Lentinan is a kind of β-1,3-glucan which extracted from the seed of lentinusedodes,this review summarize its biological activity of immunomodulation,anti-infection,antitumor activity and research foreland on lentinan.
Lentinan is a kind of β-1,3-glucan which extracted from the seed of lentinusedodes,this review summarize its biological activity of immunomodulation,anti-infection,antitumor activity and research foreland on lentinan.
s: Rosemary possesses the remarkable action of anti-oxidation, anti-tumor, resistance of human immunodeficiency virus and many antimicrobial activities.
Extracted EPS from yogurt to probe into the immune function of EPS such as anti-tumor and studied the technology of Protein-stripping during extraction. The result showed that Protein-stripping two times with Sevag after enzymolysis was the best.
Lentinan is a kind of β-1,3-glucan which extracted from the seed of lentinusedodes,this review summarize its biological activity of immunomodulation,anti-infection,antitumor activity and research foreland on lentinan.
Here, we characterize two model systems for the ex vivo activation and expansion of human T lymphocytes and describe the potential for providing broadly applicable anti tumor specificity by targeting universal tumor antigens.
Some new benzenesulfonamides, disubstituted sulfonylureas, and sulfonylthioureas substituted basically with 3-(2-thienyl or 3-pyridyl)-indeno[1,2-c]pyrazol(in)e counterpart were synthesized to be evaluated for their in vitro antitumor activity.
According to the protocol of the National Cancer Institute (NCI) in vitro disease-oriented human cells screening panel assay, 13 compounds showed promising broad spectrum antitumor activity.
To obtain an anti-tumor peptide of Tumstatin and detect its biological activity, the nucleotide sequence encoding 185-203 amino acids (19peptide) of Tumstatin was synthesized and inserted into the fusion protein vector pTYB2.
Some new benzenesulfonamides, disubstituted sulfonylureas, and sulfonylthioureas substituted basically with 3-(2-thienyl or 3-pyridyl)-indeno[1,2-c]pyrazol(in)e counterpart were synthesized to be evaluated for their in vitro antitumor activity.
According to the protocol of the National Cancer Institute (NCI) in vitro disease-oriented human cells screening panel assay, 13 compounds showed promising broad spectrum antitumor activity.