines G and H (7-8). Alkaloids 1 and 2 are voaphylline-vobasinyl type bisindole alkaloids, a structural type previously unknown, while 3-6 exhibited cytotoxicity against three human cancer cell lines HeLa, MCF-7, and SW480 with IC50 values ranging from 1.42 to 11.35 µM.


Subject(s)
Antineoplastic Agents, Phytogenic/isolation & purification , Antineoplastic Agents, Phytogenic/pharmacology , Secologanin Tryptamine Alkaloids/isolation & purification , Secologanin Tryptamine Alkaloids/pharmacology , Tabernaemontana/chemistry , Antineoplastic Agents, Phytogenic/chemistry , Drug Screening Assays, Antitumor , Humans , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Secologanin Tryptamine Alkaloids/chemistry
3.
Zhong Yao Cai ; 35(5): 803-7, 2012 May.
Article in Chinese | MEDLINE | ID: mdl-23213746

ABSTRACT

OBJECTIVE: To prepare positive-ionized liposome gel containing paeonol and study its stability and cutaneous permeation kinetics in vitro. METHODS: Prepared the liposome gel by dispersion-ultrasonic and gridding method, and studied the stability with the impact factor experiments. Compared the permeation rate of liposome gel with conventional gel in vitro using the Franz-diffusion cell. RESULTS: Mean diameter of the liposome was (132.7 +/- 14.1) nm with Zeta potential of (+33.54 +/- 1.95) mV and mean entrapment efficiency of (73.04 +/- 1.24)% (n=3), and the content of paeonol was (3.17 +/- 0.13) mg/g (n=3). The liposome gel had a promising appearance. It was stable at the humidity and the room temperature while was sensitive at the light and the temperature from 40 degrees C to 60 degrees C. The cumulative penetration amounts of the liposome gel was higher than that of the conventional gel (P < 0.05). Its cutaneous penetration rate and cumulative amounts in skin were higher than those of the conventional gel (P < 0.05). CONCLUSION: The positive-ionized liposome gel containing paeonol is stable and feasibly prepared. It can enhance the cutaneous permeation efficiency and guarantee the persistent release rate.


Subject(s)
Acetophenones/administration & dosage , Acetophenones/pharmacokinetics , Drug Carriers/chemistry , Liposomes , Skin Absorption , Acetophenones/chemistry , Administration, Cutaneous , Animals , Drug Compounding/methods , Drug Stability , Drugs, Chinese Herbal/administration & dosage , Drugs, Chinese Herbal/chemistry , Drugs, Chinese Herbal/pharmacokinetics , Female , Gels , Male , Mice , Particle Size , Permeability , Reproducibility of Results , Scutellaria baicalensis/chemistry , Skin/metabolism , Spectrophotometry, Ultraviolet
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