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Pentadecapeptide

ID:508405 View:1009 Collection
Date Listed: 2017-04-26 15:34:14 Country: China»Guangdong»guangzhou
Poster: yesi Company: Guangzhou Kafen Biotech Co.,Ltd.
Location: Guangzhou Panyu city world Website: Guangzhou Kafen Biotech Co.,Ltd.
Email: kevin@rawroid.com Mobile: 08602031121521
Fax: 86-27-6888669 MSN:

High Quality Peptide Pentadecapeptide Bpc 157 1.Basic info. Product Name:Pentadecapeptide BPC 157 Alias:Booly Protection Compound 15 CAS NO.:*-51-0 MF: C62H98N16O22 MW: 1419.* Purity: 99% Specification: 2mg/vial Appearance: White Lyophilized Powder 2.Product description: BPC 157 has a strong anti-inflammatory activity in both acute and chronic inflammation models. In fact, preliminary results in clinical trials suggest that BPC 157 may become an important therapeutic tool for the treatment of inflammatory bowel disease. BPC 157 was shown to accelerate wound healing and to have a marked angiogenic effect. In addition, it significantly facilitates the healing of bone fracture in rats. This peptide also exhibits an osteogenic effect significantly improving the healing of segmental bone defect. BPC 157 accelerates the healing of transected rat Achilles tendon and transected rat quadriceps muscle. FITC-phalloidin staining was able to demonstrate that BPC 157 induces F-actin formation in fibroblasts. Likewise, Western blot analysis was able to detect the production and activation of paxillin and FAK proteins. The western blot analysis also showed that BPC 157 increases the extent of phosphorylation of paxillin and FAK proteins without affecting the amounts produced. 3.Application: Stable gastric pentadecapeptide BPC 157 (GEPPPGKPADDAGLV, M.W. 1419) may be the new drug stable in human gastric juice, effective both in the upper and lower GI tract, and free of side effects. BPC 157, in addition to an antiulcer effect efficient in therapy of inflammatory bowel disease (IBD) (PL *) so far only tested in clinical phase II, has a very safe profile, and exhibited a particular wound healing effect. It also has shown to interact with the NO-saystem, providing endothelium protection and angiogenic effect, even in severely impaired conditions (i.e., it stimulated expression of early growth response 1 gene responsible for cytokine and factor gener

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