摘要:
Disclosed herein are isoxazole derivatives and uses thereof. Serving as agonists of Wnt, the isoxazole derivatives activate Wnt/β-catenin signaling and thus can be used in the treatment and prevention of diseases related to the signal transduction. Also, pharmaceutically acceptable salts of the isoxazole derivatives are disclosed.
摘要:
There is provided a pharmaceutical composition for prevention and treatment of restenosis comprising isoxazole derivatives. The pharmaceutical composition includes a therapeutic effective amount of isoxazole derivatives represented by Formula 1 or pharmaceutically available salts thereof. The pharmaceutical composition may be useful to prevent and treat vascular restenosis since the pharmaceutical composition shows an anti-restenosis activity and accelerates the re-endothelization.
摘要:
An apparatus and method for optimizing a data rate in a wireless communication system supporting Hybrid Automatic Repeat reQuest (HARQ) are provided. The method includes estimating Channel State Information (CSI) of a signal to be transmitted, by using other CSIs received in a previous cycle; determining an instantaneous data rate, at which the CSI is transmitted with an optimal data rate, and the amount of redundancy information to be retransmitted; and retransmitting the redundancy information of the signal according to the amount of redundancy information and the instantaneous data rate, if a receiving end requests signal retransmission. Accordingly, the packet can be transmitted with the optimal data rate.
摘要:
DNA sequences encoding antiviral proteins, amarandin 1 and 2 from Amaranthus viridis is disclosed. Expression vectors encoding amarandin 1 or 2 and transformed host cells are also disclosed.
摘要:
A CDNA clone encoding amarandin-S, a eukaryotic ribosome-inactivating protein (RIP) having antiviral activity is disclosed. Also disclosed are hybrid vectors encoding the cDNA and host cells transformed with the vector.
摘要:
Provided is a pharmaceutical composition for prevention and treatment of drug or alcohol addiction or bipolar disorder, comprising sodium phenylbutyrate (PBA). The pharmaceutical composition for prevention and treatment of drug or alcohol addiction or bipolar disorder in accordance with the present invention provides effects capable of inhibiting increases in locomotor activity which is a behavioral indicator of drug or alcohol addiction or bipolar disorder, by controlling a level of a neurotransmitter via regulation of expression of a neurotransmitter transporter.
摘要:
Provided is a pharmaceutical composition for prevention and treatment of drug or alcohol addiction or bipolar disorder, comprising sodium phenylbutyrate (PBA). The pharmaceutical composition for prevention and treatment of drug or alcohol addiction or bipolar disorder in accordance with the present invention provides effects capable of inhibiting increases in locomotor activity which is a behavioral indicator of drug or alcohol addiction or bipolar disorder, by controlling a level of a neurotransmitter via regulation of expression of a neurotransmitter transporter.
摘要:
Provided are an oxazole hydroxamic acid derivative and a pharmaceutically useful salt thereof as a histone deacetylase inhibitor The oxazole hydroxamic acid derivative and pharmaceutically useful salt thereof, prepared in accordance with the present invention, can treat and/or prevent various cancers and inflammatory diseases caused by histone deacetylase.
摘要:
The present invention provides isolated nucleic acid constructs comprising a plant strong constitutive promoter operably linked to a heterologous nucleic acid which encodes a desired polypeptide in transgenic plant tissues. Said constructs are capable of conferring the highest expression of the desired polypeptides in plant root tissue and plant leaf tissue when used as a construct for a heterologous coding sequence in chimeric gene. After any chimeric gene can be linked to said construct, the resulting vector can be introduced into plant tissues, thereby intentionally modifying plants and making the resulting plants produce foreign substances therein.
摘要:
Provided are an oxazole hydroxamic acid derivatives and pharmaceutically useful salt thereof as a histone deacetylase inhibitor. The oxazole hydroxamic acid derivative and pharmaceutically useful salt thereof, prepared in accordance with the present invention, can treat and/or prevent various cancers and inflammatory diseases caused by histone deacetylase.