Abstract:
PURPOSE: An anticancer drug composition including resveratrol derivative compound separated from grape stem shell is provided to prevent and treat all kinds of cancers including lung cancer, ovarian cancer, melanoma, central nervous system tumor, colon carcinoma, and leukemia. CONSTITUTION: An anticancer drug composition includes vitisinol C, vitisinol E, cis-vitisin A, vitisin B, vitisin C, a pharmaceutically acceptable salt and isomer or a mixture thererof, and grape stem shell extract including thereof as an active ingredient. The grape stem shell extract is obtained by extracting methanol, methanol aqueous solution, ethanol, ethanol aqueous solution, butanol, dichloromethane, ethyl acetate or a mixture thereof. The cancer is lung cancer, ovarian cancer, melanoma or colon carcinoma. A health enhancement food having cancer cell growth inhibition efficacy contains vitisinol C, vitisinol E, cis-viticin A, viticin B, viticin C, pharmaceutically acceptable salt, isomer or a mixture thereof, and grapes stem shell extract including the same. The food is in beverage form. The grape stem shell extract is obtained by the following steps: extracting the grape stem shell by methanol and suspending the obtained extract in distilled water; partitioning thereof by dichloromethane; and extracting the obtained water layer by ethyl acetate.
pseudacorus ) 종자 추출물 및 이로부터 분리 정제된 레스베라트롤 화합물인 아이리스페린 A(irisferin A), 아이리스페린 B(irisferin B), 아이리스페린 C(irisferin C) 및 이들의 혼합물로 이루어진 그룹으로부터 선택된 어느 하나를 약제학적으로 허용되는 담체와 함께 함유하는 항암제 조성물에 관한 것으로, 본 발명의 조성물은 폐암, 난소암, 흑색종, 중추신경계암, 결장암, 백혈병 등 각종 악성종양의 예방 및 치료제로 사용될 수 있다.
Abstract:
PURPOSE: An anticancer drug composition which includes resveratrol derivative compound separated from iris tectorum seeds is provided to be used as therapeutic agent for various malign tumors. CONSTITUTION: An anticancer drug composition contains irisferin A, irisferin B, irisferin C, a pharmaceutically acceptable salt, isomer or a mixture thereof, or iris pseudacorus seed extract including the same as an active ingredient. The iris pseudacorus seed extract is obtained by extracting the iris pseudacorus seed with methanol, methanol aqueous solution, ethanol, ethanol water solution, butanol, dichloromethane, ethyl acetate or a mixture thereof. The cancer is lung cancer, ovarian cancer, melanoma, central nervous system cancer or colon carcinoma. A health supplement having the anti-cancer cell growth obstruction efficacy is irisferin A, irisferin B, irisferin C, a pharmaceutically acceptable salt, isomer or a mixture thereof, or iris pseudacorus seed extract including the same.
Abstract:
본 발명은 도라지 막분리 추출물 또는 플라티코시드 E를 유효성분으로 함유하는 아토피 피부염의 예방 또는 치료용 약학적 조성물에 관한 것으로, 본 발명에 따른 도라지 막분리 추출물 또는 플라티코시드 E는 아토피 증상을 완화시킬 뿐만 아니라, 염증세포 침윤, 괴사 딱지의 발생, 조직의 두께 및 비만세포 수를 감소시키고, 혈중 IgE 함량 및 IL-4 함량을 용량의존적으로 감소시킴으로써 아토피 피부염을 예방 또는 치료하는데 유용하게 사용할 수 있다.
Abstract:
PURPOSE: A pharmaceutical composition containing Paeonia lactiflora seed extract, fraction thereof, or compound isolated from the same is provided to suppress BACE-1 activity and to treat and prevent neurodegenerative diseases. CONSTITUTION: A pharmaceutical composition for preventing or treating neurodegenerative diseases contains Paeonia lactiflora seed extract as an active ingredient. The neurodegenerative diseases include Alzheimer's dieses, Parkinsons's disease, progressive supranuclear palsy. The extract is prepared using water, alcohol of C1-C4, or mixture solvent thereof. The pharmaceutical composition contains Paeonia lactiflora seed fraction as an active ingredient. The pharmaceutical composition also contains compounds as an active ingredient. The method for preparing the compounds comprises: a step of adding water, C1-C3 alcohol, or mixture thereof to the Paeonia lactiflora seeds to prepare Paeonia lactiflora seed extract; a step of fractioning the extract with water, dichloromethane, and ethyl acetate to prepare a fraction; a step of performing silicagel column chromatography of the fraction.
Abstract:
PURPOSE: A composition containing Plumbagin as an active ingredient for preventing Sicyos angulatus is provided to suppress KAPAS(7-keto-8-aminopelargonic acid synthase) which is important for plant growth. CONSTITUTION: A herbicidal composition for preventing Sicyos angulatus contains Plumbagin as an active ingredient. Plumbagin is derived from Plumbago auriculata and is denoted by chemical formula 1. Plumbagin suppresses KAPAS activity by being treated in a concentration of 500-2,500 ug/ml. A method for eliminating Sicyos angulatus comprises a step of treating Sicyos angulatus, seeds thereof, or a habitat thereof with the herbicidal composition.
Abstract:
PURPOSE: A method for preparing crude saponin composition with improved purity and enhanced effective saponin content is provided. CONSTITUTION: A method for preparing crude saponin composition with improved purity and enhanced effective saponin content from platycodon grandiflorum or extract thereof comprises: a step of extracting platycodon grandiflorum using distilled water, low alcohol of C1-C3, ethyl acetate, hexane, dichloromethane or mixture solvent thereof; a step of dissolving the extract in a distilled water and adsorbing saponin ingredient; a step of eluting the adsorbed saponin with ethanol or methanol solution to obtain saponin; and a step of purifying saponin using an organic solvent.
Abstract:
PURPOSE: A Paeonia lactiflora seed extract, a fraction thereof, or a compound isolated therefrom, and a pharmaceutical composition containing the same are provided to suppress the activation of beta-secretase (BECE-1) and to prevent or treat neurodegenerative diseases. CONSTITUTION: A pharmaceutical composition for preventing or treating neurodegenerative diseases contains one or more kinds of compounds selected among compounds of chemical formulas 1-8, as active ingredients. A method for preparing the compounds of chemical formulas 1-8 comprises the steps of: adding water, C1-C4 alcohols, or a mixture thereof to Paeonia lactiflora seeds and obtaining a Paeonia lactiflora seed extract; fractioning the extract with water, dichloromethane, and ethyl acetate and obtaining a fraction; and isolating compounds by performing silicagel column chromatography of the fraction and purifying the compounds.