Abstract:
본 발명은 스네일-p53 간의 결합을 저해하는 화합물 및 이를 유효성분으로 함유하는 암질환 치료제에 관한 것으로, 상기 스네일-p53 간의 결합 저해제는 K-Ras 돌연변이 세포주에서 p53의 발현을 유도함으로써 췌장암, 폐암, 담관암 및 대장암과 같이 진단이나 치료가 용이하지 않은 K-Ras 돌연변이성 암질환을 효과적으로 치료하거나 예방할 수 있다.
Abstract:
PURPOSE: A specific drug transmission method of K-Ras mutant cell is provided to detect cancer caused by K-Ras mutant in initial, to be very useful for the treatment of cancer, thereby extending the survival rate of cancer patients. CONSTITUTION: A specific drug transmission method comprises: a step of treating DNA bonding domain of p53 and drug for transferring to cells, and a step of transferring drug to neighbored K-Ras mutant cell by endocytosis by the DNA bonding domain of p53.
Abstract:
PURPOSE: A chemical inhibitor for the bond between snail-p53 is provided to effectively treat K-Ras mutagenic cancer disease by inducing the revelation of the p-53 in K-Ras mutant cell strain. CONSTITUTION: A chemical inhibitor has a structure marked as a chemical formula 1. In the chemical formula 1, m is an integer of 0-10, n and p is 0 or 1. In the chemical formula 1, Z is selected from a group comprising NH(CH2)qCH3, -OH, 4-phenylpiperidine group, isobutylamine, and isobutyloxy group and q is integer of 0-9. A pharmaceutical composition for treating cancer disease contains a compound for inhibiting the bond of snail-p53 as an active ingredient.
Abstract:
PURPOSE: A pharmaceutical composition for preventing or treating aging-related diseases and a method for screening a binding inhibitor are provided to effectively treat or prevent diseases caused by progerin and to specifically select a drug which suppresses binding between progerin and lamin A. CONSTITUTION: A compound of chemical formula 1 or 2 or a pharmaceutically acceptable salt thereof is provided. A pharmaceutical composition for preventing or treating aging-related diseases contains the compound of chemical formula 1 or 2 or a pharmaceutically acceptable salt thereof as an active ingredient. A method for screening a therapeutic agent for treating aging-related diseases comprises the step of selecting candidate drugs which suppress binding between progerin and lamin A.
Abstract:
PURPOSE: A production method of an environment-friendly edible film is provided to mix a specific plasticizer with an excellent physical property and a cross-linking agent with persimmon skin for producing the edible film. CONSTITUTION: Persimmon skin is finely cut, and a persimmon skin solution is produced. A plasticizer and a cross-linking agent are mixed with the persimmon skin solution to obtain a persimmon skin film solution. The persimmon skin solution is coated into a thickness of 0.1 mm, and dried. The cutting step is performed by using an autoclave, a homogenizer, and a high pressure homogenizer. 3-10 wt% of persimmon skin is added for the total amount of edible film. The persimmon skin solution is produced by the following steps: processing the persimmon skin using the autoclave at 100-140°C and in the pressure of 0.05-0.15 MPa for 15 minutes; and homogenizing the processed persimmon skin using the homogenizer for 5-30 minutes, and high pressure homogenizing the persimmon skin under 10,000-15,000 psi for 1-10 times. [Reference numerals] (AA) Collect persimmon skins produced during processing persimmons; (BB) Wash the persimmon skins with water and dry at 50°C for 48 hours; (CC) Pulverize the dried skins and select the powder of persimmon skins under the size of 80 mesh; (DD) Produce 5 weight% of a persimmon skin solution; (EE) Process the solution in a sterilizer at 121°C, 0.1 MPa for 15 minutes; (FF) Homogenize the solution in a homogenizer at 20,000 rpm; (GG) High-pressure Homogenize the solution in a high-pressure homogenizer at 13,000 psi for 20 minutes; (HH) Remove bubbles; (II) Add 1.5 weight% cane sugar; (JJ) Add 0.01 weight% of cinnamon aldehyde; (KK) Stir the solution for 1 hour; (LL) Divide the solution at the thickness of 0.1 mm on a module; (MM) Dry at room temperature; (NN) Edible persimmon skin film
Abstract:
본 발명은 5,8-디메톡시-1,4-나프토퀴논 (5,8-Dimethxy-1,4-naphthoquinone, DMNQ) 의 유도체인 2-치환-5,8-디메톡시-1,4-나프토퀴논(2-substituted-5,8-dimethoxy-1,4-naphthoquinone) 화합물에 관한 것으로 상기 화합물은 혈소판 유래 성장인자(platelet derived growth factor, PDGF)를 억제함으로써 심혈관 질환의 예방 및 치료용 조성물로 유용하게 이용될 수 있다.